Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1060 |
| ensemblid | ENSG00000145241.11 |
| hgncid | 1854 |
| symbol | CENPC |
| name | centromere protein C |
| refseq_nuc | NM_001812.4 |
| refseq_prot | NP_001803.2 |
| ensembl_nuc | ENST00000273853.11 |
| ensembl_prot | ENSP00000273853.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 67468762 |
| end | 67545503 |
| strand | - |
| ver | v1.2 |
| region | chr4:67468762-67545503 |
| region5000 | chr4:67463762-67550503 |
| regionname0 | CENPC_chr4_67468762_67545503 |
| regionname5000 | CENPC_chr4_67463762_67550503 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 943 | 209 | 42 | 45 | 93 | 9 | 19 | 66 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0002 | 1/0 | 943 | 102 | 30 | 12 | 41 | 5 | 13 | 34 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0003 | 0/0 | 943 | 8 | 0 | 4 | 0 | 4 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0004 | 0/0 | 943 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0005 | 0/0 | 943 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0006 | 0/0 | 943 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0007 | 0/0 | 943 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0008 | 0/0 | 943 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0009 | 0/0 | 943 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0010 | 0/0 | 943 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0011 | 0/0 | 943 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| a0012 | 0/0 | 943 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | MAASG others(938): Show |
chr4 | 67463762 | 67550503 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2829 | 208 | 41 | 45 | 93 | 9 | 19 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0001c0012 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0002c0002 | 1/0 | 2829 | 101 | 29 | 12 | 41 | 5 | 13 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0002c0014 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0003c0003 | 0/0 | 2829 | 8 | 0 | 4 | 0 | 4 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0004c0004 | 0/0 | 2829 | 4 | 4 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0005c0005 | 0/0 | 2829 | 3 | 2 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0006c0009 | 0/0 | 2829 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0007c0006 | 0/0 | 2829 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0008c0008 | 0/0 | 2829 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0009c0010 | 0/0 | 2829 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0010c0007 | 0/0 | 2829 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0011c0011 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 | ||
| a0012c0013 | 0/0 | 2829 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | ATGGC others(2824): Show |
chr4 | 67463762 | 67550503 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6832 | 111 | 18 | 17 | 59 | 5 | 11 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0004 | 0/0 | 6830 | 28 | 8 | 15 | 2 | 2 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6825): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0005 | 0/0 | 6832 | 28 | 1 | 7 | 16 | 0 | 4 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0006 | 0/0 | 6833 | 8 | 1 | 3 | 3 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0008 | 0/0 | 6831 | 5 | 4 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6826): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0009 | 0/0 | 6833 | 5 | 0 | 0 | 4 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0012 | 0/0 | 6831 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6826): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0013 | 0/0 | 6832 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0016 | 0/0 | 6832 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0018 | 0/0 | 6832 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0019 | 0/0 | 6831 | 2 | 1 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6826): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0021 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0022 | 0/0 | 6833 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0025 | 0/0 | 6833 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0027 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0028 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0029 | 0/0 | 6831 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6826): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0030 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0031 | 0/0 | 6832 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0034 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0035 | 0/0 | 6833 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0036 | 0/0 | 6833 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6828): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0037 | 0/0 | 6834 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6829): Show |
chr4 | 67463762 | 67550503 |
| a0001c0001t0039 | 0/0 | 6832 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0001c0012t0012 | 0/0 | 6831 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6826): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0002 | 0/0 | 6822 | 46 | 5 | 9 | 27 | 3 | 2 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0003 | 1/0 | 6823 | 39 | 16 | 3 | 12 | 2 | 5 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6818): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0007 | 0/0 | 6822 | 5 | 1 | 0 | 0 | 0 | 4 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0010 | 0/0 | 6823 | 4 | 4 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6818): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0011 | 0/0 | 6823 | 3 | 1 | 0 | 1 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6818): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0020 | 0/0 | 6823 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6818): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0023 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0024 | 0/0 | 6822 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0002c0002t0026 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0002c0014t0003 | 0/0 | 6823 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6818): Show |
chr4 | 67463762 | 67550503 |
| a0003c0003t0004 | 0/0 | 6830 | 8 | 0 | 4 | 0 | 4 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6825): Show |
chr4 | 67463762 | 67550503 |
| a0004c0004t0001 | 0/0 | 6832 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0004c0004t0032 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0004c0004t0033 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0005c0005t0002 | 0/0 | 6822 | 3 | 2 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0006c0009t0014 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0007c0006t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0007c0006t0038 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0008c0008t0015 | 0/0 | 6822 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| a0009c0010t0017 | 0/0 | 6832 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0010c0007t0001 | 0/0 | 6832 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0011c0011t0001 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6827): Show |
chr4 | 67463762 | 67550503 |
| a0012c0013t0007 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | AGCTC others(6817): Show |
chr4 | 67463762 | 67550503 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0012g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0016g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0018g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0019g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0021g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0022g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0025g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0027g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0028g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0029g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0030g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0031g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0034g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0035g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0036g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0037g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0001t0039g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0001c0012t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0007g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0007g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0020g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0023g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0024g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0002t0026g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0002c0014t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0003c0003t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0004c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0004c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0004c0004t0032g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0004c0004t0033g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0005c0005t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0005c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0005c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0006c0009t0014g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0006c0009t0014g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0007c0006t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0007c0006t0038g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0008c0008t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0008c0008t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0009c0010t0017g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0009c0010t0017g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0010c0007t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0011c0011t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| a0012c0013t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0004 | g0132 | EUR | GBR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0060 | EUR | GBR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0279 | EUR | GBR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00140 | hp2 | a0003 | c0003 | t0004 | g0137 | EUR | GBR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | FIN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0034 | EUR | FIN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00544 | hp1 | a0001 | c0001 | t0016 | g0005 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0219 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | CHS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0081 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0017 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01167 | hp1 | a0005 | c0005 | t0002 | g0063 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01243 | hp1 | a0001 | c0001 | t0035 | g0257 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0226 | AMR | PUR | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01257 | hp1 | a0003 | c0003 | t0004 | g0131 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01361 | hp2 | a0003 | c0003 | t0004 | g0248 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0190 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01515 | hp1 | a0002 | c0002 | t0003 | g0230 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0121 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01516 | hp1 | a0003 | c0003 | t0004 | g0139 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0032 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0231 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01517 | hp2 | a0003 | c0003 | t0004 | g0140 | EUR | IBS | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01884 | hp1 | a0006 | c0009 | t0014 | g0245 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01891 | hp1 | a0001 | c0001 | t0025 | g0251 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0323 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0123 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01975 | hp2 | a0001 | c0001 | t0037 | g0328 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0180 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02056 | hp1 | a0001 | c0001 | t0027 | g0107 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02083 | hp2 | a0001 | c0001 | t0022 | g0197 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | KHV | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02145 | hp1 | a0006 | c0009 | t0014 | g0246 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02145 | hp2 | a0001 | c0001 | t0019 | g0130 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0205 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CDX | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0232 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02280 | hp2 | a0004 | c0004 | t0033 | g0320 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02293 | hp1 | a0001 | c0001 | t0036 | g0325 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0327 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02300 | hp2 | a0003 | c0003 | t0004 | g0247 | AMR | PEL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02615 | hp1 | a0005 | c0005 | t0002 | g0064 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0224 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02717 | hp1 | a0004 | c0004 | t0032 | g0277 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0319 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0153 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0082 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0316 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0278 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02818 | hp2 | a0002 | c0002 | t0020 | g0010 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02886 | hp1 | a0002 | c0002 | t0010 | g0077 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0223 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0217 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0239 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02922 | hp1 | a0008 | c0008 | t0015 | g0011 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0264 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0255 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02965 | hp2 | a0009 | c0010 | t0017 | g0244 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0265 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02976 | hp1 | a0011 | c0011 | t0001 | g0274 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0008 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0229 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03017 | hp2 | a0002 | c0002 | t0007 | g0071 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0227 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03139 | hp2 | a0002 | c0002 | t0010 | g0075 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03195 | hp1 | a0008 | c0008 | t0015 | g0012 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03195 | hp2 | a0002 | c0002 | t0010 | g0076 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03209 | hp1 | a0002 | c0014 | t0003 | g0240 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03209 | hp2 | a0002 | c0002 | t0007 | g0069 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0237 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03225 | hp2 | a0002 | c0002 | t0011 | g0062 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0235 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0242 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03453 | hp2 | a0007 | c0006 | t0038 | g0177 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0090 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03486 | hp2 | a0001 | c0012 | t0012 | g0253 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0155 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03516 | hp2 | a0001 | c0001 | t0018 | g0268 | AFR | ESN | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0241 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03540 | hp2 | a0012 | c0013 | t0007 | g0074 | AFR | GWD | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0238 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03579 | hp2 | a0005 | c0005 | t0002 | g0065 | AFR | MSL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03704 | hp2 | a0002 | c0002 | t0023 | g0072 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03710 | hp2 | a0001 | c0001 | t0031 | g0162 | SAS | PJL | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03834 | hp1 | a0002 | c0002 | t0007 | g0016 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03834 | hp2 | a0001 | c0001 | t0028 | g0160 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03927 | hp1 | a0002 | c0002 | t0007 | g0073 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0196 | SAS | BEB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0228 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0233 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0096 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0203 | SAS | STU | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18906 | hp2 | a0009 | c0010 | t0017 | g0243 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0234 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18954 | hp2 | a0001 | c0001 | t0029 | g0106 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0220 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18957 | hp2 | a0010 | c0007 | t0001 | g0006 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18968 | hp2 | a0001 | c0001 | t0034 | g0314 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18972 | hp1 | a0001 | c0001 | t0039 | g0212 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18974 | hp1 | a0001 | c0001 | t0009 | g0110 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18974 | hp2 | a0002 | c0002 | t0011 | g0044 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18983 | hp1 | a0002 | c0002 | t0003 | g0222 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18987 | hp2 | a0001 | c0001 | t0009 | g0181 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18988 | hp2 | a0010 | c0007 | t0001 | g0006 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18995 | hp2 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0324 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19009 | hp2 | a0001 | c0001 | t0009 | g0114 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0225 | AFR | LWK | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19060 | hp1 | a0001 | c0001 | t0009 | g0183 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19066 | hp2 | a0001 | c0001 | t0016 | g0005 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19072 | hp2 | a0002 | c0002 | t0024 | g0218 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19084 | hp1 | a0001 | c0001 | t0030 | g0252 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0254 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0236 | AFR | YRI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0250 | AFR | ASW | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20129 | hp2 | a0002 | c0002 | t0026 | g0068 | AFR | ASW | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | TSI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20752 | hp2 | a0001 | c0001 | t0019 | g0089 | EUR | TSI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0142 | EUR | TSI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20905 | hp1 | a0002 | c0002 | t0007 | g0070 | SAS | GIH | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20905 | hp2 | a0002 | c0002 | t0011 | g0322 | SAS | GIH | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0326 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0138 | AMR | CLM | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0266 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02486 | hp1 | a0007 | c0006 | t0001 | g0176 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG02559 | hp2 | a0002 | c0002 | t0010 | g0078 | AFR | ACB | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0013 | AFR | USA | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | USA | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | USA | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | USA | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0105 | REF | REF | CENPC_chr4_67463762_67550503 | CENPC | chr4 | 67463762 | 67550503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67472648 | C | T | 1 | a0012 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2789G>A | p.Arg930Gln | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2937/6823 | 2789/2832 | 930/943 | chr4 | 67472648 | |||
| chr4:67474905 | G | A | 1 | a0007 | 2 | HG02486.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.2744C>T | p.Ser915Leu | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/19 | 2892/6823 | 2744/2832 | 915/943 | chr4 | 67474905 | |||
| chr4:67508908 | C | T | 1 | a0008 | 2 | HG02922.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.1810G>A | p.Val604Ile | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/19 | 1958/6823 | 1810/2832 | 604/943 | chr4 | 67508908 | |||
| chr4:67508923 | C | T | 1 | a0006 | 2 | HG01884.hp1 HG02145.hp1 |
missense_variant | MODERATE | c.1795G>A | p.Gly599Ser | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/19 | 1943/6823 | 1795/2832 | 599/943 | chr4 | 67508923 | |||
| chr4:67509063 | A | G | 1 | a0011 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1655T>C | p.Met552Thr | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/19 | 1803/6823 | 1655/2832 | 552/943 | chr4 | 67509063 | |||
| chr4:67512569 | C | A | 1 | a0005 | 3 | HG01167.hp1 HG02615.hp1 HG03579.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1445G>T | p.Gly482Val | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/19 | 1593/6823 | 1445/2832 | 482/943 | chr4 | 67512569 | |||
| chr4:67514124 | T | C | 1 | a0004 | 4 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.1394A>G | p.His465Arg | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/19 | 1542/6823 | 1394/2832 | 465/943 | chr4 | 67514124 | |||
| chr4:67514352 | C | T | 1 | a0003 | 8 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(5): Show |
missense_variant | MODERATE | c.1166G>A | p.Gly389Asp | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/19 | 1314/6823 | 1166/2832 | 389/943 | chr4 | 67514352 | |||
| chr4:67514416 | G | A | 1 | a0010 | 2 | NA18957.hp2 NA18988.hp2 |
missense_variant | MODERATE | c.1102C>T | p.His368Tyr | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/19 | 1250/6823 | 1102/2832 | 368/943 | chr4 | 67514416 | |||
| chr4:67514497 | G | A | 8 | a0001 a0003 a0004 others(5): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.1021C>T | p.Leu341Phe | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/19 | 1169/6823 | 1021/2832 | 341/943 | chr4 | 67514497 | |||
| chr4:67539851 | G | C | 2 | a0006 a0009 |
4 | HG01884.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.220C>G | p.Pro74Ala | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/19 | 368/6823 | 220/2832 | 74/943 | chr4 | 67539851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67474955 | G | A | 1 | a0001c0012 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.2694C>T | p.Asp898Asp | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/19 | 2842/6823 | 2694/2832 | 898/943 | chr4 | 67474955 | |||
| chr4:67489994 | T | G | 1 | a0002c0014 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2643A>C | p.Gly881Gly | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/19 | 2791/6823 | 2643/2832 | 881/943 | chr4 | 67489994 | |||
| chr4:67508879 | C | T | 9 | a0001c0001 a0001c0012 a0003c0003 others(6): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
synonymous_variant | LOW | c.1839G>A | p.Ser613Ser | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/19 | 1987/6823 | 1839/2832 | 613/943 | chr4 | 67508879 | |||
| chr4:67518290 | C | T | 9 | a0001c0001 a0001c0012 a0003c0003 others(6): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
synonymous_variant | LOW | c.696G>A | p.Ser232Ser | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/19 | 844/6823 | 696/2832 | 232/943 | chr4 | 67518290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67468934 | T | A | 1 | a0001c0001t0025 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3671A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3671 | chr4 | 67468934 | ||||||
| chr4:67469054 | A | C | 1 | a0002c0002t0010 | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3551T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3551 | chr4 | 67469054 | ||||||
| chr4:67469112 | G | A | 1 | a0001c0001t0035 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3493C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3493 | chr4 | 67469112 | ||||||
| chr4:67469119 | T | C | 1 | a0004c0004t0033 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3486A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3486 | chr4 | 67469119 | ||||||
| chr4:67469190 | C | T | 1 | a0006c0009t0014 | 2 | HG01884.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3415G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3415 | chr4 | 67469190 | ||||||
| chr4:67469240 | G | A | 1 | a0002c0002t0010 | 4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3365C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3365 | chr4 | 67469240 | ||||||
| chr4:67469326 | C | G | 4 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0025 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3279 | chr4 | 67469326 | ||||||
| chr4:67469514 | T | G | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3091A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 3091 | chr4 | 67469514 | ||||||
| chr4:67469623 | A | G | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2982T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2982 | chr4 | 67469623 | ||||||
| chr4:67469634 | T | C | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2971 | chr4 | 67469634 | ||||||
| chr4:67469638 | C | T | 1 | a0001c0001t0030 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2967G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2967 | chr4 | 67469638 | ||||||
| chr4:67469671 | G | A | 1 | a0002c0002t0026 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2934C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2934 | chr4 | 67469671 | ||||||
| chr4:67469680 | G | A | 6 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0016 others(3): Show |
38 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2925C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2925 | chr4 | 67469680 | ||||||
| chr4:67469786 | G | A | 1 | a0006c0009t0014 | 2 | HG01884.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2819C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2819 | chr4 | 67469786 | ||||||
| chr4:67469823 | C | T | 1 | a0001c0001t0018 | 2 | HG02809.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2782G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2782 | chr4 | 67469823 | ||||||
| chr4:67469905 | TC | T | 4 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0025 others(1): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2699delG | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2699 | chr4 | 67469905 | ||||||
| chr4:67469915 | T | C | 1 | a0001c0001t0036 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2690A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2690 | chr4 | 67469915 | ||||||
| chr4:67470125 | T | G | 1 | a0001c0001t0031 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2480A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2480 | chr4 | 67470125 | ||||||
| chr4:67470162 | A | G | 1 | a0008c0008t0015 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2443T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2443 | chr4 | 67470162 | ||||||
| chr4:67470253 | T | C | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2352A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2352 | chr4 | 67470253 | ||||||
| chr4:67470254 | G | A | 1 | a0001c0001t0025 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2351C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2351 | chr4 | 67470254 | ||||||
| chr4:67470322 | A | G | 3 | a0001c0001t0004 a0001c0001t0019 a0003c0003t0004 |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2283T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2283 | chr4 | 67470322 | ||||||
| chr4:67470497 | G | A | 3 | a0004c0004t0032 a0004c0004t0033 a0008c0008t0015 |
4 | HG02280.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2108C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2108 | chr4 | 67470497 | ||||||
| chr4:67470518 | G | A | 1 | a0001c0001t0034 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2087 | chr4 | 67470518 | ||||||
| chr4:67470572 | CA | C | 9 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0023 others(6): Show |
62 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2032delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2032 | chr4 | 67470572 | ||||||
| chr4:67470583 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0037 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2021_*2022insCTTT others(9): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2021 | chr4 | 67470583 | ||||||
| chr4:67470583 | A | AAAAAAAA others(5): Show |
7 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0019 others(4): Show |
19 | HG00140.hp1 HG00558.hp2 HG01123.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2021_*2022insCTTT others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2021 | chr4 | 67470583 | ||||||
| chr4:67470583 | A | AAAAAAAA others(4): Show |
24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*2021_*2022insCTTT others(7): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2021 | chr4 | 67470583 | ||||||
| chr4:67470583 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0008 a0001c0001t0029 |
6 | HG02109.hp1 HG02717.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2021_*2022insCTTT others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 2021 | chr4 | 67470583 | ||||||
| chr4:67470733 | C | T | 1 | a0001c0001t0028 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1872G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1872 | chr4 | 67470733 | ||||||
| chr4:67470861 | A | T | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1744T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1744 | chr4 | 67470861 | ||||||
| chr4:67471003 | C | G | 1 | a0009c0010t0017 | 2 | HG02965.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1602G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1602 | chr4 | 67471003 | ||||||
| chr4:67471003 | CAA | C | 3 | a0001c0001t0004 a0001c0001t0019 a0003c0003t0004 |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1600_*1601delTT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1600 | chr4 | 67471003 | ||||||
| chr4:67471013 | T | C | 3 | a0001c0001t0004 a0001c0001t0019 a0003c0003t0004 |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1592A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1592 | chr4 | 67471013 | ||||||
| chr4:67471066 | A | C | 1 | a0009c0010t0017 | 2 | HG02965.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1539T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 1539 | chr4 | 67471066 | ||||||
| chr4:67471682 | T | C | 9 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0010 others(6): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*923A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 923 | chr4 | 67471682 | ||||||
| chr4:67471717 | A | G | 35 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(32): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*888T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 888 | chr4 | 67471717 | ||||||
| chr4:67472073 | A | G | 1 | a0001c0001t0027 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*532T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 532 | chr4 | 67472073 | ||||||
| chr4:67472188 | C | T | 1 | a0002c0002t0023 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*417G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 417 | chr4 | 67472188 | ||||||
| chr4:67472223 | T | C | 1 | a0001c0001t0021 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 382 | chr4 | 67472223 | ||||||
| chr4:67472257 | T | A | 9 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0010 others(6): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*348A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 348 | chr4 | 67472257 | ||||||
| chr4:67472291 | T | G | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(30): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*314A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 314 | chr4 | 67472291 | ||||||
| chr4:67472306 | C | G | 1 | a0001c0001t0016 | 2 | HG00544.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 299 | chr4 | 67472306 | ||||||
| chr4:67472444 | ATG | A | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(30): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*159_*160delCA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 159 | chr4 | 67472444 | ||||||
| chr4:67472464 | T | C | 1 | a0007c0006t0038 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 141 | chr4 | 67472464 | ||||||
| chr4:67472481 | G | C | 44 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(41): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*124C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 124 | chr4 | 67472481 | ||||||
| chr4:67472529 | G | T | 3 | a0002c0002t0007 a0002c0002t0023 a0012c0013t0007 |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 76 | chr4 | 67472529 | ||||||
| chr4:67472563 | A | G | 1 | a0001c0001t0022 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 42 | chr4 | 67472563 | ||||||
| chr4:67472563 | A | T | 1 | a0001c0001t0013 | 2 | HG01884.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*42T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 42 | chr4 | 67472563 | ||||||
| chr4:67472566 | T | C | 1 | a0001c0001t0039 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 39 | chr4 | 67472566 | ||||||
| chr4:67472580 | C | T | 1 | a0001c0001t0021 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 19/19 | 25 | chr4 | 67472580 | ||||||
| chr4:67545453 | A | C | 1 | a0002c0002t0020 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/19 | 98 | chr4 | 67545453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67472705 | T | G | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2762-30A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67472705 | |||||||
| chr4:67472749 | C | T | 1 | a0001c0001t0005g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2762-74G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67472749 | |||||||
| chr4:67472917 | A | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2762-242T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67472917 | |||||||
| chr4:67472961 | C | T | 1 | a0001c0001t0006g0326 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2762-286G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67472961 | |||||||
| chr4:67473007 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2762-332C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473007 | |||||||
| chr4:67473077 | T | C | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2762-402A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473077 | |||||||
| chr4:67473081 | C | T | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2762-406G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473081 | |||||||
| chr4:67473084 | A | T | 280 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(277): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2762-409T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473084 | |||||||
| chr4:67473085 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2762-410A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473085 | |||||||
| chr4:67473191 | T | C | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2762-516A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473191 | |||||||
| chr4:67473221 | G | A | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2762-546C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473221 | |||||||
| chr4:67473459 | C | T | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2762-784G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473459 | |||||||
| chr4:67473573 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0213 a0001c0001t0001g0215 others(1): Show |
4 | HG00597.hp1 HG02129.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2762-898C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473573 | |||||||
| chr4:67473595 | C | G | 7 | a0001c0001t0004g0088 a0001c0001t0004g0133 a0001c0001t0004g0141 others(4): Show |
7 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2762-920G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473595 | |||||||
| chr4:67473706 | C | T | 1 | a0002c0002t0011g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2762-1031G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473706 | |||||||
| chr4:67473707 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2762-1032C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473707 | |||||||
| chr4:67473748 | T | C | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2762-1073A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67473748 | |||||||
| chr4:67474071 | AT | A | 294 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(291): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2761+816delA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474071 | |||||||
| chr4:67474089 | G | C | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2761+799C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474089 | |||||||
| chr4:67474213 | C | T | 1 | a0002c0002t0002g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2761+675G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474213 | |||||||
| chr4:67474221 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2761+667G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474221 | |||||||
| chr4:67474494 | G | A | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2761+394C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474494 | |||||||
| chr4:67474528 | C | T | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2761+360G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474528 | |||||||
| chr4:67474590 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0122 a0001c0001t0001g0169 others(1): Show |
4 | HG00280.hp1 NA18941.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.2761+298G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474590 | |||||||
| chr4:67474591 | G | A | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2761+297C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474591 | |||||||
| chr4:67474881 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
splice_region_variant&intron_variant | LOW | c.2761+7C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 18/18 | chr4 | 67474881 | |||||||
| chr4:67475032 | A | C | 5 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2671-54T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475032 | |||||||
| chr4:67475047 | T | A | 1 | a0002c0002t0002g0028 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2671-69A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475047 | |||||||
| chr4:67475165 | G | T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2671-187C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475165 | |||||||
| chr4:67475224 | G | A | 1 | a0003c0003t0004g0247 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2671-246C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475224 | |||||||
| chr4:67475345 | A | G | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2671-367T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475345 | |||||||
| chr4:67475361 | C | T | 2 | a0003c0003t0004g0131 a0003c0003t0004g0132 |
2 | HG00099.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2671-383G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475361 | |||||||
| chr4:67475420 | G | A | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2671-442C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475420 | |||||||
| chr4:67475440 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2671-462C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475440 | |||||||
| chr4:67475678 | A | C | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2671-700T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475678 | |||||||
| chr4:67475684 | C | T | 4 | a0001c0001t0013g0090 a0001c0001t0013g0091 a0009c0010t0017g0243 others(1): Show |
4 | HG01884.hp2 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-706G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475684 | |||||||
| chr4:67475686 | C | G | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2671-708G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475686 | |||||||
| chr4:67475687 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2671-709G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475687 | |||||||
| chr4:67475815 | T | C | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2671-837A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475815 | |||||||
| chr4:67475878 | C | T | 2 | a0004c0004t0032g0277 a0004c0004t0033g0320 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2671-900G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475878 | |||||||
| chr4:67475881 | G | A | 19 | a0002c0002t0003g0007 a0002c0002t0003g0017 a0002c0002t0003g0219 others(16): Show |
20 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.2671-903C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67475881 | |||||||
| chr4:67476008 | C | T | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2671-1030G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476008 | |||||||
| chr4:67476346 | T | C | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2671-1368A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476346 | |||||||
| chr4:67476413 | G | A | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-1435C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476413 | |||||||
| chr4:67476565 | C | A | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2671-1587G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476565 | |||||||
| chr4:67476649 | C | T | 3 | a0001c0001t0005g0112 a0001c0001t0005g0113 a0001c0001t0009g0114 |
3 | NA19007.hp1 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2671-1671G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476649 | |||||||
| chr4:67476711 | T | TA | 3 | a0001c0001t0025g0251 a0006c0009t0014g0245 a0006c0009t0014g0246 |
3 | HG01884.hp1 HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2671-1734dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476711 | |||||||
| chr4:67476835 | A | C | 1 | a0001c0001t0004g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2671-1857T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476835 | |||||||
| chr4:67476852 | C | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
8 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2671-1874G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476852 | |||||||
| chr4:67476981 | A | G | 1 | a0009c0010t0017g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2671-2003T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67476981 | |||||||
| chr4:67477027 | A | G | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2671-2049T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477027 | |||||||
| chr4:67477058 | A | G | 1 | a0001c0001t0037g0328 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2671-2080T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477058 | |||||||
| chr4:67477131 | G | A | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG01943.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2671-2153C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477131 | |||||||
| chr4:67477237 | C | A | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2671-2259G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477237 | |||||||
| chr4:67477264 | A | T | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2671-2286T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477264 | |||||||
| chr4:67477419 | A | G | 1 | a0001c0001t0008g0305 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2671-2441T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477419 | |||||||
| chr4:67477450 | A | C | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2671-2472T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477450 | |||||||
| chr4:67477635 | T | C | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2671-2657A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477635 | |||||||
| chr4:67477673 | C | A | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2671-2695G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477673 | |||||||
| chr4:67477801 | T | A | 4 | a0001c0001t0001g0284 a0001c0001t0013g0090 a0001c0001t0013g0091 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-2823A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477801 | |||||||
| chr4:67477831 | C | T | 1 | a0001c0001t0006g0216 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2671-2853G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477831 | |||||||
| chr4:67477939 | G | A | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2671-2961C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67477939 | |||||||
| chr4:67478144 | A | C | 1 | a0001c0001t0004g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2671-3166T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478144 | |||||||
| chr4:67478263 | C | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2671-3285G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478263 | |||||||
| chr4:67478378 | G | C | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2671-3400C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478378 | |||||||
| chr4:67478600 | T | C | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2671-3622A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478600 | |||||||
| chr4:67478629 | A | AAC | 46 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0022 others(43): Show |
48 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2671-3653_2671-365 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478629 | |||||||
| chr4:67478629 | A | AACAC | 7 | a0002c0002t0002g0023 a0002c0002t0002g0034 a0002c0002t0002g0052 others(4): Show |
7 | HG00323.hp2 HG01109.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.2671-3655_2671-365 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478629 | |||||||
| chr4:67478629 | AAC | A | 50 | a0001c0001t0001g0286 a0001c0001t0001g0308 a0001c0001t0004g0001 others(47): Show |
54 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.2671-3653_2671-365 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478629 | |||||||
| chr4:67478629 | AACAC | A | 68 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(65): Show |
68 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.2671-3655_2671-365 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478629 | |||||||
| chr4:67478649 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2671-3671G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478649 | |||||||
| chr4:67478666 | A | ACACACAC others(9): Show |
1 | a0001c0001t0005g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2671-3689_2671-368 others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478666 | A | ACACACAC others(7): Show |
1 | a0006c0009t0014g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2671-3689_2671-368 others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478666 | A | ACACACAC others(5): Show |
2 | a0001c0001t0025g0251 a0006c0009t0014g0245 |
2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2671-3689_2671-368 others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478666 | A | ACACC | 5 | a0001c0001t0001g0120 a0001c0001t0012g0254 a0001c0001t0012g0255 others(2): Show |
5 | HG01070.hp1 HG01884.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2671-3689_2671-368 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478666 | A | ACC | 21 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0102 others(18): Show |
21 | HG00280.hp1 HG00733.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2671-3690_2671-368 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478666 | A | C | 196 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(193): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2671-3688T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478666 | |||||||
| chr4:67478757 | C | T | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2671-3779G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478757 | |||||||
| chr4:67478763 | A | G | 1 | a0002c0002t0003g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2671-3785T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478763 | |||||||
| chr4:67478868 | A | G | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2671-3890T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478868 | |||||||
| chr4:67478926 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2671-3948A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478926 | |||||||
| chr4:67478998 | G | T | 11 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0035 others(8): Show |
13 | HG02132.hp1 NA18975.hp1 NA18977.hp1 others(10): Show |
intron_variant | MODIFIER | c.2671-4020C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67478998 | |||||||
| chr4:67479103 | G | A | 1 | a0011c0011t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2671-4125C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67479103 | |||||||
| chr4:67479440 | G | A | 1 | a0002c0002t0003g0084 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2671-4462C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67479440 | |||||||
| chr4:67479911 | G | A | 1 | a0001c0001t0006g0216 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2671-4933C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67479911 | |||||||
| chr4:67480027 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2671-5049T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480027 | |||||||
| chr4:67480179 | A | C | 223 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(220): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2671-5201T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480179 | |||||||
| chr4:67480375 | C | T | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2671-5397G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480375 | |||||||
| chr4:67480492 | C | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0188 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2671-5514G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480492 | |||||||
| chr4:67480506 | A | G | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2671-5528T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480506 | |||||||
| chr4:67480532 | A | G | 1 | a0001c0001t0013g0091 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2671-5554T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480532 | |||||||
| chr4:67480739 | C | G | 1 | a0001c0001t0006g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2671-5761G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480739 | |||||||
| chr4:67480739 | C | T | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.2671-5761G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480739 | |||||||
| chr4:67480766 | C | T | 1 | a0002c0002t0003g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2671-5788G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480766 | |||||||
| chr4:67480951 | C | T | 1 | a0001c0001t0005g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2671-5973G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67480951 | |||||||
| chr4:67481100 | G | C | 1 | a0002c0002t0011g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2671-6122C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481100 | |||||||
| chr4:67481185 | C | T | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2671-6207G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481185 | |||||||
| chr4:67481212 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2671-6234T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481212 | |||||||
| chr4:67481275 | A | G | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2671-6297T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481275 | |||||||
| chr4:67481432 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0288 |
2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.2671-6454C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481432 | |||||||
| chr4:67481699 | C | A | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.2671-6721G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481699 | |||||||
| chr4:67481838 | C | G | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-6860G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481838 | |||||||
| chr4:67481858 | C | G | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2671-6880G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67481858 | |||||||
| chr4:67482254 | C | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2671-7276G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482254 | |||||||
| chr4:67482475 | A | C | 1 | a0002c0002t0002g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2670+7492T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482475 | |||||||
| chr4:67482531 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2670+7436C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482531 | |||||||
| chr4:67482586 | T | C | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2670+7381A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482586 | |||||||
| chr4:67482880 | T | G | 1 | a0002c0002t0003g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2670+7087A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482880 | |||||||
| chr4:67482921 | C | A | 7 | a0002c0002t0007g0016 a0002c0002t0007g0069 a0002c0002t0007g0070 others(4): Show |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670+7046G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482921 | |||||||
| chr4:67482925 | CAT | C | 13 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(10): Show |
16 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2670+7040_2670+704 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67482925 | |||||||
| chr4:67483005 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2670+6962G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483005 | |||||||
| chr4:67483082 | G | C | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670+6885C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483082 | |||||||
| chr4:67483208 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG00597.hp1 HG00597.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670+6759C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483208 | |||||||
| chr4:67483283 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2670+6684C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483283 | |||||||
| chr4:67483359 | GA | G | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2670+6607delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483359 | |||||||
| chr4:67483430 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2670+6537T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483430 | |||||||
| chr4:67483470 | A | G | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2670+6497T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483470 | |||||||
| chr4:67483548 | T | TA | 34 | a0001c0001t0001g0311 a0001c0001t0004g0001 a0001c0001t0004g0004 others(31): Show |
37 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.2670+6418dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483548 | |||||||
| chr4:67483550 | A | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2670+6417T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483550 | |||||||
| chr4:67483597 | T | G | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2670+6370A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483597 | |||||||
| chr4:67483765 | CA | C | 62 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(59): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2670+6201delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67483765 | |||||||
| chr4:67484052 | C | G | 4 | a0002c0002t0003g0224 a0002c0002t0003g0225 a0002c0002t0003g0226 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+5915G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484052 | |||||||
| chr4:67484420 | C | A | 3 | a0001c0001t0025g0251 a0006c0009t0014g0245 a0006c0009t0014g0246 |
3 | HG01884.hp1 HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2670+5547G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484420 | |||||||
| chr4:67484547 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2670+5420A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484547 | |||||||
| chr4:67484571 | C | A | 13 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(10): Show |
16 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2670+5396G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484571 | |||||||
| chr4:67484590 | T | C | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2670+5377A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484590 | |||||||
| chr4:67484645 | G | T | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2670+5322C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484645 | |||||||
| chr4:67484673 | A | G | 53 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(50): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2670+5294T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484673 | |||||||
| chr4:67484832 | G | A | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2670+5135C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484832 | |||||||
| chr4:67484897 | T | C | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2670+5070A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484897 | |||||||
| chr4:67484928 | T | C | 222 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(219): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2670+5039A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484928 | |||||||
| chr4:67484949 | C | T | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2670+5018G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67484949 | |||||||
| chr4:67485041 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2670+4926A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485041 | |||||||
| chr4:67485080 | G | A | 1 | a0002c0002t0002g0029 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2670+4887C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485080 | |||||||
| chr4:67485110 | C | A | 107 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(104): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2670+4857G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485110 | |||||||
| chr4:67485175 | A | AATTC | 10 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0287 others(7): Show |
10 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.2670+4791_2670+479 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485175 | |||||||
| chr4:67485176 | C | T | 10 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0287 others(7): Show |
10 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.2670+4791G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485176 | |||||||
| chr4:67485326 | T | C | 1 | a0002c0002t0002g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2670+4641A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485326 | |||||||
| chr4:67485469 | A | AC | 217 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(214): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2670+4497dupG | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485469 | |||||||
| chr4:67485567 | G | A | 1 | a0002c0002t0002g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2670+4400C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67485567 | |||||||
| chr4:67486007 | T | C | 219 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(216): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2670+3960A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486007 | |||||||
| chr4:67486212 | T | A | 107 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(104): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2670+3755A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486212 | |||||||
| chr4:67486634 | G | A | 1 | a0001c0001t0005g0117 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2670+3333C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486634 | |||||||
| chr4:67486670 | T | C | 2 | a0001c0001t0018g0268 a0001c0001t0018g0316 |
2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2670+3297A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486670 | |||||||
| chr4:67486812 | A | G | 1 | a0002c0002t0007g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2670+3155T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486812 | |||||||
| chr4:67486966 | A | G | 315 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(312): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.2670+3001T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486966 | |||||||
| chr4:67486968 | G | GT | 9 | a0001c0001t0001g0285 a0001c0001t0001g0288 a0001c0001t0001g0308 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.2670+2998dupA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486968 | |||||||
| chr4:67486968 | G | GTT | 75 | a0001c0001t0001g0150 a0001c0001t0001g0184 a0001c0001t0001g0256 others(72): Show |
75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.2670+2997_2670+299 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486968 | |||||||
| chr4:67486968 | G | GTTT | 136 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(133): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2670+2996_2670+299 others(7): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486968 | |||||||
| chr4:67486968 | G | GTTTT | 8 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0174 others(5): Show |
8 | HG00323.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2670+2995_2670+299 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67486968 | |||||||
| chr4:67487072 | C | G | 107 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(104): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2670+2895G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487072 | |||||||
| chr4:67487114 | C | G | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2670+2853G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487114 | |||||||
| chr4:67487217 | T | G | 5 | a0001c0001t0013g0090 a0001c0001t0013g0091 a0001c0001t0025g0251 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670+2750A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487217 | |||||||
| chr4:67487225 | TACCTAAT others(1037): Show |
T | 5 | a0001c0001t0013g0090 a0001c0001t0013g0091 a0001c0001t0025g0251 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670+1698_2670+274 others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487225 | |||||||
| chr4:67487317 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2670+2650C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487317 | |||||||
| chr4:67487546 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2670+2421C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487546 | |||||||
| chr4:67487676 | T | C | 1 | a0002c0002t0011g0322 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2670+2291A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487676 | |||||||
| chr4:67487744 | C | T | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2670+2223G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487744 | |||||||
| chr4:67487851 | T | C | 1 | a0001c0001t0004g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2670+2116A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487851 | |||||||
| chr4:67487896 | C | T | 4 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0035 others(1): Show |
6 | NA18977.hp1 NA18988.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.2670+2071G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67487896 | |||||||
| chr4:67488040 | A | G | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.2670+1927T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67488040 | |||||||
| chr4:67488166 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2670+1801G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67488166 | |||||||
| chr4:67488317 | C | A | 1 | a0003c0003t0004g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2670+1650G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67488317 | |||||||
| chr4:67488463 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2670+1504A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67488463 | |||||||
| chr4:67488737 | A | G | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2670+1230T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67488737 | |||||||
| chr4:67489146 | A | G | 6 | a0001c0001t0006g0323 a0001c0001t0006g0324 a0001c0001t0006g0326 others(3): Show |
6 | HG01123.hp1 HG01943.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2670+821T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489146 | |||||||
| chr4:67489197 | T | TAC | 40 | a0001c0001t0001g0163 a0001c0001t0005g0080 a0001c0001t0005g0108 others(37): Show |
41 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2670+768_2670+769d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489197 | |||||||
| chr4:67489197 | T | TACAC | 19 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0102 others(16): Show |
19 | HG00280.hp1 HG01256.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2670+766_2670+769d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489197 | |||||||
| chr4:67489197 | TAC | T | 187 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0260 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2670+768_2670+769d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489197 | |||||||
| chr4:67489221 | CAT | C | 3 | a0001c0001t0004g0097 a0001c0001t0028g0160 a0001c0001t0031g0162 |
3 | HG03710.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2670+744_2670+745d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489221 | |||||||
| chr4:67489223 | T | C | 105 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(102): Show |
107 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2670+744A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489223 | |||||||
| chr4:67489248 | T | G | 1 | a0002c0002t0003g0087 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2670+719A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489248 | |||||||
| chr4:67489304 | AAAG | A | 4 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+660_2670+662d others(5): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489304 | |||||||
| chr4:67489340 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2670+627G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489340 | |||||||
| chr4:67489393 | C | T | 223 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(220): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2670+574G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489393 | |||||||
| chr4:67489411 | G | GCT | 219 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(216): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2670+554_2670+555d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489411 | |||||||
| chr4:67489418 | C | G | 1 | a0001c0001t0004g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2670+549G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489418 | |||||||
| chr4:67489421 | G | A | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2670+546C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489421 | |||||||
| chr4:67489422 | A | G | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2670+545T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489422 | |||||||
| chr4:67489516 | T | A | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2670+451A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489516 | |||||||
| chr4:67489707 | C | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2670+260G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 17/18 | chr4 | 67489707 | |||||||
| chr4:67490164 | T | C | 2 | a0001c0001t0004g0135 a0001c0001t0004g0136 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2516-43A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490164 | |||||||
| chr4:67490246 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2516-125T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490246 | |||||||
| chr4:67490487 | T | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2516-366A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490487 | |||||||
| chr4:67490735 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2516-614G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490735 | |||||||
| chr4:67490837 | A | AAT | 3 | a0001c0001t0005g0155 a0002c0002t0003g0008 a0002c0002t0010g0075 |
4 | HG02280.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2516-718_2516-717d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490837 | |||||||
| chr4:67490837 | A | AATATATA others(3): Show |
1 | a0005c0005t0002g0063 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2516-726_2516-717d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490837 | |||||||
| chr4:67490837 | A | T | 3 | a0001c0001t0028g0160 a0001c0001t0031g0162 a0001c0012t0012g0253 |
3 | HG03486.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2516-716T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490837 | |||||||
| chr4:67490837 | AAT | A | 4 | a0002c0002t0003g0009 a0002c0002t0003g0217 a0002c0002t0003g0238 others(1): Show |
5 | HG02486.hp2 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2516-718_2516-717d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490837 | |||||||
| chr4:67490837 | AATATATA others(3): Show |
A | 18 | a0002c0002t0003g0007 a0002c0002t0003g0219 a0002c0002t0003g0220 others(15): Show |
19 | HG00544.hp2 HG01243.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.2516-726_2516-717d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490837 | |||||||
| chr4:67490841 | T | A | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2516-720A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490841 | |||||||
| chr4:67490855 | TATATATA others(19): Show |
T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2516-760_2516-735d others(28): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490855 | |||||||
| chr4:67490861 | T | G | 37 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(34): Show |
40 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2516-740A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490861 | |||||||
| chr4:67490863 | T | A | 37 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(34): Show |
40 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2516-742A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490863 | |||||||
| chr4:67490863 | T | G | 70 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(67): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2516-742A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490863 | |||||||
| chr4:67490865 | T | A | 70 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(67): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2516-744A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490865 | |||||||
| chr4:67490865 | T | G | 17 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0273 others(14): Show |
17 | HG00733.hp1 HG01243.hp1 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2516-744A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490865 | |||||||
| chr4:67490867 | T | A | 17 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0273 others(14): Show |
17 | HG00733.hp1 HG01243.hp1 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2516-746A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490867 | |||||||
| chr4:67490867 | T | G | 15 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0156 others(12): Show |
15 | HG00323.hp1 HG02647.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.2516-746A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490867 | |||||||
| chr4:67490867 | TATATATA others(7): Show |
T | 37 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(34): Show |
40 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2516-760_2516-747d others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490867 | |||||||
| chr4:67490869 | T | A | 15 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0156 others(12): Show |
15 | HG00323.hp1 HG02647.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.2516-748A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490869 | |||||||
| chr4:67490869 | T | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(44): Show |
47 | HG00423.hp2 HG00597.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.2516-748A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490869 | |||||||
| chr4:67490869 | TATATATA others(5): Show |
T | 70 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(67): Show |
70 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.2516-760_2516-749d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490869 | |||||||
| chr4:67490871 | T | A | 47 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(44): Show |
47 | HG00423.hp2 HG00597.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.2516-750A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490871 | |||||||
| chr4:67490871 | T | G | 57 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0161 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2516-750A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490871 | |||||||
| chr4:67490871 | TATATATA others(3): Show |
T | 17 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0273 others(14): Show |
17 | HG00733.hp1 HG01243.hp1 HG02735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2516-760_2516-751d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490871 | |||||||
| chr4:67490873 | T | A | 57 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0161 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2516-752A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490873 | |||||||
| chr4:67490873 | T | G | 34 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0173 others(31): Show |
36 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2516-752A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490873 | |||||||
| chr4:67490873 | TATATAGA others(1): Show |
T | 15 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0156 others(12): Show |
15 | HG00323.hp1 HG02647.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.2516-760_2516-753d others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490873 | |||||||
| chr4:67490875 | T | A | 34 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0173 others(31): Show |
36 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2516-754A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490875 | |||||||
| chr4:67490875 | T | G | 7 | a0001c0001t0001g0186 a0001c0001t0005g0180 a0002c0002t0002g0055 others(4): Show |
8 | HG00438.hp2 HG01978.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-754A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490875 | |||||||
| chr4:67490875 | TATAGAA | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(44): Show |
47 | HG00423.hp2 HG00597.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.2516-760_2516-755d others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490875 | |||||||
| chr4:67490877 | T | A | 7 | a0001c0001t0001g0186 a0001c0001t0005g0180 a0002c0002t0002g0055 others(4): Show |
8 | HG00438.hp2 HG01978.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-756A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490877 | |||||||
| chr4:67490877 | T | G | 3 | a0001c0001t0005g0115 a0002c0002t0007g0070 a0002c0002t0010g0076 |
3 | HG02451.hp1 HG03195.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2516-756A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490877 | |||||||
| chr4:67490877 | TAG | T | 34 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0173 others(31): Show |
36 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2516-758_2516-757d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490877 | |||||||
| chr4:67490879 | G | A | 3 | a0001c0001t0005g0115 a0002c0002t0007g0070 a0002c0002t0010g0076 |
3 | HG02451.hp1 HG03195.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2516-758C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490879 | |||||||
| chr4:67490879 | G | T | 7 | a0001c0001t0001g0186 a0001c0001t0005g0180 a0002c0002t0002g0055 others(4): Show |
8 | HG00438.hp2 HG01978.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2516-758C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490879 | |||||||
| chr4:67490879 | GAAAT | G | 57 | a0001c0001t0001g0122 a0001c0001t0001g0147 a0001c0001t0001g0161 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2516-762_2516-759d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490879 | |||||||
| chr4:67490881 | A | T | 44 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0173 others(41): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2516-760T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490881 | |||||||
| chr4:67490883 | T | G | 227 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(224): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2516-762A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490883 | |||||||
| chr4:67490883 | T | TAG | 3 | a0001c0001t0005g0115 a0002c0002t0007g0070 a0002c0002t0010g0076 |
3 | HG02451.hp1 HG03195.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2516-763_2516-762i others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490883 | |||||||
| chr4:67490883 | T | TATAG | 6 | a0001c0001t0005g0108 a0001c0001t0005g0155 a0001c0012t0012g0253 others(3): Show |
6 | HG00673.hp2 HG01167.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2516-763_2516-762i others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490883 | |||||||
| chr4:67490897 | T | G | 5 | a0001c0001t0001g0258 a0001c0001t0013g0090 a0001c0001t0013g0091 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2516-776A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490897 | |||||||
| chr4:67490938 | G | T | 1 | a0001c0001t0005g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2516-817C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67490938 | |||||||
| chr4:67491109 | C | T | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2516-988G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491109 | |||||||
| chr4:67491392 | G | A | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2515+788C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491392 | |||||||
| chr4:67491415 | T | C | 1 | a0005c0005t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2515+765A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491415 | |||||||
| chr4:67491431 | T | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2515+749A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491431 | |||||||
| chr4:67491445 | TCA | T | 3 | a0001c0001t0005g0108 a0001c0001t0005g0155 a0001c0001t0005g0199 |
3 | HG00673.hp2 HG01175.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2515+733_2515+734d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491445 | |||||||
| chr4:67491445 | TCATA | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0159 a0001c0001t0005g0117 |
3 | NA19030.hp1 NA19086.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2515+731_2515+734d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491445 | |||||||
| chr4:67491446 | C | CATATAT | 4 | a0001c0001t0001g0300 a0001c0001t0001g0306 a0001c0001t0001g0308 others(1): Show |
4 | HG02818.hp2 HG03491.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+728_2515+733d others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | C | G | 107 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(104): Show |
109 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.2515+734G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CAT | C | 10 | a0001c0001t0004g0143 a0001c0001t0021g0250 a0001c0012t0012g0253 others(7): Show |
10 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2515+732_2515+733d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CATATATA others(3): Show |
C | 10 | a0001c0001t0004g0097 a0001c0001t0004g0129 a0001c0001t0004g0134 others(7): Show |
10 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.2515+724_2515+733d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CATATATA others(5): Show |
C | 2 | a0001c0001t0004g0018 a0001c0001t0004g0128 |
2 | HG02165.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2515+722_2515+733d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CATATATA others(11): Show |
C | 1 | a0002c0002t0010g0076 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2515+716_2515+733d others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CATATATA others(13): Show |
C | 2 | a0002c0002t0010g0075 a0002c0002t0010g0077 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2515+714_2515+733d others(22): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491446 | CATATATA others(15): Show |
C | 1 | a0002c0002t0010g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2515+712_2515+733d others(24): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491446 | |||||||
| chr4:67491448 | T | G | 3 | a0001c0001t0005g0108 a0001c0001t0005g0155 a0001c0001t0005g0199 |
3 | HG00673.hp2 HG01175.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2515+732A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491448 | |||||||
| chr4:67491450 | T | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0159 a0001c0001t0005g0117 |
3 | NA19030.hp1 NA19086.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2515+730A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491450 | |||||||
| chr4:67491461 | A | ATATAGAG others(43): Show |
1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2515+718_2515+719i others(52): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491461 | |||||||
| chr4:67491464 | T | G | 4 | a0002c0002t0002g0022 a0002c0002t0002g0025 a0002c0002t0002g0034 others(1): Show |
4 | HG00323.hp2 NA18942.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+716A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491464 | |||||||
| chr4:67491464 | T | TAGAGAGA others(3): Show |
1 | a0002c0002t0002g0050 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2515+715_2515+716i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491464 | |||||||
| chr4:67491464 | T | TAGAGAGA others(59): Show |
1 | a0002c0002t0003g0085 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2515+715_2515+716i others(68): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491464 | |||||||
| chr4:67491465 | A | AGAGAGAG others(45): Show |
1 | a0002c0002t0003g0087 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2515+714_2515+715i others(54): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491465 | |||||||
| chr4:67491466 | T | G | 10 | a0001c0001t0001g0275 a0001c0001t0005g0199 a0002c0002t0002g0022 others(7): Show |
10 | HG00323.hp2 HG00558.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2515+714A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491466 | |||||||
| chr4:67491466 | T | TAGAGAGA others(1): Show |
3 | a0002c0002t0002g0021 a0002c0002t0002g0046 a0002c0002t0002g0047 |
3 | HG00408.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2515+713_2515+714i others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491466 | |||||||
| chr4:67491466 | T | TAGAGAGA others(3): Show |
2 | a0002c0002t0002g0030 a0002c0002t0002g0048 |
2 | HG03831.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.2515+713_2515+714i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491466 | |||||||
| chr4:67491466 | T | TAGAGAGA others(5): Show |
1 | a0002c0002t0002g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2515+713_2515+714i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491466 | |||||||
| chr4:67491466 | T | TAGAGAGA others(57): Show |
1 | a0002c0002t0003g0084 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2515+713_2515+714i others(66): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491466 | |||||||
| chr4:67491468 | T | G | 22 | a0001c0001t0001g0275 a0001c0001t0005g0151 a0001c0001t0005g0154 others(19): Show |
22 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2515+712A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491468 | |||||||
| chr4:67491468 | T | TAGAGAGA others(11): Show |
1 | a0002c0002t0003g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2515+711_2515+712i others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491468 | |||||||
| chr4:67491468 | T | TAGAGAGA others(59): Show |
1 | a0002c0002t0003g0081 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2515+711_2515+712i others(68): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491468 | |||||||
| chr4:67491468 | TATATATA others(7): Show |
T | 3 | a0001c0001t0004g0135 a0003c0003t0004g0139 a0003c0003t0004g0140 |
3 | HG01516.hp1 HG01517.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2515+698_2515+711d others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491468 | |||||||
| chr4:67491468 | TATATATA others(11): Show |
T | 1 | a0001c0001t0012g0255 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2515+694_2515+711d others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491468 | |||||||
| chr4:67491469 | A | AGAGAGAG others(43): Show |
1 | a0002c0002t0003g0083 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2515+710_2515+711i others(52): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491469 | |||||||
| chr4:67491470 | T | G | 45 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0188 others(42): Show |
46 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.2515+710A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | T | TAGAG | 5 | a0002c0002t0002g0002 a0002c0002t0002g0028 a0002c0002t0002g0054 others(2): Show |
6 | HG00099.hp2 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2515+709_2515+710i others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | T | TAGAGAGA others(3): Show |
3 | a0002c0002t0002g0041 a0002c0002t0003g0231 a0005c0005t0002g0063 |
3 | HG01167.hp1 HG01517.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2515+709_2515+710i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | T | TAGAGAGA others(5): Show |
2 | a0001c0001t0036g0325 a0002c0002t0002g0029 |
2 | HG01261.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2515+709_2515+710i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | T | TAGAGAGA others(7): Show |
1 | a0001c0001t0006g0323 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2515+709_2515+710i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | TATATATA others(5): Show |
T | 1 | a0001c0001t0019g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2515+698_2515+709d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0099 a0003c0003t0004g0247 |
2 | HG02300.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2515+696_2515+709d others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | TATATATA others(11): Show |
T | 1 | a0001c0001t0012g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2515+692_2515+709d others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491470 | TATATATA others(13): Show |
T | 1 | a0001c0001t0004g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2515+690_2515+709d others(22): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491470 | |||||||
| chr4:67491472 | T | G | 76 | a0001c0001t0001g0100 a0001c0001t0001g0120 a0001c0001t0001g0147 others(73): Show |
79 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2515+708A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | T | TAGAGAGA others(3): Show |
2 | a0001c0001t0037g0328 a0002c0002t0002g0040 |
2 | HG01975.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2515+707_2515+708i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | T | TAGAGAGA others(9): Show |
2 | a0001c0001t0001g0295 a0001c0001t0006g0326 |
2 | HG01123.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2515+707_2515+708i others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0261 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2515+707_2515+708i others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | T | TAGAGAGA others(15): Show |
1 | a0001c0001t0001g0291 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2515+707_2515+708i others(24): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | TATATATA others(3): Show |
T | 1 | a0001c0001t0004g0094 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2515+698_2515+707d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | TATATATA others(5): Show |
T | 3 | a0001c0001t0004g0127 a0003c0003t0004g0248 a0004c0004t0033g0320 |
3 | HG01167.hp2 HG01361.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2515+696_2515+707d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491472 | TATATATA others(9): Show |
T | 2 | a0001c0001t0004g0019 a0001c0001t0004g0020 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2515+692_2515+707d others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491472 | |||||||
| chr4:67491474 | T | G | 109 | a0001c0001t0001g0079 a0001c0001t0001g0100 a0001c0001t0001g0120 others(106): Show |
112 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2515+706A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(1): Show |
5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0002c0002t0002g0037 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.2515+705_2515+706i others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2515+705_2515+706i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0273 a0002c0002t0002g0039 a0002c0002t0003g0235 |
3 | HG03239.hp1 NA18906.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.2515+705_2515+706i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(9): Show |
2 | a0001c0001t0001g0271 a0005c0005t0002g0064 |
2 | HG02615.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2515+705_2515+706i others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0298 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2515+705_2515+706i others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(15): Show |
1 | a0001c0001t0001g0282 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2515+705_2515+706i others(24): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | T | TAGAGAGA others(53): Show |
1 | a0002c0002t0003g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2515+705_2515+706i others(62): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | TATATATA others(3): Show |
T | 2 | a0001c0001t0004g0004 a0001c0001t0004g0095 |
3 | HG01346.hp2 HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2515+696_2515+705d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | TATATATA others(5): Show |
T | 1 | a0001c0001t0004g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2515+694_2515+705d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491474 | TATATATA others(11): Show |
T | 1 | a0001c0001t0018g0268 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2515+688_2515+705d others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491474 | |||||||
| chr4:67491476 | T | G | 154 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(151): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2515+704A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAG | 3 | a0001c0001t0001g0287 a0002c0002t0003g0241 a0002c0002t0011g0044 |
3 | HG03540.hp1 NA18974.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2515+703_2515+704i others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAGA others(1): Show |
3 | a0002c0002t0002g0042 a0002c0002t0002g0058 a0002c0002t0003g0233 |
3 | HG04199.hp1 NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2515+703_2515+704i others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAGA others(3): Show |
1 | a0002c0002t0023g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2515+703_2515+704i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAGA others(5): Show |
2 | a0001c0001t0006g0324 a0002c0002t0003g0017 |
2 | HG01106.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2515+703_2515+704i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAGA others(7): Show |
2 | a0001c0001t0001g0272 a0001c0001t0006g0327 |
2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2515+703_2515+704i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | T | TAGAGAGA others(15): Show |
1 | a0001c0001t0006g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2515+703_2515+704i others(24): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491476 | TATATAGA others(3): Show |
T | 4 | a0001c0001t0004g0001 a0001c0001t0004g0121 a0001c0001t0004g0142 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2515+694_2515+703d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491476 | |||||||
| chr4:67491478 | T | G | 185 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.2515+702A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAG | 4 | a0002c0002t0002g0045 a0002c0002t0002g0061 a0002c0002t0003g0219 others(1): Show |
4 | HG00544.hp2 HG02896.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+701_2515+702i others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAGA others(5): Show |
3 | a0001c0001t0001g0256 a0001c0001t0001g0270 a0001c0001t0001g0290 |
3 | HG02040.hp1 HG02056.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2515+701_2515+702i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAGA others(7): Show |
1 | a0002c0002t0007g0073 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2515+701_2515+702i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAGA others(9): Show |
1 | a0001c0001t0001g0260 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2515+701_2515+702i others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAGA others(13): Show |
1 | a0001c0001t0001g0312 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2515+701_2515+702i others(22): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | T | TAGAGAGA others(19): Show |
1 | a0001c0001t0001g0292 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2515+701_2515+702i others(28): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | TATAGAGA others(3): Show |
T | 1 | a0001c0001t0004g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2515+692_2515+701d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491478 | TATAGAGA others(5): Show |
T | 1 | a0001c0001t0004g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2515+690_2515+701d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491478 | |||||||
| chr4:67491480 | T | G | 219 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2515+700A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TAGAGAGA others(3): Show |
4 | a0001c0001t0001g0286 a0001c0001t0001g0294 a0001c0001t0001g0309 others(1): Show |
4 | HG00408.hp2 HG02738.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+690_2515+699d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0288 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2515+688_2515+699d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TAGAGAGA others(7): Show |
2 | a0001c0001t0001g0289 a0002c0002t0007g0071 |
2 | HG03017.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.2515+686_2515+699d others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0297 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2515+682_2515+699d others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATAGAGA others(1): Show |
3 | a0001c0001t0001g0156 a0002c0002t0002g0036 a0002c0002t0011g0062 |
3 | HG03225.hp2 HG03927.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2515+699_2515+700i others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATAGAGA others(3): Show |
2 | a0001c0001t0001g0285 a0002c0014t0003g0240 |
2 | HG00438.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2515+699_2515+700i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATAGAGA others(5): Show |
2 | a0001c0001t0005g0115 a0002c0002t0007g0069 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2515+699_2515+700i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATAGAGA others(7): Show |
2 | a0001c0001t0001g0296 a0001c0001t0008g0305 |
2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2515+699_2515+700i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATAGAGA others(19): Show |
1 | a0001c0001t0001g0315 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2515+699_2515+700i others(28): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATAGA others(3): Show |
1 | a0001c0001t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2515+699_2515+700i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATAGA others(7): Show |
4 | a0001c0001t0001g0258 a0001c0001t0001g0269 a0001c0001t0001g0293 others(1): Show |
4 | HG01255.hp1 HG01496.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+699_2515+700i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATAGA others(13): Show |
1 | a0001c0001t0001g0307 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(22): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0304 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(7): Show |
1 | a0001c0001t0006g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2515+699_2515+700i others(20): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(17): Show |
1 | a0001c0001t0034g0314 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2515+699_2515+700i others(26): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0303 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(9): Show |
1 | a0002c0002t0003g0223 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0302 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2515+699_2515+700i others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | TAG | T | 3 | a0001c0001t0001g0283 a0002c0002t0003g0228 a0004c0004t0032g0277 |
3 | HG02717.hp1 HG04115.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.2515+698_2515+699d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | TAGAG | T | 3 | a0001c0001t0008g0265 a0004c0004t0001g0013 a0004c0004t0001g0278 |
3 | HG02818.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2515+696_2515+699d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0004g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2515+690_2515+699d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491480 | TAGAGAGA others(9): Show |
T | 1 | a0001c0001t0018g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2515+684_2515+699d others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491480 | |||||||
| chr4:67491482 | G | T | 10 | a0001c0001t0001g0300 a0001c0001t0001g0306 a0002c0002t0003g0007 others(7): Show |
12 | HG02280.hp1 HG02818.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.2515+698C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491482 | |||||||
| chr4:67491484 | G | T | 4 | a0002c0002t0003g0008 a0002c0002t0003g0228 a0009c0010t0017g0243 others(1): Show |
5 | HG02280.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2515+696C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491484 | |||||||
| chr4:67491486 | G | T | 3 | a0001c0001t0008g0265 a0002c0002t0003g0008 a0004c0004t0001g0278 |
4 | HG02280.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2515+694C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491486 | |||||||
| chr4:67491488 | G | T | 2 | a0001c0001t0008g0265 a0002c0002t0003g0236 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2515+692C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491488 | |||||||
| chr4:67491490 | G | T | 1 | a0001c0001t0008g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2515+690C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491490 | |||||||
| chr4:67491498 | G | T | 1 | a0001c0001t0018g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2515+682C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491498 | |||||||
| chr4:67491509 | A | G | 1 | a0001c0001t0005g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2515+671T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491509 | |||||||
| chr4:67491511 | A | AGAGAG | 3 | a0001c0001t0001g0103 a0001c0001t0009g0183 a0001c0001t0022g0197 |
3 | HG01258.hp2 HG02083.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2515+664_2515+668d others(7): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGAGAGAG others(4): Show |
1 | a0001c0001t0001g0194 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2515+658_2515+668d others(13): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGAGAGAG others(3): Show |
3 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0211 |
3 | HG02647.hp1 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2515+668_2515+669i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGAGAGAG others(1): Show |
14 | a0001c0001t0001g0124 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.2515+668_2515+669i others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGAGAGG | 25 | a0001c0001t0001g0125 a0001c0001t0001g0147 a0001c0001t0001g0163 others(22): Show |
25 | HG00423.hp2 HG01346.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.2515+668_2515+669i others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGAGG | 24 | a0001c0001t0001g0079 a0001c0001t0001g0102 a0001c0001t0001g0148 others(21): Show |
25 | HG00609.hp2 HG01256.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2515+668_2515+669i others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | AGG | 9 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0101 others(6): Show |
10 | HG00280.hp1 HG00544.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2515+668_2515+669i others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491511 | A | G | 22 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0104 others(19): Show |
22 | HG00673.hp2 HG00733.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2515+669T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491511 | |||||||
| chr4:67491513 | A | AGAGAGAG others(3): Show |
1 | a0001c0001t0013g0091 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2515+666_2515+667i others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491513 | |||||||
| chr4:67491517 | A | C | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2515+663T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491517 | |||||||
| chr4:67491519 | A | C | 1 | a0006c0009t0014g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2515+661T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491519 | |||||||
| chr4:67491521 | A | C | 4 | a0006c0009t0014g0245 a0006c0009t0014g0246 a0009c0010t0017g0243 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2515+659T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491521 | |||||||
| chr4:67491523 | A | C | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2515+657T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491523 | |||||||
| chr4:67491525 | A | AGAGAGAG others(5): Show |
1 | a0001c0001t0001g0281 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2515+654_2515+655i others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491525 | |||||||
| chr4:67491525 | A | C | 4 | a0006c0009t0014g0245 a0006c0009t0014g0246 a0009c0010t0017g0243 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2515+655T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491525 | |||||||
| chr4:67491527 | A | AGAGAGAG others(9): Show |
1 | a0002c0002t0002g0026 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2515+652_2515+653i others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491527 | |||||||
| chr4:67491527 | A | C | 39 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(36): Show |
42 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.2515+653T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491527 | |||||||
| chr4:67491634 | A | G | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2515+546T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491634 | |||||||
| chr4:67491849 | A | G | 1 | a0001c0001t0005g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2515+331T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67491849 | |||||||
| chr4:67492096 | A | G | 223 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(220): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2515+84T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 16/18 | chr4 | 67492096 | |||||||
| chr4:67492442 | A | G | 3 | a0002c0002t0002g0045 a0002c0002t0002g0058 a0002c0002t0011g0044 |
3 | NA18967.hp2 NA18974.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2420-167T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 15/18 | chr4 | 67492442 | |||||||
| chr4:67492568 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2420-293C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 15/18 | chr4 | 67492568 | |||||||
| chr4:67492572 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2419+297A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 15/18 | chr4 | 67492572 | |||||||
| chr4:67492613 | G | A | 223 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(220): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2419+256C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 15/18 | chr4 | 67492613 | |||||||
| chr4:67493263 | TA | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0207 a0001c0001t0001g0299 others(8): Show |
11 | HG01167.hp2 HG01255.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2291-267delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 14/18 | chr4 | 67493263 | |||||||
| chr4:67493499 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2290+385T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 14/18 | chr4 | 67493499 | |||||||
| chr4:67493733 | T | G | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2290+151A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 14/18 | chr4 | 67493733 | |||||||
| chr4:67493781 | G | A | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.2290+103C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 14/18 | chr4 | 67493781 | |||||||
| chr4:67494351 | G | A | 7 | a0002c0002t0003g0081 a0002c0002t0003g0082 a0002c0002t0003g0083 others(4): Show |
7 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2186-363C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494351 | |||||||
| chr4:67494388 | G | A | 7 | a0002c0002t0003g0081 a0002c0002t0003g0082 a0002c0002t0003g0083 others(4): Show |
7 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2186-400C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494388 | |||||||
| chr4:67494412 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2186-424G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494412 | |||||||
| chr4:67494587 | A | ATC | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2185+570_2185+571d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494587 | |||||||
| chr4:67494645 | C | T | 3 | a0004c0004t0001g0278 a0004c0004t0032g0277 a0004c0004t0033g0320 |
3 | HG02280.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2185+514G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494645 | |||||||
| chr4:67494717 | T | C | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2185+442A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494717 | |||||||
| chr4:67494838 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2185+321C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494838 | |||||||
| chr4:67494972 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2185+187G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494972 | |||||||
| chr4:67494976 | T | C | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2185+183A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 13/18 | chr4 | 67494976 | |||||||
| chr4:67495228 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2132-16C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495228 | |||||||
| chr4:67495232 | A | G | 3 | a0001c0001t0013g0090 a0001c0001t0013g0091 a0001c0001t0025g0251 |
3 | HG01884.hp2 HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2132-20T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495232 | |||||||
| chr4:67495237 | A | G | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2132-25T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495237 | |||||||
| chr4:67495303 | T | C | 1 | a0001c0001t0005g0152 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2132-91A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495303 | |||||||
| chr4:67495411 | G | T | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2132-199C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495411 | |||||||
| chr4:67495436 | C | T | 7 | a0002c0002t0003g0081 a0002c0002t0003g0082 a0002c0002t0003g0083 others(4): Show |
7 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.2132-224G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495436 | |||||||
| chr4:67495522 | C | T | 15 | a0001c0001t0004g0088 a0001c0001t0004g0133 a0001c0001t0004g0141 others(12): Show |
15 | HG00099.hp1 HG00140.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2132-310G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495522 | |||||||
| chr4:67495546 | G | A | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2132-334C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495546 | |||||||
| chr4:67495636 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2132-424C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495636 | |||||||
| chr4:67495783 | T | C | 4 | a0002c0002t0002g0034 a0002c0002t0002g0052 a0002c0002t0002g0053 others(1): Show |
4 | HG00323.hp2 HG01109.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2132-571A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495783 | |||||||
| chr4:67495866 | C | T | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2132-654G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67495866 | |||||||
| chr4:67496237 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0299 |
2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2132-1025A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496237 | |||||||
| chr4:67496243 | G | A | 1 | a0002c0002t0011g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2132-1031C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496243 | |||||||
| chr4:67496334 | T | C | 1 | a0001c0001t0004g0121 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2132-1122A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496334 | |||||||
| chr4:67496460 | C | G | 2 | a0001c0001t0004g0145 a0001c0001t0004g0146 |
2 | HG01943.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2132-1248G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496460 | |||||||
| chr4:67496486 | T | C | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2132-1274A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496486 | |||||||
| chr4:67496515 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2132-1303G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496515 | |||||||
| chr4:67496516 | A | G | 225 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(222): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2132-1304T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496516 | |||||||
| chr4:67496702 | G | T | 1 | a0002c0002t0024g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2132-1490C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496702 | |||||||
| chr4:67496730 | G | A | 1 | a0001c0001t0013g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2132-1518C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496730 | |||||||
| chr4:67496768 | T | G | 1 | a0005c0005t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2132-1556A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496768 | |||||||
| chr4:67496808 | CAT | C | 3 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0012t0012g0253 |
3 | HG02965.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2132-1598_2132-159 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496808 | |||||||
| chr4:67496858 | G | A | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1646C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496858 | |||||||
| chr4:67496860 | T | A | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1648A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496860 | |||||||
| chr4:67496861 | T | C | 282 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(279): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2132-1649A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496861 | |||||||
| chr4:67496863 | A | C | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1651T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496863 | |||||||
| chr4:67496865 | A | C | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1653T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496865 | |||||||
| chr4:67496866 | A | T | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1654T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496866 | |||||||
| chr4:67496870 | T | A | 1 | a0002c0002t0003g0086 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2132-1658A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496870 | |||||||
| chr4:67496896 | C | T | 3 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0026g0068 |
3 | HG02615.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2132-1684G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496896 | |||||||
| chr4:67496989 | G | A | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2132-1777C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67496989 | |||||||
| chr4:67497105 | C | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2132-1893G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497105 | |||||||
| chr4:67497221 | C | T | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2132-2009G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497221 | |||||||
| chr4:67497327 | G | A | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2132-2115C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497327 | |||||||
| chr4:67497356 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2132-2144G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497356 | |||||||
| chr4:67497372 | C | A | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2132-2160G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497372 | |||||||
| chr4:67497443 | T | TCCAGACT others(7): Show |
1 | a0002c0002t0024g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2132-2245_2132-223 others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497443 | |||||||
| chr4:67497469 | C | A | 1 | a0001c0001t0001g0292 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2132-2257G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497469 | |||||||
| chr4:67497471 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0293 others(4): Show |
7 | HG00280.hp2 HG01255.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.2132-2259C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497471 | |||||||
| chr4:67497666 | G | A | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2132-2454C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497666 | |||||||
| chr4:67497789 | A | C | 1 | a0001c0001t0004g0121 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2132-2577T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497789 | |||||||
| chr4:67497797 | GGT | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2587_2132-258 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497797 | |||||||
| chr4:67497801 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2589C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497801 | |||||||
| chr4:67497802 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2590G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497802 | |||||||
| chr4:67497804 | C | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2592G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497804 | |||||||
| chr4:67497806 | C | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2594G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497806 | |||||||
| chr4:67497807 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2595T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497807 | |||||||
| chr4:67497808 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2596T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497808 | |||||||
| chr4:67497809 | A | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2597T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497809 | |||||||
| chr4:67497822 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2610T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497822 | |||||||
| chr4:67497843 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2132-2631T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497843 | |||||||
| chr4:67497979 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2132-2767G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67497979 | |||||||
| chr4:67498107 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-2895A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498107 | |||||||
| chr4:67498136 | C | T | 3 | a0001c0001t0001g0173 a0007c0006t0001g0176 a0007c0006t0038g0177 |
3 | HG02486.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2132-2924G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498136 | |||||||
| chr4:67498137 | G | A | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2132-2925C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498137 | |||||||
| chr4:67498148 | C | T | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2132-2936G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498148 | |||||||
| chr4:67498173 | T | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2132-2961A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498173 | |||||||
| chr4:67498186 | G | A | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2132-2974C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498186 | |||||||
| chr4:67498194 | C | A | 1 | a0001c0001t0006g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2132-2982G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498194 | |||||||
| chr4:67498226 | C | A | 1 | a0001c0001t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2132-3014G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498226 | |||||||
| chr4:67498403 | C | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG00423.hp2 HG02083.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2132-3191G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498403 | |||||||
| chr4:67498571 | T | C | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2132-3359A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498571 | |||||||
| chr4:67498710 | C | T | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2132-3498G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498710 | |||||||
| chr4:67498803 | T | C | 110 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(107): Show |
112 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.2132-3591A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67498803 | |||||||
| chr4:67499297 | G | C | 1 | a0004c0004t0033g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2132-4085C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67499297 | |||||||
| chr4:67499300 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2132-4088G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67499300 | |||||||
| chr4:67499382 | A | T | 1 | a0002c0002t0007g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2132-4170T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67499382 | |||||||
| chr4:67499608 | G | A | 1 | a0008c0008t0015g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2132-4396C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67499608 | |||||||
| chr4:67499886 | G | T | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2132-4674C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67499886 | |||||||
| chr4:67500059 | AG | A | 4 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(1): Show |
4 | HG02965.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2132-4848delC | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500059 | |||||||
| chr4:67500114 | A | G | 1 | a0001c0001t0004g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2132-4902T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500114 | |||||||
| chr4:67500169 | A | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2132-4957T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500169 | |||||||
| chr4:67500437 | C | T | 1 | a0005c0005t0002g0063 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2131+4768G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500437 | |||||||
| chr4:67500585 | G | C | 1 | a0001c0001t0034g0314 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2131+4620C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500585 | |||||||
| chr4:67500619 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG00323.hp1 HG03927.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2131+4586G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500619 | |||||||
| chr4:67500620 | C | G | 221 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(218): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.2131+4585G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500620 | |||||||
| chr4:67500827 | G | C | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2131+4378C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500827 | |||||||
| chr4:67500828 | T | C | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2131+4377A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67500828 | |||||||
| chr4:67501086 | T | C | 2 | a0001c0001t0001g0276 a0011c0011t0001g0274 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2131+4119A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67501086 | |||||||
| chr4:67501192 | C | T | 6 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.2131+4013G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67501192 | |||||||
| chr4:67501541 | C | T | 2 | a0001c0001t0004g0088 a0002c0002t0002g0055 |
2 | HG00438.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2131+3664G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67501541 | |||||||
| chr4:67501832 | G | T | 1 | a0001c0001t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2131+3373C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67501832 | |||||||
| chr4:67501941 | A | AT | 294 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(291): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2131+3263dupA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67501941 | |||||||
| chr4:67502062 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2131+3143G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502062 | |||||||
| chr4:67502091 | A | G | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2131+3114T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502091 | |||||||
| chr4:67502092 | T | C | 5 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2131+3113A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502092 | |||||||
| chr4:67502319 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2131+2886G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502319 | |||||||
| chr4:67502325 | G | A | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2131+2880C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502325 | |||||||
| chr4:67502398 | TAAAG | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2131+2803_2131+280 others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502398 | |||||||
| chr4:67502706 | A | G | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2131+2499T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502706 | |||||||
| chr4:67502765 | T | C | 1 | a0001c0001t0004g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2131+2440A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502765 | |||||||
| chr4:67502925 | C | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2131+2280G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502925 | |||||||
| chr4:67502937 | A | C | 2 | a0001c0001t0004g0019 a0001c0001t0004g0020 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2131+2268T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67502937 | |||||||
| chr4:67503079 | C | G | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG00738.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2131+2126G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503079 | |||||||
| chr4:67503159 | A | C | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2131+2046T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503159 | |||||||
| chr4:67503421 | C | T | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2131+1784G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503421 | |||||||
| chr4:67503456 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2131+1749T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503456 | |||||||
| chr4:67503713 | C | G | 3 | a0005c0005t0002g0063 a0005c0005t0002g0064 a0005c0005t0002g0065 |
3 | HG01167.hp1 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2131+1492G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503713 | |||||||
| chr4:67503831 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2131+1374A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503831 | |||||||
| chr4:67503958 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2131+1247A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503958 | |||||||
| chr4:67503972 | T | C | 1 | a0002c0002t0003g0220 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2131+1233A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67503972 | |||||||
| chr4:67504087 | T | C | 1 | a0001c0001t0004g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2131+1118A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504087 | |||||||
| chr4:67504092 | C | CA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0173 a0001c0001t0004g0018 others(8): Show |
11 | HG01081.hp2 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.2131+1112dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504092 | |||||||
| chr4:67504092 | C | CAA | 206 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(203): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2131+1111_2131+111 others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504092 | |||||||
| chr4:67504092 | C | CAAA | 9 | a0001c0001t0001g0156 a0001c0001t0001g0202 a0001c0001t0001g0295 others(6): Show |
9 | HG00621.hp1 HG01884.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.2131+1110_2131+111 others(7): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504092 | |||||||
| chr4:67504092 | CA | C | 8 | a0002c0002t0002g0037 a0002c0002t0003g0081 a0002c0002t0003g0082 others(5): Show |
8 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.2131+1112delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504092 | |||||||
| chr4:67504173 | C | G | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2131+1032G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504173 | |||||||
| chr4:67504242 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2131+963T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504242 | |||||||
| chr4:67504245 | A | G | 1 | a0001c0001t0013g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2131+960T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504245 | |||||||
| chr4:67504250 | T | C | 15 | a0002c0002t0003g0007 a0002c0002t0003g0017 a0002c0002t0003g0219 others(12): Show |
16 | HG00544.hp2 HG01106.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.2131+955A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504250 | |||||||
| chr4:67504260 | A | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0102 others(19): Show |
22 | HG00280.hp1 HG01256.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2131+945T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504260 | |||||||
| chr4:67504322 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2131+883T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504322 | |||||||
| chr4:67504553 | G | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2131+652C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504553 | |||||||
| chr4:67504620 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2131+585C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504620 | |||||||
| chr4:67504830 | A | T | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2131+375T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 12/18 | chr4 | 67504830 | |||||||
| chr4:67505456 | A | G | 7 | a0002c0002t0007g0016 a0002c0002t0007g0069 a0002c0002t0007g0070 others(4): Show |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.2052-172T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67505456 | |||||||
| chr4:67505515 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2052-231A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67505515 | |||||||
| chr4:67505622 | T | A | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2052-338A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67505622 | |||||||
| chr4:67505989 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2052-705C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67505989 | |||||||
| chr4:67506016 | C | T | 1 | a0001c0001t0006g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2052-732G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506016 | |||||||
| chr4:67506127 | C | T | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2051+661G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506127 | |||||||
| chr4:67506224 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2051+564C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506224 | |||||||
| chr4:67506292 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2051+496A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506292 | |||||||
| chr4:67506463 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2051+325A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506463 | |||||||
| chr4:67506474 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2051+314G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506474 | |||||||
| chr4:67506547 | G | T | 1 | a0002c0002t0002g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2051+241C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506547 | |||||||
| chr4:67506658 | G | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2051+130C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506658 | |||||||
| chr4:67506662 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0189 |
2 | NA18960.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2051+126A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 11/18 | chr4 | 67506662 | |||||||
| chr4:67507112 | T | C | 5 | a0002c0002t0007g0016 a0002c0002t0007g0070 a0002c0002t0007g0071 others(2): Show |
5 | HG03017.hp2 HG03704.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1905-178A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507112 | |||||||
| chr4:67507262 | A | ACC | 71 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(68): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1905-329_1905-328i others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507262 | |||||||
| chr4:67507531 | A | C | 1 | a0002c0002t0003g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1905-597T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507531 | |||||||
| chr4:67507548 | A | T | 1 | a0001c0001t0031g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1905-614T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507548 | |||||||
| chr4:67507552 | T | C | 2 | a0002c0002t0003g0007 a0002c0002t0003g0234 |
3 | NA18944.hp1 NA18971.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1905-618A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507552 | |||||||
| chr4:67507560 | T | C | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1905-626A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507560 | |||||||
| chr4:67507623 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1905-689A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507623 | |||||||
| chr4:67507762 | T | C | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1905-828A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507762 | |||||||
| chr4:67507904 | G | A | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1904+910C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67507904 | |||||||
| chr4:67508025 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1904+789A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508025 | |||||||
| chr4:67508059 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1904+755A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508059 | |||||||
| chr4:67508483 | G | A | 1 | a0001c0001t0005g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1904+331C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508483 | |||||||
| chr4:67508513 | T | TA | 55 | a0001c0001t0001g0100 a0001c0001t0001g0147 a0001c0001t0005g0155 others(52): Show |
57 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1904+300dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508513 | |||||||
| chr4:67508513 | T | TAA | 122 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(119): Show |
124 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1904+299_1904+300d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508513 | |||||||
| chr4:67508513 | T | TAAA | 68 | a0001c0001t0001g0099 a0001c0001t0001g0256 a0001c0001t0001g0258 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1904+298_1904+300d others(5): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508513 | |||||||
| chr4:67508513 | T | TAAAA | 33 | a0001c0001t0001g0296 a0001c0001t0004g0001 a0001c0001t0004g0004 others(30): Show |
36 | HG00099.hp1 HG00423.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1904+297_1904+300d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508513 | |||||||
| chr4:67508513 | T | TAAAAA | 8 | a0001c0001t0004g0020 a0001c0001t0004g0092 a0001c0001t0004g0097 others(5): Show |
8 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904+296_1904+300d others(7): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508513 | |||||||
| chr4:67508543 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1904+271G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508543 | |||||||
| chr4:67508660 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1904+154A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 10/18 | chr4 | 67508660 | |||||||
| chr4:67509207 | T | TAC | 13 | a0002c0002t0003g0007 a0002c0002t0003g0017 a0002c0002t0003g0222 others(10): Show |
14 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1613-104_1613-103d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | T | TACAC | 7 | a0002c0002t0003g0221 a0002c0002t0003g0229 a0002c0002t0003g0230 others(4): Show |
7 | HG01515.hp1 HG01517.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613-106_1613-103d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TAC | T | 18 | a0002c0002t0002g0034 a0002c0002t0002g0051 a0002c0002t0002g0052 others(15): Show |
18 | HG00323.hp2 HG00438.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1613-104_1613-103d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACAC | T | 39 | a0001c0001t0006g0323 a0001c0001t0021g0250 a0002c0002t0002g0003 others(36): Show |
41 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1613-106_1613-103d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACAC | T | 27 | a0001c0001t0001g0198 a0001c0001t0001g0299 a0001c0001t0001g0315 others(24): Show |
28 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1613-108_1613-103d others(8): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACACA others(1): Show |
T | 40 | a0001c0001t0001g0104 a0001c0001t0001g0191 a0001c0001t0001g0192 others(37): Show |
40 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1613-110_1613-103d others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACACA others(3): Show |
T | 145 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(142): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1613-112_1613-103d others(12): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACACA others(5): Show |
T | 15 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0213 others(12): Show |
15 | HG00597.hp1 HG02040.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.1613-114_1613-103d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACACA others(7): Show |
T | 3 | a0001c0001t0005g0155 a0001c0001t0006g0279 a0001c0001t0025g0251 |
3 | HG00140.hp1 HG01891.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1613-116_1613-103d others(16): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509207 | TACACACA others(9): Show |
T | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1613-118_1613-103d others(18): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509207 | |||||||
| chr4:67509255 | C | T | 3 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0002c0002t0002g0059 |
3 | HG00738.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1613-150G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509255 | |||||||
| chr4:67509402 | A | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1613-297T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509402 | |||||||
| chr4:67509456 | T | C | 2 | a0001c0001t0005g0200 a0002c0002t0007g0073 |
2 | HG03927.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1613-351A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509456 | |||||||
| chr4:67509460 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1613-355G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509460 | |||||||
| chr4:67509470 | T | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1613-365A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509470 | |||||||
| chr4:67509718 | TTAG | T | 7 | a0002c0002t0007g0016 a0002c0002t0007g0069 a0002c0002t0007g0070 others(4): Show |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1613-616_1613-614d others(5): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67509718 | |||||||
| chr4:67510349 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1613-1244C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510349 | |||||||
| chr4:67510593 | G | A | 1 | a0010c0007t0001g0006 | 2 | NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1613-1488C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510593 | |||||||
| chr4:67510761 | G | A | 2 | a0003c0003t0004g0139 a0003c0003t0004g0140 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1612+1641C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510761 | |||||||
| chr4:67510882 | A | G | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1612+1520T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510882 | |||||||
| chr4:67510922 | G | C | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1612+1480C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510922 | |||||||
| chr4:67510990 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1612+1412A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67510990 | |||||||
| chr4:67511073 | C | T | 7 | a0002c0002t0007g0016 a0002c0002t0007g0069 a0002c0002t0007g0070 others(4): Show |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612+1329G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511073 | |||||||
| chr4:67511408 | C | T | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.1612+994G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511408 | |||||||
| chr4:67511596 | G | T | 8 | a0003c0003t0004g0131 a0003c0003t0004g0132 a0003c0003t0004g0137 others(5): Show |
8 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1612+806C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511596 | |||||||
| chr4:67511632 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1612+770C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511632 | |||||||
| chr4:67511754 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1612+648T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511754 | |||||||
| chr4:67511917 | G | A | 1 | a0002c0002t0002g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1612+485C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511917 | |||||||
| chr4:67511993 | T | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1612+409A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67511993 | |||||||
| chr4:67512256 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | NA18968.hp1 NA18982.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612+146A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 9/18 | chr4 | 67512256 | |||||||
| chr4:67512668 | T | A | 1 | a0001c0001t0005g0080 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1445-99A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67512668 | |||||||
| chr4:67512741 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1445-172C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67512741 | |||||||
| chr4:67512755 | T | C | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1445-186A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67512755 | |||||||
| chr4:67512801 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1445-232A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67512801 | |||||||
| chr4:67513200 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1445-631A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513200 | |||||||
| chr4:67513203 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1445-634G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513203 | |||||||
| chr4:67513213 | G | A | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1445-644C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513213 | |||||||
| chr4:67513268 | T | TG | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1445-700dupC | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513268 | |||||||
| chr4:67513332 | A | C | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1444+742T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513332 | |||||||
| chr4:67513334 | T | A | 1 | a0001c0001t0001g0311 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1444+740A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513334 | |||||||
| chr4:67513372 | T | C | 1 | a0002c0002t0002g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1444+702A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513372 | |||||||
| chr4:67513373 | T | C | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1444+701A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513373 | |||||||
| chr4:67513406 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1444+668A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513406 | |||||||
| chr4:67513466 | T | C | 1 | a0002c0002t0003g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1444+608A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513466 | |||||||
| chr4:67513471 | C | T | 2 | a0001c0001t0005g0115 a0001c0001t0005g0116 |
2 | HG00621.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1444+603G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513471 | |||||||
| chr4:67513537 | G | T | 7 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | HG00733.hp2 HG01070.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+537C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513537 | |||||||
| chr4:67513540 | T | C | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1444+534A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513540 | |||||||
| chr4:67513581 | A | G | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1444+493T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513581 | |||||||
| chr4:67513659 | T | C | 1 | a0002c0002t0003g0234 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1444+415A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513659 | |||||||
| chr4:67513856 | T | G | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444+218A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513856 | |||||||
| chr4:67513859 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1444+215T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513859 | |||||||
| chr4:67513895 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1444+179A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513895 | |||||||
| chr4:67513906 | A | G | 10 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(7): Show |
10 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1444+168T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67513906 | |||||||
| chr4:67514048 | T | C | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1444+26A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 8/18 | chr4 | 67514048 | |||||||
| chr4:67514739 | T | A | 1 | a0002c0002t0002g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.831-52A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67514739 | |||||||
| chr4:67514926 | T | C | 1 | a0001c0001t0037g0328 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.831-239A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67514926 | |||||||
| chr4:67514990 | C | T | 1 | a0002c0002t0020g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.831-303G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67514990 | |||||||
| chr4:67515006 | C | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.831-319G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515006 | |||||||
| chr4:67515056 | A | G | 1 | a0001c0001t0005g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.831-369T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515056 | |||||||
| chr4:67515057 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.831-370A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515057 | |||||||
| chr4:67515079 | G | A | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.831-392C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515079 | |||||||
| chr4:67515180 | AGGAGGCC others(2409): Show |
A | 4 | a0006c0009t0014g0245 a0006c0009t0014g0246 a0009c0010t0017g0243 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.830+560_831-494del | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515180 | |||||||
| chr4:67515242 | G | T | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.831-555C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515242 | |||||||
| chr4:67515258 | G | C | 1 | a0001c0001t0006g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.831-571C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515258 | |||||||
| chr4:67515497 | G | A | 4 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(1): Show |
4 | HG02083.hp1 NA18966.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-810C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515497 | |||||||
| chr4:67515501 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.831-814C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515501 | |||||||
| chr4:67515504 | G | C | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.831-817C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515504 | |||||||
| chr4:67515649 | T | C | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.831-962A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515649 | |||||||
| chr4:67515716 | T | C | 220 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(217): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.831-1029A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515716 | |||||||
| chr4:67515750 | T | C | 1 | a0001c0001t0005g0310 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.831-1063A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515750 | |||||||
| chr4:67515923 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.831-1236A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515923 | |||||||
| chr4:67515929 | T | C | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.831-1242A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67515929 | |||||||
| chr4:67516485 | A | G | 1 | a0001c0001t0005g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.830+1671T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67516485 | |||||||
| chr4:67516528 | C | T | 1 | a0002c0002t0011g0322 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.830+1628G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67516528 | |||||||
| chr4:67516536 | C | T | 1 | a0002c0002t0023g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.830+1620G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67516536 | |||||||
| chr4:67516667 | A | G | 220 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(217): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.830+1489T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67516667 | |||||||
| chr4:67516918 | T | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.830+1238A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67516918 | |||||||
| chr4:67517119 | C | A | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.830+1037G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517119 | |||||||
| chr4:67517414 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG00597.hp2 HG02129.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.830+742C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517414 | |||||||
| chr4:67517423 | A | G | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.830+733T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517423 | |||||||
| chr4:67517520 | C | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.830+636G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517520 | |||||||
| chr4:67517560 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.830+596C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517560 | |||||||
| chr4:67517575 | A | T | 220 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(217): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.830+581T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517575 | |||||||
| chr4:67517626 | T | A | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.830+530A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517626 | |||||||
| chr4:67517635 | C | T | 1 | a0003c0003t0004g0247 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.830+521G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517635 | |||||||
| chr4:67517699 | G | A | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG00738.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.830+457C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517699 | |||||||
| chr4:67517730 | C | T | 1 | a0001c0001t0035g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.830+426G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517730 | |||||||
| chr4:67517755 | T | G | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.830+401A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517755 | |||||||
| chr4:67517849 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.830+307A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 7/18 | chr4 | 67517849 | |||||||
| chr4:67518405 | G | A | 1 | a0005c0005t0002g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.618-37C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518405 | |||||||
| chr4:67518410 | G | A | 1 | a0001c0001t0005g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.618-42C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518410 | |||||||
| chr4:67518422 | A | G | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.618-54T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518422 | |||||||
| chr4:67518504 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.618-136G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518504 | |||||||
| chr4:67518539 | C | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.618-171G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518539 | |||||||
| chr4:67518556 | T | C | 17 | a0001c0001t0004g0088 a0001c0001t0004g0133 a0001c0001t0004g0141 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.618-188A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518556 | |||||||
| chr4:67518882 | C | A | 1 | a0001c0001t0005g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.617+335G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518882 | |||||||
| chr4:67518884 | C | G | 105 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(102): Show |
107 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.617+333G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518884 | |||||||
| chr4:67518894 | C | T | 1 | a0001c0001t0018g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.617+323G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67518894 | |||||||
| chr4:67519004 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.617+213A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67519004 | |||||||
| chr4:67519097 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.617+120A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67519097 | |||||||
| chr4:67519143 | G | T | 220 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(217): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.617+74C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 6/18 | chr4 | 67519143 | |||||||
| chr4:67519654 | T | C | 17 | a0001c0001t0004g0088 a0001c0001t0004g0133 a0001c0001t0004g0141 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-152A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67519654 | |||||||
| chr4:67519751 | A | G | 1 | a0001c0001t0004g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.332-249T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67519751 | |||||||
| chr4:67520057 | C | T | 13 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(10): Show |
16 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-555G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520057 | |||||||
| chr4:67520102 | G | A | 57 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(54): Show |
59 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.332-600C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520102 | |||||||
| chr4:67520179 | C | T | 5 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-677G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520179 | |||||||
| chr4:67520364 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-862A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520364 | |||||||
| chr4:67520504 | C | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.332-1002G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520504 | |||||||
| chr4:67520510 | C | T | 73 | a0001c0001t0001g0204 a0001c0001t0001g0256 a0001c0001t0001g0258 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.332-1008G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520510 | |||||||
| chr4:67520848 | C | T | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-1346G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67520848 | |||||||
| chr4:67521022 | C | CAAAT | 7 | a0002c0002t0002g0042 a0002c0002t0002g0060 a0002c0002t0003g0081 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-1524_332-1521d others(6): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521022 | |||||||
| chr4:67521022 | C | CAAATAAA others(1): Show |
53 | a0002c0002t0002g0003 a0002c0002t0002g0021 a0002c0002t0002g0022 others(50): Show |
54 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.332-1528_332-1521d others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521022 | |||||||
| chr4:67521022 | C | CAAATAAA others(5): Show |
2 | a0002c0002t0002g0002 a0002c0002t0002g0035 |
3 | NA18977.hp1 NA18988.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.332-1532_332-1521d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521022 | |||||||
| chr4:67521022 | CAAATAAA others(1): Show |
C | 5 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-1528_332-1521d others(10): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521022 | |||||||
| chr4:67521022 | CAAATAAA others(5): Show |
C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-1532_332-1521d others(14): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521022 | |||||||
| chr4:67521038 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-1536A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521038 | |||||||
| chr4:67521106 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.332-1604A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521106 | |||||||
| chr4:67521204 | C | CA | 283 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(280): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.332-1703dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521204 | |||||||
| chr4:67521277 | CAAT | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.332-1778_332-1776d others(5): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521277 | |||||||
| chr4:67521343 | T | C | 73 | a0001c0001t0001g0204 a0001c0001t0001g0256 a0001c0001t0001g0258 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.332-1841A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521343 | |||||||
| chr4:67521585 | T | A | 2 | a0002c0002t0003g0081 a0002c0002t0003g0082 |
2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.332-2083A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521585 | |||||||
| chr4:67521643 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-2141G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521643 | |||||||
| chr4:67521989 | G | A | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332-2487C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67521989 | |||||||
| chr4:67522566 | G | C | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332-3064C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522566 | |||||||
| chr4:67522594 | T | C | 56 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(53): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.332-3092A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522594 | |||||||
| chr4:67522678 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.332-3176C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522678 | |||||||
| chr4:67522766 | A | G | 325 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(322): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.332-3264T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522766 | |||||||
| chr4:67522817 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.332-3315A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522817 | |||||||
| chr4:67522831 | C | T | 2 | a0005c0005t0002g0063 a0005c0005t0002g0064 |
2 | HG01167.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.332-3329G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522831 | |||||||
| chr4:67522870 | T | C | 288 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.332-3368A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67522870 | |||||||
| chr4:67523223 | G | T | 3 | a0001c0001t0005g0112 a0001c0001t0005g0113 a0001c0001t0009g0114 |
3 | NA19007.hp1 NA19009.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.332-3721C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523223 | |||||||
| chr4:67523261 | C | T | 13 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(10): Show |
16 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-3759G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523261 | |||||||
| chr4:67523264 | G | T | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.332-3762C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523264 | |||||||
| chr4:67523269 | C | T | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.332-3767G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523269 | |||||||
| chr4:67523303 | A | ACT | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-3803_332-3802d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523303 | |||||||
| chr4:67523653 | T | TAC | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.332-4153_332-4152d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67523653 | |||||||
| chr4:67524095 | C | T | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.332-4593G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524095 | |||||||
| chr4:67524123 | C | T | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.332-4621G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524123 | |||||||
| chr4:67524367 | GGAAGAGA | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-4872_332-4866d others(9): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524367 | |||||||
| chr4:67524433 | C | T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.332-4931G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524433 | |||||||
| chr4:67524534 | C | T | 1 | a0001c0001t0006g0323 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.332-5032G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524534 | |||||||
| chr4:67524623 | C | A | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332-5121G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524623 | |||||||
| chr4:67524733 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.332-5231A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67524733 | |||||||
| chr4:67525230 | G | A | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.331+5585C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525230 | |||||||
| chr4:67525253 | G | A | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+5562C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525253 | |||||||
| chr4:67525302 | G | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+5513C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525302 | |||||||
| chr4:67525508 | T | C | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.331+5307A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525508 | |||||||
| chr4:67525654 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+5161A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525654 | |||||||
| chr4:67525884 | C | T | 1 | a0004c0004t0033g0320 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+4931G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525884 | |||||||
| chr4:67525963 | G | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+4852C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67525963 | |||||||
| chr4:67526076 | A | C | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.331+4739T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526076 | |||||||
| chr4:67526139 | G | A | 5 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+4676C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526139 | |||||||
| chr4:67526167 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.331+4648C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526167 | |||||||
| chr4:67526203 | CA | C | 11 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0035 others(8): Show |
13 | HG02132.hp1 NA18975.hp1 NA18977.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+4611delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526203 | |||||||
| chr4:67526231 | A | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+4584T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526231 | |||||||
| chr4:67526266 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+4549A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526266 | |||||||
| chr4:67526335 | A | G | 1 | a0001c0001t0005g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.331+4480T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526335 | |||||||
| chr4:67526338 | AT | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+4476delA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526338 | |||||||
| chr4:67526339 | T | A | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.331+4476A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526339 | |||||||
| chr4:67526824 | T | C | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.331+3991A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526824 | |||||||
| chr4:67526934 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.331+3881C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526934 | |||||||
| chr4:67526959 | A | T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.331+3856T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67526959 | |||||||
| chr4:67527279 | T | A | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.331+3536A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527279 | |||||||
| chr4:67527329 | G | A | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.331+3486C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527329 | |||||||
| chr4:67527395 | T | G | 1 | a0001c0001t0004g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331+3420A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527395 | |||||||
| chr4:67527471 | A | T | 1 | a0001c0001t0005g0111 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.331+3344T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527471 | |||||||
| chr4:67527472 | C | G | 295 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.331+3343G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527472 | |||||||
| chr4:67527493 | C | CTT | 58 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0022 others(55): Show |
60 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.331+3320_331+3321d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527493 | |||||||
| chr4:67527493 | CT | C | 96 | a0001c0001t0001g0126 a0001c0001t0001g0156 a0001c0001t0001g0207 others(93): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.331+3321delA | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527493 | |||||||
| chr4:67527493 | CTT | C | 115 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(112): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.331+3320_331+3321d others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527493 | |||||||
| chr4:67527700 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.331+3115A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527700 | |||||||
| chr4:67527896 | C | T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.331+2919G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527896 | |||||||
| chr4:67527901 | A | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+2914T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67527901 | |||||||
| chr4:67528182 | C | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+2633G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528182 | |||||||
| chr4:67528292 | C | T | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.331+2523G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528292 | |||||||
| chr4:67528347 | T | G | 1 | a0001c0001t0005g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.331+2468A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528347 | |||||||
| chr4:67528532 | T | A | 1 | a0001c0001t0005g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.331+2283A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528532 | |||||||
| chr4:67528724 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.331+2091G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528724 | |||||||
| chr4:67528846 | T | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.331+1969A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528846 | |||||||
| chr4:67528906 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+1909A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528906 | |||||||
| chr4:67528999 | A | G | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+1816T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67528999 | |||||||
| chr4:67529175 | G | A | 7 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0207 others(4): Show |
7 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+1640C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529175 | |||||||
| chr4:67529328 | A | C | 1 | a0002c0002t0002g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.331+1487T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529328 | |||||||
| chr4:67529347 | C | T | 1 | a0002c0002t0011g0322 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.331+1468G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529347 | |||||||
| chr4:67529489 | C | A | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.331+1326G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529489 | |||||||
| chr4:67529508 | T | A | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.331+1307A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529508 | |||||||
| chr4:67529511 | A | G | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.331+1304T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529511 | |||||||
| chr4:67529580 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.331+1235G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529580 | |||||||
| chr4:67529705 | C | T | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.331+1110G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529705 | |||||||
| chr4:67529914 | A | C | 1 | a0001c0001t0005g0080 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.331+901T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529914 | |||||||
| chr4:67529914 | AAAGT | A | 14 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(11): Show |
14 | HG00408.hp2 HG02083.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+897_331+900del others(4): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67529914 | |||||||
| chr4:67530059 | C | T | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331+756G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530059 | |||||||
| chr4:67530064 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.331+751G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530064 | |||||||
| chr4:67530071 | C | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+744G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530071 | |||||||
| chr4:67530077 | A | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.331+738T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530077 | |||||||
| chr4:67530229 | G | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+586C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530229 | |||||||
| chr4:67530413 | C | T | 7 | a0002c0002t0003g0081 a0002c0002t0003g0082 a0002c0002t0003g0083 others(4): Show |
7 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+402G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530413 | |||||||
| chr4:67530417 | C | G | 5 | a0002c0002t0007g0016 a0002c0002t0007g0070 a0002c0002t0007g0071 others(2): Show |
5 | HG03017.hp2 HG03704.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+398G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530417 | |||||||
| chr4:67530454 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.331+361A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530454 | |||||||
| chr4:67530587 | A | G | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.331+228T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530587 | |||||||
| chr4:67530669 | A | T | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.331+146T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530669 | |||||||
| chr4:67530807 | G | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
splice_region_variant&intron_variant | LOW | c.331+8C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 5/18 | chr4 | 67530807 | |||||||
| chr4:67531232 | G | A | 1 | a0001c0001t0004g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.232-318C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531232 | |||||||
| chr4:67531280 | C | G | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.232-366G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531280 | |||||||
| chr4:67531312 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.232-398G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531312 | |||||||
| chr4:67531354 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.232-440A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531354 | |||||||
| chr4:67531421 | C | T | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0029 others(5): Show |
8 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.232-507G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531421 | |||||||
| chr4:67531455 | C | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0088 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.232-541G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531455 | |||||||
| chr4:67531738 | A | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-824T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531738 | |||||||
| chr4:67531738 | A | G | 218 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(215): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.232-824T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531738 | |||||||
| chr4:67531933 | T | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-1019A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67531933 | |||||||
| chr4:67532132 | G | A | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.232-1218C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532132 | |||||||
| chr4:67532274 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-1360A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532274 | |||||||
| chr4:67532312 | G | T | 188 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(185): Show |
190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.232-1398C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532312 | |||||||
| chr4:67532340 | A | G | 126 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(123): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.232-1426T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532340 | |||||||
| chr4:67532344 | G | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-1430C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532344 | |||||||
| chr4:67532480 | A | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.232-1566T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532480 | |||||||
| chr4:67532646 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232-1732C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532646 | |||||||
| chr4:67532767 | A | G | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.232-1853T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532767 | |||||||
| chr4:67532861 | C | T | 1 | a0009c0010t0017g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.232-1947G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67532861 | |||||||
| chr4:67533045 | A | G | 229 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(226): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.232-2131T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533045 | |||||||
| chr4:67533170 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.232-2256A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533170 | |||||||
| chr4:67533206 | C | G | 3 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0027g0107 |
3 | HG00673.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.232-2292G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533206 | |||||||
| chr4:67533600 | T | C | 2 | a0009c0010t0017g0243 a0009c0010t0017g0244 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.232-2686A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533600 | |||||||
| chr4:67533749 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-2835T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533749 | |||||||
| chr4:67533888 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232-2974T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67533888 | |||||||
| chr4:67534028 | T | C | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.232-3114A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534028 | |||||||
| chr4:67534064 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-3150A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534064 | |||||||
| chr4:67534119 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG00597.hp1 HG00597.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-3205C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534119 | |||||||
| chr4:67534123 | G | C | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.232-3209C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534123 | |||||||
| chr4:67534346 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-3432C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534346 | |||||||
| chr4:67534347 | C | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-3433G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534347 | |||||||
| chr4:67534378 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-3464A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534378 | |||||||
| chr4:67534675 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.232-3761C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534675 | |||||||
| chr4:67534785 | G | C | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.232-3871C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534785 | |||||||
| chr4:67534921 | T | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.232-4007A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67534921 | |||||||
| chr4:67535028 | T | A | 1 | a0001c0001t0025g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.232-4114A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535028 | |||||||
| chr4:67535460 | C | T | 35 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0018 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.231+4380G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535460 | |||||||
| chr4:67535481 | A | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.231+4359T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535481 | |||||||
| chr4:67535520 | C | G | 5 | a0002c0002t0003g0219 a0002c0002t0003g0220 a0002c0002t0003g0221 others(2): Show |
5 | HG00544.hp2 NA18957.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+4320G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535520 | |||||||
| chr4:67535520 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.231+4320G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535520 | |||||||
| chr4:67535541 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18982.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.231+4299C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535541 | |||||||
| chr4:67535623 | A | T | 1 | a0002c0002t0024g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.231+4217T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535623 | |||||||
| chr4:67535732 | T | A | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.231+4108A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535732 | |||||||
| chr4:67535738 | T | C | 7 | a0002c0002t0003g0081 a0002c0002t0003g0082 a0002c0002t0003g0083 others(4): Show |
7 | HG00733.hp1 HG02735.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+4102A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535738 | |||||||
| chr4:67535828 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.231+4012C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535828 | |||||||
| chr4:67535836 | A | T | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.231+4004T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67535836 | |||||||
| chr4:67536060 | G | A | 106 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(103): Show |
108 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.231+3780C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536060 | |||||||
| chr4:67536178 | T | C | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.231+3662A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536178 | |||||||
| chr4:67536248 | T | C | 4 | a0002c0002t0002g0061 a0002c0002t0002g0066 a0002c0002t0002g0067 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+3592A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536248 | |||||||
| chr4:67536276 | T | TA | 4 | a0006c0009t0014g0245 a0006c0009t0014g0246 a0009c0010t0017g0243 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+3563dupT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536276 | |||||||
| chr4:67536288 | T | C | 8 | a0001c0001t0001g0315 a0001c0001t0006g0323 a0001c0001t0006g0324 others(5): Show |
8 | HG01123.hp1 HG01943.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.231+3552A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536288 | |||||||
| chr4:67536607 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.231+3233T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67536607 | |||||||
| chr4:67537027 | TA | T | 12 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0124 others(9): Show |
12 | HG00280.hp1 HG01070.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+2812delT | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537027 | |||||||
| chr4:67537104 | C | T | 4 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(1): Show |
4 | HG00621.hp2 NA18942.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+2736G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537104 | |||||||
| chr4:67537244 | A | C | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.231+2596T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537244 | |||||||
| chr4:67537249 | A | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.231+2591T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537249 | |||||||
| chr4:67537256 | A | T | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.231+2584T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537256 | |||||||
| chr4:67537384 | C | T | 14 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0005g0111 others(11): Show |
14 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.231+2456G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537384 | |||||||
| chr4:67537502 | T | A | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.231+2338A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537502 | |||||||
| chr4:67537521 | G | A | 224 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0098 others(221): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.231+2319C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537521 | |||||||
| chr4:67537608 | C | A | 1 | a0001c0001t0018g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.231+2232G>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537608 | |||||||
| chr4:67537718 | C | T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+2122G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67537718 | |||||||
| chr4:67538042 | T | G | 31 | a0002c0002t0003g0007 a0002c0002t0003g0008 a0002c0002t0003g0009 others(28): Show |
34 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.231+1798A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67538042 | |||||||
| chr4:67538314 | T | C | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+1526A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67538314 | |||||||
| chr4:67538367 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.231+1473T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67538367 | |||||||
| chr4:67538729 | G | A | 62 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(59): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.231+1111C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67538729 | |||||||
| chr4:67538971 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.231+869A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67538971 | |||||||
| chr4:67539052 | A | G | 1 | a0002c0002t0007g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.231+788T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539052 | |||||||
| chr4:67539119 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.231+721G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539119 | |||||||
| chr4:67539120 | T | G | 1 | a0002c0002t0002g0059 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.231+720A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539120 | |||||||
| chr4:67539232 | G | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | NA18968.hp1 NA18982.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+608C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539232 | |||||||
| chr4:67539423 | A | G | 1 | a0001c0001t0004g0097 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.231+417T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539423 | |||||||
| chr4:67539496 | A | G | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.231+344T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539496 | |||||||
| chr4:67539503 | G | A | 7 | a0002c0002t0007g0016 a0002c0002t0007g0069 a0002c0002t0007g0070 others(4): Show |
7 | HG03017.hp2 HG03209.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+337C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539503 | |||||||
| chr4:67539629 | A | G | 1 | a0001c0001t0009g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.231+211T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539629 | |||||||
| chr4:67539706 | T | C | 102 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(99): Show |
107 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.231+134A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539706 | |||||||
| chr4:67539715 | A | G | 6 | a0001c0001t0004g0001 a0001c0001t0004g0004 a0001c0001t0004g0092 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.231+125T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 4/18 | chr4 | 67539715 | |||||||
| chr4:67540271 | G | C | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.137-337C>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540271 | |||||||
| chr4:67540307 | T | C | 5 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(2): Show |
5 | NA18987.hp1 NA18995.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-373A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540307 | |||||||
| chr4:67540400 | G | A | 2 | a0006c0009t0014g0245 a0006c0009t0014g0246 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.137-466C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540400 | |||||||
| chr4:67540758 | C | T | 1 | a0001c0001t0035g0257 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+222G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540758 | |||||||
| chr4:67540797 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+183C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540797 | |||||||
| chr4:67540871 | A | G | 1 | a0001c0001t0021g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136+109T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540871 | |||||||
| chr4:67540891 | A | G | 2 | a0001c0001t0013g0090 a0001c0001t0013g0091 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.136+89T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540891 | |||||||
| chr4:67540908 | TATTA | T | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.136+68_136+71delTA others(2): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 3/18 | chr4 | 67540908 | |||||||
| chr4:67541143 | A | C | 2 | a0001c0001t0004g0088 a0001c0001t0019g0089 |
2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.66-93T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67541143 | |||||||
| chr4:67541164 | A | G | 43 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(40): Show |
45 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.66-114T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67541164 | |||||||
| chr4:67541640 | T | C | 2 | a0003c0003t0004g0247 a0003c0003t0004g0248 |
2 | HG01361.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.66-590A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67541640 | |||||||
| chr4:67541941 | TACA | T | 71 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(68): Show |
73 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.66-894_66-892delTG others(1): Show |
CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67541941 | |||||||
| chr4:67542261 | T | G | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.66-1211A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67542261 | |||||||
| chr4:67542290 | A | G | 1 | a0002c0002t0002g0021 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.66-1240T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67542290 | |||||||
| chr4:67542725 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.65+1424A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67542725 | |||||||
| chr4:67542759 | A | C | 1 | a0001c0001t0005g0080 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.65+1390T>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67542759 | |||||||
| chr4:67542854 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.65+1295G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67542854 | |||||||
| chr4:67543277 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.65+872T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67543277 | |||||||
| chr4:67543403 | T | A | 5 | a0001c0001t0012g0254 a0001c0001t0012g0255 a0001c0001t0021g0250 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.65+746A>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67543403 | |||||||
| chr4:67543442 | T | C | 4 | a0002c0002t0010g0075 a0002c0002t0010g0076 a0002c0002t0010g0077 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.65+707A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67543442 | |||||||
| chr4:67543591 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.65+558A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67543591 | |||||||
| chr4:67543916 | G | A | 2 | a0001c0001t0008g0319 a0004c0004t0033g0320 |
2 | HG02280.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.65+233C>T | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 2/18 | chr4 | 67543916 | |||||||
| chr4:67544291 | C | T | 64 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0021 others(61): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.19-96G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544291 | |||||||
| chr4:67544490 | T | C | 1 | a0001c0001t0030g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.19-295A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544490 | |||||||
| chr4:67544510 | T | C | 1 | a0001c0012t0012g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19-315A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544510 | |||||||
| chr4:67544687 | C | G | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19-492G>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544687 | |||||||
| chr4:67544715 | T | C | 2 | a0001c0001t0012g0254 a0001c0001t0012g0255 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19-520A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544715 | |||||||
| chr4:67544888 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0020 |
3 | HG01891.hp2 HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.18+450G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544888 | |||||||
| chr4:67544895 | T | C | 72 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(69): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.18+443A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544895 | |||||||
| chr4:67544898 | C | T | 1 | a0002c0002t0003g0017 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.18+440G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67544898 | |||||||
| chr4:67545022 | G | T | 1 | a0002c0002t0007g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+316C>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545022 | |||||||
| chr4:67545079 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.18+259A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545079 | |||||||
| chr4:67545238 | A | T | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18+100T>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545238 | |||||||
| chr4:67545273 | C | T | 1 | a0004c0004t0001g0013 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18+65G>A | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545273 | |||||||
| chr4:67545308 | A | G | 2 | a0008c0008t0015g0011 a0008c0008t0015g0012 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.18+30T>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545308 | |||||||
| chr4:67545310 | T | C | 1 | a0002c0002t0011g0322 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.18+28A>G | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545310 | |||||||
| chr4:67545315 | T | G | 6 | a0001c0001t0006g0323 a0001c0001t0006g0324 a0001c0001t0006g0326 others(3): Show |
6 | HG01123.hp1 HG01943.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+23A>C | CENPC | ENSG00000145241.11 | transcript | ENST00000273853.11 | protein_coding | 1/18 | chr4 | 67545315 |