Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79682 |
| ensemblid | ENSG00000151725.12 |
| hgncid | 21348 |
| symbol | CENPU |
| name | centromere protein U |
| refseq_nuc | NM_024629.4 |
| refseq_prot | NP_078905.2 |
| ensembl_nuc | ENST00000281453.10 |
| ensembl_prot | ENSP00000281453.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 184694085 |
| end | 184734096 |
| strand | - |
| ver | v1.2 |
| region | chr4:184694085-184734096 |
| region5000 | chr4:184689085-184739096 |
| regionname0 | CENPU_chr4_184694085_184734096 |
| regionname5000 | CENPU_chr4_184689085_184739096 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 418 | 158 | 46 | 23 | 64 | 8 | 15 | 56 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0002 | 0/0 | 418 | 126 | 5 | 22 | 88 | 3 | 8 | 66 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0003 | 0/0 | 418 | 22 | 15 | 5 | 0 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0004 | 0/0 | 418 | 18 | 5 | 8 | 0 | 0 | 5 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0005 | 0/0 | 418 | 18 | 16 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0006 | 0/0 | 418 | 10 | 2 | 6 | 0 | 1 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0007 | 0/0 | 389 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MKDKA others(384): Show |
chr4 | 184689085 | 184739096 |
| a0008 | 0/0 | 418 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0009 | 0/0 | 418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| a0010 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | MAPRG others(413): Show |
chr4 | 184689085 | 184739096 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1254 | 158 | 46 | 23 | 64 | 8 | 15 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0002c0002 | 0/0 | 1254 | 125 | 4 | 22 | 88 | 3 | 8 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0002c0012 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0003c0003 | 0/0 | 1254 | 19 | 15 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0003c0008 | 0/0 | 1254 | 3 | 0 | 1 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0004c0005 | 0/0 | 1254 | 14 | 1 | 8 | 0 | 0 | 5 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0004c0007 | 0/0 | 1254 | 4 | 4 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0005c0004 | 0/0 | 1254 | 18 | 16 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0006c0006 | 0/0 | 1254 | 10 | 2 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0007c0009 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATAGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0008c0010 | 0/0 | 1254 | 2 | 0 | 0 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0009c0011 | 0/0 | 1254 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 | ||
| a0010c0013 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | ATGGC others(1249): Show |
chr4 | 184689085 | 184739096 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2494 | 132 | 26 | 22 | 59 | 8 | 15 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0002 | 0/0 | 2498 | 3 | 1 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0006 | 0/0 | 2498 | 8 | 8 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0007 | 0/0 | 2498 | 6 | 4 | 1 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0010 | 0/0 | 2494 | 3 | 3 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0012 | 0/0 | 2498 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0013 | 0/0 | 2494 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | CGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0015 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0001c0001t0017 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0002c0002t0001 | 0/0 | 2494 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0002c0002t0002 | 0/0 | 2498 | 115 | 4 | 20 | 81 | 3 | 7 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0002c0002t0008 | 0/0 | 2494 | 6 | 0 | 2 | 3 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0002c0002t0011 | 0/0 | 2498 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0002c0012t0007 | 0/0 | 2498 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0003c0003t0003 | 0/0 | 2485 | 19 | 15 | 4 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2480): Show |
chr4 | 184689085 | 184739096 |
| a0003c0008t0004 | 0/0 | 2490 | 3 | 0 | 1 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2485): Show |
chr4 | 184689085 | 184739096 |
| a0004c0005t0004 | 0/0 | 2490 | 13 | 0 | 8 | 0 | 0 | 5 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2485): Show |
chr4 | 184689085 | 184739096 |
| a0004c0005t0016 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0004c0007t0003 | 0/0 | 2485 | 4 | 4 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2480): Show |
chr4 | 184689085 | 184739096 |
| a0005c0004t0001 | 0/0 | 2494 | 12 | 11 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0005c0004t0009 | 0/0 | 2490 | 5 | 5 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2485): Show |
chr4 | 184689085 | 184739096 |
| a0005c0004t0014 | 0/0 | 2490 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2485): Show |
chr4 | 184689085 | 184739096 |
| a0006c0006t0005 | 0/0 | 2494 | 10 | 2 | 6 | 0 | 1 | 1 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0007c0009t0001 | 0/0 | 2494 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0008c0010t0001 | 0/0 | 2494 | 2 | 0 | 0 | 0 | 0 | 2 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| a0009c0011t0002 | 0/0 | 2498 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2493): Show |
chr4 | 184689085 | 184739096 |
| a0010c0013t0005 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | AGCTT others(2489): Show |
chr4 | 184689085 | 184739096 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0001c0001t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0002 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0002t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0002c0012t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0008t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0008t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0003c0008t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0003 | 0/0 | 7 | 0 | 3 | 0 | 0 | 4 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0005t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0007t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0007t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0007t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0004c0007t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0005c0004t0014g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0006c0006t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0007c0009t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0008c0010t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0008c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0009c0011t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| a0010c0013t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0113 | EUR | FIN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00639 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00642 | hp1 | a0004 | c0005 | t0004 | g0003 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | CHS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00733 | hp1 | a0005 | c0004 | t0001 | g0298 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00733 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00735 | hp1 | a0004 | c0005 | t0004 | g0285 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01074 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01074 | hp2 | a0006 | c0006 | t0005 | g0008 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01081 | hp1 | a0003 | c0003 | t0003 | g0276 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0266 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01167 | hp1 | a0003 | c0003 | t0003 | g0270 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01167 | hp2 | a0006 | c0006 | t0005 | g0130 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01169 | hp1 | a0006 | c0006 | t0005 | g0127 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01243 | hp1 | a0004 | c0005 | t0004 | g0301 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01256 | hp1 | a0004 | c0005 | t0004 | g0003 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01358 | hp2 | a0004 | c0005 | t0004 | g0287 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01433 | hp2 | a0006 | c0006 | t0005 | g0129 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01496 | hp1 | a0003 | c0008 | t0004 | g0158 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0007 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01884 | hp1 | a0003 | c0003 | t0003 | g0277 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01891 | hp2 | a0002 | c0012 | t0007 | g0132 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01952 | hp1 | a0002 | c0002 | t0008 | g0068 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01975 | hp2 | a0005 | c0004 | t0014 | g0293 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02004 | hp1 | a0002 | c0002 | t0008 | g0063 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02055 | hp1 | a0004 | c0005 | t0016 | g0284 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02071 | hp1 | a0002 | c0002 | t0008 | g0088 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02145 | hp2 | a0005 | c0004 | t0001 | g0290 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02148 | hp1 | a0004 | c0005 | t0004 | g0286 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | CDX | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02165 | hp2 | a0001 | c0001 | t0013 | g0177 | EAS | CDX | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02273 | hp1 | a0004 | c0005 | t0004 | g0283 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02280 | hp2 | a0004 | c0007 | t0003 | g0281 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0255 | AMR | PEL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02451 | hp2 | a0006 | c0006 | t0005 | g0017 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02523 | hp2 | a0002 | c0002 | t0008 | g0033 | EAS | KHV | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02572 | hp2 | a0005 | c0004 | t0009 | g0295 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0268 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02622 | hp1 | a0003 | c0003 | t0003 | g0274 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02622 | hp2 | a0005 | c0004 | t0001 | g0289 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0204 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02630 | hp2 | a0005 | c0004 | t0001 | g0031 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02647 | hp1 | a0005 | c0004 | t0009 | g0291 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02717 | hp2 | a0005 | c0004 | t0001 | g0297 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0244 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02735 | hp2 | a0004 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02809 | hp2 | a0004 | c0007 | t0003 | g0280 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02895 | hp2 | a0005 | c0004 | t0001 | g0030 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0262 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02897 | hp1 | a0005 | c0004 | t0001 | g0030 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0259 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02922 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02922 | hp2 | a0005 | c0004 | t0009 | g0292 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02965 | hp2 | a0005 | c0004 | t0001 | g0029 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02970 | hp1 | a0006 | c0006 | t0005 | g0017 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0147 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03041 | hp2 | a0005 | c0004 | t0001 | g0299 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03130 | hp2 | a0003 | c0003 | t0003 | g0267 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03139 | hp1 | a0007 | c0009 | t0001 | g0012 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03139 | hp2 | a0004 | c0007 | t0003 | g0279 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0265 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0250 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03225 | hp1 | a0005 | c0004 | t0001 | g0300 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03225 | hp2 | a0003 | c0003 | t0003 | g0273 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0243 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0253 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03491 | hp1 | a0004 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0150 | AFR | ESN | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03540 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03579 | hp1 | a0005 | c0004 | t0001 | g0031 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03579 | hp2 | a0007 | c0009 | t0001 | g0012 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03688 | hp1 | a0008 | c0010 | t0001 | g0140 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03688 | hp2 | a0006 | c0006 | t0005 | g0131 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03704 | hp1 | a0004 | c0005 | t0004 | g0003 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03710 | hp1 | a0009 | c0011 | t0002 | g0054 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03710 | hp2 | a0008 | c0010 | t0001 | g0138 | SAS | PJL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03927 | hp1 | a0003 | c0008 | t0004 | g0247 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04184 | hp1 | a0003 | c0008 | t0004 | g0241 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04184 | hp2 | a0002 | c0002 | t0008 | g0043 | SAS | BEB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04204 | hp2 | a0004 | c0005 | t0004 | g0003 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG04228 | hp2 | a0004 | c0005 | t0004 | g0288 | SAS | STU | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18522 | hp1 | a0005 | c0004 | t0001 | g0029 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0258 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | CHB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0149 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18949 | hp1 | a0002 | c0002 | t0008 | g0047 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18961 | hp2 | a0002 | c0002 | t0011 | g0110 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18990 | hp1 | a0001 | c0001 | t0013 | g0194 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19030 | hp1 | a0010 | c0013 | t0005 | g0126 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19043 | hp2 | a0005 | c0004 | t0009 | g0294 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19079 | hp1 | a0002 | c0002 | t0011 | g0109 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19240 | hp1 | a0004 | c0007 | t0003 | g0282 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0269 | AFR | YRI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0272 | AFR | ASW | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ASW | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20805 | hp1 | a0006 | c0006 | t0005 | g0128 | EUR | TSI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | GIH | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01123 | hp1 | a0004 | c0005 | t0004 | g0003 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0052 | AMR | CLM | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0275 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02486 | hp1 | a0005 | c0004 | t0009 | g0296 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0251 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | USA | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| NA21309 | hp2 | a0003 | c0003 | t0003 | g0271 | AFR | LWK | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0230 | REF | REF | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0248 | REF | REF | CENPU_chr4_184689085_184739096 | CENPU | chr4 | 184689085 | 184739096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184702404 | C | T | 1 | a0005 | 18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
missense_variant | MODERATE | c.835G>A | p.Ala279Thr | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 869/2494 | 835/1257 | 279/418 | chr4 | 184702404 | |||
| chr4:184702410 | C | A | 1 | a0008 | 2 | HG03688.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.829G>T | p.Ala277Ser | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 863/2494 | 829/1257 | 277/418 | chr4 | 184702410 | |||
| chr4:184712989 | A | G | 1 | a0009 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.643T>C | p.Ser215Pro | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/13 | 677/2494 | 643/1257 | 215/418 | chr4 | 184712989 | |||
| chr4:184712990 | T | C | 4 | a0003 a0004 a0006 others(1): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
missense_variant | MODERATE | c.642A>G | p.Ile214Met | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/13 | 676/2494 | 642/1257 | 214/418 | chr4 | 184712990 | |||
| chr4:184716509 | G | A | 1 | a0010 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.506C>T | p.Ala169Val | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/13 | 540/2494 | 506/1257 | 169/418 | chr4 | 184716509 | |||
| chr4:184716545 | A | G | 4 | a0003 a0004 a0006 others(1): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
missense_variant | MODERATE | c.470T>C | p.Ile157Thr | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/13 | 504/2494 | 470/1257 | 157/418 | chr4 | 184716545 | |||
| chr4:184734017 | C | T | 4 | a0002 a0006 a0009 others(1): Show |
138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
missense_variant&splice_region_variant | MODERATE | c.46G>A | p.Gly16Ser | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 80/2494 | 46/1257 | 16/418 | chr4 | 184734017 | |||
| chr4:184734038 | G | C | 2 | a0004 a0005 |
36 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
missense_variant | MODERATE | c.25C>G | p.Pro9Ala | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 59/2494 | 25/1257 | 9/418 | chr4 | 184734038 | |||
| chr4:184734060 | C | T | 1 | a0007 | 2 | HG03139.hp1 HG03579.hp2 |
start_lost | HIGH | c.3G>A | p.Met1? | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 37/2494 | 3/1257 | 1/418 | chr4 | 184734060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184702375 | T | C | 2 | a0003c0003 a0004c0007 |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
synonymous_variant | LOW | c.864A>G | p.Gln288Gln | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/13 | 898/2494 | 864/1257 | 288/418 | chr4 | 184702375 | |||
| chr4:184729000 | G | A | 6 | a0003c0003 a0003c0008 a0004c0005 others(3): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
synonymous_variant | LOW | c.132C>T | p.Phe44Phe | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/13 | 166/2494 | 132/1257 | 44/418 | chr4 | 184729000 | |||
| chr4:184734036 | C | G | 2 | a0002c0002 a0009c0011 |
126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
synonymous_variant | LOW | c.27G>C | p.Pro9Pro | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 61/2494 | 27/1257 | 9/418 | chr4 | 184734036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184694173 | G | T | 3 | a0001c0001t0015 a0003c0003t0003 a0004c0007t0003 |
24 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 1115 | chr4 | 184694173 | ||||||
| chr4:184694378 | A | T | 8 | a0001c0001t0015 a0003c0003t0003 a0003c0008t0004 others(5): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*910T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 910 | chr4 | 184694378 | ||||||
| chr4:184694404 | T | G | 1 | a0004c0005t0016 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 884 | chr4 | 184694404 | ||||||
| chr4:184694413 | G | GTATC | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(5): Show |
138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*871_*874dupGATA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 874 | chr4 | 184694413 | ||||||
| chr4:184694461 | C | G | 1 | a0002c0002t0011 | 2 | NA18961.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*827G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 827 | chr4 | 184694461 | ||||||
| chr4:184694537 | ACAGATGA others(2): Show |
A | 2 | a0003c0003t0003 a0004c0007t0003 |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*750delCTTCAT others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 742 | chr4 | 184694537 | ||||||
| chr4:184694610 | C | A | 9 | a0001c0001t0015 a0001c0001t0017 a0003c0003t0003 others(6): Show |
53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*678G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 678 | chr4 | 184694610 | ||||||
| chr4:184694614 | T | G | 9 | a0001c0001t0015 a0001c0001t0017 a0003c0003t0003 others(6): Show |
53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 674 | chr4 | 184694614 | ||||||
| chr4:184694842 | T | A | 1 | a0001c0001t0012 | 2 | HG03209.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*446A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 446 | chr4 | 184694842 | ||||||
| chr4:184694938 | T | C | 1 | a0001c0001t0010 | 3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*350A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 350 | chr4 | 184694938 | ||||||
| chr4:184694966 | G | A | 1 | a0005c0004t0014 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 322 | chr4 | 184694966 | ||||||
| chr4:184694970 | TATTA | T | 2 | a0003c0008t0004 a0004c0005t0004 |
16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*314_*317delTAAT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 314 | chr4 | 184694970 | ||||||
| chr4:184695013 | A | C | 8 | a0001c0001t0015 a0003c0003t0003 a0003c0008t0004 others(5): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*275T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 275 | chr4 | 184695013 | ||||||
| chr4:184695065 | TACTC | T | 2 | a0005c0004t0009 a0005c0004t0014 |
6 | HG01975.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*219_*222delGAGT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 219 | chr4 | 184695065 | ||||||
| chr4:184695146 | C | G | 1 | a0001c0001t0006 | 8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 142 | chr4 | 184695146 | ||||||
| chr4:184695284 | C | T | 6 | a0001c0001t0002 a0001c0001t0012 a0002c0002t0002 others(3): Show |
129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 13/13 | 4 | chr4 | 184695284 | ||||||
| chr4:184734096 | T | G | 1 | a0001c0001t0013 | 2 | HG02165.hp2 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/13 | 34 | chr4 | 184734096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:184695415 | A | G | 5 | a0001c0001t0015g0204 a0004c0007t0003g0279 a0004c0007t0003g0280 others(2): Show |
5 | HG02280.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-14T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695415 | |||||||
| chr4:184695477 | T | C | 41 | a0001c0001t0015g0204 a0003c0003t0003g0027 a0003c0003t0003g0028 others(38): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-76A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695477 | |||||||
| chr4:184695660 | T | C | 41 | a0001c0001t0015g0204 a0003c0003t0003g0027 a0003c0003t0003g0028 others(38): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-259A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695660 | |||||||
| chr4:184695705 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1144-304A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695705 | |||||||
| chr4:184695851 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1144-450G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184695851 | |||||||
| chr4:184696191 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1144-790G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696191 | |||||||
| chr4:184696363 | T | C | 2 | a0001c0001t0012g0250 a0001c0001t0012g0251 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1144-962A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696363 | |||||||
| chr4:184696371 | A | G | 40 | a0001c0001t0015g0204 a0003c0003t0003g0027 a0003c0003t0003g0028 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1144-970T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696371 | |||||||
| chr4:184696375 | T | C | 41 | a0001c0001t0015g0204 a0003c0003t0003g0027 a0003c0003t0003g0028 others(38): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1144-974A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696375 | |||||||
| chr4:184696482 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144-1081A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696482 | |||||||
| chr4:184696631 | C | T | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1143+1016G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696631 | |||||||
| chr4:184696693 | T | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+954A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696693 | |||||||
| chr4:184696694 | A | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+953T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696694 | |||||||
| chr4:184696699 | T | TA | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+947_1143+948i others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696699 | |||||||
| chr4:184696781 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+866T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696781 | |||||||
| chr4:184696845 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+802G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696845 | |||||||
| chr4:184696883 | C | CT | 92 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1143+763dupA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | |||||||
| chr4:184696883 | C | T | 1 | a0005c0004t0001g0030 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+764G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | |||||||
| chr4:184696883 | CT | C | 40 | a0002c0002t0002g0079 a0003c0003t0003g0027 a0003c0003t0003g0028 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+763delA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696883 | |||||||
| chr4:184696999 | GCCT | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+645_1143+647d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184696999 | |||||||
| chr4:184697118 | G | C | 1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1143+529C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697118 | |||||||
| chr4:184697188 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1143+459A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697188 | |||||||
| chr4:184697219 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1143+428G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697219 | |||||||
| chr4:184697227 | T | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1143+420A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697227 | |||||||
| chr4:184697354 | TCAATTGA others(65): Show |
T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0227 |
2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1143+221_1143+292d others(74): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697354 | |||||||
| chr4:184697425 | C | T | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1143+222G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697425 | |||||||
| chr4:184697452 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1143+195G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697452 | |||||||
| chr4:184697468 | G | A | 1 | a0001c0001t0012g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143+179C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697468 | |||||||
| chr4:184697535 | CTG | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1143+110_1143+111d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697535 | |||||||
| chr4:184697623 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1143+24C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 12/12 | chr4 | 184697623 | |||||||
| chr4:184697865 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.987-62A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184697865 | |||||||
| chr4:184697941 | G | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.987-138C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184697941 | |||||||
| chr4:184698127 | C | T | 47 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(44): Show |
58 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.987-324G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698127 | |||||||
| chr4:184698128 | A | G | 47 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(44): Show |
58 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.987-325T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698128 | |||||||
| chr4:184698133 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.987-330G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698133 | |||||||
| chr4:184698206 | A | G | 23 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(20): Show |
25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.987-403T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698206 | |||||||
| chr4:184698278 | G | C | 1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.987-475C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698278 | |||||||
| chr4:184698343 | G | A | 23 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(20): Show |
25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.987-540C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698343 | |||||||
| chr4:184698413 | A | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-610T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698413 | |||||||
| chr4:184698447 | G | A | 1 | a0002c0012t0007g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.987-644C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698447 | |||||||
| chr4:184698466 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.987-663A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698466 | |||||||
| chr4:184698511 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-708G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698511 | |||||||
| chr4:184698512 | G | A | 4 | a0005c0004t0001g0030 a0005c0004t0001g0031 a0005c0004t0001g0299 others(1): Show |
6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.987-709C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698512 | |||||||
| chr4:184698549 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.987-746G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698549 | |||||||
| chr4:184698607 | G | A | 22 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(19): Show |
25 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.987-804C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698607 | |||||||
| chr4:184698698 | C | T | 1 | a0002c0002t0008g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.987-895G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698698 | |||||||
| chr4:184698738 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.987-935C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698738 | |||||||
| chr4:184698792 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.987-989G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698792 | |||||||
| chr4:184698813 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1010T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698813 | |||||||
| chr4:184698887 | C | CT | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1085_987-1084i others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698887 | |||||||
| chr4:184698954 | G | T | 147 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(144): Show |
181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.987-1151C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698954 | |||||||
| chr4:184698959 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1156A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184698959 | |||||||
| chr4:184699037 | C | G | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.987-1234G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699037 | |||||||
| chr4:184699055 | C | T | 6 | a0001c0001t0002g0152 a0002c0002t0002g0041 a0002c0002t0002g0075 others(3): Show |
6 | HG00621.hp1 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.987-1252G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699055 | |||||||
| chr4:184699102 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.987-1299G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699102 | |||||||
| chr4:184699154 | T | C | 1 | a0005c0004t0009g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.987-1351A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699154 | |||||||
| chr4:184699187 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.987-1384C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699187 | |||||||
| chr4:184699247 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.987-1444C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699247 | |||||||
| chr4:184699262 | G | A | 1 | a0002c0002t0002g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.987-1459C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699262 | |||||||
| chr4:184699286 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.987-1483G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699286 | |||||||
| chr4:184699309 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.987-1506C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699309 | |||||||
| chr4:184699331 | A | AAAAT | 3 | a0001c0001t0001g0134 a0002c0002t0002g0049 a0002c0002t0002g0101 |
3 | HG01993.hp1 HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.986+1485_986+1488d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699331 | |||||||
| chr4:184699350 | A | G | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.986+1470T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699350 | |||||||
| chr4:184699356 | A | AAATAAAA others(1): Show |
39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.986+1463_986+1464i others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699356 | |||||||
| chr4:184699356 | A | AAATAAAT others(9): Show |
1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.986+1463_986+1464i others(18): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699356 | |||||||
| chr4:184699469 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+1351C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699469 | |||||||
| chr4:184699597 | C | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+1223G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699597 | |||||||
| chr4:184699636 | T | G | 1 | a0009c0011t0002g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.986+1184A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699636 | |||||||
| chr4:184699668 | C | CTCTT | 17 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(14): Show |
26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.986+1151_986+1152i others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699668 | |||||||
| chr4:184699668 | C | CTTTT | 22 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(19): Show |
24 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.986+1148_986+1151d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699668 | |||||||
| chr4:184699746 | C | T | 17 | a0002c0002t0002g0013 a0002c0002t0002g0042 a0002c0002t0002g0044 others(14): Show |
18 | HG01243.hp2 HG01257.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.986+1074G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699746 | |||||||
| chr4:184699863 | G | A | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.986+957C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699863 | |||||||
| chr4:184699872 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+948C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699872 | |||||||
| chr4:184699908 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.986+912G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699908 | |||||||
| chr4:184699952 | C | T | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.986+868G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699952 | |||||||
| chr4:184699968 | T | A | 3 | a0005c0004t0009g0294 a0005c0004t0009g0295 a0005c0004t0014g0293 |
3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.986+852A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699968 | |||||||
| chr4:184699999 | A | G | 2 | a0005c0004t0009g0291 a0005c0004t0009g0292 |
2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.986+821T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184699999 | |||||||
| chr4:184700076 | G | A | 1 | a0005c0004t0014g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.986+744C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700076 | |||||||
| chr4:184700095 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+725G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700095 | |||||||
| chr4:184700212 | C | T | 2 | a0001c0001t0006g0259 a0001c0001t0006g0262 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.986+608G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700212 | |||||||
| chr4:184700294 | T | TAAC | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+523_986+525dup others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700294 | |||||||
| chr4:184700300 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+520T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700300 | |||||||
| chr4:184700348 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0227 |
2 | HG00741.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.986+472C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700348 | |||||||
| chr4:184700423 | C | G | 104 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0017g0150 others(101): Show |
127 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.986+397G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700423 | |||||||
| chr4:184700514 | CCAAGCAG others(2): Show |
C | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.986+297_986+305del others(9): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700514 | |||||||
| chr4:184700525 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.986+295T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700525 | |||||||
| chr4:184700538 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.986+282A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700538 | |||||||
| chr4:184700550 | A | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+270T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700550 | |||||||
| chr4:184700572 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+248A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700572 | |||||||
| chr4:184700698 | C | T | 1 | a0001c0001t0010g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.986+122G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700698 | |||||||
| chr4:184700739 | G | T | 1 | a0002c0002t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.986+81C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700739 | |||||||
| chr4:184700771 | A | T | 1 | a0003c0003t0003g0266 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986+49T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 11/12 | chr4 | 184700771 | |||||||
| chr4:184700892 | C | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.925-11G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184700892 | |||||||
| chr4:184700917 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.925-36C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184700917 | |||||||
| chr4:184701173 | A | C | 41 | a0001c0001t0015g0204 a0003c0003t0003g0027 a0003c0003t0003g0028 others(38): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.925-292T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701173 | |||||||
| chr4:184701248 | A | G | 17 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(14): Show |
26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.925-367T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701248 | |||||||
| chr4:184701279 | A | C | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.925-398T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701279 | |||||||
| chr4:184701355 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.925-474A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701355 | |||||||
| chr4:184701366 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.925-485G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701366 | |||||||
| chr4:184701391 | C | A | 1 | a0002c0002t0011g0110 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.925-510G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701391 | |||||||
| chr4:184701625 | A | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.924+464T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701625 | |||||||
| chr4:184701805 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.924+284G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701805 | |||||||
| chr4:184701871 | C | T | 2 | a0005c0004t0001g0289 a0005c0004t0001g0290 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.924+218G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701871 | |||||||
| chr4:184701981 | T | G | 1 | a0003c0003t0003g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.924+108A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184701981 | |||||||
| chr4:184702050 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.924+39C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 10/12 | chr4 | 184702050 | |||||||
| chr4:184702158 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.877-22G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/12 | chr4 | 184702158 | |||||||
| chr4:184702207 | A | C | 1 | a0002c0002t0002g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.877-71T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 9/12 | chr4 | 184702207 | |||||||
| chr4:184702557 | TA | T | 41 | a0002c0002t0002g0079 a0003c0003t0003g0027 a0003c0003t0003g0028 others(38): Show |
52 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.798-117delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702557 | |||||||
| chr4:184702634 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-193A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702634 | |||||||
| chr4:184702691 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-250T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702691 | |||||||
| chr4:184702763 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-322G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702763 | |||||||
| chr4:184702809 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-368A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702809 | |||||||
| chr4:184702819 | C | T | 57 | a0001c0001t0001g0024 a0001c0001t0001g0157 a0001c0001t0001g0169 others(54): Show |
69 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.798-378G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702819 | |||||||
| chr4:184702822 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798-381A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702822 | |||||||
| chr4:184702835 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-394C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702835 | |||||||
| chr4:184702866 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-425G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702866 | |||||||
| chr4:184702893 | G | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-452C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702893 | |||||||
| chr4:184702975 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-534C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702975 | |||||||
| chr4:184702996 | C | T | 1 | a0002c0002t0008g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.798-555G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184702996 | |||||||
| chr4:184703066 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-625A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703066 | |||||||
| chr4:184703075 | TG | T | 6 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0004c0007t0003g0279 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.798-635delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703075 | |||||||
| chr4:184703084 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-643G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703084 | |||||||
| chr4:184703127 | A | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-686T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703127 | |||||||
| chr4:184703182 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-741G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703182 | |||||||
| chr4:184703234 | T | C | 174 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(171): Show |
211 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.798-793A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703234 | |||||||
| chr4:184703246 | T | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798-805A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703246 | |||||||
| chr4:184703385 | ACTGCCTC others(4): Show |
A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0174 |
3 | HG01257.hp1 HG01258.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.798-955_798-945del others(11): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703385 | |||||||
| chr4:184703426 | G | A | 7 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(4): Show |
8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.798-985C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703426 | |||||||
| chr4:184703444 | T | C | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.798-1003A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703444 | |||||||
| chr4:184703599 | A | C | 9 | a0002c0002t0002g0005 a0002c0002t0002g0016 a0002c0002t0002g0073 others(6): Show |
13 | HG02129.hp1 NA18747.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-1158T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703599 | |||||||
| chr4:184703607 | A | T | 1 | a0002c0012t0007g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798-1166T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703607 | |||||||
| chr4:184703796 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-1355A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703796 | |||||||
| chr4:184703898 | C | T | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.798-1457G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703898 | |||||||
| chr4:184703965 | G | A | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.798-1524C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703965 | |||||||
| chr4:184703969 | TA | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1529delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184703969 | |||||||
| chr4:184704023 | G | A | 2 | a0002c0002t0002g0061 a0002c0002t0002g0064 |
2 | NA18960.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.798-1582C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704023 | |||||||
| chr4:184704086 | CTT | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1647_798-1646d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704086 | |||||||
| chr4:184704193 | C | T | 9 | a0002c0002t0002g0005 a0002c0002t0002g0016 a0002c0002t0002g0073 others(6): Show |
13 | HG02129.hp1 NA18747.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.798-1752G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704193 | |||||||
| chr4:184704236 | C | T | 42 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 others(39): Show |
53 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.798-1795G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704236 | |||||||
| chr4:184704243 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-1802A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704243 | |||||||
| chr4:184704369 | T | C | 147 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(144): Show |
181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.798-1928A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704369 | |||||||
| chr4:184704383 | T | C | 1 | a0002c0002t0002g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.798-1942A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704383 | |||||||
| chr4:184704445 | G | A | 4 | a0001c0001t0007g0252 a0001c0001t0007g0253 a0001c0001t0007g0255 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-2004C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704445 | |||||||
| chr4:184704503 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.798-2062T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704503 | |||||||
| chr4:184704516 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.798-2075A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704516 | |||||||
| chr4:184704583 | A | ACC | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.798-2143_798-2142i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704583 | |||||||
| chr4:184704584 | C | CATATGAC others(7): Show |
1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-2144_798-2143i others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704584 | |||||||
| chr4:184704850 | G | T | 106 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(103): Show |
129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.798-2409C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184704850 | |||||||
| chr4:184705225 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-2784T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705225 | |||||||
| chr4:184705357 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-2916G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705357 | |||||||
| chr4:184705388 | G | A | 173 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(170): Show |
210 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(207): Show |
intron_variant | MODIFIER | c.798-2947C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705388 | |||||||
| chr4:184705435 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.798-2994C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705435 | |||||||
| chr4:184705451 | C | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3010G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705451 | |||||||
| chr4:184705488 | A | G | 1 | a0002c0002t0002g0041 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.798-3047T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705488 | |||||||
| chr4:184705579 | T | TA | 36 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(33): Show |
47 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.798-3139dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705579 | |||||||
| chr4:184705579 | TA | T | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.798-3139delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705579 | |||||||
| chr4:184705628 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.798-3187A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705628 | |||||||
| chr4:184705874 | T | G | 1 | a0001c0001t0007g0234 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.798-3433A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705874 | |||||||
| chr4:184705978 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3537C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184705978 | |||||||
| chr4:184706044 | C | T | 18 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(15): Show |
27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.798-3603G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706044 | |||||||
| chr4:184706108 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.798-3667A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706108 | |||||||
| chr4:184706150 | T | TA | 19 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(16): Show |
28 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.798-3710dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706150 | |||||||
| chr4:184706150 | T | TAA | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.798-3711_798-3710d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706150 | |||||||
| chr4:184706262 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3810A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706262 | |||||||
| chr4:184706327 | C | T | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+3745G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706327 | |||||||
| chr4:184706471 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0228 |
3 | NA18939.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.797+3601G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706471 | |||||||
| chr4:184706568 | C | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.797+3504G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706568 | |||||||
| chr4:184706592 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3480T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706592 | |||||||
| chr4:184706607 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3465C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706607 | |||||||
| chr4:184706866 | ACTGCAGC others(504): Show |
A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
6 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.797+2695_797+3205d others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706866 | |||||||
| chr4:184706937 | T | C | 7 | a0006c0006t0005g0008 a0006c0006t0005g0017 a0006c0006t0005g0127 others(4): Show |
10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.797+3135A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706937 | |||||||
| chr4:184706999 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+3073A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184706999 | |||||||
| chr4:184707157 | G | C | 1 | a0002c0002t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.797+2915C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707157 | |||||||
| chr4:184707161 | C | G | 1 | a0002c0002t0002g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.797+2911G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707161 | |||||||
| chr4:184707250 | G | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18990.hp2 NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.797+2822C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707250 | |||||||
| chr4:184707251 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+2821T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707251 | |||||||
| chr4:184707252 | A | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+2820T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707252 | |||||||
| chr4:184707303 | A | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.797+2769T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707303 | |||||||
| chr4:184707480 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.797+2592C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707480 | |||||||
| chr4:184707556 | G | C | 1 | a0003c0003t0003g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.797+2516C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707556 | |||||||
| chr4:184707688 | G | A | 1 | a0002c0002t0002g0113 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.797+2384C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707688 | |||||||
| chr4:184707812 | G | A | 1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.797+2260C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707812 | |||||||
| chr4:184707830 | G | C | 2 | a0001c0001t0012g0250 a0001c0001t0012g0251 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.797+2242C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707830 | |||||||
| chr4:184707951 | G | A | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.797+2121C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184707951 | |||||||
| chr4:184708015 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+2057C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708015 | |||||||
| chr4:184708049 | C | T | 4 | a0004c0007t0003g0279 a0004c0007t0003g0280 a0004c0007t0003g0281 others(1): Show |
4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.797+2023G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708049 | |||||||
| chr4:184708092 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.797+1980G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708092 | |||||||
| chr4:184708096 | T | C | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.797+1976A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708096 | |||||||
| chr4:184708178 | G | A | 5 | a0001c0001t0002g0152 a0002c0002t0002g0075 a0002c0002t0002g0077 others(2): Show |
5 | HG00621.hp1 HG02165.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.797+1894C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708178 | |||||||
| chr4:184708185 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.797+1887C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708185 | |||||||
| chr4:184708204 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1868A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708204 | |||||||
| chr4:184708211 | AG | A | 6 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0004c0007t0003g0279 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.797+1860delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708211 | |||||||
| chr4:184708212 | G | A | 34 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(31): Show |
45 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.797+1860C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708212 | |||||||
| chr4:184708219 | T | A | 103 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0002c0002t0002g0001 others(100): Show |
126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.797+1853A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708219 | |||||||
| chr4:184708222 | CA | C | 209 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(206): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.797+1849delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | |||||||
| chr4:184708222 | CAA | C | 24 | a0001c0001t0001g0024 a0001c0001t0001g0148 a0001c0001t0001g0157 others(21): Show |
25 | HG00099.hp2 HG01081.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.797+1848_797+1849d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | |||||||
| chr4:184708222 | CAAAAAAA others(6): Show |
C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1837_797+1849d others(15): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708222 | |||||||
| chr4:184708230 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00639.hp1 HG00738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.797+1842T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708230 | |||||||
| chr4:184708252 | T | A | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1820A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708252 | |||||||
| chr4:184708480 | A | T | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.797+1592T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708480 | |||||||
| chr4:184708533 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.797+1539G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708533 | |||||||
| chr4:184708534 | AAAG | A | 17 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(14): Show |
26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.797+1535_797+1537d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708534 | |||||||
| chr4:184708537 | G | GA | 10 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0035 others(7): Show |
18 | HG00558.hp2 HG00621.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1534dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708537 | |||||||
| chr4:184708614 | C | T | 6 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0004c0007t0003g0279 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.797+1458G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708614 | |||||||
| chr4:184708635 | A | T | 103 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0002c0002t0002g0001 others(100): Show |
126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.797+1437T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708635 | |||||||
| chr4:184708651 | C | A | 17 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(14): Show |
26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.797+1421G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708651 | |||||||
| chr4:184708718 | A | C | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.797+1354T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708718 | |||||||
| chr4:184708775 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.797+1297G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708775 | |||||||
| chr4:184708857 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1215A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708857 | |||||||
| chr4:184708871 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+1201C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184708871 | |||||||
| chr4:184709018 | AAAAGTT | A | 61 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0002c0002t0002g0002 others(58): Show |
73 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.797+1048_797+1053d others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709018 | |||||||
| chr4:184709122 | G | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.797+950C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709122 | |||||||
| chr4:184709162 | G | A | 2 | a0006c0006t0005g0127 a0006c0006t0005g0130 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.797+910C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709162 | |||||||
| chr4:184709227 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+845C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709227 | |||||||
| chr4:184709348 | G | A | 1 | a0002c0002t0002g0064 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.797+724C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709348 | |||||||
| chr4:184709378 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+694A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709378 | |||||||
| chr4:184709444 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+628A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709444 | |||||||
| chr4:184709485 | C | CA | 48 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(45): Show |
60 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.797+586dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709485 | |||||||
| chr4:184709646 | T | C | 1 | a0002c0002t0002g0062 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.797+426A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709646 | |||||||
| chr4:184709656 | T | C | 2 | a0002c0002t0002g0087 a0002c0002t0002g0090 |
2 | NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.797+416A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709656 | |||||||
| chr4:184709726 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+346A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709726 | |||||||
| chr4:184709736 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.797+336A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709736 | |||||||
| chr4:184709794 | T | A | 3 | a0001c0001t0001g0205 a0001c0001t0015g0204 a0002c0002t0002g0125 |
3 | HG02630.hp1 HG02647.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.797+278A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709794 | |||||||
| chr4:184709830 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.797+242A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709830 | |||||||
| chr4:184709892 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0168 |
3 | NA18966.hp1 NA19075.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.797+180A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184709892 | |||||||
| chr4:184710010 | G | T | 1 | a0001c0001t0010g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.797+62C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 8/12 | chr4 | 184710010 | |||||||
| chr4:184710184 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.689-4T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710184 | |||||||
| chr4:184710314 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-134A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710314 | |||||||
| chr4:184710322 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18961.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.689-142A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710322 | |||||||
| chr4:184710345 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.689-165A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710345 | |||||||
| chr4:184710361 | A | C | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.689-181T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710361 | |||||||
| chr4:184710550 | G | A | 2 | a0002c0002t0002g0091 a0002c0002t0002g0108 |
2 | NA19001.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.689-370C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710550 | |||||||
| chr4:184710667 | C | CA | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-488_689-487ins others(1): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710667 | |||||||
| chr4:184710844 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-664A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710844 | |||||||
| chr4:184710859 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-679C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710859 | |||||||
| chr4:184710865 | T | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-685A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184710865 | |||||||
| chr4:184711004 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-824G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711004 | |||||||
| chr4:184711005 | G | A | 12 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(9): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.689-825C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711005 | |||||||
| chr4:184711010 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.689-830A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711010 | |||||||
| chr4:184711087 | G | GCTAACC | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-908_689-907ins others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711087 | |||||||
| chr4:184711090 | C | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-910G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711090 | |||||||
| chr4:184711092 | A | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-912T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711092 | |||||||
| chr4:184711093 | G | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-913C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711093 | |||||||
| chr4:184711095 | A | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-915T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711095 | |||||||
| chr4:184711097 | T | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-917A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711097 | |||||||
| chr4:184711099 | T | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-919A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711099 | |||||||
| chr4:184711102 | C | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-922G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711102 | |||||||
| chr4:184711131 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689-951G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711131 | |||||||
| chr4:184711132 | G | A | 1 | a0005c0004t0009g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.689-952C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711132 | |||||||
| chr4:184711135 | T | G | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-955A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711135 | |||||||
| chr4:184711273 | T | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.689-1093A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711273 | |||||||
| chr4:184711324 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-1144A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711324 | |||||||
| chr4:184711547 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.689-1367G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711547 | |||||||
| chr4:184711736 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.688+1208A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711736 | |||||||
| chr4:184711807 | C | T | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.688+1137G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711807 | |||||||
| chr4:184711811 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+1133G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711811 | |||||||
| chr4:184711875 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.688+1069G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184711875 | |||||||
| chr4:184712031 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.688+913C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712031 | |||||||
| chr4:184712036 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+908C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712036 | |||||||
| chr4:184712069 | G | C | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.688+875C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712069 | |||||||
| chr4:184712119 | C | CA | 50 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0023 others(47): Show |
59 | HG00099.hp1 HG00733.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.688+824dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712119 | C | CAAAAA | 13 | a0003c0003t0003g0028 a0003c0003t0003g0265 a0003c0003t0003g0267 others(10): Show |
14 | HG01081.hp1 HG01167.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.688+820_688+824dup others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712119 | C | CAAAAAA | 8 | a0003c0003t0003g0027 a0003c0003t0003g0266 a0003c0008t0004g0158 others(5): Show |
12 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.688+819_688+824dup others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712119 | C | CAAAAAAA | 14 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0003c0008t0004g0241 others(11): Show |
20 | HG00642.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.688+818_688+824dup others(7): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712119 | C | CAAAAAAA others(3): Show |
1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.688+815_688+824dup others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712119 | CA | C | 8 | a0001c0001t0001g0179 a0001c0001t0001g0203 a0001c0001t0001g0205 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.688+824delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712119 | |||||||
| chr4:184712171 | C | G | 1 | a0005c0004t0009g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.688+773G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712171 | |||||||
| chr4:184712310 | T | C | 2 | a0002c0002t0011g0109 a0002c0002t0011g0110 |
2 | NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.688+634A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712310 | |||||||
| chr4:184712379 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.688+565C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712379 | |||||||
| chr4:184712392 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+552T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712392 | |||||||
| chr4:184712427 | G | A | 1 | a0002c0012t0007g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.688+517C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712427 | |||||||
| chr4:184712711 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.688+233C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712711 | |||||||
| chr4:184712919 | C | A | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+25G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 7/12 | chr4 | 184712919 | |||||||
| chr4:184713017 | CA | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.619-5delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713017 | |||||||
| chr4:184713064 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-51T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713064 | |||||||
| chr4:184713087 | C | A | 1 | a0002c0002t0002g0100 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.619-74G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713087 | |||||||
| chr4:184713219 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-206G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713219 | |||||||
| chr4:184713599 | G | A | 1 | a0002c0002t0002g0092 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.619-586C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713599 | |||||||
| chr4:184713683 | T | C | 283 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(280): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.619-670A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713683 | |||||||
| chr4:184713705 | A | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-692T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713705 | |||||||
| chr4:184713714 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.619-701A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713714 | |||||||
| chr4:184713722 | A | G | 1 | a0005c0004t0009g0291 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.619-709T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713722 | |||||||
| chr4:184713864 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-851C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184713864 | |||||||
| chr4:184714004 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-991G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714004 | |||||||
| chr4:184714005 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-992A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714005 | |||||||
| chr4:184714095 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1082T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714095 | |||||||
| chr4:184714157 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.619-1144G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714157 | |||||||
| chr4:184714181 | A | G | 2 | a0002c0002t0002g0078 a0002c0002t0002g0114 |
2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.619-1168T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714181 | |||||||
| chr4:184714210 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.619-1197T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714210 | |||||||
| chr4:184714265 | A | C | 1 | a0002c0002t0002g0077 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.619-1252T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714265 | |||||||
| chr4:184714310 | G | C | 1 | a0002c0002t0002g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-1297C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714310 | |||||||
| chr4:184714363 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.619-1350A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714363 | |||||||
| chr4:184714427 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1414C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714427 | |||||||
| chr4:184714552 | T | C | 1 | a0002c0002t0002g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.619-1539A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714552 | |||||||
| chr4:184714612 | T | A | 284 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(281): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.619-1599A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714612 | |||||||
| chr4:184714680 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.619-1667A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714680 | |||||||
| chr4:184714868 | A | G | 33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(30): Show |
40 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.618+1529T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714868 | |||||||
| chr4:184714905 | CAGTA | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.618+1488_618+1491d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714905 | |||||||
| chr4:184714909 | A | G | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1488T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714909 | |||||||
| chr4:184714926 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1471G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714926 | |||||||
| chr4:184714942 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1455C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714942 | |||||||
| chr4:184714951 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1446A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184714951 | |||||||
| chr4:184715024 | T | C | 1 | a0001c0001t0006g0263 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.618+1373A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715024 | |||||||
| chr4:184715063 | T | A | 148 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(145): Show |
182 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.618+1334A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715063 | |||||||
| chr4:184715120 | A | C | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.618+1277T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715120 | |||||||
| chr4:184715126 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1271G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715126 | |||||||
| chr4:184715137 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.618+1260C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715137 | |||||||
| chr4:184715242 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+1155C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715242 | |||||||
| chr4:184715251 | A | G | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.618+1146T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715251 | |||||||
| chr4:184715305 | G | A | 6 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0004c0007t0003g0279 others(3): Show |
6 | HG02280.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+1092C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715305 | |||||||
| chr4:184715323 | A | G | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.618+1074T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715323 | |||||||
| chr4:184715388 | T | C | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(5): Show |
9 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+1009A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715388 | |||||||
| chr4:184715397 | C | CA | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+999dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715397 | |||||||
| chr4:184715405 | G | A | 1 | a0002c0002t0002g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.618+992C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715405 | |||||||
| chr4:184715414 | G | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+983C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715414 | |||||||
| chr4:184715427 | T | C | 3 | a0002c0002t0008g0047 a0002c0002t0008g0063 a0002c0002t0008g0068 |
3 | HG01952.hp1 HG02004.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.618+970A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715427 | |||||||
| chr4:184715432 | C | T | 3 | a0005c0004t0009g0294 a0005c0004t0009g0295 a0005c0004t0014g0293 |
3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.618+965G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715432 | |||||||
| chr4:184715462 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.618+935C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715462 | |||||||
| chr4:184715495 | T | C | 17 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(14): Show |
26 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.618+902A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715495 | |||||||
| chr4:184715548 | C | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+849G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715548 | |||||||
| chr4:184715609 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.618+788C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715609 | |||||||
| chr4:184715654 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.618+743C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715654 | |||||||
| chr4:184715678 | A | C | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+719T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715678 | |||||||
| chr4:184715926 | GCT | G | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+469_618+470del others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715926 | |||||||
| chr4:184715927 | C | T | 269 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(266): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.618+470G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715927 | |||||||
| chr4:184715937 | G | GT | 116 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0144 others(113): Show |
140 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.618+459dupA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | |||||||
| chr4:184715937 | G | T | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+460C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | |||||||
| chr4:184715937 | GTTT | G | 25 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0003c0008t0004g0158 others(22): Show |
34 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.618+457_618+459del others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715937 | |||||||
| chr4:184715940 | T | G | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618+457A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715940 | |||||||
| chr4:184715941 | T | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+456A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715941 | |||||||
| chr4:184715955 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+442G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715955 | |||||||
| chr4:184715994 | G | A | 2 | a0005c0004t0009g0291 a0005c0004t0009g0292 |
2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.618+403C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184715994 | |||||||
| chr4:184716193 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.618+204G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716193 | |||||||
| chr4:184716227 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+170C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716227 | |||||||
| chr4:184716232 | G | A | 1 | a0002c0002t0002g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+165C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716232 | |||||||
| chr4:184716264 | C | T | 169 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(166): Show |
206 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(203): Show |
intron_variant | MODIFIER | c.618+133G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716264 | |||||||
| chr4:184716369 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.618+28G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716369 | |||||||
| chr4:184716389 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.618+8C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 6/12 | chr4 | 184716389 | |||||||
| chr4:184716727 | T | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-94A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716727 | |||||||
| chr4:184716740 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-107G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716740 | |||||||
| chr4:184716750 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-117A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716750 | |||||||
| chr4:184716970 | G | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+166C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184716970 | |||||||
| chr4:184717010 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0178 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.381+126C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717010 | |||||||
| chr4:184717077 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.381+59G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717077 | |||||||
| chr4:184717126 | T | G | 1 | a0001c0001t0010g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+10A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 5/12 | chr4 | 184717126 | |||||||
| chr4:184717240 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-44A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717240 | |||||||
| chr4:184717353 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-157C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717353 | |||||||
| chr4:184717569 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-373C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717569 | |||||||
| chr4:184717675 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-479A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717675 | |||||||
| chr4:184717682 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0184 a0001c0001t0001g0186 others(1): Show |
4 | HG02738.hp1 HG03239.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-486T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717682 | |||||||
| chr4:184717699 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-503C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717699 | |||||||
| chr4:184717714 | A | C | 1 | a0002c0002t0002g0102 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.321-518T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717714 | |||||||
| chr4:184717722 | C | T | 147 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(144): Show |
181 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.321-526G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717722 | |||||||
| chr4:184717746 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-550C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717746 | |||||||
| chr4:184717800 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-604T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717800 | |||||||
| chr4:184717848 | A | G | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-652T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717848 | |||||||
| chr4:184717848 | A | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-652T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717848 | |||||||
| chr4:184717924 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-728G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717924 | |||||||
| chr4:184717941 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-745G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717941 | |||||||
| chr4:184717977 | T | A | 1 | a0002c0002t0002g0038 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.321-781A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717977 | |||||||
| chr4:184717980 | A | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-784T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184717980 | |||||||
| chr4:184718015 | G | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-819C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718015 | |||||||
| chr4:184718038 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-842G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718038 | |||||||
| chr4:184718179 | G | A | 1 | a0002c0002t0002g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.321-983C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718179 | |||||||
| chr4:184718301 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-1105G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718301 | |||||||
| chr4:184718321 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1125G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718321 | |||||||
| chr4:184718348 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1152A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718348 | |||||||
| chr4:184718371 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1175C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718371 | |||||||
| chr4:184718566 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1370T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718566 | |||||||
| chr4:184718574 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1378A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718574 | |||||||
| chr4:184718588 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1392C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718588 | |||||||
| chr4:184718608 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1412T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718608 | |||||||
| chr4:184718705 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.321-1509G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718705 | |||||||
| chr4:184718740 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1544T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718740 | |||||||
| chr4:184718749 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1553C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718749 | |||||||
| chr4:184718807 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1611G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718807 | |||||||
| chr4:184718843 | A | G | 1 | a0005c0004t0009g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321-1647T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718843 | |||||||
| chr4:184718846 | G | A | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.321-1650C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718846 | |||||||
| chr4:184718850 | A | G | 284 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(281): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.321-1654T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718850 | |||||||
| chr4:184718903 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1707G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718903 | |||||||
| chr4:184718924 | G | A | 1 | a0003c0003t0003g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.321-1728C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184718924 | |||||||
| chr4:184719062 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-1866A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719062 | |||||||
| chr4:184719094 | A | G | 2 | a0005c0004t0009g0291 a0005c0004t0009g0292 |
2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.321-1898T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719094 | |||||||
| chr4:184719276 | C | T | 1 | a0001c0001t0007g0252 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.321-2080G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719276 | |||||||
| chr4:184719377 | A | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-2181T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719377 | |||||||
| chr4:184719494 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2298G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719494 | |||||||
| chr4:184719530 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2334C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719530 | |||||||
| chr4:184719563 | C | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-2367G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719563 | |||||||
| chr4:184719619 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2423T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719619 | |||||||
| chr4:184719638 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-2442A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719638 | |||||||
| chr4:184719658 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.321-2462A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719658 | |||||||
| chr4:184719686 | C | G | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-2490G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719686 | |||||||
| chr4:184719798 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.321-2602G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719798 | |||||||
| chr4:184719798 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.321-2602G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719798 | |||||||
| chr4:184719931 | A | G | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.321-2735T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719931 | |||||||
| chr4:184719971 | C | T | 7 | a0006c0006t0005g0008 a0006c0006t0005g0017 a0006c0006t0005g0127 others(4): Show |
10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.321-2775G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184719971 | |||||||
| chr4:184720172 | TTAAC | T | 18 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(15): Show |
27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.321-2980_321-2977d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720172 | |||||||
| chr4:184720229 | G | T | 1 | a0005c0004t0009g0294 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321-3033C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720229 | |||||||
| chr4:184720236 | A | G | 1 | a0005c0004t0009g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321-3040T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720236 | |||||||
| chr4:184720343 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-3147C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720343 | |||||||
| chr4:184720383 | G | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0163 others(12): Show |
18 | HG02015.hp2 HG02083.hp2 HG03831.hp2 others(15): Show |
intron_variant | MODIFIER | c.321-3187C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720383 | |||||||
| chr4:184720402 | A | T | 3 | a0002c0002t0002g0013 a0002c0002t0002g0058 a0002c0002t0002g0066 |
4 | HG01243.hp2 HG01257.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-3206T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720402 | |||||||
| chr4:184720414 | G | A | 51 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(48): Show |
59 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.321-3218C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720414 | |||||||
| chr4:184720474 | G | A | 3 | a0001c0001t0002g0264 a0001c0001t0012g0250 a0001c0001t0012g0251 |
3 | HG03209.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.321-3278C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720474 | |||||||
| chr4:184720557 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.321-3361A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720557 | |||||||
| chr4:184720844 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.321-3648A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184720844 | |||||||
| chr4:184721020 | T | C | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.321-3824A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721020 | |||||||
| chr4:184721181 | T | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3776A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721181 | |||||||
| chr4:184721227 | T | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0233 others(4): Show |
7 | HG00639.hp1 HG00738.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+3730A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721227 | |||||||
| chr4:184721245 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.320+3712T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721245 | |||||||
| chr4:184721423 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3534G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721423 | |||||||
| chr4:184721457 | T | TAA | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.320+3498_320+3499d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | |||||||
| chr4:184721457 | T | TAAA | 111 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0141 others(108): Show |
138 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.320+3497_320+3499d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | |||||||
| chr4:184721457 | T | TAAAA | 25 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00280.hp1 HG00609.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.320+3496_320+3499d others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | |||||||
| chr4:184721457 | T | TAAAAAAA others(1): Show |
14 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(11): Show |
16 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+3492_320+3499d others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721457 | |||||||
| chr4:184721478 | AG | A | 16 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(13): Show |
25 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.320+3478delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721478 | |||||||
| chr4:184721479 | G | A | 20 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.320+3478C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721479 | |||||||
| chr4:184721554 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.320+3403C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721554 | |||||||
| chr4:184721614 | G | C | 10 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(7): Show |
16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+3343C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721614 | |||||||
| chr4:184721620 | CTAGATT | C | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3331_320+3336d others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721620 | |||||||
| chr4:184721711 | G | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3246C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721711 | |||||||
| chr4:184721715 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3242G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721715 | |||||||
| chr4:184721740 | C | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.320+3217G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721740 | |||||||
| chr4:184721789 | A | G | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+3168T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721789 | |||||||
| chr4:184721806 | T | G | 1 | a0002c0002t0002g0087 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.320+3151A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721806 | |||||||
| chr4:184721848 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+3109T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721848 | |||||||
| chr4:184721934 | G | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(281): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.320+3023C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721934 | |||||||
| chr4:184721957 | C | A | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(5): Show |
9 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+3000G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721957 | |||||||
| chr4:184721988 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.320+2969G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184721988 | |||||||
| chr4:184722007 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2950T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722007 | |||||||
| chr4:184722015 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+2942T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722015 | |||||||
| chr4:184722069 | T | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2888A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722069 | |||||||
| chr4:184722099 | T | C | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+2858A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722099 | |||||||
| chr4:184722131 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320+2826A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722131 | |||||||
| chr4:184722182 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2775G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722182 | |||||||
| chr4:184722417 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2540A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722417 | |||||||
| chr4:184722542 | C | T | 1 | a0002c0002t0002g0087 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.320+2415G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722542 | |||||||
| chr4:184722543 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320+2414C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722543 | |||||||
| chr4:184722588 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2369C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722588 | |||||||
| chr4:184722621 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2336C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722621 | |||||||
| chr4:184722624 | C | G | 1 | a0003c0003t0003g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320+2333G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722624 | |||||||
| chr4:184722670 | CAA | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0055 a0002c0002t0002g0065 |
5 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+2285_320+2286d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722670 | |||||||
| chr4:184722703 | A | G | 1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.320+2254T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722703 | |||||||
| chr4:184722708 | A | G | 38 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(35): Show |
49 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.320+2249T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722708 | |||||||
| chr4:184722718 | A | AAC | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.320+2238_320+2239i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722718 | |||||||
| chr4:184722724 | A | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0143 others(3): Show |
6 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+2233T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722724 | |||||||
| chr4:184722791 | A | G | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+2166T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722791 | |||||||
| chr4:184722797 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.320+2160A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722797 | |||||||
| chr4:184722822 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.320+2135G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722822 | |||||||
| chr4:184722830 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+2127C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722830 | |||||||
| chr4:184722830 | G | C | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+2127C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722830 | |||||||
| chr4:184722863 | A | G | 1 | a0001c0001t0012g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320+2094T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722863 | |||||||
| chr4:184722989 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1968C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184722989 | |||||||
| chr4:184723237 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1720C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723237 | |||||||
| chr4:184723263 | G | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1694C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723263 | |||||||
| chr4:184723339 | TTAA | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.320+1615_320+1617d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723339 | |||||||
| chr4:184723363 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1594A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723363 | |||||||
| chr4:184723425 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | NA18973.hp1 NA18979.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.320+1532A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723425 | |||||||
| chr4:184723507 | C | CAT | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1449_320+1450i others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723507 | |||||||
| chr4:184723579 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.320+1378T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723579 | |||||||
| chr4:184723615 | G | A | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.320+1342C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723615 | |||||||
| chr4:184723659 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1298A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723659 | |||||||
| chr4:184723676 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.320+1281A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723676 | |||||||
| chr4:184723735 | C | T | 1 | a0002c0012t0007g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.320+1222G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723735 | |||||||
| chr4:184723756 | T | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.320+1201A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723756 | |||||||
| chr4:184723772 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1185C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723772 | |||||||
| chr4:184723775 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320+1182C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723775 | |||||||
| chr4:184723782 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+1175T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723782 | |||||||
| chr4:184723841 | CA | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.320+1115delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | |||||||
| chr4:184723841 | CAA | C | 190 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(187): Show |
232 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.320+1114_320+1115d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | |||||||
| chr4:184723841 | CAAA | C | 12 | a0001c0001t0006g0262 a0002c0002t0002g0039 a0002c0002t0002g0074 others(9): Show |
12 | HG01975.hp2 HG02165.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+1113_320+1115d others(5): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723841 | |||||||
| chr4:184723857 | A | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG01515.hp1 HG01517.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.320+1100T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723857 | |||||||
| chr4:184723930 | T | C | 1 | a0002c0002t0002g0099 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.320+1027A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723930 | |||||||
| chr4:184723958 | A | G | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+999T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184723958 | |||||||
| chr4:184724040 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+917T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724040 | |||||||
| chr4:184724050 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+907T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724050 | |||||||
| chr4:184724061 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+896C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724061 | |||||||
| chr4:184724069 | C | G | 4 | a0001c0001t0001g0278 a0001c0001t0010g0146 a0001c0001t0010g0147 others(1): Show |
4 | HG02970.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+888G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724069 | |||||||
| chr4:184724071 | T | C | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.320+886A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724071 | |||||||
| chr4:184724080 | T | C | 1 | a0003c0003t0003g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.320+877A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724080 | |||||||
| chr4:184724118 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+839G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724118 | |||||||
| chr4:184724134 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.320+823G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724134 | |||||||
| chr4:184724138 | C | T | 18 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(15): Show |
27 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.320+819G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724138 | |||||||
| chr4:184724148 | C | T | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.320+809G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724148 | |||||||
| chr4:184724173 | G | C | 12 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(9): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+784C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724173 | |||||||
| chr4:184724265 | C | CA | 12 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(9): Show |
13 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+691dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724265 | |||||||
| chr4:184724284 | A | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.320+673T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724284 | |||||||
| chr4:184724356 | C | T | 1 | a0002c0002t0002g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.320+601G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724356 | |||||||
| chr4:184724390 | G | GATA | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+564_320+566dup others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724390 | |||||||
| chr4:184724418 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+539G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724418 | |||||||
| chr4:184724629 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.320+328A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724629 | |||||||
| chr4:184724681 | A | C | 3 | a0005c0004t0009g0294 a0005c0004t0009g0295 a0005c0004t0014g0293 |
3 | HG01975.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.320+276T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724681 | |||||||
| chr4:184724789 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.320+168G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 4/12 | chr4 | 184724789 | |||||||
| chr4:184725214 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.215-152A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725214 | |||||||
| chr4:184725322 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-260G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725322 | |||||||
| chr4:184725329 | A | G | 1 | a0001c0001t0006g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.215-267T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725329 | |||||||
| chr4:184725351 | C | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-289G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725351 | |||||||
| chr4:184725409 | G | A | 1 | a0002c0002t0008g0068 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.215-347C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725409 | |||||||
| chr4:184725421 | T | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | NA18969.hp2 NA19057.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.215-359A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725421 | |||||||
| chr4:184725624 | C | T | 3 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 |
3 | HG02970.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.215-562G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725624 | |||||||
| chr4:184725766 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-704G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725766 | |||||||
| chr4:184725808 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-746A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725808 | |||||||
| chr4:184725953 | G | C | 106 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0007g0234 others(103): Show |
129 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-891C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725953 | |||||||
| chr4:184725963 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.215-901G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184725963 | |||||||
| chr4:184726064 | T | G | 1 | a0002c0012t0007g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1002A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726064 | |||||||
| chr4:184726085 | T | C | 1 | a0001c0001t0007g0256 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.215-1023A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726085 | |||||||
| chr4:184726146 | C | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1084G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726146 | |||||||
| chr4:184726191 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1129C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726191 | |||||||
| chr4:184726241 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1179G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726241 | |||||||
| chr4:184726260 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1198T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726260 | |||||||
| chr4:184726371 | G | GA | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-1310dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726371 | |||||||
| chr4:184726441 | T | C | 7 | a0006c0006t0005g0008 a0006c0006t0005g0017 a0006c0006t0005g0127 others(4): Show |
10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.215-1379A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726441 | |||||||
| chr4:184726484 | A | C | 5 | a0001c0001t0001g0184 a0004c0007t0003g0279 a0004c0007t0003g0280 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-1422T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726484 | |||||||
| chr4:184726499 | G | C | 1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.215-1437C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726499 | |||||||
| chr4:184726544 | G | GCTGGTGG others(7): Show |
1 | a0001c0001t0001g0196 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.215-1496_215-1483d others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726544 | |||||||
| chr4:184726577 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1515T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726577 | |||||||
| chr4:184726696 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1634T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726696 | |||||||
| chr4:184726748 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1686C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726748 | |||||||
| chr4:184726753 | TAA | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.215-1693_215-1692d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726753 | |||||||
| chr4:184726861 | G | A | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.215-1799C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726861 | |||||||
| chr4:184726921 | G | A | 2 | a0002c0002t0002g0086 a0002c0002t0002g0100 |
2 | NA18970.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.215-1859C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726921 | |||||||
| chr4:184726974 | T | TG | 52 | a0001c0001t0001g0142 a0001c0001t0001g0249 a0001c0001t0001g0254 others(49): Show |
68 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.215-1913dupC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | |||||||
| chr4:184726974 | T | TGG | 15 | a0001c0001t0001g0144 a0001c0001t0006g0026 a0001c0001t0006g0261 others(12): Show |
19 | HG00558.hp1 HG00738.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.215-1914_215-1913d others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | |||||||
| chr4:184726974 | TG | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.215-1913delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | |||||||
| chr4:184726974 | TGGGGG | T | 38 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(35): Show |
49 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.215-1917_215-1913d others(7): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726974 | |||||||
| chr4:184726978 | G | A | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.215-1916C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726978 | |||||||
| chr4:184726980 | G | T | 15 | a0005c0004t0001g0029 a0005c0004t0001g0030 a0005c0004t0001g0031 others(12): Show |
18 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.215-1918C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726980 | |||||||
| chr4:184726983 | G | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.215-1921C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726983 | |||||||
| chr4:184726988 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215-1926C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184726988 | |||||||
| chr4:184727007 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.214+1911G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727007 | |||||||
| chr4:184727041 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1877T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727041 | |||||||
| chr4:184727047 | T | C | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.214+1871A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727047 | |||||||
| chr4:184727048 | G | A | 1 | a0002c0002t0002g0099 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.214+1870C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727048 | |||||||
| chr4:184727116 | C | CA | 9 | a0001c0001t0001g0212 a0001c0001t0010g0146 a0001c0001t0010g0147 others(6): Show |
9 | HG01975.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.214+1801dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | |||||||
| chr4:184727116 | C | CAAAAAAA | 20 | a0003c0003t0003g0243 a0003c0003t0003g0244 a0003c0008t0004g0158 others(17): Show |
29 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.214+1795_214+1801d others(9): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | |||||||
| chr4:184727116 | C | CAAAAAAA others(1): Show |
15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+1794_214+1801d others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727116 | |||||||
| chr4:184727117 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
7 | NA18965.hp2 NA18981.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+1801T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727117 | |||||||
| chr4:184727121 | A | G | 2 | a0001c0001t0002g0151 a0002c0002t0002g0038 |
2 | NA19074.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.214+1797T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727121 | |||||||
| chr4:184727335 | A | G | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.214+1583T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727335 | |||||||
| chr4:184727356 | G | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1562C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727356 | |||||||
| chr4:184727424 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.214+1494A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727424 | |||||||
| chr4:184727456 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1462T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727456 | |||||||
| chr4:184727457 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1461A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727457 | |||||||
| chr4:184727560 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1358A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727560 | |||||||
| chr4:184727714 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1204A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727714 | |||||||
| chr4:184727723 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1195G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727723 | |||||||
| chr4:184727817 | A | G | 2 | a0004c0005t0016g0284 a0010c0013t0005g0126 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.214+1101T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727817 | |||||||
| chr4:184727823 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1095G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727823 | |||||||
| chr4:184727843 | G | A | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1075C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727843 | |||||||
| chr4:184727844 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+1074A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727844 | |||||||
| chr4:184727975 | G | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.214+943C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727975 | |||||||
| chr4:184727987 | G | C | 1 | a0001c0001t0001g0189 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214+931C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184727987 | |||||||
| chr4:184728071 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214+847G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728071 | |||||||
| chr4:184728150 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.214+768A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728150 | |||||||
| chr4:184728256 | T | C | 16 | a0001c0001t0007g0234 a0002c0002t0002g0014 a0002c0002t0002g0015 others(13): Show |
18 | HG00609.hp2 HG00738.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+662A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728256 | |||||||
| chr4:184728277 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+641T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728277 | |||||||
| chr4:184728305 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+613T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728305 | |||||||
| chr4:184728335 | T | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.214+583A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728335 | |||||||
| chr4:184728376 | A | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.214+542T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728376 | |||||||
| chr4:184728397 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+521T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728397 | |||||||
| chr4:184728507 | G | T | 19 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(16): Show |
28 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+411C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728507 | |||||||
| chr4:184728673 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+245G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728673 | |||||||
| chr4:184728698 | T | C | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.214+220A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728698 | |||||||
| chr4:184728712 | C | A | 148 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(145): Show |
182 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.214+206G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728712 | |||||||
| chr4:184728724 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.214+194A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728724 | |||||||
| chr4:184728841 | A | C | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.214+77T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 3/12 | chr4 | 184728841 | |||||||
| chr4:184729122 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-87G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729122 | |||||||
| chr4:184729239 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.97-204A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729239 | |||||||
| chr4:184729304 | A | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-269T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729304 | |||||||
| chr4:184729667 | A | C | 107 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0264 others(104): Show |
130 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.97-632T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729667 | |||||||
| chr4:184729695 | T | C | 4 | a0004c0007t0003g0279 a0004c0007t0003g0280 a0004c0007t0003g0281 others(1): Show |
4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-660A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729695 | |||||||
| chr4:184729741 | T | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-706A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729741 | |||||||
| chr4:184729787 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-752T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729787 | |||||||
| chr4:184729902 | T | C | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.97-867A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184729902 | |||||||
| chr4:184730074 | C | A | 1 | a0002c0002t0008g0068 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.96+846G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730074 | |||||||
| chr4:184730109 | G | A | 5 | a0005c0004t0001g0029 a0005c0004t0001g0289 a0005c0004t0001g0290 others(2): Show |
6 | HG00733.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+811C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730109 | |||||||
| chr4:184730248 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | NA18962.hp1 NA19001.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.96+672G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730248 | |||||||
| chr4:184730262 | C | T | 39 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(36): Show |
50 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.96+658G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730262 | |||||||
| chr4:184730297 | G | T | 65 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0002c0002t0002g0002 others(62): Show |
77 | HG00280.hp1 HG00558.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.96+623C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730297 | |||||||
| chr4:184730463 | A | G | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+457T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730463 | |||||||
| chr4:184730484 | C | T | 40 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(37): Show |
51 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.96+436G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730484 | |||||||
| chr4:184730505 | G | A | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.96+415C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730505 | |||||||
| chr4:184730507 | T | TAAAGAAA others(314): Show |
1 | a0003c0003t0003g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(319): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(318): Show |
10 | a0003c0008t0004g0158 a0003c0008t0004g0241 a0003c0008t0004g0247 others(7): Show |
16 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+412_96+413insTT others(323): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(322): Show |
2 | a0003c0003t0003g0265 a0004c0007t0003g0279 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(327): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(325): Show |
7 | a0003c0003t0003g0027 a0003c0003t0003g0266 a0004c0007t0003g0280 others(4): Show |
11 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+412_96+413insTT others(330): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(326): Show |
1 | a0006c0006t0005g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(331): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(328): Show |
2 | a0006c0006t0005g0127 a0006c0006t0005g0130 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(333): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(334): Show |
1 | a0003c0003t0003g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(339): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(338): Show |
2 | a0003c0003t0003g0028 a0004c0007t0003g0281 |
3 | HG02280.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(343): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(339): Show |
2 | a0003c0003t0003g0267 a0004c0007t0003g0282 |
2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(344): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(343): Show |
1 | a0003c0003t0003g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(348): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(344): Show |
3 | a0003c0003t0003g0269 a0003c0003t0003g0270 a0003c0003t0003g0271 |
3 | HG01167.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(349): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(346): Show |
1 | a0003c0003t0003g0272 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(351): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(351): Show |
1 | a0003c0003t0003g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.96+412_96+413insTT others(356): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(353): Show |
1 | a0003c0003t0003g0274 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(358): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(355): Show |
2 | a0003c0003t0003g0275 a0003c0003t0003g0276 |
2 | HG01081.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.96+412_96+413insTT others(360): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730507 | T | TAAAGAAA others(360): Show |
1 | a0003c0003t0003g0277 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+412_96+413insTT others(365): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730507 | |||||||
| chr4:184730518 | A | ACATGCGG others(322): Show |
1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+401_96+402insCG others(327): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730518 | |||||||
| chr4:184730518 | A | ACATGCGG others(323): Show |
1 | a0004c0005t0016g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+401_96+402insCG others(328): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730518 | |||||||
| chr4:184730590 | T | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02083.hp2 NA18939.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.96+330A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730590 | |||||||
| chr4:184730601 | TA | T | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.96+318delT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730601 | |||||||
| chr4:184730602 | A | C | 2 | a0004c0005t0016g0284 a0010c0013t0005g0126 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.96+318T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 2/12 | chr4 | 184730602 | |||||||
| chr4:184730993 | G | A | 112 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.48-25C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184730993 | |||||||
| chr4:184731047 | G | A | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-79C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731047 | |||||||
| chr4:184731070 | AC | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(238): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.48-103delG | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731070 | |||||||
| chr4:184731071 | C | A | 3 | a0001c0001t0017g0150 a0002c0002t0002g0105 a0010c0013t0005g0126 |
3 | HG02615.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.48-103G>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731071 | |||||||
| chr4:184731148 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.48-180G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731148 | |||||||
| chr4:184731195 | G | A | 3 | a0002c0002t0002g0111 a0002c0002t0011g0109 a0002c0002t0011g0110 |
3 | NA18961.hp2 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.48-227C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731195 | |||||||
| chr4:184731234 | C | G | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-266G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731234 | |||||||
| chr4:184731305 | C | T | 1 | a0002c0002t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.48-337G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731305 | |||||||
| chr4:184731400 | G | A | 21 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0243 others(18): Show |
23 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.48-432C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731400 | |||||||
| chr4:184731540 | G | A | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-572C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731540 | |||||||
| chr4:184731554 | A | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-586T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731554 | |||||||
| chr4:184731590 | A | G | 1 | a0002c0002t0002g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.48-622T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731590 | |||||||
| chr4:184731594 | C | T | 1 | a0010c0013t0005g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.48-626G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731594 | |||||||
| chr4:184731673 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0242 |
4 | HG00099.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-705G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731673 | |||||||
| chr4:184731676 | G | C | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-708C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731676 | |||||||
| chr4:184731677 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.48-709C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731677 | |||||||
| chr4:184731717 | A | T | 135 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.48-749T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731717 | |||||||
| chr4:184731761 | C | T | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-793G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731761 | |||||||
| chr4:184731813 | T | A | 1 | a0001c0001t0017g0150 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.48-845A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731813 | |||||||
| chr4:184731820 | A | G | 103 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0002c0002t0002g0001 others(100): Show |
126 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.48-852T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731820 | |||||||
| chr4:184731838 | C | G | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-870G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731838 | |||||||
| chr4:184731847 | C | T | 284 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(281): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.48-879G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731847 | |||||||
| chr4:184731881 | C | CTGTGTGT others(9): Show |
2 | a0001c0001t0001g0160 a0001c0001t0017g0150 |
2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48-914_48-913insCA others(14): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731881 | |||||||
| chr4:184731883 | C | CTG | 29 | a0001c0001t0001g0231 a0001c0001t0001g0240 a0001c0001t0007g0252 others(26): Show |
33 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.48-917_48-916dupCA | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0010g0146 a0001c0001t0010g0147 a0001c0001t0010g0149 others(1): Show |
4 | HG02970.hp2 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-923_48-916dupCA others(6): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(3): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0024 others(38): Show |
49 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.48-925_48-916dupCA others(8): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(5): Show |
70 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0202 others(67): Show |
84 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.48-927_48-916dupCA others(10): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(7): Show |
45 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
58 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.48-929_48-916dupCA others(12): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(9): Show |
35 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0141 others(32): Show |
40 | HG00621.hp2 HG00733.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.48-931_48-916dupCA others(14): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(11): Show |
16 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0183 others(13): Show |
17 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.48-933_48-916dupCA others(16): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(13): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
17 | HG00738.hp1 HG02015.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.48-935_48-916dupCA others(18): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(15): Show |
13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0164 others(10): Show |
15 | HG01168.hp2 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.48-937_48-916dupCA others(20): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(17): Show |
2 | a0001c0001t0001g0163 a0005c0004t0014g0293 |
2 | HG01975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.48-939_48-916dupCA others(22): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | CTGTGTGT others(19): Show |
2 | a0005c0004t0009g0291 a0005c0004t0009g0292 |
2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.48-941_48-916dupCA others(24): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731883 | C | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0232 a0001c0001t0017g0150 |
3 | HG02572.hp1 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48-915G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731883 | |||||||
| chr4:184731904 | T | TGC | 7 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(4): Show |
8 | HG02280.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.48-937_48-936insGC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731904 | |||||||
| chr4:184731966 | G | A | 1 | a0002c0002t0002g0121 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.48-998C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184731966 | |||||||
| chr4:184732074 | T | C | 1 | a0001c0001t0007g0234 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.48-1106A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732074 | |||||||
| chr4:184732107 | A | G | 1 | a0003c0003t0003g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.48-1139T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732107 | |||||||
| chr4:184732197 | T | A | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.48-1229A>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732197 | |||||||
| chr4:184732222 | A | G | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(2): Show |
6 | HG02056.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.48-1254T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732222 | |||||||
| chr4:184732248 | T | TA | 243 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(240): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.48-1281dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732248 | |||||||
| chr4:184732366 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48-1398G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732366 | |||||||
| chr4:184732414 | C | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(236): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.48-1446G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732414 | |||||||
| chr4:184732486 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.48-1518C>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732486 | |||||||
| chr4:184732542 | G | A | 246 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(243): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.47+1474C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732542 | |||||||
| chr4:184732568 | G | A | 2 | a0004c0007t0003g0281 a0004c0007t0003g0282 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.47+1448C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732568 | |||||||
| chr4:184732611 | C | T | 2 | a0002c0002t0002g0037 a0002c0002t0008g0033 |
2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.47+1405G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732611 | |||||||
| chr4:184732618 | T | TG | 117 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.47+1397dupC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732618 | |||||||
| chr4:184732618 | TG | T | 15 | a0003c0008t0004g0247 a0004c0005t0004g0003 a0004c0005t0004g0283 others(12): Show |
24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+1397delC | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732618 | |||||||
| chr4:184732655 | C | G | 247 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(244): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.47+1361G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732655 | |||||||
| chr4:184732672 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.47+1344C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732672 | |||||||
| chr4:184732770 | C | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.47+1246G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732770 | |||||||
| chr4:184732919 | T | C | 7 | a0006c0006t0005g0008 a0006c0006t0005g0017 a0006c0006t0005g0127 others(4): Show |
10 | HG00639.hp2 HG00733.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.47+1097A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732919 | |||||||
| chr4:184732985 | C | CA | 11 | a0001c0001t0006g0026 a0001c0001t0006g0258 a0001c0001t0006g0259 others(8): Show |
12 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.47+1030dupT | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | |||||||
| chr4:184732985 | CAA | C | 123 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(120): Show |
147 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.47+1029_47+1030del others(2): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | |||||||
| chr4:184732985 | CAAA | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(134): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.47+1028_47+1030del others(3): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | |||||||
| chr4:184732985 | CAAAA | C | 12 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
18 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+1027_47+1030del others(4): Show |
CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184732985 | |||||||
| chr4:184733046 | T | C | 1 | a0004c0005t0004g0288 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.47+970A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733046 | |||||||
| chr4:184733083 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.47+933T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733083 | |||||||
| chr4:184733147 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+869G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733147 | |||||||
| chr4:184733166 | C | T | 115 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(112): Show |
138 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.47+850G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733166 | |||||||
| chr4:184733220 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(280): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.47+796T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733220 | |||||||
| chr4:184733359 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0242 |
4 | HG00099.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+657C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733359 | |||||||
| chr4:184733497 | T | C | 15 | a0003c0003t0003g0027 a0003c0003t0003g0028 a0003c0003t0003g0265 others(12): Show |
17 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.47+519A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733497 | |||||||
| chr4:184733511 | A | C | 4 | a0001c0001t0001g0148 a0001c0001t0010g0146 a0001c0001t0010g0147 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.47+505T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733511 | |||||||
| chr4:184733513 | A | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.47+503T>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733513 | |||||||
| chr4:184733522 | G | C | 298 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(295): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.47+494C>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733522 | |||||||
| chr4:184733529 | T | C | 134 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(131): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.47+487A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733529 | |||||||
| chr4:184733556 | C | T | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+460G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733556 | |||||||
| chr4:184733569 | T | C | 167 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(164): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.47+447A>G | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733569 | |||||||
| chr4:184733598 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.47+418T>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733598 | |||||||
| chr4:184733643 | G | A | 19 | a0004c0007t0003g0279 a0004c0007t0003g0280 a0004c0007t0003g0281 others(16): Show |
22 | HG00733.hp1 HG01975.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.47+373C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733643 | |||||||
| chr4:184733661 | A | G | 7 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
7 | HG02602.hp2 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.47+355T>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733661 | |||||||
| chr4:184733673 | T | G | 15 | a0003c0008t0004g0247 a0004c0005t0004g0003 a0004c0005t0004g0283 others(12): Show |
24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.47+343A>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733673 | |||||||
| chr4:184733683 | C | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.47+333G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733683 | |||||||
| chr4:184733802 | C | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG01928.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.47+214G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733802 | |||||||
| chr4:184733804 | C | T | 1 | a0004c0005t0004g0283 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.47+212G>A | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733804 | |||||||
| chr4:184733937 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.47+79C>T | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733937 | |||||||
| chr4:184733985 | C | G | 4 | a0004c0007t0003g0279 a0004c0007t0003g0280 a0004c0007t0003g0281 others(1): Show |
4 | HG02280.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+31G>C | CENPU | ENSG00000151725.12 | transcript | ENST00000281453.10 | protein_coding | 1/12 | chr4 | 184733985 |