Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55165 |
| ensemblid | ENSG00000138180.16 |
| hgncid | 1161 |
| symbol | CEP55 |
| name | centrosomal protein 55 |
| refseq_nuc | NM_018131.5 |
| refseq_prot | NP_060601.4 |
| ensembl_nuc | ENST00000371485.8 |
| ensembl_prot | ENSP00000360540.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 93496612 |
| end | 93529092 |
| strand | + |
| ver | v1.2 |
| region | chr10:93496612-93529092 |
| region5000 | chr10:93491612-93534092 |
| regionname0 | CEP55_chr10_93496612_93529092 |
| regionname5000 | CEP55_chr10_93491612_93534092 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 464 | 144 | 19 | 34 | 61 | 6 | 23 | 46 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0002 | 0/0 | 464 | 72 | 12 | 3 | 50 | 2 | 5 | 34 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0003 | 0/0 | 464 | 49 | 11 | 12 | 24 | 1 | 1 | 18 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0004 | 0/0 | 464 | 24 | 3 | 0 | 18 | 0 | 3 | 14 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0005 | 0/0 | 464 | 17 | 0 | 8 | 8 | 0 | 1 | 5 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0006 | 0/0 | 464 | 17 | 3 | 6 | 3 | 1 | 4 | 3 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0007 | 0/0 | 464 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0008 | 0/0 | 464 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0009 | 0/0 | 464 | 8 | 0 | 3 | 0 | 2 | 3 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0010 | 1/0 | 464 | 7 | 5 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0011 | 0/0 | 464 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0012 | 0/0 | 464 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0013 | 0/0 | 464 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0014 | 0/0 | 464 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0015 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0016 | 0/0 | 464 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0017 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0018 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0019 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| a0020 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | MSSRS others(459): Show |
chr10 | 93491612 | 93534092 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1392 | 143 | 19 | 34 | 61 | 6 | 22 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0001c0022 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0002c0002 | 0/0 | 1392 | 69 | 9 | 3 | 50 | 2 | 5 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0002c0013 | 0/0 | 1392 | 3 | 3 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0003c0003 | 0/0 | 1392 | 49 | 11 | 12 | 24 | 1 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0004c0004 | 0/0 | 1392 | 24 | 3 | 0 | 18 | 0 | 3 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0005c0005 | 0/0 | 1392 | 17 | 0 | 8 | 8 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0006c0006 | 0/0 | 1392 | 17 | 3 | 6 | 3 | 1 | 4 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0007c0007 | 0/0 | 1392 | 13 | 12 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0008c0008 | 0/0 | 1392 | 12 | 12 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0009c0010 | 0/0 | 1392 | 6 | 0 | 1 | 0 | 2 | 3 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0009c0015 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0010c0009 | 1/0 | 1392 | 7 | 5 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0011c0011 | 0/0 | 1392 | 6 | 6 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0012c0012 | 0/0 | 1392 | 4 | 4 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0013c0017 | 0/0 | 1392 | 2 | 1 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0013c0023 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0014c0018 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0015c0016 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0016c0014 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0017c0019 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0018c0021 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0019c0024 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 | ||
| a0020c0020 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | ATGTC others(1387): Show |
chr10 | 93491612 | 93534092 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2657 | 137 | 19 | 34 | 57 | 6 | 20 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0001c0001t0002 | 0/0 | 2658 | 5 | 0 | 0 | 4 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0001c0001t0010 | 0/0 | 2657 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0001c0022t0001 | 0/0 | 2657 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0002c0002t0001 | 0/0 | 2657 | 6 | 0 | 2 | 4 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0002c0002t0002 | 0/0 | 2658 | 62 | 9 | 1 | 45 | 2 | 5 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0002c0002t0007 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0002c0013t0005 | 0/0 | 2657 | 3 | 3 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0001 | 0/0 | 2657 | 3 | 3 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0002 | 0/0 | 2658 | 41 | 3 | 12 | 24 | 1 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0004 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0005 | 0/0 | 2657 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0008 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0003c0003t0009 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0004c0004t0001 | 0/0 | 2657 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0004c0004t0002 | 0/0 | 2658 | 23 | 3 | 0 | 17 | 0 | 3 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0005c0005t0001 | 0/0 | 2657 | 17 | 0 | 8 | 8 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0006c0006t0001 | 0/0 | 2657 | 16 | 3 | 5 | 3 | 1 | 4 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0006c0006t0002 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0007c0007t0003 | 0/0 | 2658 | 11 | 10 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0007c0007t0006 | 0/0 | 2658 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0008c0008t0002 | 0/0 | 2658 | 11 | 11 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0008c0008t0006 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0009c0010t0002 | 0/0 | 2658 | 6 | 0 | 1 | 0 | 2 | 3 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0009c0015t0002 | 0/0 | 2658 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0010c0009t0002 | 1/0 | 2658 | 7 | 5 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0011c0011t0001 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0011c0011t0002 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0011c0011t0004 | 0/0 | 2657 | 3 | 3 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0011c0011t0006 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0012c0012t0002 | 0/0 | 2658 | 4 | 4 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0013c0017t0002 | 0/0 | 2658 | 2 | 1 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0013c0023t0002 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0014c0018t0001 | 0/0 | 2657 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0015c0016t0002 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0015c0016t0004 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0016c0014t0002 | 0/0 | 2658 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0017c0019t0001 | 0/0 | 2657 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| a0018c0021t0002 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0019c0024t0002 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2653): Show |
chr10 | 93491612 | 93534092 |
| a0020c0020t0001 | 0/0 | 2657 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | AAACT others(2652): Show |
chr10 | 93491612 | 93534092 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 4 | 8 | 4 | 1 | 2 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0001c0022t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0003 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0013t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0013t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0002c0013t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0010 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0003c0003t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0004c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0005c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0006c0006t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0007c0007t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0008c0008t0002g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0008c0008t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0008c0008t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0008c0008t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0008c0008t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0010t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0010t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0010t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0010t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0010t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0015t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0009c0015t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0010c0009t0002g0007 | 1/0 | 7 | 5 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0011c0011t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0012c0012t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0012c0012t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0012c0012t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0013c0017t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0013c0017t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0013c0023t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0014c0018t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0015c0016t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0015c0016t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0016c0014t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0017c0019t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0018c0021t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0019c0024t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| a0020c0020t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0010 | t0002 | g0197 | EUR | GBR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00140 | hp1 | a0009 | c0010 | t0002 | g0042 | EUR | GBR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0096 | EUR | FIN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00408 | hp1 | a0003 | c0003 | t0002 | g0010 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00438 | hp2 | a0005 | c0005 | t0001 | g0152 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0046 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00621 | hp1 | a0005 | c0005 | t0001 | g0180 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00735 | hp1 | a0005 | c0005 | t0001 | g0016 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00741 | hp1 | a0017 | c0019 | t0001 | g0242 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG00741 | hp2 | a0009 | c0015 | t0002 | g0229 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0241 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01070 | hp2 | a0005 | c0005 | t0001 | g0127 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0046 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01074 | hp1 | a0009 | c0010 | t0002 | g0200 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01081 | hp1 | a0009 | c0015 | t0002 | g0256 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01081 | hp2 | a0005 | c0005 | t0001 | g0016 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01099 | hp1 | a0013 | c0017 | t0002 | g0090 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0235 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01167 | hp2 | a0014 | c0018 | t0001 | g0029 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01168 | hp1 | a0006 | c0006 | t0001 | g0028 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01169 | hp2 | a0014 | c0018 | t0001 | g0029 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0169 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01192 | hp2 | a0006 | c0006 | t0001 | g0077 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01243 | hp2 | a0007 | c0007 | t0003 | g0054 | AMR | PUR | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01255 | hp1 | a0006 | c0006 | t0001 | g0014 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01257 | hp2 | a0006 | c0006 | t0001 | g0028 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01261 | hp2 | a0006 | c0006 | t0001 | g0111 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01346 | hp2 | a0003 | c0003 | t0002 | g0010 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01361 | hp1 | a0006 | c0006 | t0002 | g0112 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0156 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01433 | hp1 | a0010 | c0009 | t0002 | g0007 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0214 | EUR | IBS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01891 | hp2 | a0012 | c0012 | t0002 | g0022 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01928 | hp1 | a0005 | c0005 | t0001 | g0036 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0039 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01975 | hp1 | a0003 | c0003 | t0002 | g0145 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG01981 | hp2 | a0005 | c0005 | t0001 | g0036 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02004 | hp2 | a0005 | c0005 | t0001 | g0162 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02040 | hp1 | a0003 | c0003 | t0002 | g0227 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02055 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02056 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02071 | hp2 | a0003 | c0003 | t0002 | g0039 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0190 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02129 | hp1 | a0004 | c0004 | t0002 | g0040 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02132 | hp1 | a0005 | c0005 | t0001 | g0164 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02145 | hp2 | a0018 | c0021 | t0002 | g0055 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02148 | hp1 | a0005 | c0005 | t0001 | g0163 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02148 | hp2 | a0005 | c0005 | t0001 | g0184 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02155 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | CDX | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | CDX | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02257 | hp1 | a0007 | c0007 | t0003 | g0009 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02257 | hp2 | a0004 | c0004 | t0002 | g0033 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0102 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02258 | hp2 | a0007 | c0007 | t0006 | g0192 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02273 | hp1 | a0003 | c0003 | t0002 | g0010 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02280 | hp1 | a0011 | c0011 | t0004 | g0059 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0168 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02572 | hp2 | a0007 | c0007 | t0003 | g0009 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02602 | hp1 | a0006 | c0006 | t0001 | g0078 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02615 | hp1 | a0008 | c0008 | t0002 | g0069 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02615 | hp2 | a0007 | c0007 | t0003 | g0009 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02622 | hp1 | a0003 | c0003 | t0005 | g0134 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02622 | hp2 | a0011 | c0011 | t0004 | g0061 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02630 | hp2 | a0006 | c0006 | t0001 | g0032 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02683 | hp1 | a0009 | c0010 | t0002 | g0198 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02683 | hp2 | a0005 | c0005 | t0001 | g0196 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02717 | hp1 | a0011 | c0011 | t0001 | g0070 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02717 | hp2 | a0006 | c0006 | t0001 | g0032 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02723 | hp1 | a0007 | c0007 | t0003 | g0009 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02735 | hp2 | a0004 | c0004 | t0002 | g0172 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02809 | hp1 | a0007 | c0007 | t0003 | g0056 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02818 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02818 | hp2 | a0004 | c0004 | t0002 | g0187 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02886 | hp1 | a0007 | c0007 | t0003 | g0009 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02886 | hp2 | a0015 | c0016 | t0004 | g0049 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02895 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02896 | hp1 | a0016 | c0014 | t0002 | g0045 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02897 | hp1 | a0008 | c0008 | t0002 | g0023 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02897 | hp2 | a0016 | c0014 | t0002 | g0045 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02922 | hp2 | a0007 | c0007 | t0003 | g0057 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02965 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02970 | hp1 | a0015 | c0016 | t0002 | g0194 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02970 | hp2 | a0007 | c0007 | t0003 | g0204 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02976 | hp2 | a0012 | c0012 | t0002 | g0022 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03041 | hp2 | a0007 | c0007 | t0003 | g0212 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03130 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03130 | hp2 | a0003 | c0003 | t0008 | g0205 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03139 | hp1 | a0010 | c0009 | t0002 | g0007 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03139 | hp2 | a0003 | c0003 | t0009 | g0063 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03209 | hp1 | a0002 | c0013 | t0005 | g0116 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03209 | hp2 | a0008 | c0008 | t0002 | g0068 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03225 | hp1 | a0013 | c0017 | t0002 | g0122 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03225 | hp2 | a0002 | c0013 | t0005 | g0103 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03453 | hp1 | a0011 | c0011 | t0006 | g0060 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0033 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03486 | hp1 | a0012 | c0012 | t0002 | g0067 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03486 | hp2 | a0011 | c0011 | t0004 | g0062 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0210 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03540 | hp1 | a0003 | c0003 | t0005 | g0232 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03540 | hp2 | a0010 | c0009 | t0002 | g0007 | AFR | GWD | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0072 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03579 | hp2 | a0008 | c0008 | t0002 | g0006 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03654 | hp1 | a0009 | c0010 | t0002 | g0042 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03654 | hp2 | a0003 | c0003 | t0002 | g0236 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03688 | hp2 | a0006 | c0006 | t0001 | g0014 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03831 | hp2 | a0004 | c0004 | t0002 | g0037 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03834 | hp2 | a0004 | c0004 | t0002 | g0037 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0114 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03942 | hp2 | a0006 | c0006 | t0001 | g0105 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04199 | hp1 | a0009 | c0010 | t0002 | g0199 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04204 | hp2 | a0006 | c0006 | t0001 | g0014 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04228 | hp1 | a0001 | c0022 | t0001 | g0238 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18522 | hp1 | a0010 | c0009 | t0002 | g0007 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18522 | hp2 | a0008 | c0008 | t0002 | g0023 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0239 | EAS | CHB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | CHB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | CHB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18747 | hp2 | a0004 | c0004 | t0002 | g0041 | EAS | CHB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18906 | hp2 | a0010 | c0009 | t0002 | g0007 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18943 | hp2 | a0004 | c0004 | t0002 | g0175 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18946 | hp1 | a0004 | c0004 | t0002 | g0189 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18947 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18947 | hp2 | a0005 | c0005 | t0001 | g0182 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18949 | hp1 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18950 | hp1 | a0002 | c0002 | t0007 | g0106 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18950 | hp2 | a0004 | c0004 | t0002 | g0151 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18951 | hp2 | a0003 | c0003 | t0002 | g0186 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18952 | hp1 | a0006 | c0006 | t0001 | g0091 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18965 | hp1 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18965 | hp2 | a0006 | c0006 | t0001 | g0125 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18972 | hp2 | a0005 | c0005 | t0001 | g0181 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18974 | hp2 | a0003 | c0003 | t0002 | g0183 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18977 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18977 | hp2 | a0004 | c0004 | t0002 | g0138 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18981 | hp2 | a0005 | c0005 | t0001 | g0132 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18983 | hp1 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18987 | hp1 | a0004 | c0004 | t0002 | g0019 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18989 | hp1 | a0006 | c0006 | t0001 | g0110 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19003 | hp2 | a0004 | c0004 | t0001 | g0179 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19004 | hp1 | a0004 | c0004 | t0002 | g0040 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19004 | hp2 | a0005 | c0005 | t0001 | g0159 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19006 | hp2 | a0003 | c0003 | t0002 | g0171 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19009 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19012 | hp1 | a0004 | c0004 | t0002 | g0158 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19030 | hp1 | a0010 | c0009 | t0002 | g0007 | AFR | LWK | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19030 | hp2 | a0007 | c0007 | t0003 | g0064 | AFR | LWK | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19043 | hp1 | a0002 | c0013 | t0005 | g0002 | AFR | LWK | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19043 | hp2 | a0013 | c0023 | t0002 | g0193 | AFR | LWK | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19054 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19063 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19063 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19066 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19068 | hp2 | a0005 | c0005 | t0001 | g0016 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19074 | hp2 | a0004 | c0004 | t0002 | g0041 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19079 | hp2 | a0019 | c0024 | t0002 | g0108 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19082 | hp1 | a0004 | c0004 | t0002 | g0155 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0148 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19086 | hp2 | a0020 | c0020 | t0001 | g0004 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0228 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19091 | hp2 | a0003 | c0003 | t0002 | g0136 | EAS | JPT | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19240 | hp1 | a0007 | c0007 | t0006 | g0058 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | YRI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20129 | hp1 | a0008 | c0008 | t0006 | g0065 | AFR | ASW | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | ASW | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0085 | EUR | TSI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20805 | hp1 | a0006 | c0006 | t0001 | g0088 | EUR | TSI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02109 | hp1 | a0011 | c0011 | t0002 | g0053 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02486 | hp1 | a0006 | c0006 | t0001 | g0082 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02486 | hp2 | a0012 | c0012 | t0002 | g0066 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02559 | hp1 | a0008 | c0008 | t0002 | g0006 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0021 | AFR | ACB | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0021 | AFR | MSL | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | USA | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0050 | AFR | USA | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0230 | REF | REF | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| homoSapiens | grch38p0 | a0010 | c0009 | t0002 | g0007 | REF | REF | CEP55_chr10_93491612_93534092 | CEP55 | chr10 | 93491612 | 93534092 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:93500121 | G | A | 1 | a0017 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.70G>A | p.Glu24Lys | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/9 | 394/2658 | 70/1395 | 24/464 | chr10 | 93500121 | |||
| chr10:93500222 | C | G | 7 | a0002 a0006 a0008 others(4): Show |
111 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(108): Show |
missense_variant | MODERATE | c.171C>G | p.His57Gln | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/9 | 495/2658 | 171/1395 | 57/464 | chr10 | 93500222 | |||
| chr10:93500226 | C | T | 2 | a0008 a0012 |
16 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(13): Show |
missense_variant | MODERATE | c.175C>T | p.Leu59Phe | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/9 | 499/2658 | 175/1395 | 59/464 | chr10 | 93500226 | |||
| chr10:93503224 | A | G | 19 | a0001 a0002 a0003 others(16): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
missense_variant | MODERATE | c.295A>G | p.Thr99Ala | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/9 | 619/2658 | 295/1395 | 99/464 | chr10 | 93503224 | |||
| chr10:93503307 | C | A | 1 | a0020 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.378C>A | p.Asp126Glu | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/9 | 702/2658 | 378/1395 | 126/464 | chr10 | 93503307 | |||
| chr10:93507042 | A | G | 1 | a0015 | 2 | HG02886.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.514A>G | p.Ile172Val | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/9 | 838/2658 | 514/1395 | 172/464 | chr10 | 93507042 | |||
| chr10:93515516 | C | A | 1 | a0016 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.640C>A | p.His214Asn | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/9 | 964/2658 | 640/1395 | 214/464 | chr10 | 93515516 | |||
| chr10:93516935 | G | A | 3 | a0007 a0015 a0018 |
16 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
missense_variant&splice_region_variant | MODERATE | c.680G>A | p.Gly227Asp | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/9 | 1004/2658 | 680/1395 | 227/464 | chr10 | 93516935 | |||
| chr10:93516961 | T | C | 7 | a0007 a0008 a0011 others(4): Show |
39 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(36): Show |
missense_variant | MODERATE | c.706T>C | p.Cys236Arg | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/9 | 1030/2658 | 706/1395 | 236/464 | chr10 | 93516961 | |||
| chr10:93516985 | G | C | 3 | a0004 a0005 a0019 |
42 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(39): Show |
missense_variant | MODERATE | c.730G>C | p.Ala244Pro | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/9 | 1054/2658 | 730/1395 | 244/464 | chr10 | 93516985 | |||
| chr10:93518926 | G | A | 1 | a0009 | 8 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(5): Show |
missense_variant | MODERATE | c.1043G>A | p.Arg348Lys | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/9 | 1367/2658 | 1043/1395 | 348/464 | chr10 | 93518926 | |||
| chr10:93519749 | A | T | 7 | a0001 a0005 a0006 others(4): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
missense_variant | MODERATE | c.1133A>T | p.His378Leu | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/9 | 1457/2658 | 1133/1395 | 378/464 | chr10 | 93519749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:93500210 | T | C | 1 | a0002c0013 | 3 | HG03209.hp1 HG03225.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.159T>C | p.Asp53Asp | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/9 | 483/2658 | 159/1395 | 53/464 | chr10 | 93500210 | |||
| chr10:93503133 | T | A | 1 | a0009c0010 | 6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
synonymous_variant | LOW | c.204T>A | p.Ala68Ala | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/9 | 528/2658 | 204/1395 | 68/464 | chr10 | 93503133 | |||
| chr10:93503223 | C | T | 1 | a0001c0022 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.294C>T | p.Thr98Thr | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/9 | 618/2658 | 294/1395 | 98/464 | chr10 | 93503223 | |||
| chr10:93528030 | C | T | 1 | a0013c0023 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1272C>T | p.Ala424Ala | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 1596/2658 | 1272/1395 | 424/464 | chr10 | 93528030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:93528261 | A | G | 1 | a0001c0001t0010 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 108 | chr10 | 93528261 | ||||||
| chr10:93528396 | AC | A | 2 | a0002c0013t0005 a0003c0003t0005 |
5 | HG02622.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*244delC | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 244 | chr10 | 93528396 | ||||||
| chr10:93528445 | C | T | 4 | a0003c0003t0004 a0003c0003t0009 a0011c0011t0004 others(1): Show |
6 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 292 | chr10 | 93528445 | ||||||
| chr10:93528501 | GT | G | 12 | a0001c0001t0001 a0001c0001t0010 a0001c0022t0001 others(9): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*352delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 352 | INFO_REALIGN_3_PRIME | chr10 | 93528501 | |||||
| chr10:93528547 | G | A | 1 | a0007c0007t0003 | 11 | HG01243.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*394G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 394 | chr10 | 93528547 | ||||||
| chr10:93528624 | AT | A | 4 | a0003c0003t0004 a0003c0003t0009 a0011c0011t0004 others(1): Show |
6 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*481delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chr10 | 93528624 | |||||
| chr10:93528641 | G | A | 8 | a0003c0003t0004 a0003c0003t0009 a0007c0007t0003 others(5): Show |
21 | HG01243.hp2 HG02257.hp1 HG02258.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 488 | chr10 | 93528641 | ||||||
| chr10:93528703 | C | T | 1 | a0003c0003t0009 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 550 | chr10 | 93528703 | ||||||
| chr10:93528715 | G | C | 1 | a0002c0002t0007 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 562 | chr10 | 93528715 | ||||||
| chr10:93529011 | T | C | 1 | a0003c0003t0008 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*858T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 9/9 | 858 | chr10 | 93529011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:93497045 | T | C | 2 | a0003c0003t0002g0050 a0015c0016t0004g0049 |
2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-13+122T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497045 | |||||||
| chr10:93497069 | C | CT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(71): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.-13+153dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93497069 | ||||||
| chr10:93497118 | A | G | 1 | a0005c0005t0001g0196 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-13+195A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497118 | |||||||
| chr10:93497195 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | NA18968.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-13+272T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497195 | |||||||
| chr10:93497235 | T | G | 14 | a0003c0003t0002g0021 a0003c0003t0009g0063 a0007c0007t0003g0009 others(11): Show |
19 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-13+312T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497235 | |||||||
| chr10:93497361 | G | A | 12 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(9): Show |
21 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+438G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497361 | |||||||
| chr10:93497414 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-13+491C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497414 | |||||||
| chr10:93497422 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(66): Show |
98 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-13+499C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497422 | |||||||
| chr10:93497527 | G | T | 1 | a0015c0016t0002g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+604G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497527 | |||||||
| chr10:93497582 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(90): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-13+659A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497582 | |||||||
| chr10:93497638 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+715G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497638 | |||||||
| chr10:93497751 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+828A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497751 | |||||||
| chr10:93497782 | G | T | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-13+859G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497782 | |||||||
| chr10:93497797 | A | G | 2 | a0015c0016t0002g0194 a0015c0016t0004g0049 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-13+874A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497797 | |||||||
| chr10:93497952 | C | G | 2 | a0015c0016t0002g0194 a0015c0016t0004g0049 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-13+1029C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497952 | |||||||
| chr10:93497983 | G | T | 3 | a0013c0023t0002g0193 a0015c0016t0002g0194 a0015c0016t0004g0049 |
3 | HG02886.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+1060G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93497983 | |||||||
| chr10:93498047 | G | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(68): Show |
100 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-13+1124G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498047 | |||||||
| chr10:93498128 | C | A | 5 | a0009c0010t0002g0042 a0009c0010t0002g0197 a0009c0010t0002g0198 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+1205C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498128 | |||||||
| chr10:93498142 | C | CA | 9 | a0001c0001t0001g0126 a0001c0001t0001g0202 a0001c0001t0001g0203 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+1230dupA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93498142 | ||||||
| chr10:93498142 | C | CAA | 89 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(86): Show |
130 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.-13+1229_-13+1230d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93498142 | ||||||
| chr10:93498218 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0128 |
4 | HG03834.hp1 NA18985.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1295G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498218 | |||||||
| chr10:93498268 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-13+1345C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498268 | |||||||
| chr10:93498283 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-13+1360T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498283 | |||||||
| chr10:93498327 | C | T | 14 | a0003c0003t0002g0021 a0003c0003t0009g0063 a0007c0007t0003g0009 others(11): Show |
19 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-13+1404C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498327 | |||||||
| chr10:93498330 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-13+1407C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498330 | |||||||
| chr10:93498514 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-12-1526A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498514 | |||||||
| chr10:93498533 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-12-1507G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498533 | |||||||
| chr10:93498692 | C | A | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-12-1348C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498692 | |||||||
| chr10:93498749 | G | T | 1 | a0001c0001t0001g0048 | 2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-12-1291G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498749 | |||||||
| chr10:93498809 | C | CT | 151 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(148): Show |
224 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-12-1217dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93498809 | ||||||
| chr10:93498946 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-12-1094T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498946 | |||||||
| chr10:93498985 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12-1055C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93498985 | |||||||
| chr10:93498989 | ATTAGAG | A | 14 | a0003c0003t0002g0021 a0003c0003t0009g0063 a0007c0007t0003g0009 others(11): Show |
19 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-1047_-12-1042d others(8): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93498989 | ||||||
| chr10:93499393 | C | G | 67 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(64): Show |
95 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-12-647C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93499393 | |||||||
| chr10:93499505 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-12-535A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93499505 | |||||||
| chr10:93499518 | C | CT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0255 a0001c0001t0001g0257 others(5): Show |
10 | HG00140.hp2 HG01081.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-501dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93499518 | ||||||
| chr10:93499518 | CT | C | 29 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0135 others(26): Show |
34 | HG00099.hp1 HG01074.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-501delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93499518 | ||||||
| chr10:93499518 | CTT | C | 68 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(65): Show |
97 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-12-502_-12-501del others(2): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 93499518 | ||||||
| chr10:93499688 | A | T | 14 | a0003c0003t0002g0021 a0003c0003t0009g0063 a0007c0007t0003g0009 others(11): Show |
19 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-352A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93499688 | |||||||
| chr10:93499884 | T | C | 1 | a0003c0003t0002g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-12-156T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93499884 | |||||||
| chr10:93500018 | C | T | 5 | a0009c0010t0002g0042 a0009c0010t0002g0197 a0009c0010t0002g0198 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-22C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 1/8 | chr10 | 93500018 | |||||||
| chr10:93500266 | G | A | 8 | a0008c0008t0002g0006 a0008c0008t0002g0023 a0008c0008t0002g0068 others(5): Show |
16 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.183+32G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500266 | |||||||
| chr10:93500281 | G | C | 1 | a0013c0023t0002g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+47G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500281 | |||||||
| chr10:93500552 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.183+318C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500552 | |||||||
| chr10:93500558 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(72): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.183+324T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500558 | |||||||
| chr10:93500744 | G | A | 1 | a0006c0006t0001g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.183+510G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500744 | |||||||
| chr10:93500749 | C | T | 79 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(76): Show |
116 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.183+515C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500749 | |||||||
| chr10:93500761 | CT | C | 20 | a0001c0001t0001g0137 a0001c0001t0001g0215 a0002c0002t0002g0124 others(17): Show |
25 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+542delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 93500761 | ||||||
| chr10:93500777 | G | A | 2 | a0015c0016t0002g0194 a0015c0016t0004g0049 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.183+543G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500777 | |||||||
| chr10:93500931 | T | C | 3 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0006c0006t0001g0078 |
3 | HG00639.hp2 HG00738.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.183+697T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93500931 | |||||||
| chr10:93501010 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.183+776G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501010 | |||||||
| chr10:93501082 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(146): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.183+848G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501082 | |||||||
| chr10:93501122 | C | T | 13 | a0003c0003t0009g0063 a0007c0007t0003g0009 a0007c0007t0003g0054 others(10): Show |
17 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.183+888C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501122 | |||||||
| chr10:93501174 | G | A | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.183+940G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501174 | |||||||
| chr10:93501208 | A | G | 79 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(76): Show |
116 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.183+974A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501208 | |||||||
| chr10:93501476 | G | T | 1 | a0003c0003t0001g0024 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.183+1242G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501476 | |||||||
| chr10:93501558 | A | T | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.183+1324A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501558 | |||||||
| chr10:93501598 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG00738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183+1364G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501598 | |||||||
| chr10:93501631 | C | T | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183+1397C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501631 | |||||||
| chr10:93501674 | A | T | 1 | a0003c0003t0005g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-1439A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501674 | |||||||
| chr10:93501678 | T | A | 1 | a0002c0002t0002g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.184-1435T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501678 | |||||||
| chr10:93501711 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0139 others(5): Show |
14 | HG03710.hp1 HG04184.hp2 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.184-1402T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501711 | |||||||
| chr10:93501735 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(85): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.184-1378C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501735 | |||||||
| chr10:93501797 | C | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-1316C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501797 | |||||||
| chr10:93501947 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.184-1166A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501947 | |||||||
| chr10:93501999 | A | G | 1 | a0004c0004t0002g0189 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.184-1114A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93501999 | |||||||
| chr10:93502002 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.184-1111G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502002 | |||||||
| chr10:93502153 | TC | T | 65 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(62): Show |
93 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.184-959delC | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502153 | |||||||
| chr10:93502252 | G | A | 1 | a0002c0002t0002g0025 | 2 | NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.184-861G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502252 | |||||||
| chr10:93502322 | A | G | 2 | a0001c0001t0001g0133 a0004c0004t0002g0033 |
3 | HG02257.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.184-791A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502322 | |||||||
| chr10:93502372 | G | C | 79 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(76): Show |
116 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.184-741G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502372 | |||||||
| chr10:93502482 | A | G | 5 | a0009c0010t0002g0042 a0009c0010t0002g0197 a0009c0010t0002g0198 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-631A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502482 | |||||||
| chr10:93502487 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184-626T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502487 | |||||||
| chr10:93502577 | G | T | 1 | a0007c0007t0006g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.184-536G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502577 | |||||||
| chr10:93502740 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(151): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.184-373G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502740 | |||||||
| chr10:93502875 | T | C | 1 | a0011c0011t0002g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.184-238T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502875 | |||||||
| chr10:93502895 | T | C | 9 | a0008c0008t0002g0006 a0008c0008t0002g0023 a0008c0008t0002g0068 others(6): Show |
17 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.184-218T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502895 | |||||||
| chr10:93502969 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-144G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 2/8 | chr10 | 93502969 | |||||||
| chr10:93503762 | G | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+374G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93503762 | |||||||
| chr10:93503846 | A | G | 1 | a0009c0010t0002g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.459+458A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93503846 | |||||||
| chr10:93503973 | CT | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0218 others(3): Show |
6 | HG01070.hp2 HG01243.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+599delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 93503973 | ||||||
| chr10:93504035 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+647G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504035 | |||||||
| chr10:93504132 | C | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+744C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504132 | |||||||
| chr10:93504241 | G | A | 78 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(75): Show |
114 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.459+853G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504241 | |||||||
| chr10:93504330 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+942G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504330 | |||||||
| chr10:93504350 | G | A | 1 | a0007c0007t0006g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.459+962G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504350 | |||||||
| chr10:93504365 | C | T | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.459+977C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504365 | |||||||
| chr10:93504388 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+1000G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504388 | |||||||
| chr10:93504472 | C | CA | 82 | a0001c0001t0001g0133 a0001c0001t0001g0255 a0002c0002t0001g0079 others(79): Show |
119 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.459+1097dupA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 93504472 | ||||||
| chr10:93504472 | C | CAA | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(69): Show |
114 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.459+1096_459+1097d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 93504472 | ||||||
| chr10:93504472 | C | CAAA | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0051 others(8): Show |
13 | HG00423.hp2 HG00438.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+1095_459+1097d others(5): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 93504472 | ||||||
| chr10:93504496 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+1108T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504496 | |||||||
| chr10:93504618 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
5 | HG00140.hp1 HG02735.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+1230C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504618 | |||||||
| chr10:93504651 | T | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(151): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.459+1263T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504651 | |||||||
| chr10:93504750 | T | G | 74 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(71): Show |
109 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.459+1362T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504750 | |||||||
| chr10:93504876 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+1488G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504876 | |||||||
| chr10:93504945 | G | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+1557G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504945 | |||||||
| chr10:93504966 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(256): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.459+1578G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504966 | |||||||
| chr10:93504967 | A | G | 1 | a0007c0007t0006g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.459+1579A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504967 | |||||||
| chr10:93504969 | G | A | 1 | a0013c0017t0002g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459+1581G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93504969 | |||||||
| chr10:93505018 | G | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+1630G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505018 | |||||||
| chr10:93505040 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(146): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.459+1652T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505040 | |||||||
| chr10:93505121 | A | G | 69 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(66): Show |
96 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.459+1733A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505121 | |||||||
| chr10:93505158 | C | T | 64 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(61): Show |
91 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.459+1770C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505158 | |||||||
| chr10:93505164 | G | A | 2 | a0015c0016t0002g0194 a0015c0016t0004g0049 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.459+1776G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505164 | |||||||
| chr10:93505176 | T | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+1788T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505176 | |||||||
| chr10:93505181 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+1793A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505181 | |||||||
| chr10:93505489 | A | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1499A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505489 | |||||||
| chr10:93505622 | T | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1366T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505622 | |||||||
| chr10:93505736 | G | A | 4 | a0009c0010t0002g0197 a0009c0010t0002g0198 a0009c0010t0002g0199 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1252G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505736 | |||||||
| chr10:93505862 | T | TG | 71 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(68): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.460-1126_460-1125i others(3): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505862 | |||||||
| chr10:93505862 | T | TTG | 6 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG02723.hp2 HG02970.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-1126_460-1125i others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93505862 | |||||||
| chr10:93506041 | C | T | 4 | a0011c0011t0004g0059 a0011c0011t0004g0061 a0011c0011t0004g0062 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-947C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506041 | |||||||
| chr10:93506050 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(85): Show |
133 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.460-938G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506050 | |||||||
| chr10:93506135 | G | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.460-853G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506135 | |||||||
| chr10:93506181 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.460-807T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506181 | |||||||
| chr10:93506211 | GGATT | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01257.hp1 HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.460-776_460-773del others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506211 | |||||||
| chr10:93506214 | T | A | 1 | a0003c0003t0002g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.460-774T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506214 | |||||||
| chr10:93506286 | A | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.460-702A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506286 | |||||||
| chr10:93506388 | T | C | 1 | a0002c0002t0002g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.460-600T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506388 | |||||||
| chr10:93506447 | T | G | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.460-541T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506447 | |||||||
| chr10:93506654 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(146): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.460-334A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506654 | |||||||
| chr10:93506715 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.460-273A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506715 | |||||||
| chr10:93506718 | C | T | 4 | a0011c0011t0004g0059 a0011c0011t0004g0061 a0011c0011t0004g0062 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-270C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506718 | |||||||
| chr10:93506761 | A | G | 1 | a0009c0010t0002g0042 | 2 | HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.460-227A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506761 | |||||||
| chr10:93506853 | C | T | 1 | a0002c0002t0002g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.460-135C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506853 | |||||||
| chr10:93506926 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(69): Show |
103 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.460-62A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506926 | |||||||
| chr10:93506985 | C | T | 1 | a0004c0004t0002g0138 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.460-3C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 3/8 | chr10 | 93506985 | |||||||
| chr10:93507225 | C | CT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(77): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+185dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93507225 | ||||||
| chr10:93507225 | C | CTT | 6 | a0001c0001t0001g0213 a0001c0001t0001g0249 a0001c0001t0001g0254 others(3): Show |
8 | HG00140.hp1 HG01074.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+184_528+185dup others(2): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93507225 | ||||||
| chr10:93507292 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.528+236T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507292 | |||||||
| chr10:93507308 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.528+252C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507308 | |||||||
| chr10:93507382 | C | T | 1 | a0015c0016t0002g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.528+326C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507382 | |||||||
| chr10:93507383 | G | A | 1 | a0013c0023t0002g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+327G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507383 | |||||||
| chr10:93507413 | G | T | 1 | a0002c0013t0005g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.528+357G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507413 | |||||||
| chr10:93507422 | A | T | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.528+366A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507422 | |||||||
| chr10:93507517 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.528+461C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507517 | |||||||
| chr10:93507533 | G | T | 19 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0002g0003 others(16): Show |
27 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.528+477G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507533 | |||||||
| chr10:93507574 | C | T | 1 | a0005c0005t0001g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.528+518C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507574 | |||||||
| chr10:93507697 | G | A | 1 | a0004c0004t0002g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.528+641G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507697 | |||||||
| chr10:93507796 | C | T | 9 | a0003c0003t0002g0183 a0004c0004t0001g0179 a0004c0004t0002g0019 others(6): Show |
13 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+740C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507796 | |||||||
| chr10:93507870 | C | T | 65 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(62): Show |
92 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.528+814C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507870 | |||||||
| chr10:93507899 | G | A | 1 | a0006c0006t0001g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+843G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507899 | |||||||
| chr10:93507922 | C | T | 65 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0087 others(62): Show |
92 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.528+866C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507922 | |||||||
| chr10:93507958 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.528+902C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507958 | |||||||
| chr10:93507962 | T | C | 1 | a0001c0001t0002g0220 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.528+906T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507962 | |||||||
| chr10:93507996 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.528+940G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93507996 | |||||||
| chr10:93508058 | C | T | 1 | a0006c0006t0001g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.528+1002C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508058 | |||||||
| chr10:93508071 | G | A | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.528+1015G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508071 | |||||||
| chr10:93508123 | G | T | 1 | a0004c0004t0002g0187 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.528+1067G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508123 | |||||||
| chr10:93508507 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(149): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.528+1451G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508507 | |||||||
| chr10:93508512 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(74): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.528+1456A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508512 | |||||||
| chr10:93508542 | A | G | 4 | a0008c0008t0006g0065 a0013c0017t0002g0122 a0015c0016t0002g0194 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+1486A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508542 | |||||||
| chr10:93508616 | T | A | 1 | a0002c0002t0002g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.528+1560T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508616 | |||||||
| chr10:93508617 | A | C | 1 | a0002c0002t0002g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.528+1561A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508617 | |||||||
| chr10:93508681 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(86): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.528+1625T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508681 | |||||||
| chr10:93508793 | C | T | 1 | a0009c0010t0002g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.528+1737C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508793 | |||||||
| chr10:93508795 | G | C | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(101): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.528+1739G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508795 | |||||||
| chr10:93508872 | T | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(169): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.528+1816T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508872 | |||||||
| chr10:93508935 | T | C | 4 | a0003c0003t0002g0050 a0003c0003t0009g0063 a0008c0008t0006g0065 others(1): Show |
4 | HG03139.hp2 HG03225.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+1879T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93508935 | |||||||
| chr10:93509097 | AGCTTACA others(3): Show |
A | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+2046_528+2055d others(12): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509097 | ||||||
| chr10:93509233 | A | G | 4 | a0011c0011t0004g0059 a0011c0011t0004g0061 a0011c0011t0004g0062 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+2177A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509233 | |||||||
| chr10:93509240 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.528+2184C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509240 | |||||||
| chr10:93509416 | C | G | 2 | a0015c0016t0002g0194 a0015c0016t0004g0049 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.528+2360C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509416 | |||||||
| chr10:93509421 | A | AGCT | 4 | a0001c0001t0001g0044 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
5 | HG00639.hp1 HG01109.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+2379_528+2381d others(5): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509421 | ||||||
| chr10:93509450 | C | T | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+2394C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509450 | |||||||
| chr10:93509468 | C | CATTATTA others(5): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0003c0003t0008g0205 others(1): Show |
4 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2434_528+2445d others(14): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509468 | ||||||
| chr10:93509468 | C | CATTATTA others(8): Show |
5 | a0001c0001t0001g0203 a0009c0010t0002g0042 a0009c0010t0002g0197 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+2431_528+2445d others(17): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509468 | ||||||
| chr10:93509468 | CATT | C | 8 | a0001c0001t0001g0188 a0001c0001t0001g0216 a0002c0002t0002g0026 others(5): Show |
9 | HG02055.hp2 HG02135.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+2443_528+2445d others(5): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509468 | ||||||
| chr10:93509468 | CATTATT | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(234): Show |
350 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.528+2440_528+2445d others(8): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93509468 | ||||||
| chr10:93509581 | T | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(255): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.528+2525T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509581 | |||||||
| chr10:93509632 | C | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+2576C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509632 | |||||||
| chr10:93509678 | G | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(153): Show |
228 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.528+2622G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509678 | |||||||
| chr10:93509805 | C | G | 3 | a0003c0003t0002g0050 a0003c0003t0009g0063 a0013c0023t0002g0193 |
3 | HG03139.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.528+2749C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509805 | |||||||
| chr10:93509981 | C | T | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+2925C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93509981 | |||||||
| chr10:93510021 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.528+2965C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510021 | |||||||
| chr10:93510041 | T | G | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.528+2985T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510041 | |||||||
| chr10:93510159 | C | T | 1 | a0003c0003t0004g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.528+3103C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510159 | |||||||
| chr10:93510240 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(63): Show |
96 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+3184A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510240 | |||||||
| chr10:93510257 | C | T | 1 | a0009c0010t0002g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.528+3201C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510257 | |||||||
| chr10:93510446 | C | T | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+3390C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510446 | |||||||
| chr10:93510452 | A | AC | 4 | a0002c0002t0002g0104 a0002c0002t0002g0118 a0003c0003t0002g0183 others(1): Show |
4 | HG01243.hp2 NA18974.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+3400dupC | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510452 | ||||||
| chr10:93510475 | CCT | C | 6 | a0003c0003t0002g0174 a0004c0004t0002g0012 a0004c0004t0002g0151 others(3): Show |
9 | NA18943.hp2 NA18946.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+3422_528+3423d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510475 | ||||||
| chr10:93510485 | C | T | 2 | a0001c0001t0001g0129 a0003c0003t0005g0134 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.528+3429C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510485 | |||||||
| chr10:93510599 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18956.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.528+3543C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510599 | |||||||
| chr10:93510645 | A | AAGATCAG others(3): Show |
1 | a0002c0002t0002g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.528+3596_528+3597i others(12): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510645 | ||||||
| chr10:93510672 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+3616G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510672 | |||||||
| chr10:93510908 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(84): Show |
132 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.528+3852G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510908 | |||||||
| chr10:93510910 | C | G | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+3854C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93510910 | |||||||
| chr10:93510937 | C | CT | 85 | a0001c0001t0001g0047 a0001c0001t0001g0218 a0001c0001t0001g0243 others(82): Show |
117 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.528+3900dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510937 | ||||||
| chr10:93510937 | C | CTT | 79 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0034 others(76): Show |
117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.528+3899_528+3900d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510937 | ||||||
| chr10:93510937 | C | CTTT | 13 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0130 others(10): Show |
21 | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.528+3898_528+3900d others(5): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93510937 | ||||||
| chr10:93511003 | G | A | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.528+3947G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511003 | |||||||
| chr10:93511008 | A | C | 3 | a0003c0003t0002g0050 a0003c0003t0009g0063 a0013c0023t0002g0193 |
3 | HG03139.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.528+3952A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511008 | |||||||
| chr10:93511067 | T | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+4011T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511067 | |||||||
| chr10:93511079 | C | T | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.528+4023C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511079 | |||||||
| chr10:93511081 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(78): Show |
123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.528+4025G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511081 | |||||||
| chr10:93511235 | G | A | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529-4170G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511235 | |||||||
| chr10:93511250 | T | A | 3 | a0003c0003t0002g0050 a0003c0003t0009g0063 a0013c0023t0002g0193 |
3 | HG03139.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.529-4155T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511250 | |||||||
| chr10:93511479 | G | A | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-3926G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511479 | |||||||
| chr10:93511515 | C | T | 2 | a0008c0008t0006g0065 a0013c0017t0002g0122 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.529-3890C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511515 | |||||||
| chr10:93511571 | C | CT | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-3832dupT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93511571 | ||||||
| chr10:93511687 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(78): Show |
123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.529-3718C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511687 | |||||||
| chr10:93511712 | C | T | 2 | a0008c0008t0006g0065 a0013c0017t0002g0122 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.529-3693C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511712 | |||||||
| chr10:93511796 | G | A | 1 | a0003c0003t0005g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.529-3609G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511796 | |||||||
| chr10:93511901 | T | C | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-3504T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511901 | |||||||
| chr10:93511915 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.529-3490G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511915 | |||||||
| chr10:93511945 | T | C | 1 | a0006c0006t0001g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.529-3460T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511945 | |||||||
| chr10:93511966 | C | T | 1 | a0017c0019t0001g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.529-3439C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93511966 | |||||||
| chr10:93512151 | C | T | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529-3254C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512151 | |||||||
| chr10:93512196 | C | T | 2 | a0003c0003t0002g0050 a0003c0003t0009g0063 |
2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.529-3209C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512196 | |||||||
| chr10:93512200 | C | T | 1 | a0008c0008t0006g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529-3205C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512200 | |||||||
| chr10:93512210 | G | A | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-3195G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512210 | |||||||
| chr10:93512226 | C | CAAAA | 10 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(7): Show |
12 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.529-3168_529-3165d others(6): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512226 | ||||||
| chr10:93512226 | C | CAAAAAA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(81): Show |
125 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.529-3170_529-3165d others(8): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512226 | ||||||
| chr10:93512226 | C | CAAAAAAA | 65 | a0001c0001t0001g0141 a0001c0001t0001g0223 a0002c0002t0001g0079 others(62): Show |
90 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.529-3171_529-3165d others(9): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512226 | ||||||
| chr10:93512226 | C | CAAAAAAA others(1): Show |
94 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(91): Show |
142 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.529-3172_529-3165d others(10): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512226 | ||||||
| chr10:93512244 | G | C | 1 | a0007c0007t0003g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529-3161G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512244 | |||||||
| chr10:93512247 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-3158G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512247 | |||||||
| chr10:93512250 | C | T | 2 | a0003c0003t0002g0050 a0003c0003t0009g0063 |
2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.529-3155C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512250 | |||||||
| chr10:93512274 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.529-3131C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512274 | |||||||
| chr10:93512514 | CA | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(107): Show |
170 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.529-2868delA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512514 | ||||||
| chr10:93512514 | CAA | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0043 others(113): Show |
170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.529-2869_529-2868d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512514 | ||||||
| chr10:93512514 | CAAA | C | 16 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0215 others(13): Show |
18 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.529-2870_529-2868d others(5): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93512514 | ||||||
| chr10:93512608 | A | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(63): Show |
96 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2797A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512608 | |||||||
| chr10:93512662 | T | A | 5 | a0009c0010t0002g0042 a0009c0010t0002g0197 a0009c0010t0002g0198 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-2743T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512662 | |||||||
| chr10:93512701 | C | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0004g0072 others(1): Show |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-2704C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512701 | |||||||
| chr10:93512713 | G | C | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-2692G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512713 | |||||||
| chr10:93512795 | G | A | 1 | a0015c0016t0004g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.529-2610G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512795 | |||||||
| chr10:93512964 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(93): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.529-2441A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93512964 | |||||||
| chr10:93513077 | C | T | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-2328C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513077 | |||||||
| chr10:93513085 | G | A | 11 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-2320G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513085 | |||||||
| chr10:93513187 | TG | T | 2 | a0002c0002t0002g0030 a0002c0002t0002g0031 |
4 | NA18979.hp2 NA18994.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2217delG | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513187 | |||||||
| chr10:93513401 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(248): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.529-2004C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513401 | |||||||
| chr10:93513462 | G | A | 64 | a0001c0001t0001g0258 a0002c0002t0001g0079 a0002c0002t0001g0080 others(61): Show |
91 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.529-1943G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513462 | |||||||
| chr10:93513527 | C | T | 1 | a0012c0012t0002g0066 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.529-1878C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513527 | |||||||
| chr10:93513573 | G | A | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-1832G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513573 | |||||||
| chr10:93513930 | C | T | 1 | a0011c0011t0002g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529-1475C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513930 | |||||||
| chr10:93513937 | G | GC | 13 | a0001c0001t0001g0224 a0002c0002t0001g0089 a0002c0002t0002g0104 others(10): Show |
17 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-1466dupC | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93513937 | ||||||
| chr10:93513940 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(255): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.529-1465T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513940 | |||||||
| chr10:93513946 | T | C | 6 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
7 | HG02559.hp2 HG02970.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1459T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513946 | |||||||
| chr10:93513947 | C | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
5 | HG02970.hp2 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-1458C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513947 | |||||||
| chr10:93513950 | CT | C | 5 | a0009c0010t0002g0042 a0009c0010t0002g0197 a0009c0010t0002g0198 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-1443delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 93513950 | ||||||
| chr10:93513951 | T | C | 33 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(30): Show |
49 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.529-1454T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93513951 | |||||||
| chr10:93514019 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.529-1386A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514019 | |||||||
| chr10:93514031 | G | A | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.529-1374G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514031 | |||||||
| chr10:93514090 | C | T | 3 | a0007c0007t0006g0192 a0015c0016t0002g0194 a0015c0016t0004g0049 |
3 | HG02258.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.529-1315C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514090 | |||||||
| chr10:93514104 | C | T | 1 | a0002c0002t0002g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.529-1301C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514104 | |||||||
| chr10:93514178 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
187 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.529-1227C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514178 | |||||||
| chr10:93514208 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.529-1197C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514208 | |||||||
| chr10:93514482 | T | C | 3 | a0007c0007t0006g0192 a0011c0011t0002g0053 a0015c0016t0002g0194 |
3 | HG02109.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.529-923T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514482 | |||||||
| chr10:93514704 | A | G | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-701A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514704 | |||||||
| chr10:93514720 | T | C | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-685T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514720 | |||||||
| chr10:93514771 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.529-634T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514771 | |||||||
| chr10:93514795 | C | G | 1 | a0011c0011t0004g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.529-610C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514795 | |||||||
| chr10:93514839 | C | T | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-566C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514839 | |||||||
| chr10:93514842 | A | G | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-563A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514842 | |||||||
| chr10:93514921 | C | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0002g0050 others(1): Show |
5 | HG02280.hp2 HG03041.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-484C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514921 | |||||||
| chr10:93514979 | G | A | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-426G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514979 | |||||||
| chr10:93514988 | G | A | 2 | a0002c0002t0002g0074 a0002c0002t0002g0086 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.529-417G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93514988 | |||||||
| chr10:93515053 | G | A | 3 | a0007c0007t0006g0192 a0015c0016t0002g0194 a0015c0016t0004g0049 |
3 | HG02258.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.529-352G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515053 | |||||||
| chr10:93515133 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(191): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.529-272C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515133 | |||||||
| chr10:93515215 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.529-190C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515215 | |||||||
| chr10:93515258 | G | A | 1 | a0004c0004t0002g0187 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-147G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515258 | |||||||
| chr10:93515268 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.529-137A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515268 | |||||||
| chr10:93515301 | A | G | 9 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(6): Show |
13 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-104A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515301 | |||||||
| chr10:93515303 | A | G | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-102A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 4/8 | chr10 | 93515303 | |||||||
| chr10:93515619 | A | G | 4 | a0011c0011t0004g0059 a0011c0011t0004g0061 a0011c0011t0004g0062 others(1): Show |
4 | HG02280.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+64A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93515619 | |||||||
| chr10:93515653 | A | G | 1 | a0001c0022t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.679+98A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93515653 | |||||||
| chr10:93515850 | T | G | 1 | a0002c0002t0007g0106 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.679+295T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93515850 | |||||||
| chr10:93515956 | A | G | 4 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0003c0003t0002g0050 others(1): Show |
5 | HG02280.hp2 HG03041.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+401A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93515956 | |||||||
| chr10:93516003 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0170 |
4 | HG00558.hp1 HG02165.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+448G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516003 | |||||||
| chr10:93516063 | A | T | 1 | a0004c0004t0002g0041 | 2 | NA18747.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.679+508A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516063 | |||||||
| chr10:93516137 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.679+582C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516137 | |||||||
| chr10:93516220 | G | T | 30 | a0004c0004t0001g0179 a0004c0004t0002g0012 a0004c0004t0002g0019 others(27): Show |
42 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.679+665G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516220 | |||||||
| chr10:93516279 | T | C | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.680-656T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516279 | |||||||
| chr10:93516285 | T | C | 1 | a0002c0002t0002g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.680-650T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516285 | |||||||
| chr10:93516320 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.680-615A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516320 | |||||||
| chr10:93516363 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0139 others(5): Show |
14 | HG03710.hp1 HG04184.hp2 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.680-572T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516363 | |||||||
| chr10:93516455 | TTC | T | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.680-460_680-459del others(2): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 93516455 | ||||||
| chr10:93516473 | CTCTT | C | 5 | a0005c0005t0001g0036 a0005c0005t0001g0127 a0005c0005t0001g0162 others(2): Show |
6 | HG01070.hp2 HG01928.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-458_680-455del others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 93516473 | ||||||
| chr10:93516514 | C | G | 3 | a0007c0007t0006g0192 a0015c0016t0002g0194 a0015c0016t0004g0049 |
3 | HG02258.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.680-421C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516514 | |||||||
| chr10:93516528 | G | C | 3 | a0007c0007t0006g0192 a0015c0016t0002g0194 a0015c0016t0004g0049 |
3 | HG02258.hp2 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.680-407G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516528 | |||||||
| chr10:93516575 | G | A | 2 | a0001c0001t0001g0129 a0003c0003t0005g0134 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680-360G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516575 | |||||||
| chr10:93516775 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.680-160T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516775 | |||||||
| chr10:93516889 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.680-46T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516889 | |||||||
| chr10:93516916 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.680-19G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 5/8 | chr10 | 93516916 | |||||||
| chr10:93517299 | G | A | 1 | a0008c0008t0002g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.993+51G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517299 | |||||||
| chr10:93517492 | C | T | 2 | a0008c0008t0006g0065 a0011c0011t0001g0070 |
2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.993+244C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517492 | |||||||
| chr10:93517573 | G | C | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.993+325G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517573 | |||||||
| chr10:93517704 | C | G | 1 | a0002c0002t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.993+456C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517704 | |||||||
| chr10:93517845 | G | A | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+597G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517845 | |||||||
| chr10:93517886 | T | A | 2 | a0001c0001t0001g0129 a0003c0003t0005g0134 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.993+638T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517886 | |||||||
| chr10:93517972 | A | T | 12 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.993+724A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517972 | |||||||
| chr10:93517988 | C | G | 43 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(40): Show |
57 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.993+740C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517988 | |||||||
| chr10:93517989 | G | A | 1 | a0007c0007t0003g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.993+741G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93517989 | |||||||
| chr10:93518028 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(2): Show |
6 | HG02559.hp2 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+780G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518028 | |||||||
| chr10:93518099 | G | A | 1 | a0004c0004t0002g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.994-778G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518099 | |||||||
| chr10:93518154 | CT | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(253): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.994-712delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 93518154 | ||||||
| chr10:93518155 | T | C | 1 | a0002c0002t0002g0104 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.994-722T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518155 | |||||||
| chr10:93518156 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(140): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.994-721T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518156 | |||||||
| chr10:93518189 | G | A | 30 | a0004c0004t0001g0179 a0004c0004t0002g0012 a0004c0004t0002g0019 others(27): Show |
42 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.994-688G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518189 | |||||||
| chr10:93518214 | A | G | 1 | a0011c0011t0002g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.994-663A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518214 | |||||||
| chr10:93518229 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.994-648A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518229 | |||||||
| chr10:93518488 | A | G | 2 | a0001c0001t0001g0237 a0006c0006t0001g0032 |
3 | HG01346.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.994-389A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518488 | |||||||
| chr10:93518594 | G | A | 12 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(9): Show |
16 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.994-283G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518594 | |||||||
| chr10:93518839 | T | C | 24 | a0004c0004t0001g0179 a0004c0004t0002g0012 a0004c0004t0002g0019 others(21): Show |
33 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.994-38T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 6/8 | chr10 | 93518839 | |||||||
| chr10:93518959 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1065+11G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93518959 | |||||||
| chr10:93519033 | C | T | 8 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(5): Show |
12 | HG01243.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1065+85C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519033 | |||||||
| chr10:93519048 | G | A | 2 | a0004c0004t0001g0179 a0004c0004t0002g0040 |
3 | HG02129.hp1 NA19003.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1065+100G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519048 | |||||||
| chr10:93519072 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(147): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1065+124A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519072 | |||||||
| chr10:93519084 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(147): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1065+136C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519084 | |||||||
| chr10:93519267 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0131 a0001c0001t0001g0149 others(2): Show |
6 | NA18957.hp2 NA18969.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065+319G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519267 | |||||||
| chr10:93519332 | G | C | 9 | a0001c0001t0001g0044 a0002c0002t0002g0074 a0003c0003t0008g0205 others(6): Show |
10 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1066-350G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519332 | |||||||
| chr10:93519414 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1066-268T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519414 | |||||||
| chr10:93519528 | C | T | 3 | a0005c0005t0001g0036 a0005c0005t0001g0127 a0005c0005t0001g0163 |
4 | HG01070.hp2 HG01928.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-154C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 7/8 | chr10 | 93519528 | |||||||
| chr10:93519842 | C | T | 5 | a0008c0008t0002g0006 a0008c0008t0002g0023 a0008c0008t0002g0068 others(2): Show |
12 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1191+35C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93519842 | |||||||
| chr10:93519843 | G | A | 3 | a0003c0003t0002g0050 a0013c0023t0002g0193 a0015c0016t0002g0194 |
3 | HG02970.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1191+36G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93519843 | |||||||
| chr10:93519896 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(256): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1191+89A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93519896 | |||||||
| chr10:93520014 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(125): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1191+207C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93520014 | |||||||
| chr10:93520161 | C | T | 1 | a0007c0007t0006g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1191+354C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93520161 | |||||||
| chr10:93520298 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1191+491G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93520298 | |||||||
| chr10:93520426 | C | CAA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1191+634_1191+635d others(4): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93520426 | ||||||
| chr10:93520560 | C | A | 3 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0011c0011t0001g0070 |
4 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+753C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93520560 | |||||||
| chr10:93520649 | G | A | 9 | a0003c0003t0002g0021 a0003c0003t0002g0050 a0003c0003t0005g0134 others(6): Show |
17 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1191+842G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93520649 | |||||||
| chr10:93521033 | C | T | 1 | a0003c0003t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1191+1226C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521033 | |||||||
| chr10:93521116 | C | T | 2 | a0013c0017t0002g0122 a0013c0023t0002g0193 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1191+1309C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521116 | |||||||
| chr10:93521121 | C | T | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+1314C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521121 | |||||||
| chr10:93521187 | CT | C | 12 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(9): Show |
16 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+1384delT | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93521187 | ||||||
| chr10:93521213 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(258): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1191+1406T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521213 | |||||||
| chr10:93521224 | G | A | 8 | a0003c0003t0002g0214 a0009c0010t0002g0042 a0009c0010t0002g0197 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+1417G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521224 | |||||||
| chr10:93521266 | C | T | 12 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(9): Show |
16 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+1459C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521266 | |||||||
| chr10:93521319 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0258 a0006c0006t0001g0028 |
4 | HG01168.hp1 HG01257.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1191+1512G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521319 | |||||||
| chr10:93521331 | C | T | 2 | a0009c0010t0002g0198 a0009c0010t0002g0199 |
2 | HG02683.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1191+1524C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521331 | |||||||
| chr10:93521440 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1191+1633C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521440 | |||||||
| chr10:93521445 | G | A | 1 | a0005c0005t0001g0163 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1191+1638G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521445 | |||||||
| chr10:93521669 | G | A | 3 | a0002c0002t0002g0109 a0002c0002t0002g0114 a0011c0011t0006g0060 |
3 | HG03017.hp2 HG03453.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1191+1862G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521669 | |||||||
| chr10:93521695 | C | T | 9 | a0003c0003t0002g0021 a0003c0003t0002g0050 a0003c0003t0005g0134 others(6): Show |
17 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1191+1888C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521695 | |||||||
| chr10:93521720 | AC | A | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+1914delC | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521720 | |||||||
| chr10:93521794 | C | T | 4 | a0009c0010t0002g0197 a0009c0010t0002g0198 a0009c0010t0002g0199 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+1987C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521794 | |||||||
| chr10:93521835 | G | A | 8 | a0003c0003t0002g0214 a0009c0010t0002g0042 a0009c0010t0002g0197 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+2028G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521835 | |||||||
| chr10:93521935 | C | A | 3 | a0003c0003t0001g0024 a0003c0003t0001g0071 a0011c0011t0001g0070 |
4 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+2128C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521935 | |||||||
| chr10:93521946 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1191+2139T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93521946 | |||||||
| chr10:93522020 | C | A | 3 | a0002c0002t0002g0083 a0002c0002t0002g0084 a0003c0003t0002g0227 |
3 | HG02040.hp1 HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1191+2213C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522020 | |||||||
| chr10:93522055 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1191+2248C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522055 | |||||||
| chr10:93522138 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(190): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1191+2331T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522138 | |||||||
| chr10:93522142 | C | A | 4 | a0009c0010t0002g0197 a0009c0010t0002g0198 a0009c0010t0002g0199 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+2335C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522142 | |||||||
| chr10:93522164 | G | A | 1 | a0002c0002t0002g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1191+2357G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522164 | |||||||
| chr10:93522201 | T | C | 2 | a0001c0001t0001g0147 a0005c0005t0001g0132 |
2 | NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1191+2394T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522201 | |||||||
| chr10:93522253 | G | A | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1191+2446G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522253 | |||||||
| chr10:93522281 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(190): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1191+2474A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522281 | |||||||
| chr10:93522314 | A | G | 8 | a0003c0003t0002g0214 a0009c0010t0002g0042 a0009c0010t0002g0197 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+2507A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522314 | |||||||
| chr10:93522346 | G | A | 5 | a0002c0002t0002g0027 a0002c0002t0002g0076 a0002c0002t0002g0095 others(2): Show |
6 | HG00423.hp1 NA18949.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+2539G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522346 | |||||||
| chr10:93522349 | C | G | 4 | a0009c0010t0002g0197 a0009c0010t0002g0198 a0009c0010t0002g0199 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+2542C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522349 | |||||||
| chr10:93522582 | G | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0128 a0002c0002t0002g0121 others(23): Show |
40 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1191+2775G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522582 | |||||||
| chr10:93522628 | A | G | 15 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(12): Show |
19 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1191+2821A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522628 | |||||||
| chr10:93522868 | C | A | 1 | a0015c0016t0004g0049 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1191+3061C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522868 | |||||||
| chr10:93522893 | G | C | 1 | a0002c0002t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1191+3086G>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93522893 | |||||||
| chr10:93523280 | G | T | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+3473G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523280 | |||||||
| chr10:93523517 | T | G | 15 | a0003c0003t0002g0050 a0003c0003t0002g0214 a0003c0003t0008g0205 others(12): Show |
23 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1191+3710T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523517 | |||||||
| chr10:93523567 | C | T | 1 | a0003c0003t0002g0183 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1191+3760C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523567 | |||||||
| chr10:93523621 | A | G | 1 | a0003c0003t0009g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1191+3814A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523621 | |||||||
| chr10:93523653 | A | G | 1 | a0004c0004t0002g0175 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1191+3846A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523653 | |||||||
| chr10:93523655 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1191+3848C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523655 | |||||||
| chr10:93523659 | C | G | 1 | a0002c0002t0002g0115 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1191+3852C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523659 | |||||||
| chr10:93523746 | A | G | 9 | a0003c0003t0002g0214 a0003c0003t0008g0205 a0009c0010t0002g0042 others(6): Show |
10 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1191+3939A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523746 | |||||||
| chr10:93523748 | C | G | 7 | a0003c0003t0002g0010 a0003c0003t0002g0039 a0003c0003t0002g0145 others(4): Show |
12 | HG00408.hp1 HG01346.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1191+3941C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523748 | |||||||
| chr10:93523781 | A | T | 1 | a0003c0003t0002g0168 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1191+3974A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523781 | |||||||
| chr10:93523796 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0234 |
3 | HG00642.hp1 HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1191+3989C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93523796 | |||||||
| chr10:93524001 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1192-3949C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524001 | |||||||
| chr10:93524082 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1192-3868C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524082 | |||||||
| chr10:93524083 | T | C | 1 | a0006c0006t0001g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1192-3867T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524083 | |||||||
| chr10:93524130 | A | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0128 a0002c0002t0002g0121 others(23): Show |
40 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1192-3820A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524130 | |||||||
| chr10:93524202 | TAAAG | T | 9 | a0003c0003t0002g0021 a0003c0003t0002g0050 a0003c0003t0005g0134 others(6): Show |
17 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1192-3745_1192-374 others(8): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93524202 | ||||||
| chr10:93524230 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1192-3720A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524230 | |||||||
| chr10:93524316 | C | T | 2 | a0001c0001t0001g0222 a0002c0002t0002g0073 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1192-3634C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524316 | |||||||
| chr10:93524358 | C | G | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1192-3592C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524358 | |||||||
| chr10:93524413 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(189): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1192-3537T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524413 | |||||||
| chr10:93524582 | C | T | 1 | a0009c0010t0002g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1192-3368C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524582 | |||||||
| chr10:93524685 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(148): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1192-3265C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524685 | |||||||
| chr10:93524721 | C | T | 8 | a0003c0003t0002g0214 a0009c0010t0002g0042 a0009c0010t0002g0197 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1192-3229C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524721 | |||||||
| chr10:93524788 | C | T | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1192-3162C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524788 | |||||||
| chr10:93524789 | G | A | 1 | a0015c0016t0002g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1192-3161G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524789 | |||||||
| chr10:93524797 | A | G | 1 | a0015c0016t0002g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1192-3153A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524797 | |||||||
| chr10:93524815 | A | G | 9 | a0003c0003t0002g0021 a0003c0003t0002g0050 a0003c0003t0005g0134 others(6): Show |
17 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1192-3135A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524815 | |||||||
| chr10:93524933 | C | T | 1 | a0013c0023t0002g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-3017C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524933 | |||||||
| chr10:93524934 | A | G | 1 | a0013c0023t0002g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-3016A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524934 | |||||||
| chr10:93524938 | C | T | 1 | a0013c0023t0002g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-3012C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93524938 | |||||||
| chr10:93525042 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(189): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1192-2908T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525042 | |||||||
| chr10:93525043 | C | A | 18 | a0003c0003t0004g0072 a0003c0003t0009g0063 a0007c0007t0003g0009 others(15): Show |
22 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1192-2907C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525043 | |||||||
| chr10:93525056 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1192-2894T>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525056 | |||||||
| chr10:93525069 | A | G | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1192-2881A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525069 | |||||||
| chr10:93525534 | G | A | 1 | a0007c0007t0006g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1192-2416G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525534 | |||||||
| chr10:93525573 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1192-2377T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525573 | |||||||
| chr10:93525619 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1192-2331G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525619 | |||||||
| chr10:93525623 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1192-2327C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525623 | |||||||
| chr10:93525779 | G | A | 1 | a0003c0003t0002g0021 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1192-2171G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525779 | |||||||
| chr10:93525882 | A | G | 26 | a0001c0001t0002g0015 a0001c0001t0002g0128 a0002c0002t0002g0121 others(23): Show |
40 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1192-2068A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525882 | |||||||
| chr10:93525958 | A | G | 1 | a0003c0003t0008g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1192-1992A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525958 | |||||||
| chr10:93525970 | A | G | 3 | a0003c0003t0004g0072 a0003c0003t0009g0063 a0015c0016t0004g0049 |
3 | HG02886.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1192-1980A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93525970 | |||||||
| chr10:93526090 | A | G | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192-1860A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526090 | |||||||
| chr10:93526151 | T | A | 2 | a0003c0003t0002g0169 a0003c0003t0002g0235 |
2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1192-1799T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526151 | |||||||
| chr10:93526265 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1192-1685T>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526265 | |||||||
| chr10:93526284 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0255 |
4 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-1666G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526284 | |||||||
| chr10:93526334 | A | G | 1 | a0003c0003t0005g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1192-1616A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526334 | |||||||
| chr10:93526354 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1192-1596T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526354 | |||||||
| chr10:93526407 | A | G | 15 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(12): Show |
19 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1192-1543A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526407 | |||||||
| chr10:93526666 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1192-1284A>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526666 | |||||||
| chr10:93526667 | AAGACTTG others(4): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1192-1282_1192-127 others(15): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526667 | |||||||
| chr10:93526686 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1192-1264A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526686 | |||||||
| chr10:93526689 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1192-1261G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526689 | |||||||
| chr10:93526715 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1192-1235A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526715 | |||||||
| chr10:93526822 | C | G | 3 | a0003c0003t0004g0072 a0003c0003t0009g0063 a0015c0016t0004g0049 |
3 | HG02886.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1192-1128C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526822 | |||||||
| chr10:93526827 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(195): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1192-1123A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526827 | |||||||
| chr10:93526960 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1192-990C>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526960 | |||||||
| chr10:93526976 | C | T | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192-974C>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93526976 | |||||||
| chr10:93527035 | A | G | 6 | a0003c0003t0002g0050 a0008c0008t0002g0006 a0008c0008t0002g0023 others(3): Show |
13 | HG01099.hp1 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192-915A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527035 | |||||||
| chr10:93527083 | TA | T | 31 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0104 others(28): Show |
45 | HG01099.hp1 HG01243.hp2 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.1192-855delA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93527083 | ||||||
| chr10:93527083 | TAAAAAA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1192-860_1192-855d others(8): Show |
CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93527083 | ||||||
| chr10:93527085 | A | T | 1 | a0003c0003t0008g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1192-865A>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527085 | |||||||
| chr10:93527104 | A | G | 1 | a0002c0002t0002g0118 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1192-846A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527104 | |||||||
| chr10:93527197 | A | G | 43 | a0001c0001t0002g0015 a0001c0001t0002g0128 a0002c0002t0002g0121 others(40): Show |
66 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1192-753A>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527197 | |||||||
| chr10:93527384 | G | A | 3 | a0003c0003t0004g0072 a0003c0003t0009g0063 a0015c0016t0004g0049 |
3 | HG02886.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1192-566G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527384 | |||||||
| chr10:93527390 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0245 |
2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1192-560T>C | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527390 | |||||||
| chr10:93527507 | G | A | 8 | a0007c0007t0003g0009 a0007c0007t0003g0054 a0007c0007t0003g0056 others(5): Show |
12 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1192-443G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527507 | |||||||
| chr10:93527534 | C | G | 26 | a0001c0001t0002g0015 a0001c0001t0002g0128 a0002c0002t0002g0121 others(23): Show |
40 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.1192-416C>G | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527534 | |||||||
| chr10:93527608 | G | T | 3 | a0003c0003t0002g0021 a0003c0003t0005g0134 a0003c0003t0005g0232 |
4 | HG02559.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-342G>T | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527608 | |||||||
| chr10:93527717 | C | CA | 17 | a0003c0003t0002g0021 a0003c0003t0002g0050 a0003c0003t0002g0214 others(14): Show |
26 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1192-227dupA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93527717 | ||||||
| chr10:93527814 | G | A | 11 | a0003c0003t0002g0021 a0003c0003t0002g0214 a0003c0003t0005g0134 others(8): Show |
13 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-136G>A | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | chr10 | 93527814 | |||||||
| chr10:93527886 | G | GA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1192-53dupA | CEP55 | ENSG00000138180.16 | transcript | ENST00000371485.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 93527886 |