Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64946 |
| ensemblid | ENSG00000153044.10 |
| hgncid | 17268 |
| symbol | CENPH |
| name | centromere protein H |
| refseq_nuc | NM_022909.4 |
| refseq_prot | NP_075060.1 |
| ensembl_nuc | ENST00000283006.7 |
| ensembl_prot | ENSP00000283006.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 69189583 |
| end | 69210357 |
| strand | + |
| ver | v1.2 |
| region | chr5:69189583-69210357 |
| region5000 | chr5:69184583-69215357 |
| regionname0 | CENPH_chr5_69189583_69210357 |
| regionname5000 | CENPH_chr5_69184583_69215357 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 247 | 385 | 92 | 75 | 162 | 8 | 46 | 122 | CENPH_chr5_69184583_69215357 | CENPH | MEEQP others(242): Show |
chr5 | 69184583 | 69215357 |
| a0002 | 0/0 | 247 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | MEEQP others(242): Show |
chr5 | 69184583 | 69215357 |
| a0003 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | MEEQP others(242): Show |
chr5 | 69184583 | 69215357 |
| a0004 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | MEEQP others(242): Show |
chr5 | 69184583 | 69215357 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 741 | 384 | 92 | 74 | 162 | 8 | 46 | CENPH_chr5_69184583_69215357 | CENPH | ATGGA others(736): Show |
chr5 | 69184583 | 69215357 | ||
| a0001c0005 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | ATGGA others(736): Show |
chr5 | 69184583 | 69215357 | ||
| a0002c0002 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | ATGGA others(736): Show |
chr5 | 69184583 | 69215357 | ||
| a0003c0003 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | ATGGA others(736): Show |
chr5 | 69184583 | 69215357 | ||
| a0004c0004 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | ATGGA others(736): Show |
chr5 | 69184583 | 69215357 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1354 | 267 | 48 | 52 | 127 | 7 | 32 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0002 | 0/0 | 1354 | 67 | 23 | 9 | 27 | 0 | 8 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0003 | 0/1 | 1354 | 43 | 19 | 12 | 7 | 1 | 3 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0004 | 0/0 | 1354 | 3 | 0 | 0 | 1 | 0 | 2 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0005 | 0/0 | 1354 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0006 | 0/0 | 1354 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0007 | 0/0 | 1354 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0001t0008 | 0/0 | 1354 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0001c0005t0001 | 0/0 | 1354 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0002c0002t0002 | 0/0 | 1354 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0003c0003t0003 | 0/0 | 1354 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| a0004c0004t0001 | 0/0 | 1354 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | CTTTT others(1349): Show |
chr5 | 69184583 | 69215357 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0002 | 0/0 | 11 | 1 | 0 | 9 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 5 | 1 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0004 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0006 | 1/0 | 6 | 0 | 5 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0001 | 0/0 | 13 | 5 | 0 | 7 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0009 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0001c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0003c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0268 | EUR | FIN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01981 | hp2 | a0001 | c0005 | t0001 | g0089 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0099 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18992 | hp2 | a0003 | c0003 | t0003 | g0252 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA18999 | hp2 | a0004 | c0004 | t0001 | g0131 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ASW | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0143 | AFR | ASW | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | GIH | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | USA | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0251 | REF | REF | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | CENPH_chr5_69184583_69215357 | CENPH | chr5 | 69184583 | 69215357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69194691 | G | A | 1 | a0002 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.235G>A | p.Glu79Lys | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/9 | 287/1354 | 235/744 | 79/247 | chr5 | 69194691 | |||
| chr5:69194694 | G | A | 1 | a0003 | 1 | NA18992.hp2 | missense_variant&splice_region_variant | MODERATE | c.238G>A | p.Ala80Thr | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/9 | 290/1354 | 238/744 | 80/247 | chr5 | 69194694 | |||
| chr5:69208270 | A | G | 1 | a0004 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.562A>G | p.Ser188Gly | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/9 | 614/1354 | 562/744 | 188/247 | chr5 | 69208270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69189727 | C | T | 1 | a0001c0005 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.93C>T | p.Ala31Ala | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/9 | 145/1354 | 93/744 | 31/247 | chr5 | 69189727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69209882 | C | T | 1 | a0001c0001t0004 | 3 | HG02027.hp2 HG03704.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 83 | chr5 | 69209882 | ||||||
| chr5:69210027 | A | C | 2 | a0001c0001t0002 a0002c0002t0002 |
68 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*228A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 228 | chr5 | 69210027 | ||||||
| chr5:69210038 | G | T | 1 | a0001c0001t0008 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 239 | chr5 | 69210038 | ||||||
| chr5:69210095 | G | A | 3 | a0001c0001t0003 a0001c0001t0008 a0003c0003t0003 |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*296G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 296 | chr5 | 69210095 | ||||||
| chr5:69210127 | T | A | 1 | a0001c0001t0005 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 328 | chr5 | 69210127 | ||||||
| chr5:69210251 | G | A | 1 | a0001c0001t0006 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 452 | chr5 | 69210251 | ||||||
| chr5:69210321 | A | G | 1 | a0001c0001t0007 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*522A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 9/9 | 522 | chr5 | 69210321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:69189869 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.134+101C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69189869 | |||||||
| chr5:69189925 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.134+157A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69189925 | |||||||
| chr5:69190122 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.134+354C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190122 | |||||||
| chr5:69190164 | A | G | 48 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(45): Show |
53 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+396A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190164 | |||||||
| chr5:69190215 | G | C | 48 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(45): Show |
53 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.134+447G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190215 | |||||||
| chr5:69190341 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.134+573A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190341 | |||||||
| chr5:69190354 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0226 |
3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.134+586G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190354 | |||||||
| chr5:69190452 | T | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | NA18612.hp2 NA18990.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+684T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190452 | |||||||
| chr5:69190465 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.134+697G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190465 | |||||||
| chr5:69190529 | T | C | 1 | a0001c0001t0006g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.134+761T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190529 | |||||||
| chr5:69190542 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.134+774A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190542 | |||||||
| chr5:69190561 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.134+793A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190561 | |||||||
| chr5:69190652 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.134+884G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190652 | |||||||
| chr5:69190797 | A | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.135-998A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190797 | |||||||
| chr5:69190936 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(5): Show |
11 | HG00099.hp1 HG01175.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.135-859T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69190936 | |||||||
| chr5:69191132 | C | G | 1 | a0001c0001t0002g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.135-663C>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191132 | |||||||
| chr5:69191229 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.135-566G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191229 | |||||||
| chr5:69191344 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.135-451C>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191344 | |||||||
| chr5:69191366 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.135-429G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191366 | |||||||
| chr5:69191423 | A | G | 1 | a0002c0002t0002g0141 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135-372A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191423 | |||||||
| chr5:69191452 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
244 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.135-343T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191452 | |||||||
| chr5:69191533 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0220 |
3 | HG01243.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.135-262A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191533 | |||||||
| chr5:69191609 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.135-186A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 1/8 | chr5 | 69191609 | |||||||
| chr5:69191862 | C | T | 1 | a0001c0001t0006g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.190+12C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69191862 | |||||||
| chr5:69191901 | T | G | 1 | a0001c0001t0003g0229 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.190+51T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69191901 | |||||||
| chr5:69191970 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.190+120C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69191970 | |||||||
| chr5:69192038 | A | G | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.190+188A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69192038 | |||||||
| chr5:69192095 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0272 |
3 | HG00738.hp2 HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.190+245C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69192095 | |||||||
| chr5:69192347 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.190+497G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69192347 | |||||||
| chr5:69192747 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.190+897G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69192747 | |||||||
| chr5:69192757 | C | CAGGCAAT others(3): Show |
1 | a0001c0001t0002g0060 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.190+908_190+917dup others(10): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69192757 | ||||||
| chr5:69192871 | C | T | 3 | a0001c0001t0003g0269 a0001c0001t0003g0270 a0001c0001t0003g0271 |
3 | NA18962.hp2 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.190+1021C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69192871 | |||||||
| chr5:69192988 | CG | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.190+1142delG | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69192988 | ||||||
| chr5:69193011 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.190+1161C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193011 | |||||||
| chr5:69193017 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
5 | HG02165.hp1 NA18994.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+1167A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193017 | |||||||
| chr5:69193147 | GTATATGT others(3): Show |
G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0218 a0001c0001t0006g0050 others(1): Show |
4 | HG01167.hp1 HG02148.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+1315_190+1324d others(12): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69193147 | ||||||
| chr5:69193183 | G | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.190+1333G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193183 | |||||||
| chr5:69193193 | GTA | G | 27 | a0001c0001t0003g0023 a0001c0001t0003g0043 a0001c0001t0003g0044 others(24): Show |
31 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.190+1351_190+1352d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69193193 | ||||||
| chr5:69193302 | A | G | 1 | a0001c0001t0007g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.191-1345A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193302 | |||||||
| chr5:69193392 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.191-1255G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193392 | |||||||
| chr5:69193393 | AG | A | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.191-1250delG | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69193393 | ||||||
| chr5:69193416 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.191-1231T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193416 | |||||||
| chr5:69193450 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.191-1197G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193450 | |||||||
| chr5:69193475 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.191-1172A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193475 | |||||||
| chr5:69193552 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.191-1095G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193552 | |||||||
| chr5:69193663 | G | GT | 56 | a0001c0001t0001g0057 a0001c0001t0001g0126 a0001c0001t0001g0127 others(53): Show |
61 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.191-968dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 69193663 | ||||||
| chr5:69193664 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.191-983T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193664 | |||||||
| chr5:69193676 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.191-971T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193676 | |||||||
| chr5:69193704 | C | A | 1 | a0001c0001t0002g0025 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.191-943C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193704 | |||||||
| chr5:69193841 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.191-806G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193841 | |||||||
| chr5:69193887 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.191-760G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193887 | |||||||
| chr5:69193904 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.191-743G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193904 | |||||||
| chr5:69193990 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.191-657A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193990 | |||||||
| chr5:69193991 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.191-656A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193991 | |||||||
| chr5:69193992 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.191-655T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193992 | |||||||
| chr5:69193995 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.191-652A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69193995 | |||||||
| chr5:69194001 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.191-646A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194001 | |||||||
| chr5:69194009 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.191-638A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194009 | |||||||
| chr5:69194220 | A | T | 1 | a0001c0001t0001g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.191-427A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194220 | |||||||
| chr5:69194245 | A | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-402A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194245 | |||||||
| chr5:69194253 | G | T | 9 | a0001c0001t0001g0051 a0001c0001t0001g0117 a0001c0001t0001g0118 others(6): Show |
9 | HG01981.hp1 HG02071.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.191-394G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194253 | |||||||
| chr5:69194313 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.191-334T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194313 | |||||||
| chr5:69194349 | A | G | 1 | a0001c0001t0002g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.191-298A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 2/8 | chr5 | 69194349 | |||||||
| chr5:69194877 | G | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+182G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69194877 | |||||||
| chr5:69194918 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0112 others(4): Show |
9 | HG00280.hp1 HG00735.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+223C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69194918 | |||||||
| chr5:69194918 | CT | C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0083 a0001c0001t0001g0084 others(13): Show |
16 | HG00738.hp1 HG01070.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.239+241delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69194918 | ||||||
| chr5:69194918 | CTT | C | 38 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(35): Show |
43 | HG00738.hp2 HG01109.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.239+240_239+241del others(2): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69194918 | ||||||
| chr5:69194937 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239+242A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69194937 | |||||||
| chr5:69195014 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18989.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.239+319G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69195014 | |||||||
| chr5:69195097 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.239+402C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69195097 | |||||||
| chr5:69195184 | G | A | 1 | a0001c0001t0003g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.239+489G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69195184 | |||||||
| chr5:69195512 | C | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.240-205C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69195512 | |||||||
| chr5:69195583 | G | A | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.240-134G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | chr5 | 69195583 | |||||||
| chr5:69195653 | AT | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0134 others(4): Show |
13 | HG01074.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.240-61delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr5 | 69195653 | ||||||
| chr5:69195805 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+14T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69195805 | |||||||
| chr5:69195887 | T | TAGTCAAG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.314+97_314+103dupA others(6): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69195887 | ||||||
| chr5:69195942 | T | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(25): Show |
37 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.314+151T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69195942 | |||||||
| chr5:69196013 | A | G | 1 | a0001c0001t0003g0249 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.314+222A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196013 | |||||||
| chr5:69196074 | G | GA | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.314+284dupA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69196074 | ||||||
| chr5:69196108 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG01496.hp2 HG02300.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+317T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196108 | |||||||
| chr5:69196280 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.314+489A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196280 | |||||||
| chr5:69196297 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+506G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196297 | |||||||
| chr5:69196370 | C | G | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.314+579C>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196370 | |||||||
| chr5:69196371 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.314+580G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196371 | |||||||
| chr5:69196373 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.314+582G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196373 | |||||||
| chr5:69196551 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.315-502A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196551 | |||||||
| chr5:69196594 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00438.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.315-459G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196594 | |||||||
| chr5:69196653 | CA | C | 8 | a0001c0001t0003g0042 a0001c0001t0003g0229 a0001c0001t0003g0243 others(5): Show |
9 | HG02258.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-391delA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 69196653 | ||||||
| chr5:69196754 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.315-299G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196754 | |||||||
| chr5:69196919 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
291 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.315-134A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 4/8 | chr5 | 69196919 | |||||||
| chr5:69197125 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.371+16T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197125 | |||||||
| chr5:69197186 | T | C | 4 | a0001c0001t0003g0229 a0001c0001t0003g0243 a0001c0001t0003g0244 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+77T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197186 | |||||||
| chr5:69197352 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.371+243G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197352 | |||||||
| chr5:69197567 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0226 |
3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.371+458C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197567 | |||||||
| chr5:69197568 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.371+459C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197568 | |||||||
| chr5:69197895 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0057 |
4 | HG00099.hp1 HG01175.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+786A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197895 | |||||||
| chr5:69197912 | TC | T | 24 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(21): Show |
29 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.371+804delC | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197912 | |||||||
| chr5:69197913 | C | CT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
51 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.371+831dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69197913 | ||||||
| chr5:69197913 | C | T | 14 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(11): Show |
14 | HG01109.hp2 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.371+804C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197913 | |||||||
| chr5:69197913 | CTT | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(30): Show |
36 | HG01167.hp1 HG01175.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.371+830_371+831del others(2): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69197913 | ||||||
| chr5:69197913 | CTTT | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.371+829_371+831del others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69197913 | ||||||
| chr5:69197946 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.371+837A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197946 | |||||||
| chr5:69197969 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.371+860G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197969 | |||||||
| chr5:69197980 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.371+871G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197980 | |||||||
| chr5:69197983 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.371+874C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69197983 | |||||||
| chr5:69198059 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.371+950T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198059 | |||||||
| chr5:69198145 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.371+1036C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198145 | |||||||
| chr5:69198166 | C | A | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.371+1057C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198166 | |||||||
| chr5:69198190 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.371+1081G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198190 | |||||||
| chr5:69198192 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.371+1083T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198192 | |||||||
| chr5:69198215 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0174 a0001c0001t0001g0175 |
5 | NA18954.hp2 NA18964.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+1106C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198215 | |||||||
| chr5:69198400 | G | A | 3 | a0001c0001t0002g0059 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG02559.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.371+1291G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198400 | |||||||
| chr5:69198435 | A | G | 5 | a0001c0001t0003g0043 a0001c0001t0003g0257 a0001c0001t0003g0258 others(2): Show |
6 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+1326A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198435 | |||||||
| chr5:69198671 | G | A | 1 | a0001c0001t0003g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.371+1562G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198671 | |||||||
| chr5:69198690 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.371+1581T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198690 | |||||||
| chr5:69198754 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.371+1645G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198754 | |||||||
| chr5:69198948 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.371+1851delA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69198948 | ||||||
| chr5:69198952 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.371+1843A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198952 | |||||||
| chr5:69198972 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0226 |
3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.371+1863G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69198972 | |||||||
| chr5:69199034 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.371+1925G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199034 | |||||||
| chr5:69199035 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.371+1926C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199035 | |||||||
| chr5:69199256 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.371+2147A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199256 | |||||||
| chr5:69199386 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371+2277G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199386 | |||||||
| chr5:69199419 | A | T | 1 | a0001c0001t0003g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.371+2310A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199419 | |||||||
| chr5:69199512 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0006g0050 a0001c0001t0007g0143 |
3 | HG01167.hp1 HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.371+2403C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199512 | |||||||
| chr5:69199514 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.371+2405T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199514 | |||||||
| chr5:69199684 | A | G | 1 | a0001c0001t0003g0241 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.371+2575A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199684 | |||||||
| chr5:69199836 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.372-2670G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69199836 | |||||||
| chr5:69200112 | C | CA | 46 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0085 others(43): Show |
48 | HG00609.hp1 HG00642.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.372-2373dupA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200112 | ||||||
| chr5:69200112 | CA | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0056 a0001c0001t0001g0109 others(4): Show |
8 | HG00099.hp1 HG02258.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.372-2373delA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200112 | ||||||
| chr5:69200124 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.372-2382A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200124 | |||||||
| chr5:69200128 | A | C | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.372-2378A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200128 | |||||||
| chr5:69200138 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.372-2368A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200138 | |||||||
| chr5:69200157 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.372-2349C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200157 | |||||||
| chr5:69200387 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.372-2119C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200387 | |||||||
| chr5:69200615 | T | C | 27 | a0001c0001t0003g0023 a0001c0001t0003g0043 a0001c0001t0003g0044 others(24): Show |
31 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.372-1891T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200615 | |||||||
| chr5:69200625 | T | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.372-1881T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200625 | |||||||
| chr5:69200660 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(30): Show |
45 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.372-1846A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200660 | |||||||
| chr5:69200714 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.372-1792C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200714 | |||||||
| chr5:69200719 | C | CT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0003g0042 others(7): Show |
14 | HG01074.hp1 HG01175.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.372-1753dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0051 others(13): Show |
23 | HG00099.hp1 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.372-1754_372-1753d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0024 others(21): Show |
38 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.372-1755_372-1753d others(5): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0084 others(8): Show |
18 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.372-1756_372-1753d others(6): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0105 others(9): Show |
13 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.372-1757_372-1753d others(7): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0107 others(3): Show |
7 | HG00741.hp2 HG01255.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.372-1758_372-1753d others(8): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01099.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.372-1764_372-1753d others(14): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0046 a0001c0001t0001g0179 a0001c0001t0001g0190 |
3 | NA18612.hp2 NA18959.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.372-1765_372-1753d others(15): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0047 others(9): Show |
18 | HG00621.hp2 HG00735.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.372-1766_372-1753d others(16): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0150 others(5): Show |
14 | HG00438.hp2 HG00741.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.372-1767_372-1753d others(17): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0176 a0001c0001t0001g0197 a0001c0001t0001g0213 others(1): Show |
4 | HG00438.hp1 HG01167.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-1768_372-1753d others(18): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0177 |
2 | NA19005.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.372-1769_372-1753d others(19): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0208 others(1): Show |
4 | HG04184.hp1 NA18985.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-1771_372-1753d others(21): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0151 others(1): Show |
8 | HG01070.hp1 HG02132.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.372-1772_372-1753d others(22): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0152 |
5 | HG01071.hp2 HG01496.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.372-1773_372-1753d others(23): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0201 a0001c0001t0001g0214 others(1): Show |
5 | HG00323.hp2 NA18956.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.372-1774_372-1753d others(24): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.372-1776_372-1753d others(26): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0203 a0001c0001t0001g0218 |
3 | HG01978.hp2 HG02148.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.372-1777_372-1753d others(27): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0038 | 2 | HG02572.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.372-1779_372-1753d others(29): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.372-1781_372-1753d others(31): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CT | C | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
12 | HG01257.hp2 HG01258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.372-1753delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTT | C | 16 | a0001c0001t0001g0219 a0001c0001t0001g0237 a0001c0001t0003g0044 others(13): Show |
17 | HG00323.hp1 HG00738.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.372-1754_372-1753d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0172 a0001c0001t0002g0080 |
3 | HG03017.hp1 NA18985.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.372-1763_372-1753d others(13): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(5): Show |
C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(60): Show |
98 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.372-1764_372-1753d others(14): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(6): Show |
C | 17 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0134 others(14): Show |
27 | HG00733.hp1 HG01074.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.372-1765_372-1753d others(15): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0007g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.372-1766_372-1753d others(16): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.372-1767_372-1753d others(17): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0095 others(1): Show |
6 | HG01081.hp2 HG01106.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.372-1768_372-1753d others(18): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200719 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0144 a0001c0001t0001g0226 |
4 | HG01891.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-1769_372-1753d others(19): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200719 | ||||||
| chr5:69200798 | C | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.372-1708C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200798 | |||||||
| chr5:69200828 | T | TC | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
291 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.372-1676dupC | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 69200828 | ||||||
| chr5:69200953 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.372-1553G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69200953 | |||||||
| chr5:69201336 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.372-1170C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69201336 | |||||||
| chr5:69201462 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.372-1044A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69201462 | |||||||
| chr5:69201892 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.372-614G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69201892 | |||||||
| chr5:69202026 | G | C | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.372-480G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69202026 | |||||||
| chr5:69202261 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.372-245A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69202261 | |||||||
| chr5:69202381 | T | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0134 others(4): Show |
13 | HG01074.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-125T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69202381 | |||||||
| chr5:69202468 | A | G | 1 | a0001c0001t0006g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.372-38A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 5/8 | chr5 | 69202468 | |||||||
| chr5:69202820 | T | G | 10 | a0001c0001t0001g0130 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
10 | HG00741.hp2 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-99T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 6/8 | chr5 | 69202820 | |||||||
| chr5:69202848 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.436-71A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 6/8 | chr5 | 69202848 | |||||||
| chr5:69203179 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+209G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203179 | |||||||
| chr5:69203358 | A | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.487+388A>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203358 | |||||||
| chr5:69203374 | AT | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.487+413delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69203374 | ||||||
| chr5:69203379 | T | A | 1 | a0001c0001t0003g0246 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.487+409T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203379 | |||||||
| chr5:69203389 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG03669.hp1 NA18981.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+419C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203389 | |||||||
| chr5:69203452 | C | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.487+482C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203452 | |||||||
| chr5:69203672 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.487+702G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203672 | |||||||
| chr5:69203877 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.487+907A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203877 | |||||||
| chr5:69203878 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.487+908T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203878 | |||||||
| chr5:69203980 | C | CTA | 10 | a0001c0001t0001g0034 a0001c0001t0001g0148 a0001c0001t0001g0155 others(7): Show |
11 | HG01433.hp1 HG01496.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1023_487+1024d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69203980 | ||||||
| chr5:69203989 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0002g0222 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1019T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203989 | |||||||
| chr5:69203991 | T | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
177 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.487+1021T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203991 | |||||||
| chr5:69203991 | T | TAG | 5 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0004g0161 others(2): Show |
5 | HG00597.hp1 HG02027.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1022_487+1023i others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69203991 | ||||||
| chr5:69203993 | T | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.487+1023T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203993 | |||||||
| chr5:69203993 | T | TAG | 13 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(10): Show |
21 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1031_487+1032d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69203993 | ||||||
| chr5:69203995 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0208 |
3 | HG02258.hp1 HG03225.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.487+1025G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69203995 | |||||||
| chr5:69204009 | ATATATAT others(35): Show |
A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(26): Show |
39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.487+1053_487+1094d others(44): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204009 | ||||||
| chr5:69204012 | TATATATA others(52): Show |
T | 1 | a0001c0001t0001g0206 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.487+1053_487+1111d others(61): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204012 | ||||||
| chr5:69204022 | T | TA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(47): Show |
83 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.487+1052_487+1053i others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(4): Show |
68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.487+1052_487+1053i others(13): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(284): Show |
1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(293): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(301): Show |
1 | a0001c0001t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(310): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(316): Show |
1 | a0001c0001t0001g0119 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(325): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(361): Show |
1 | a0001c0001t0001g0118 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(370): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(419): Show |
1 | a0001c0001t0001g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+1052_487+1053i others(428): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(316): Show |
1 | a0001c0001t0001g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.487+1052_487+1053i others(325): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(331): Show |
1 | a0001c0001t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(340): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(346): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0124 |
2 | HG02148.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.487+1052_487+1053i others(355): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(361): Show |
1 | a0001c0001t0001g0101 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.487+1052_487+1053i others(370): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(376): Show |
1 | a0001c0001t0001g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.487+1052_487+1053i others(385): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | T | TATATAAA others(282): Show |
1 | a0001c0001t0001g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.487+1052_487+1053i others(291): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204022 | |||||||
| chr5:69204022 | TTA | T | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.487+1061_487+1062d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204022 | ||||||
| chr5:69204025 | T | TA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.487+1056dupA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204025 | ||||||
| chr5:69204027 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(47): Show |
83 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.487+1057T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204027 | |||||||
| chr5:69204032 | A | AT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(58): Show |
94 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.487+1062_487+1063i others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204032 | |||||||
| chr5:69204034 | T | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.487+1064T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204034 | |||||||
| chr5:69204034 | T | G | 11 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0101 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1064T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204034 | |||||||
| chr5:69204035 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(58): Show |
94 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.487+1065T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204035 | |||||||
| chr5:69204042 | A | AATTTC | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.487+1072_487+1073i others(7): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204042 | |||||||
| chr5:69204043 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(47): Show |
83 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.487+1073T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204043 | |||||||
| chr5:69204044 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.487+1074T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204044 | |||||||
| chr5:69204049 | T | G | 11 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0101 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1079T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204049 | |||||||
| chr5:69204051 | T | A | 11 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0101 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1081T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204051 | T | TAATTTCT others(36): Show |
42 | a0001c0001t0001g0001 a0001c0001t0002g0001 a0001c0001t0002g0009 others(39): Show |
67 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.487+1081_487+1082i others(45): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204051 | T | TAATTTCT others(51): Show |
6 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0134 others(3): Show |
12 | HG01074.hp2 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+1081_487+1082i others(60): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204051 | T | TAATTTCT others(388): Show |
1 | a0004c0004t0001g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487+1081_487+1082i others(397): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204051 | T | TAATTTCT others(257): Show |
1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.487+1081_487+1082i others(266): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204051 | T | TAATTTCT others(66): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0028 |
2 | HG03654.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.487+1081_487+1082i others(75): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204051 | |||||||
| chr5:69204060 | T | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.487+1090T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204060 | |||||||
| chr5:69204061 | A | AG | 61 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(58): Show |
94 | HG00609.hp1 HG00639.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.487+1091_487+1092i others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204061 | |||||||
| chr5:69204062 | A | AT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.487+1092_487+1093i others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204062 | |||||||
| chr5:69204062 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0137 |
2 | HG02647.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.487+1092A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204062 | |||||||
| chr5:69204063 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.487+1093A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204063 | |||||||
| chr5:69204070 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.487+1100T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204070 | |||||||
| chr5:69204070 | TA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(46): Show |
82 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.487+1102delA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204070 | ||||||
| chr5:69204071 | A | AGAATATA others(3): Show |
1 | a0001c0001t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(12): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(332): Show |
1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(341): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(280): Show |
1 | a0001c0001t0001g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(289): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(325): Show |
1 | a0001c0001t0001g0132 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(334): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(233): Show |
1 | a0001c0001t0001g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(242): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(265): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0032 |
2 | HG03491.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(274): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(280): Show |
1 | a0001c0001t0001g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(289): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(295): Show |
1 | a0001c0001t0001g0002 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(304): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(310): Show |
1 | a0001c0001t0001g0002 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(319): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(400): Show |
1 | a0001c0001t0001g0012 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(409): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(132): Show |
1 | a0001c0001t0001g0012 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(141): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(342): Show |
1 | a0001c0001t0001g0012 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(351): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | AGAATATA others(254): Show |
1 | a0001c0001t0001g0091 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(263): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(276): Show |
1 | a0001c0001t0001g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(285): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(222): Show |
1 | a0001c0001t0001g0232 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(231): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(368): Show |
1 | a0001c0001t0001g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(377): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(205): Show |
1 | a0001c0001t0001g0018 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(214): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(235): Show |
1 | a0001c0001t0001g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(244): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(222): Show |
1 | a0001c0001t0001g0019 | 2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(231): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(237): Show |
1 | a0001c0001t0001g0019 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(246): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(312): Show |
1 | a0001c0005t0001g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(321): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(233): Show |
1 | a0001c0001t0001g0018 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(242): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(250): Show |
1 | a0001c0001t0001g0018 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(259): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(263): Show |
1 | a0001c0001t0001g0084 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(272): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(310): Show |
1 | a0001c0001t0001g0004 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(319): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(445): Show |
1 | a0001c0001t0001g0127 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(454): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(340): Show |
1 | a0001c0001t0001g0120 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(349): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(291): Show |
1 | a0001c0001t0001g0085 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(300): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(278): Show |
1 | a0001c0001t0001g0086 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(287): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(293): Show |
1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(302): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(295): Show |
1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(304): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(400): Show |
1 | a0001c0001t0001g0100 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(409): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(445): Show |
1 | a0001c0001t0001g0002 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(454): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(267): Show |
1 | a0001c0001t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(276): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(282): Show |
1 | a0001c0001t0001g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(291): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(297): Show |
1 | a0001c0001t0001g0109 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(306): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(447): Show |
1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(456): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(237): Show |
1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(246): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(417): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(426): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(149): Show |
1 | a0001c0001t0001g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(158): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(194): Show |
1 | a0001c0001t0001g0092 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(203): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(282): Show |
1 | a0001c0001t0001g0003 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(291): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(312): Show |
1 | a0001c0001t0001g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(321): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(209): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0094 |
2 | HG02109.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(218): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(297): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0087 |
2 | NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(306): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(224): Show |
1 | a0001c0001t0001g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(233): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(312): Show |
1 | a0001c0001t0001g0002 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(321): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(239): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0030 others(1): Show |
5 | HG00280.hp1 HG02027.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1101_487+1102i others(248): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(254): Show |
1 | a0001c0001t0001g0003 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(263): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(295): Show |
1 | a0001c0001t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(304): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(269): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0102 |
3 | HG03927.hp1 NA19002.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(278): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(284): Show |
2 | a0001c0001t0001g0003 a0001c0001t0005g0099 |
2 | HG04199.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(293): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(299): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0024 others(2): Show |
7 | HG01255.hp2 HG01257.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1101_487+1102i others(308): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(314): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0052 |
3 | HG02738.hp2 HG02895.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(323): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(329): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0093 a0001c0001t0001g0096 |
3 | HG03486.hp1 HG03834.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(338): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(344): Show |
1 | a0001c0001t0001g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(353): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(359): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0057 a0001c0001t0001g0098 |
3 | HG01175.hp2 HG01192.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(368): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(374): Show |
1 | a0001c0001t0001g0003 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(383): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(389): Show |
1 | a0001c0001t0001g0003 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(398): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(419): Show |
1 | a0001c0001t0001g0105 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(428): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(325): Show |
1 | a0001c0001t0001g0002 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(334): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(389): Show |
1 | a0001c0001t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(398): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(271): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0056 |
2 | HG00099.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.487+1101_487+1102i others(280): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(316): Show |
1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(325): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(331): Show |
1 | a0001c0001t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(340): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(278): Show |
1 | a0001c0001t0001g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(287): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(359): Show |
1 | a0001c0001t0001g0002 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(368): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(263): Show |
1 | a0001c0001t0001g0126 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(272): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(402): Show |
1 | a0001c0001t0001g0004 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(411): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(346): Show |
1 | a0001c0001t0001g0113 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(355): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(344): Show |
1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(353): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(331): Show |
1 | a0001c0001t0001g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(340): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(299): Show |
1 | a0001c0001t0001g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(308): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(299): Show |
1 | a0001c0001t0001g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(308): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(278): Show |
1 | a0001c0001t0001g0235 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(287): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(310): Show |
1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.487+1101_487+1102i others(319): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATAGAATA others(318): Show |
1 | a0001c0001t0001g0002 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(327): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATATAGAA others(5): Show |
10 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0101 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+1101_487+1102i others(14): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204071 | A | ATGTAGAA others(5): Show |
1 | a0001c0001t0001g0119 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.487+1101_487+1102i others(14): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204071 | |||||||
| chr5:69204075 | T | A | 1 | a0004c0004t0001g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487+1105T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204075 | |||||||
| chr5:69204078 | A | AG | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.487+1108_487+1109i others(3): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204078 | |||||||
| chr5:69204079 | A | T | 1 | a0004c0004t0001g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.487+1109A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204079 | |||||||
| chr5:69204250 | A | T | 1 | a0001c0001t0003g0241 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.487+1280A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204250 | |||||||
| chr5:69204479 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.487+1509C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204479 | |||||||
| chr5:69204496 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487+1526C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204496 | |||||||
| chr5:69204597 | C | CT | 13 | a0001c0001t0001g0036 a0001c0001t0001g0166 a0001c0001t0001g0170 others(10): Show |
14 | HG00597.hp2 HG00735.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.487+1651dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204597 | C | CTTTTT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0085 others(11): Show |
18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.487+1647_487+1651d others(7): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204597 | C | CTTTTTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.487+1646_487+1651d others(8): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204597 | C | CTTTTTTT | 38 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0063 others(35): Show |
48 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.487+1645_487+1651d others(9): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204597 | CTTTT | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
6 | HG01261.hp1 HG03710.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1648_487+1651d others(6): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204597 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0148 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+1642_487+1651d others(12): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204597 | ||||||
| chr5:69204690 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.487+1720C>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204690 | |||||||
| chr5:69204702 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.487+1732T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204702 | |||||||
| chr5:69204730 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.487+1760G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204730 | |||||||
| chr5:69204842 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.487+1872G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204842 | |||||||
| chr5:69204919 | C | CT | 66 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(63): Show |
80 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.487+1966dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69204919 | ||||||
| chr5:69204925 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1955T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69204925 | |||||||
| chr5:69205219 | A | G | 1 | a0001c0001t0003g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.487+2249A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205219 | |||||||
| chr5:69205258 | C | CGCTCT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.487+2290_487+2294d others(7): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69205258 | ||||||
| chr5:69205277 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0005t0001g0089 |
5 | HG01081.hp2 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+2307G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205277 | |||||||
| chr5:69205289 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.487+2319G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205289 | |||||||
| chr5:69205352 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.487+2382C>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205352 | |||||||
| chr5:69205529 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.487+2559T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205529 | |||||||
| chr5:69205702 | C | CT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.488-2470dupT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69205702 | ||||||
| chr5:69205702 | C | CTT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0039 others(44): Show |
75 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.488-2471_488-2470d others(4): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69205702 | ||||||
| chr5:69205702 | C | CTTT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0110 others(9): Show |
19 | HG00741.hp2 HG01074.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.488-2472_488-2470d others(5): Show |
CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69205702 | ||||||
| chr5:69205702 | CT | C | 37 | a0001c0001t0001g0185 a0001c0001t0001g0226 a0001c0001t0003g0023 others(34): Show |
42 | HG00738.hp2 HG01109.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.488-2470delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69205702 | ||||||
| chr5:69205850 | A | G | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-2346A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205850 | |||||||
| chr5:69205869 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(26): Show |
39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.488-2327C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205869 | |||||||
| chr5:69205870 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0190 |
3 | HG00621.hp2 NA18949.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.488-2326G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205870 | |||||||
| chr5:69205877 | T | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0060 a0001c0001t0002g0070 others(1): Show |
6 | NA18960.hp1 NA18992.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-2319T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205877 | |||||||
| chr5:69205977 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.488-2219G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69205977 | |||||||
| chr5:69206005 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(26): Show |
39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.488-2191G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206005 | |||||||
| chr5:69206064 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.488-2132C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206064 | |||||||
| chr5:69206111 | C | T | 1 | a0001c0001t0006g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.488-2085C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206111 | |||||||
| chr5:69206145 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.488-2051G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206145 | |||||||
| chr5:69206173 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.488-2023A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206173 | |||||||
| chr5:69206327 | G | A | 39 | a0001c0001t0003g0023 a0001c0001t0003g0042 a0001c0001t0003g0043 others(36): Show |
44 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.488-1869G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206327 | |||||||
| chr5:69206343 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
248 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.488-1853A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206343 | |||||||
| chr5:69206382 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.488-1814C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206382 | |||||||
| chr5:69206390 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.488-1806C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206390 | |||||||
| chr5:69206470 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.488-1726C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206470 | |||||||
| chr5:69206838 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19082.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.488-1358A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69206838 | |||||||
| chr5:69206880 | T | TC | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.488-1311dupC | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69206880 | ||||||
| chr5:69207026 | A | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.488-1170A>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207026 | |||||||
| chr5:69207201 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.488-995T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207201 | |||||||
| chr5:69207276 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.488-920G>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207276 | |||||||
| chr5:69207385 | C | T | 3 | a0001c0001t0003g0255 a0001c0001t0003g0261 a0001c0001t0003g0264 |
3 | HG01168.hp2 HG01952.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.488-811C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207385 | |||||||
| chr5:69207533 | C | T | 1 | a0001c0001t0003g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.488-663C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207533 | |||||||
| chr5:69207545 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0007g0143 |
2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.488-651C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207545 | |||||||
| chr5:69207706 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.488-490C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207706 | |||||||
| chr5:69207856 | TA | T | 4 | a0001c0001t0003g0253 a0001c0001t0003g0255 a0001c0001t0003g0261 others(1): Show |
4 | HG01168.hp2 HG01952.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.488-338delA | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 69207856 | ||||||
| chr5:69207928 | T | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488-268T>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207928 | |||||||
| chr5:69207932 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.488-264A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69207932 | |||||||
| chr5:69208098 | A | G | 5 | a0001c0001t0003g0043 a0001c0001t0003g0257 a0001c0001t0003g0258 others(2): Show |
6 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.488-98A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 7/8 | chr5 | 69208098 | |||||||
| chr5:69208423 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0033 others(26): Show |
39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.651+64G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208423 | |||||||
| chr5:69208504 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.651+145G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208504 | |||||||
| chr5:69208522 | C | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02280.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.651+163C>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208522 | |||||||
| chr5:69208549 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.651+190G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208549 | |||||||
| chr5:69208601 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
6 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+242C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208601 | |||||||
| chr5:69208602 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0134 others(4): Show |
13 | HG01074.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.651+243G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208602 | |||||||
| chr5:69208620 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.651+261A>G | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208620 | |||||||
| chr5:69208820 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0220 |
3 | HG01243.hp2 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.651+461C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208820 | |||||||
| chr5:69208833 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.651+474T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208833 | |||||||
| chr5:69208969 | GT | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.651+616delT | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr5 | 69208969 | ||||||
| chr5:69208972 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
197 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.651+613T>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69208972 | |||||||
| chr5:69209140 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
293 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.652-567C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209140 | |||||||
| chr5:69209252 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0079 |
2 | NA18945.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.652-455G>A | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209252 | |||||||
| chr5:69209270 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.652-437C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209270 | |||||||
| chr5:69209304 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.652-403T>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209304 | |||||||
| chr5:69209402 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0194 |
2 | HG01099.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.652-305G>C | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209402 | |||||||
| chr5:69209535 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.652-172C>T | CENPH | ENSG00000153044.10 | transcript | ENST00000283006.7 | protein_coding | 8/8 | chr5 | 69209535 |