Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7272 |
| ensemblid | ENSG00000112742.10 |
| hgncid | 12401 |
| symbol | TTK |
| name | TTK protein kinase |
| refseq_nuc | NM_003318.5 |
| refseq_prot | NP_003309.2 |
| ensembl_nuc | ENST00000369798.7 |
| ensembl_prot | ENSP00000358813.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 80004649 |
| end | 80042527 |
| strand | + |
| ver | v1.2 |
| region | chr6:80004649-80042527 |
| region5000 | chr6:79999649-80047527 |
| regionname0 | TTK_chr6_80004649_80042527 |
| regionname5000 | TTK_chr6_79999649_80047527 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 857 | 319 | 86 | 49 | 128 | 10 | 44 | 105 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| a0002 | 0/0 | 857 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| a0003 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| a0004 | 0/0 | 857 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| a0005 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| a0006 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | MESED others(852): Show |
chr6 | 79999649 | 80047527 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2571 | 284 | 68 | 44 | 126 | 7 | 37 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0001c0002 | 0/0 | 2571 | 16 | 0 | 5 | 2 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0001c0003 | 0/0 | 2571 | 8 | 8 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0001c0004 | 0/0 | 2571 | 7 | 7 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0001c0005 | 0/0 | 2571 | 3 | 2 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0001c0008 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0002c0006 | 0/0 | 2571 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0003c0010 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0003c0011 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0004c0007 | 0/0 | 2571 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0005c0012 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 | ||
| a0006c0009 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | ATGGA others(2566): Show |
chr6 | 79999649 | 80047527 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2966 | 258 | 45 | 42 | 126 | 6 | 37 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0001t0002 | 0/0 | 2966 | 23 | 22 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0001t0005 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0001t0007 | 0/0 | 2966 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0001t0008 | 0/0 | 2966 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0002t0003 | 0/0 | 2966 | 15 | 0 | 5 | 1 | 3 | 6 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0002t0006 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0003t0001 | 0/0 | 2966 | 8 | 8 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0004t0001 | 0/0 | 2966 | 7 | 7 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0005t0004 | 0/0 | 2966 | 3 | 2 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0001c0008t0004 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0002c0006t0001 | 0/0 | 2966 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0003c0010t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0003c0011t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0004c0007t0001 | 0/0 | 2966 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0005c0012t0001 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| a0006c0009t0001 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | CAAAC others(2961): Show |
chr6 | 79999649 | 80047527 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 2 | 2 | 12 | 1 | 3 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0002 | 0/0 | 9 | 4 | 0 | 3 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 3 | 1 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 3 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0007 | 1/0 | 6 | 2 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0014 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0002t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0005t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0005t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0005t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0001c0008t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0002c0006t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0003c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0003c0011t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0004c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0004c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0005c0012t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| a0006c0009t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0100 | EUR | GBR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00673 | hp1 | a0001 | c0002 | t0006 | g0175 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00733 | hp2 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01069 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01071 | hp1 | a0002 | c0006 | t0001 | g0020 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0045 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0176 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0043 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0043 | EUR | IBS | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0111 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02129 | hp2 | a0003 | c0011 | t0001 | g0006 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0187 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02280 | hp2 | a0005 | c0012 | t0001 | g0103 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0171 | AMR | PEL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0184 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0044 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0180 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0181 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03195 | hp2 | a0006 | c0009 | t0001 | g0178 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0019 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03516 | hp1 | a0001 | c0005 | t0004 | g0188 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03579 | hp1 | a0001 | c0005 | t0004 | g0191 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0177 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0044 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0172 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04204 | hp2 | a0001 | c0005 | t0004 | g0190 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0185 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18945 | hp1 | a0004 | c0007 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18960 | hp2 | a0004 | c0007 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18983 | hp1 | a0003 | c0010 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19030 | hp1 | a0001 | c0008 | t0004 | g0186 | AFR | LWK | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0182 | AFR | YRI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0173 | EUR | TSI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | GIH | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0066 | REF | REF | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | TTK_chr6_79999649_80047527 | TTK | chr6 | 79999649 | 80047527 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:80007902 | C | T | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.233C>T | p.Pro78Leu | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/22 | 300/2966 | 233/2574 | 78/857 | chr6 | 80007902 | |||
| chr6:80007959 | C | T | 1 | a0002 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.290C>T | p.Ala97Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/22 | 357/2966 | 290/2574 | 97/857 | chr6 | 80007959 | |||
| chr6:80011736 | A | G | 1 | a0003 | 2 | HG02129.hp2 NA18983.hp1 |
missense_variant | MODERATE | c.736A>G | p.Met246Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/22 | 803/2966 | 736/2574 | 246/857 | chr6 | 80011736 | |||
| chr6:80014544 | C | G | 1 | a0006 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1066C>G | p.Leu356Val | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/22 | 1133/2966 | 1066/2574 | 356/857 | chr6 | 80014544 | |||
| chr6:80027896 | C | T | 1 | a0004 | 2 | NA18945.hp1 NA18960.hp2 |
missense_variant | MODERATE | c.1406C>T | p.Pro469Leu | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/22 | 1473/2966 | 1406/2574 | 469/857 | chr6 | 80027896 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:80022445 | G | A | 1 | a0001c0004 | 7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.1230G>A | p.Pro410Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/22 | 1297/2966 | 1230/2574 | 410/857 | chr6 | 80022445 | |||
| chr6:80026431 | A | G | 1 | a0001c0003 | 8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1311A>G | p.Pro437Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/22 | 1378/2966 | 1311/2574 | 437/857 | chr6 | 80026431 | |||
| chr6:80031526 | A | T | 3 | a0001c0002 a0001c0005 a0001c0008 |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
synonymous_variant | LOW | c.1581A>T | p.Ile527Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/22 | 1648/2966 | 1581/2574 | 527/857 | chr6 | 80031526 | |||
| chr6:80035287 | C | T | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1794C>T | p.Ile598Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/22 | 1861/2966 | 1794/2574 | 598/857 | chr6 | 80035287 | |||
| chr6:80036479 | T | C | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1929T>C | p.Ile643Ile | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/22 | 1996/2966 | 1929/2574 | 643/857 | chr6 | 80036479 | |||
| chr6:80036524 | A | C | 1 | a0003c0011 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1974A>C | p.Gly658Gly | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/22 | 2041/2966 | 1974/2574 | 658/857 | chr6 | 80036524 | |||
| chr6:80040255 | A | C | 1 | a0001c0002 | 16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
synonymous_variant | LOW | c.2367A>C | p.Pro789Pro | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/22 | 2434/2966 | 2367/2574 | 789/857 | chr6 | 80040255 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:80004671 | T | C | 1 | a0001c0001t0002 | 23 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-45T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1173 | chr6 | 80004671 | ||||||
| chr6:80004676 | G | C | 1 | a0001c0001t0005 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1168 | chr6 | 80004676 | ||||||
| chr6:80004681 | A | G | 1 | a0001c0001t0008 | 1 | HG01952.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/22 | 1163 | chr6 | 80004681 | ||||||
| chr6:80042225 | G | A | 4 | a0001c0002t0003 a0001c0002t0006 a0001c0005t0004 others(1): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 23 | chr6 | 80042225 | ||||||
| chr6:80042354 | G | A | 1 | a0001c0001t0007 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 152 | chr6 | 80042354 | ||||||
| chr6:80042377 | C | T | 2 | a0001c0002t0003 a0001c0002t0006 |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 175 | chr6 | 80042377 | ||||||
| chr6:80042424 | A | T | 1 | a0001c0002t0006 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 22/22 | 222 | chr6 | 80042424 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:80004778 | T | C | 13 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(10): Show |
23 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-3+65T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80004778 | |||||||
| chr6:80004793 | G | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3+80G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80004793 | |||||||
| chr6:80005051 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-3+338C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005051 | |||||||
| chr6:80005060 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-3+347A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005060 | |||||||
| chr6:80005089 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+376G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005089 | |||||||
| chr6:80005147 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+434G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005147 | |||||||
| chr6:80005200 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3+487C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005200 | |||||||
| chr6:80005203 | T | TTTG | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(2): Show |
7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+491_-3+492insTG others(1): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 80005203 | ||||||
| chr6:80005446 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-396G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005446 | |||||||
| chr6:80005475 | C | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-2-367C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005475 | |||||||
| chr6:80005550 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.-2-292T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | chr6 | 80005550 | |||||||
| chr6:80005556 | AT | A | 11 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(8): Show |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-278delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 80005556 | ||||||
| chr6:80006038 | A | G | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.139+56A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006038 | |||||||
| chr6:80006042 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139+60A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006042 | |||||||
| chr6:80006121 | T | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.139+139T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006121 | |||||||
| chr6:80006212 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.139+230A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006212 | |||||||
| chr6:80006515 | C | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.139+533C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006515 | |||||||
| chr6:80006612 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.139+630T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006612 | |||||||
| chr6:80006872 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.139+890G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006872 | |||||||
| chr6:80006903 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.140-906A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80006903 | |||||||
| chr6:80007178 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.140-631C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007178 | |||||||
| chr6:80007219 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.140-590G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007219 | |||||||
| chr6:80007487 | G | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.140-322G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007487 | |||||||
| chr6:80007499 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.140-310C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007499 | |||||||
| chr6:80007571 | G | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.140-238G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007571 | |||||||
| chr6:80007614 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0168 others(1): Show |
6 | HG03834.hp1 NA18945.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-195C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007614 | |||||||
| chr6:80007629 | A | T | 14 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0012 others(11): Show |
24 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.140-180A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 2/21 | chr6 | 80007629 | |||||||
| chr6:80008113 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.362+82G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 3/21 | chr6 | 80008113 | |||||||
| chr6:80008539 | T | C | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.469+47T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008539 | |||||||
| chr6:80008628 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.469+136A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008628 | |||||||
| chr6:80008630 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.469+138A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008630 | |||||||
| chr6:80008796 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.469+304G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80008796 | |||||||
| chr6:80008929 | C | CTG | 8 | a0001c0001t0001g0032 a0001c0001t0001g0097 a0001c0001t0001g0109 others(5): Show |
9 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.469+475_469+476dup others(2): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTG | 6 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0002t0003g0171 others(3): Show |
8 | HG01071.hp2 HG02300.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+473_469+476dup others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTG | 5 | a0001c0002t0003g0019 a0001c0002t0003g0172 a0001c0003t0001g0010 others(2): Show |
11 | HG00733.hp1 HG01106.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.469+471_469+476dup others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(1): Show |
10 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0113 others(7): Show |
13 | HG00558.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+469_469+476dup others(8): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(3): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0107 others(18): Show |
30 | HG00558.hp2 HG00673.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.469+467_469+476dup others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(5): Show |
29 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0041 others(26): Show |
40 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.469+465_469+476dup others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(7): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(22): Show |
51 | HG00323.hp2 HG00673.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.469+463_469+476dup others(14): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(9): Show |
11 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(8): Show |
15 | HG01167.hp1 HG01496.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.469+461_469+476dup others(16): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(11): Show |
7 | a0001c0001t0001g0042 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
8 | HG01891.hp1 HG01952.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+459_469+476dup others(18): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | C | CTGTGTGT others(13): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0165 a0001c0001t0001g0166 |
4 | HG01496.hp2 HG01515.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+457_469+476dup others(20): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTG | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
77 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.469+475_469+476del others(2): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTGTG | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0059 others(8): Show |
13 | HG01175.hp1 HG01192.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+473_469+476del others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTGTGTG | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0081 a0001c0001t0001g0105 |
3 | HG03225.hp1 NA18973.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.469+471_469+476del others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTGTGTGT others(1): Show |
C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.469+469_469+476del others(8): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+467_469+476del others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80008929 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+465_469+476del others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 80008929 | ||||||
| chr6:80009619 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.469+1127T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009619 | |||||||
| chr6:80009695 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.470-1119A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009695 | |||||||
| chr6:80009746 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0058 others(3): Show |
10 | HG00408.hp1 HG02132.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-1068T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009746 | |||||||
| chr6:80009773 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-1041C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009773 | |||||||
| chr6:80009798 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-1016G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009798 | |||||||
| chr6:80009831 | A | G | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-983A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009831 | |||||||
| chr6:80009859 | C | G | 1 | a0001c0002t0003g0045 | 2 | HG01074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.470-955C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80009859 | |||||||
| chr6:80010067 | C | T | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-747C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010067 | |||||||
| chr6:80010349 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18950.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.470-465A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010349 | |||||||
| chr6:80010506 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.470-308C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010506 | |||||||
| chr6:80010569 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.470-245C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010569 | |||||||
| chr6:80010670 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0140 others(3): Show |
8 | HG02083.hp2 NA18952.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-144A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010670 | |||||||
| chr6:80010770 | G | GTA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-44_470-43insTA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010770 | |||||||
| chr6:80010771 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-43C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010771 | |||||||
| chr6:80010773 | T | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-41T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010773 | |||||||
| chr6:80010774 | T | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.470-40T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010774 | |||||||
| chr6:80010785 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.470-29A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 4/21 | chr6 | 80010785 | |||||||
| chr6:80010970 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.613+13G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80010970 | |||||||
| chr6:80011016 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.613+59G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011016 | |||||||
| chr6:80011025 | A | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.613+68A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011025 | |||||||
| chr6:80011056 | G | A | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.613+99G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011056 | |||||||
| chr6:80011163 | A | G | 1 | a0001c0003t0001g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.613+206A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011163 | |||||||
| chr6:80011188 | AT | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.614-233delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 80011188 | ||||||
| chr6:80011310 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.614-124A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011310 | |||||||
| chr6:80011315 | T | A | 23 | a0001c0001t0001g0179 a0001c0001t0002g0012 a0001c0001t0002g0015 others(20): Show |
39 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.614-119T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011315 | |||||||
| chr6:80011328 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.614-106A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 5/21 | chr6 | 80011328 | |||||||
| chr6:80011806 | G | C | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.801+5G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/21 | chr6 | 80011806 | |||||||
| chr6:80011812 | T | G | 1 | a0001c0001t0001g0022 | 3 | NA19001.hp1 NA19076.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.801+11T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 7/21 | chr6 | 80011812 | |||||||
| chr6:80012015 | C | T | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.896+35C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012015 | |||||||
| chr6:80012138 | T | C | 17 | a0001c0001t0001g0142 a0001c0001t0001g0162 a0001c0002t0003g0019 others(14): Show |
22 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.896+158T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012138 | |||||||
| chr6:80012212 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0007g0100 |
2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.896+232T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012212 | |||||||
| chr6:80012290 | C | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
190 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.896+310C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012290 | |||||||
| chr6:80012316 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.896+336C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012316 | |||||||
| chr6:80012411 | C | A | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.896+431C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012411 | |||||||
| chr6:80012639 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.897-640T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012639 | |||||||
| chr6:80012654 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.897-625C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012654 | |||||||
| chr6:80012789 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.897-490A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012789 | |||||||
| chr6:80012909 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.897-370T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012909 | |||||||
| chr6:80012912 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.897-367G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80012912 | |||||||
| chr6:80013140 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.897-139C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 8/21 | chr6 | 80013140 | |||||||
| chr6:80013427 | C | T | 5 | a0001c0004t0001g0021 a0001c0004t0001g0180 a0001c0004t0001g0181 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+61C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013427 | |||||||
| chr6:80013481 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.984+115T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013481 | |||||||
| chr6:80013512 | C | A | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.984+146C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013512 | |||||||
| chr6:80013573 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.984+207A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013573 | |||||||
| chr6:80013666 | G | A | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.984+300G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013666 | |||||||
| chr6:80013686 | G | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.984+320G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013686 | |||||||
| chr6:80013763 | G | A | 2 | a0001c0004t0001g0180 a0001c0004t0001g0185 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.984+397G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013763 | |||||||
| chr6:80013880 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.984+514T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013880 | |||||||
| chr6:80013915 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0007g0100 |
2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.985-548G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80013915 | |||||||
| chr6:80014030 | A | G | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.985-433A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014030 | |||||||
| chr6:80014085 | G | C | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.985-378G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014085 | |||||||
| chr6:80014213 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01257.hp1 HG01943.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.985-250T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014213 | |||||||
| chr6:80014439 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.985-24T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 9/21 | chr6 | 80014439 | |||||||
| chr6:80014595 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+9A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014595 | |||||||
| chr6:80014654 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1108+68A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014654 | |||||||
| chr6:80014686 | T | C | 1 | a0001c0003t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1108+100T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014686 | |||||||
| chr6:80014745 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+159C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014745 | |||||||
| chr6:80014815 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1108+229T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014815 | |||||||
| chr6:80014827 | T | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+241T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014827 | |||||||
| chr6:80014949 | C | T | 11 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(8): Show |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1108+363C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014949 | |||||||
| chr6:80014976 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG01106.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1108+390T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80014976 | |||||||
| chr6:80015034 | C | T | 1 | a0001c0002t0003g0045 | 2 | HG01074.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1108+448C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015034 | |||||||
| chr6:80015038 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1108+452A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015038 | |||||||
| chr6:80015141 | A | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1108+555A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015141 | |||||||
| chr6:80015189 | T | TGGG | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+604_1108+606d others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80015189 | ||||||
| chr6:80015256 | A | G | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1108+670A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015256 | |||||||
| chr6:80015283 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0071 |
4 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108+697G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015283 | |||||||
| chr6:80015290 | G | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1108+704G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015290 | |||||||
| chr6:80015335 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+749T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015335 | |||||||
| chr6:80015574 | C | A | 3 | a0001c0005t0004g0188 a0001c0005t0004g0190 a0001c0005t0004g0191 |
3 | HG03516.hp1 HG03579.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1108+988C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015574 | |||||||
| chr6:80015780 | T | C | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1108+1194T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015780 | |||||||
| chr6:80015799 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0161 |
3 | HG01167.hp1 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1108+1213A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015799 | |||||||
| chr6:80015892 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+1306C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015892 | |||||||
| chr6:80015942 | C | A | 1 | a0001c0004t0001g0187 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1108+1356C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80015942 | |||||||
| chr6:80016096 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1108+1510T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016096 | |||||||
| chr6:80016209 | G | C | 1 | a0001c0001t0001g0046 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1108+1623G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016209 | |||||||
| chr6:80016276 | C | G | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1108+1690C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016276 | |||||||
| chr6:80016276 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1108+1690C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016276 | |||||||
| chr6:80016277 | T | G | 1 | a0001c0001t0002g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1108+1691T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016277 | |||||||
| chr6:80016390 | C | T | 1 | a0001c0003t0001g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1108+1804C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016390 | |||||||
| chr6:80016444 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+1858G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016444 | |||||||
| chr6:80016461 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1108+1875A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016461 | |||||||
| chr6:80016676 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1108+2090C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016676 | |||||||
| chr6:80016721 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1108+2135G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80016721 | |||||||
| chr6:80017053 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1108+2467T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017053 | |||||||
| chr6:80017071 | C | T | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1108+2485C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017071 | |||||||
| chr6:80017107 | A | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1108+2521A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017107 | |||||||
| chr6:80017313 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1108+2727T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017313 | |||||||
| chr6:80017434 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1108+2848A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017434 | |||||||
| chr6:80017487 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+2901C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017487 | |||||||
| chr6:80017555 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1108+2969A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017555 | |||||||
| chr6:80017781 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+3195C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017781 | |||||||
| chr6:80017822 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1108+3236C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80017822 | |||||||
| chr6:80018107 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1108+3521C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018107 | |||||||
| chr6:80018182 | C | CA | 7 | a0001c0001t0001g0059 a0001c0004t0001g0021 a0001c0004t0001g0180 others(4): Show |
11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108+3608dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018182 | ||||||
| chr6:80018182 | CA | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0099 a0001c0001t0007g0100 others(4): Show |
11 | HG00140.hp2 HG01943.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108+3608delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018182 | ||||||
| chr6:80018199 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1108+3613G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018199 | |||||||
| chr6:80018236 | A | T | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1108+3650A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018236 | |||||||
| chr6:80018239 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1108+3653T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018239 | |||||||
| chr6:80018445 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1108+3859A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018445 | |||||||
| chr6:80018461 | CA | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
217 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.1109-3850delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018461 | ||||||
| chr6:80018578 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1109-3746C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018578 | |||||||
| chr6:80018621 | C | T | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1109-3703C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018621 | |||||||
| chr6:80018626 | CA | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0024 others(57): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1109-3676delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018626 | ||||||
| chr6:80018626 | CAA | C | 11 | a0001c0001t0001g0082 a0001c0001t0002g0051 a0001c0002t0003g0019 others(8): Show |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1109-3677_1109-367 others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80018626 | ||||||
| chr6:80018648 | A | AG | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG00741.hp1 HG02071.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-3676_1109-367 others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018648 | |||||||
| chr6:80018648 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1109-3676A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018648 | |||||||
| chr6:80018649 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1109-3675T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018649 | |||||||
| chr6:80018690 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0158 |
2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1109-3634A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80018690 | |||||||
| chr6:80019074 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1109-3250A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019074 | |||||||
| chr6:80019087 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-3237C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019087 | |||||||
| chr6:80019217 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1109-3107A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80019217 | |||||||
| chr6:80020053 | T | TACATATA others(1): Show |
139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-2266_1109-225 others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 80020053 | ||||||
| chr6:80020195 | G | T | 1 | a0001c0005t0004g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1109-2129G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020195 | |||||||
| chr6:80020282 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1109-2042A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020282 | |||||||
| chr6:80020545 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-1779A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020545 | |||||||
| chr6:80020788 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1109-1536A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020788 | |||||||
| chr6:80020852 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
221 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1109-1472A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80020852 | |||||||
| chr6:80021004 | C | T | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1109-1320C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021004 | |||||||
| chr6:80021131 | C | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-1193C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021131 | |||||||
| chr6:80021159 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1109-1165T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021159 | |||||||
| chr6:80021249 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.1109-1075G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021249 | |||||||
| chr6:80021297 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1109-1027A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021297 | |||||||
| chr6:80021349 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
7 | NA18954.hp2 NA18984.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109-975C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021349 | |||||||
| chr6:80021432 | GGCACCAC others(6): Show |
G | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1109-891_1109-879d others(15): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021432 | |||||||
| chr6:80021485 | A | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0165 a0001c0001t0005g0147 |
4 | HG03130.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-839A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021485 | |||||||
| chr6:80021958 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
129 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1109-366A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80021958 | |||||||
| chr6:80022032 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1109-292A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022032 | |||||||
| chr6:80022131 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0075 |
6 | HG02129.hp1 NA18968.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-193A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022131 | |||||||
| chr6:80022139 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1109-185T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022139 | |||||||
| chr6:80022141 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0121 others(1): Show |
4 | NA18956.hp2 NA18991.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109-183T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022141 | |||||||
| chr6:80022294 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1109-30G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 10/21 | chr6 | 80022294 | |||||||
| chr6:80022524 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(7): Show |
22 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1257+52C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022524 | |||||||
| chr6:80022525 | G | A | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1257+53G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022525 | |||||||
| chr6:80022639 | A | G | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+167A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022639 | |||||||
| chr6:80022813 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1257+341G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022813 | |||||||
| chr6:80022887 | C | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
220 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1257+415C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022887 | |||||||
| chr6:80022954 | C | T | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1257+482C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80022954 | |||||||
| chr6:80023036 | C | G | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257+564C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023036 | |||||||
| chr6:80023055 | A | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0162 |
2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1257+583A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023055 | |||||||
| chr6:80023331 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
190 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1257+859C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023331 | |||||||
| chr6:80023365 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1257+893G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023365 | |||||||
| chr6:80023366 | G | T | 7 | a0001c0001t0001g0179 a0001c0004t0001g0021 a0001c0004t0001g0180 others(4): Show |
9 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+894G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023366 | |||||||
| chr6:80023399 | T | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0160 a0001c0003t0001g0010 others(3): Show |
10 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1257+927T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023399 | |||||||
| chr6:80023449 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+977C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023449 | |||||||
| chr6:80023453 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+981T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023453 | |||||||
| chr6:80023461 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1257+989T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023461 | |||||||
| chr6:80023465 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1257+993C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023465 | |||||||
| chr6:80023512 | GA | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1257+1042delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80023512 | ||||||
| chr6:80023535 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
175 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1257+1063G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023535 | |||||||
| chr6:80023562 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0091 |
4 | HG02809.hp2 HG03516.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+1090C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80023562 | |||||||
| chr6:80024003 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1257+1531T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024003 | |||||||
| chr6:80024030 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1257+1558T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024030 | |||||||
| chr6:80024167 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1257+1695A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024167 | |||||||
| chr6:80024192 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1257+1720G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024192 | |||||||
| chr6:80024259 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257+1787G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024259 | |||||||
| chr6:80024286 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0082 a0001c0001t0001g0083 |
4 | HG02257.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257+1814C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024286 | |||||||
| chr6:80024475 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1258-1903T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024475 | |||||||
| chr6:80024481 | G | A | 1 | a0001c0002t0006g0175 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1258-1897G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80024481 | |||||||
| chr6:80024860 | G | GTCCAGAC others(10): Show |
1 | a0001c0001t0001g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1258-1515_1258-149 others(21): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80024860 | ||||||
| chr6:80025040 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1258-1338A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025040 | |||||||
| chr6:80025153 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1258-1225G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025153 | |||||||
| chr6:80025178 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1258-1200G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025178 | |||||||
| chr6:80025226 | T | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18942.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1258-1152T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025226 | |||||||
| chr6:80025262 | C | T | 1 | a0001c0001t0001g0048 | 2 | NA19006.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1258-1116C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025262 | |||||||
| chr6:80025448 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0126 |
2 | HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1258-930A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025448 | |||||||
| chr6:80025518 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1258-860T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025518 | |||||||
| chr6:80025605 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1258-773G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80025605 | |||||||
| chr6:80025859 | C | CT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0074 others(4): Show |
10 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1258-503dupT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025859 | ||||||
| chr6:80025859 | CT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1258-503delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025859 | ||||||
| chr6:80025896 | AAG | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(2): Show |
7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-480_1258-479d others(4): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025896 | ||||||
| chr6:80025991 | TGAG | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1258-383_1258-381d others(5): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 80025991 | ||||||
| chr6:80026277 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1258-101A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 11/21 | chr6 | 80026277 | |||||||
| chr6:80027027 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0007g0100 |
2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1394+513G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027027 | |||||||
| chr6:80027218 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1395-667G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027218 | |||||||
| chr6:80027270 | A | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395-615A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027270 | |||||||
| chr6:80027493 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1395-392C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027493 | |||||||
| chr6:80027544 | A | G | 5 | a0001c0004t0001g0021 a0001c0004t0001g0180 a0001c0004t0001g0181 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1395-341A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027544 | |||||||
| chr6:80027576 | G | A | 11 | a0001c0001t0001g0179 a0001c0003t0001g0010 a0001c0003t0001g0182 others(8): Show |
17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1395-309G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027576 | |||||||
| chr6:80027617 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0144 a0001c0001t0001g0157 others(1): Show |
11 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1395-268C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027617 | |||||||
| chr6:80027805 | A | G | 1 | a0005c0012t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1395-80A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027805 | |||||||
| chr6:80027865 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1395-20A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 12/21 | chr6 | 80027865 | |||||||
| chr6:80028027 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1521+16T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028027 | |||||||
| chr6:80028036 | G | T | 1 | a0001c0002t0003g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1521+25G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028036 | |||||||
| chr6:80028051 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+40C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028051 | |||||||
| chr6:80028057 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1521+46G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028057 | |||||||
| chr6:80028086 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0194 a0001c0001t0001g0197 others(1): Show |
6 | HG01891.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+75A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028086 | |||||||
| chr6:80028167 | C | T | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1521+156C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028167 | |||||||
| chr6:80028297 | T | TTTTA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
24 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.1521+318_1521+321d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80028297 | ||||||
| chr6:80028297 | TTTTA | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
214 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1521+318_1521+321d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80028297 | ||||||
| chr6:80028379 | G | A | 12 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1521+368G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028379 | |||||||
| chr6:80028389 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1521+378G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028389 | |||||||
| chr6:80028413 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+402G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028413 | |||||||
| chr6:80028465 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1521+454G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028465 | |||||||
| chr6:80028609 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+598C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028609 | |||||||
| chr6:80028621 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1521+610G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028621 | |||||||
| chr6:80028715 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1521+704T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028715 | |||||||
| chr6:80028916 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
174 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.1521+905G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80028916 | |||||||
| chr6:80029011 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+1000G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029011 | |||||||
| chr6:80029111 | A | G | 1 | a0001c0004t0001g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1521+1100A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029111 | |||||||
| chr6:80029175 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1521+1164G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029175 | |||||||
| chr6:80029268 | A | C | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1521+1257A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029268 | |||||||
| chr6:80029449 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1521+1438C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029449 | |||||||
| chr6:80029460 | C | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
221 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1521+1449C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029460 | |||||||
| chr6:80029682 | A | C | 1 | a0001c0003t0001g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1521+1671A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029682 | |||||||
| chr6:80029718 | G | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
7 | NA18954.hp2 NA18984.hp1 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1521+1707G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80029718 | |||||||
| chr6:80030042 | A | G | 5 | a0001c0004t0001g0021 a0001c0004t0001g0180 a0001c0004t0001g0181 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522-1425A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030042 | |||||||
| chr6:80030057 | G | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1522-1410G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030057 | |||||||
| chr6:80030059 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1522-1408A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030059 | |||||||
| chr6:80030063 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1522-1404C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030063 | |||||||
| chr6:80030115 | A | T | 1 | a0001c0002t0003g0174 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1522-1352A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030115 | |||||||
| chr6:80030184 | T | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1522-1283T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030184 | |||||||
| chr6:80030217 | CT | C | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1522-1245delT | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80030217 | ||||||
| chr6:80030331 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0007g0100 |
2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1522-1136G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030331 | |||||||
| chr6:80030470 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
130 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1522-997G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030470 | |||||||
| chr6:80030484 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
21 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1522-983A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030484 | |||||||
| chr6:80030535 | C | G | 1 | a0001c0003t0001g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1522-932C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030535 | |||||||
| chr6:80030722 | A | C | 5 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0134 others(2): Show |
5 | HG01175.hp2 HG02145.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-745A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030722 | |||||||
| chr6:80030742 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1522-725T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030742 | |||||||
| chr6:80030903 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1522-564C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80030903 | |||||||
| chr6:80031044 | C | CA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1522-408dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80031044 | ||||||
| chr6:80031044 | CA | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0121 others(6): Show |
11 | HG00741.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1522-408delA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 80031044 | ||||||
| chr6:80031077 | A | C | 5 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0025 others(2): Show |
10 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522-390A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80031077 | |||||||
| chr6:80031361 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1522-106T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 13/21 | chr6 | 80031361 | |||||||
| chr6:80031611 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+52G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031611 | |||||||
| chr6:80031688 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1614+129A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031688 | |||||||
| chr6:80031701 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1614+142C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031701 | |||||||
| chr6:80031711 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1614+152C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031711 | |||||||
| chr6:80031731 | A | T | 11 | a0001c0001t0001g0179 a0001c0003t0001g0010 a0001c0003t0001g0182 others(8): Show |
17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1614+172A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031731 | |||||||
| chr6:80031736 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1614+177T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031736 | |||||||
| chr6:80031753 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
125 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1614+194A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031753 | |||||||
| chr6:80031836 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1614+277G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031836 | |||||||
| chr6:80031901 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+342C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80031901 | |||||||
| chr6:80032207 | C | A | 1 | a0006c0009t0001g0178 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1614+648C>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032207 | |||||||
| chr6:80032285 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1614+726C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032285 | |||||||
| chr6:80032384 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+825A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032384 | |||||||
| chr6:80032451 | T | G | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1614+892T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032451 | |||||||
| chr6:80032638 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1079A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032638 | |||||||
| chr6:80032657 | T | TA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
28 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1614+1099dupA | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 80032657 | ||||||
| chr6:80032822 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1614+1263A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032822 | |||||||
| chr6:80032840 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1614+1281C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032840 | |||||||
| chr6:80032871 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1312G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032871 | |||||||
| chr6:80032914 | A | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1355A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80032914 | |||||||
| chr6:80033163 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1614+1604A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033163 | |||||||
| chr6:80033180 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1614+1621A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033180 | |||||||
| chr6:80033393 | G | A | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1615-1592G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033393 | |||||||
| chr6:80033466 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1519T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033466 | |||||||
| chr6:80033488 | A | C | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1615-1497A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033488 | |||||||
| chr6:80033571 | A | G | 11 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(8): Show |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1615-1414A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033571 | |||||||
| chr6:80033615 | G | A | 2 | a0001c0001t0001g0179 a0006c0009t0001g0178 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1615-1370G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033615 | |||||||
| chr6:80033705 | A | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1280A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033705 | |||||||
| chr6:80033739 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1246C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033739 | |||||||
| chr6:80033763 | C | CATGTGT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1615-1219_1615-121 others(10): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 80033763 | ||||||
| chr6:80033814 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1615-1171A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033814 | |||||||
| chr6:80033849 | C | T | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-1136C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033849 | |||||||
| chr6:80033950 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-1035A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80033950 | |||||||
| chr6:80034388 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1615-597G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034388 | |||||||
| chr6:80034399 | C | T | 11 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(8): Show |
16 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1615-586C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034399 | |||||||
| chr6:80034461 | T | G | 1 | a0001c0001t0001g0023 | 3 | HG01168.hp2 HG01433.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1615-524T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034461 | |||||||
| chr6:80034553 | G | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
220 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1615-432G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034553 | |||||||
| chr6:80034647 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1615-338A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034647 | |||||||
| chr6:80034648 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1615-337G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034648 | |||||||
| chr6:80034853 | C | G | 1 | a0001c0001t0001g0032 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1615-132C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034853 | |||||||
| chr6:80034921 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1615-64T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 14/21 | chr6 | 80034921 | |||||||
| chr6:80035438 | A | G | 11 | a0001c0001t0001g0179 a0001c0003t0001g0010 a0001c0003t0001g0182 others(8): Show |
17 | HG02257.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1924+21A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035438 | |||||||
| chr6:80035589 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1924+172C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035589 | |||||||
| chr6:80035614 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1924+197C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035614 | |||||||
| chr6:80035692 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1924+275A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035692 | |||||||
| chr6:80035721 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1924+304G>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035721 | |||||||
| chr6:80035795 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1924+378G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80035795 | |||||||
| chr6:80036262 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1925-213A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 16/21 | chr6 | 80036262 | |||||||
| chr6:80036681 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2049+82T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036681 | |||||||
| chr6:80036861 | A | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2049+262A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036861 | |||||||
| chr6:80036872 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2049+273C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036872 | |||||||
| chr6:80036873 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2049+274G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036873 | |||||||
| chr6:80036885 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2049+286T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036885 | |||||||
| chr6:80036956 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2049+357A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80036956 | |||||||
| chr6:80037258 | A | G | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2049+659A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037258 | |||||||
| chr6:80037493 | G | A | 1 | a0001c0002t0003g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2050-474G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037493 | |||||||
| chr6:80037561 | G | A | 1 | a0001c0001t0001g0039 | 2 | NA18952.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2050-406G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037561 | |||||||
| chr6:80037636 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2050-331G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037636 | |||||||
| chr6:80037661 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
218 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.2050-306A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037661 | |||||||
| chr6:80037716 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2050-251C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037716 | |||||||
| chr6:80037760 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2050-207G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037760 | |||||||
| chr6:80037792 | A | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2050-175A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037792 | |||||||
| chr6:80037865 | T | TATA | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0102 others(2): Show |
7 | HG02280.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050-72_2050-70dup others(3): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | ||||||
| chr6:80037865 | TATA | T | 21 | a0001c0001t0001g0132 a0001c0001t0001g0148 a0001c0001t0002g0012 others(18): Show |
34 | HG01074.hp1 HG01109.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2050-72_2050-70del others(3): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | ||||||
| chr6:80037865 | TATAATA | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.2050-75_2050-70del others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | ||||||
| chr6:80037865 | TATAATAA others(2): Show |
T | 10 | a0001c0001t0001g0124 a0001c0001t0001g0150 a0001c0002t0003g0019 others(7): Show |
13 | HG00673.hp1 HG00733.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2050-78_2050-70del others(9): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | ||||||
| chr6:80037865 | TATAATAA others(5): Show |
T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0058 others(3): Show |
10 | HG00408.hp1 HG02132.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.2050-81_2050-70del others(12): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr6 | 80037865 | ||||||
| chr6:80037895 | A | C | 1 | a0001c0008t0004g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2050-72A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037895 | |||||||
| chr6:80037903 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2050-64A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 17/21 | chr6 | 80037903 | |||||||
| chr6:80038100 | C | G | 2 | a0001c0001t0002g0051 a0001c0001t0002g0056 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2130+53C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038100 | |||||||
| chr6:80038187 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2130+140G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038187 | |||||||
| chr6:80038220 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
21 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.2130+173C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038220 | |||||||
| chr6:80038317 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2130+270G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038317 | |||||||
| chr6:80038488 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2130+441T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038488 | |||||||
| chr6:80038525 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2130+478T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038525 | |||||||
| chr6:80038594 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2130+547G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038594 | |||||||
| chr6:80038719 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18977.hp1 NA19003.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2130+672G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038719 | |||||||
| chr6:80038900 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
251 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.2131-796G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80038900 | |||||||
| chr6:80039062 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2131-634A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039062 | |||||||
| chr6:80039208 | G | A | 4 | a0001c0003t0001g0010 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
8 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2131-488G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039208 | |||||||
| chr6:80039489 | A | G | 15 | a0001c0002t0003g0019 a0001c0002t0003g0043 a0001c0002t0003g0044 others(12): Show |
20 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2131-207A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039489 | |||||||
| chr6:80039673 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
27 | HG01167.hp2 HG01168.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.2131-23G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 18/21 | chr6 | 80039673 | |||||||
| chr6:80039958 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2307+86G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 19/21 | chr6 | 80039958 | |||||||
| chr6:80040168 | T | C | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2308-28T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 19/21 | chr6 | 80040168 | |||||||
| chr6:80040289 | T | A | 4 | a0001c0005t0004g0188 a0001c0005t0004g0190 a0001c0005t0004g0191 others(1): Show |
4 | HG03516.hp1 HG03579.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2392+9T>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040289 | |||||||
| chr6:80040376 | C | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2392+96C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040376 | |||||||
| chr6:80040532 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2393-74T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040532 | |||||||
| chr6:80040573 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2393-33C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040573 | |||||||
| chr6:80040575 | G | T | 1 | a0002c0006t0001g0020 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2393-31G>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 20/21 | chr6 | 80040575 | |||||||
| chr6:80040745 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2490+42A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040745 | |||||||
| chr6:80040864 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2490+161C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040864 | |||||||
| chr6:80040935 | C | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2490+232C>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80040935 | |||||||
| chr6:80041016 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
212 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.2490+313T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041016 | |||||||
| chr6:80041281 | A | T | 1 | a0001c0004t0001g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2490+578A>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041281 | |||||||
| chr6:80041308 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2490+605C>T | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041308 | |||||||
| chr6:80041413 | T | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18942.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.2491-706T>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041413 | |||||||
| chr6:80041551 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0156 |
3 | NA18950.hp1 NA18975.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2491-568T>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041551 | |||||||
| chr6:80041658 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2491-461G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041658 | |||||||
| chr6:80041814 | CTTTA | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0083 |
3 | HG02257.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2491-300_2491-297d others(6): Show |
TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 80041814 | ||||||
| chr6:80041866 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0061 |
2 | HG01175.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2491-253A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041866 | |||||||
| chr6:80041975 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2491-144A>G | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80041975 | |||||||
| chr6:80042030 | A | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | NA19057.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2491-89A>C | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80042030 | |||||||
| chr6:80042063 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
173 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2491-56G>A | TTK | ENSG00000112742.10 | transcript | ENST00000369798.7 | protein_coding | 21/21 | chr6 | 80042063 |