Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54840 |
| ensemblid | ENSG00000137074.20 |
| hgncid | 15984 |
| symbol | APTX |
| name | aprataxin |
| refseq_nuc | NM_001195248.2 |
| refseq_prot | NP_001182177.2 |
| ensembl_nuc | ENST00000379817.7 |
| ensembl_prot | ENSP00000369145.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 32972616 |
| end | 33001628 |
| strand | - |
| ver | v1.2 |
| region | chr9:32972616-33001628 |
| region5000 | chr9:32967616-33006628 |
| regionname0 | APTX_chr9_32972616_33001628 |
| regionname5000 | APTX_chr9_32967616_33006628 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 342 | 382 | 88 | 63 | 177 | 10 | 42 | 139 | APTX_chr9_32967616_33006628 | APTX | MMRVC others(337): Show |
chr9 | 32967616 | 33006628 |
| a0002 | 0/0 | 342 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | MMRVC others(337): Show |
chr9 | 32967616 | 33006628 |
| a0003 | 0/0 | 342 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | MMRVC others(337): Show |
chr9 | 32967616 | 33006628 |
| a0004 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | MMRVC others(337): Show |
chr9 | 32967616 | 33006628 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1026 | 379 | 86 | 63 | 176 | 10 | 42 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 | ||
| a0001c0004 | 0/0 | 1026 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 | ||
| a0001c0005 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 | ||
| a0002c0002 | 0/0 | 1026 | 3 | 3 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 | ||
| a0003c0003 | 0/0 | 1026 | 2 | 1 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 | ||
| a0004c0006 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | ATGAT others(1021): Show |
chr9 | 32967616 | 33006628 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1977 | 367 | 76 | 62 | 176 | 10 | 41 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0001t0002 | 0/0 | 1977 | 6 | 5 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0001t0003 | 0/0 | 1977 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0001t0004 | 0/0 | 1977 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0001t0006 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0001t0007 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0004t0001 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0004t0005 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0001c0005t0001 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0002c0002t0001 | 0/0 | 1977 | 3 | 3 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0003c0003t0001 | 0/0 | 1977 | 2 | 1 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| a0004c0006t0001 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | AGCGC others(1972): Show |
chr9 | 32967616 | 33006628 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 5 | 7 | 16 | 2 | 7 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 2 | 11 | 1 | 3 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0003 | 0/0 | 14 | 1 | 1 | 12 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 2 | 4 | 0 | 3 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 4 | 0 | 3 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0008 | 0/0 | 7 | 1 | 2 | 3 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0009 | 0/0 | 6 | 2 | 2 | 1 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0017 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0004t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0001c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| a0004c0006t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0222 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0224 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02647 | hp1 | a0001 | c0004 | t0005 | g0192 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0099 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18959 | hp2 | a0001 | c0005 | t0001 | g0085 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19000 | hp1 | a0004 | c0006 | t0001 | g0196 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | LWK | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ASW | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ASW | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | GIH | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | MSL | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | USA | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | USA | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0046 | REF | REF | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0051 | REF | REF | APTX_chr9_32967616_33006628 | APTX | chr9 | 32967616 | 33006628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:32984805 | C | T | 1 | a0002 | 3 | HG02818.hp2 HG06807.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.596G>A | p.Arg199His | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/8 | 662/1977 | 596/1029 | 199/342 | chr9 | 32984805 | |||
| chr9:32987596 | G | T | 1 | a0003 | 2 | HG01256.hp1 HG02145.hp2 |
missense_variant | MODERATE | c.431C>A | p.Ser144Tyr | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/8 | 497/1977 | 431/1029 | 144/342 | chr9 | 32987596 | |||
| chr9:32987688 | C | A | 1 | a0004 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.339G>T | p.Arg113Ser | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/8 | 405/1977 | 339/1029 | 113/342 | chr9 | 32987688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:32984711 | C | T | 1 | a0001c0005 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.690G>A | p.Val230Val | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/8 | 756/1977 | 690/1029 | 230/342 | chr9 | 32984711 | |||
| chr9:32987709 | G | A | 1 | a0001c0004 | 2 | HG02647.hp1 HG02723.hp2 |
synonymous_variant | LOW | c.318C>T | p.Asn106Asn | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/8 | 384/1977 | 318/1029 | 106/342 | chr9 | 32987709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:32972692 | C | T | 1 | a0001c0001t0002 | 6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*806G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 806 | chr9 | 32972692 | ||||||
| chr9:32972742 | C | T | 1 | a0001c0001t0004 | 2 | HG02965.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*756G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 756 | chr9 | 32972742 | ||||||
| chr9:32972892 | C | T | 1 | a0001c0001t0002 | 6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*606G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 606 | chr9 | 32972892 | ||||||
| chr9:32973042 | G | C | 1 | a0001c0001t0006 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 456 | chr9 | 32973042 | ||||||
| chr9:32973044 | C | G | 1 | a0001c0001t0003 | 2 | HG03471.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*454G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 454 | chr9 | 32973044 | ||||||
| chr9:32973311 | C | G | 1 | a0001c0001t0002 | 6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 187 | chr9 | 32973311 | ||||||
| chr9:32973357 | C | T | 1 | a0001c0004t0005 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 141 | chr9 | 32973357 | ||||||
| chr9:32973471 | C | A | 1 | a0001c0001t0007 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 8/8 | 27 | chr9 | 32973471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:32973711 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.875-60delT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32973711 | |||||||
| chr9:32973779 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(31): Show |
51 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.875-127G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32973779 | |||||||
| chr9:32973860 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.875-208G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32973860 | |||||||
| chr9:32974094 | A | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+364T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32974094 | |||||||
| chr9:32974217 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.874+241T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32974217 | |||||||
| chr9:32974374 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.874+84G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 7/7 | chr9 | 32974374 | |||||||
| chr9:32974572 | G | GA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.771-12dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974572 | |||||||
| chr9:32974586 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.771-25C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974586 | |||||||
| chr9:32974666 | T | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-105A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974666 | |||||||
| chr9:32974680 | T | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-119A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974680 | |||||||
| chr9:32974711 | T | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-150A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974711 | |||||||
| chr9:32974715 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.771-154A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974715 | |||||||
| chr9:32974735 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.771-174T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974735 | |||||||
| chr9:32974749 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.771-188A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974749 | |||||||
| chr9:32974752 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.771-191T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974752 | |||||||
| chr9:32974813 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.771-252C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974813 | |||||||
| chr9:32974844 | C | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-283G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974844 | |||||||
| chr9:32974887 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.771-326G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974887 | |||||||
| chr9:32974974 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.771-413G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32974974 | |||||||
| chr9:32975010 | G | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-449C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975010 | |||||||
| chr9:32975026 | G | A | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-465C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975026 | |||||||
| chr9:32975064 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.771-503A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975064 | |||||||
| chr9:32975212 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.771-651T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975212 | |||||||
| chr9:32975289 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.771-728C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975289 | |||||||
| chr9:32975313 | ACT | A | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.771-754_771-753del others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975313 | |||||||
| chr9:32975398 | A | T | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-837T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975398 | |||||||
| chr9:32975432 | C | T | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-871G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975432 | |||||||
| chr9:32975474 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.771-913C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975474 | |||||||
| chr9:32975776 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.771-1215A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975776 | |||||||
| chr9:32975983 | T | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.771-1422A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975983 | |||||||
| chr9:32975988 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.771-1427A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975988 | |||||||
| chr9:32975994 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.771-1433G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975994 | |||||||
| chr9:32975999 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.771-1438G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32975999 | |||||||
| chr9:32976296 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.771-1735G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976296 | |||||||
| chr9:32976444 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-1883A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976444 | |||||||
| chr9:32976446 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-1885T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976446 | |||||||
| chr9:32976512 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.771-1951A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976512 | |||||||
| chr9:32976522 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
72 | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.771-1961G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976522 | |||||||
| chr9:32976694 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-2133G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976694 | |||||||
| chr9:32976835 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-2274T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32976835 | |||||||
| chr9:32977033 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.771-2472G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977033 | |||||||
| chr9:32977034 | G | A | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.771-2473C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977034 | |||||||
| chr9:32977076 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-2515C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977076 | |||||||
| chr9:32977106 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-2545A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977106 | |||||||
| chr9:32977186 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0107 others(4): Show |
11 | NA18940.hp2 NA18952.hp1 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.771-2625T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977186 | |||||||
| chr9:32977303 | T | C | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-2742A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977303 | |||||||
| chr9:32977408 | G | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0223 others(8): Show |
13 | HG01243.hp1 HG01256.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.771-2847C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977408 | |||||||
| chr9:32977416 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0140 |
3 | HG00544.hp1 HG02165.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.771-2855G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977416 | |||||||
| chr9:32977421 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.771-2860G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977421 | |||||||
| chr9:32977463 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.771-2902C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977463 | |||||||
| chr9:32977489 | A | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.771-2928T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977489 | |||||||
| chr9:32977510 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.771-2949A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977510 | |||||||
| chr9:32977543 | GA | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.771-2983delT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977543 | |||||||
| chr9:32977544 | A | G | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.771-2983T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977544 | |||||||
| chr9:32977636 | G | C | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.771-3075C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977636 | |||||||
| chr9:32977651 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.771-3090G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977651 | |||||||
| chr9:32977729 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-3168C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977729 | |||||||
| chr9:32977775 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.771-3214C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977775 | |||||||
| chr9:32977787 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-3226G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977787 | |||||||
| chr9:32977855 | G | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.771-3294C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977855 | |||||||
| chr9:32977953 | G | A | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.771-3392C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977953 | |||||||
| chr9:32977997 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-3436A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32977997 | |||||||
| chr9:32978048 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.771-3487T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978048 | |||||||
| chr9:32978152 | G | C | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-3591C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978152 | |||||||
| chr9:32978190 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.771-3629A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978190 | |||||||
| chr9:32978192 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.771-3631G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978192 | |||||||
| chr9:32978193 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-3632C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978193 | |||||||
| chr9:32978223 | C | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.771-3662G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978223 | |||||||
| chr9:32978257 | C | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-3696G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978257 | |||||||
| chr9:32978326 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-3765A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978326 | |||||||
| chr9:32978498 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0002g0135 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.771-3937G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978498 | |||||||
| chr9:32978572 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
6 | HG03491.hp1 HG03492.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-4011C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978572 | |||||||
| chr9:32978642 | A | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
73 | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.771-4081T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978642 | |||||||
| chr9:32978763 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.771-4202C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978763 | |||||||
| chr9:32978808 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(60): Show |
113 | HG00438.hp2 HG00544.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.771-4247G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978808 | |||||||
| chr9:32978853 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.771-4292A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32978853 | |||||||
| chr9:32979035 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-4474T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979035 | |||||||
| chr9:32979046 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-4485A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979046 | |||||||
| chr9:32979161 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.771-4600A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979161 | |||||||
| chr9:32979254 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.771-4693G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979254 | |||||||
| chr9:32979325 | G | T | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-4764C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979325 | |||||||
| chr9:32979331 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.771-4770C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979331 | |||||||
| chr9:32979378 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-4817A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979378 | |||||||
| chr9:32979394 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.771-4833C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979394 | |||||||
| chr9:32979451 | T | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.771-4890A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979451 | |||||||
| chr9:32979541 | G | A | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.771-4980C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979541 | |||||||
| chr9:32979871 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.770+4760T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979871 | |||||||
| chr9:32979986 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.770+4645T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32979986 | |||||||
| chr9:32980018 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.770+4613C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980018 | |||||||
| chr9:32980096 | T | TA | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+4534dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980096 | |||||||
| chr9:32980128 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.770+4503T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980128 | |||||||
| chr9:32980166 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.770+4465A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980166 | |||||||
| chr9:32980184 | C | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+4447G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980184 | |||||||
| chr9:32980210 | G | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+4421C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980210 | |||||||
| chr9:32980299 | G | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+4332C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980299 | |||||||
| chr9:32980336 | A | G | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+4295T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980336 | |||||||
| chr9:32980422 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0161 a0001c0001t0001g0172 others(2): Show |
6 | HG01074.hp1 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.770+4209G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980422 | |||||||
| chr9:32980542 | C | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+4089G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980542 | |||||||
| chr9:32980562 | T | C | 9 | a0001c0001t0001g0223 a0001c0001t0002g0134 a0001c0001t0002g0135 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+4069A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980562 | |||||||
| chr9:32980896 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.770+3735C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32980896 | |||||||
| chr9:32981037 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770+3594G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981037 | |||||||
| chr9:32981186 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.770+3445C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981186 | |||||||
| chr9:32981297 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.770+3334T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981297 | |||||||
| chr9:32981395 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.770+3236C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981395 | |||||||
| chr9:32981423 | T | C | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0002g0134 others(5): Show |
10 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+3208A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981423 | |||||||
| chr9:32981597 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+3034G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981597 | |||||||
| chr9:32981672 | A | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0002g0134 others(5): Show |
10 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.770+2959T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981672 | |||||||
| chr9:32981807 | C | T | 1 | a0001c0005t0001g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.770+2824G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981807 | |||||||
| chr9:32981808 | G | A | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+2823C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981808 | |||||||
| chr9:32981910 | A | G | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.770+2721T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981910 | |||||||
| chr9:32981927 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.770+2704A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981927 | |||||||
| chr9:32981934 | C | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
12 | HG00423.hp1 HG00621.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.770+2697G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981934 | |||||||
| chr9:32981994 | T | TA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
22 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.770+2636dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981994 | |||||||
| chr9:32981998 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.770+2633T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32981998 | |||||||
| chr9:32982022 | G | A | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.770+2609C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982022 | |||||||
| chr9:32982255 | C | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
71 | HG00544.hp2 HG00741.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.770+2376G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982255 | |||||||
| chr9:32982425 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.770+2206C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982425 | |||||||
| chr9:32982450 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.770+2181A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982450 | |||||||
| chr9:32982544 | CTTGT | C | 4 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0004t0001g0191 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+2083_770+2086d others(6): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982544 | |||||||
| chr9:32982689 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.770+1942G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982689 | |||||||
| chr9:32982740 | C | T | 9 | a0001c0001t0001g0223 a0001c0001t0002g0137 a0001c0001t0002g0138 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+1891G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982740 | |||||||
| chr9:32982749 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.770+1882G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982749 | |||||||
| chr9:32982750 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770+1881C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982750 | |||||||
| chr9:32982781 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0155 a0001c0001t0001g0156 |
4 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+1850A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982781 | |||||||
| chr9:32982933 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+1698T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982933 | |||||||
| chr9:32982947 | T | TC | 3 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0092 |
3 | HG02055.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.770+1683_770+1684i others(3): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982947 | |||||||
| chr9:32982947 | TTTC | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.770+1681_770+1683d others(5): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32982947 | |||||||
| chr9:32983006 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.770+1625C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983006 | |||||||
| chr9:32983245 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA18984.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.770+1386C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983245 | |||||||
| chr9:32983366 | T | TTAAC | 3 | a0001c0001t0001g0038 a0001c0001t0001g0155 a0001c0001t0001g0156 |
4 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+1261_770+1264d others(6): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983366 | |||||||
| chr9:32983373 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(67): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.770+1258C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983373 | |||||||
| chr9:32983398 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.770+1233C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983398 | |||||||
| chr9:32983430 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.770+1201A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983430 | |||||||
| chr9:32983444 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.770+1187T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983444 | |||||||
| chr9:32983445 | A | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.770+1186T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983445 | |||||||
| chr9:32983586 | G | C | 1 | a0001c0001t0001g0014 | 4 | NA18951.hp2 NA18970.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+1045C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983586 | |||||||
| chr9:32983837 | T | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.770+794A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983837 | |||||||
| chr9:32983866 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.770+765C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32983866 | |||||||
| chr9:32984074 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(32): Show |
66 | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.770+557A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984074 | |||||||
| chr9:32984096 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0193 a0001c0001t0001g0221 |
4 | HG02074.hp1 HG02135.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+535C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984096 | |||||||
| chr9:32984264 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.770+367C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984264 | |||||||
| chr9:32984393 | A | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(66): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.770+238T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984393 | |||||||
| chr9:32984408 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.770+223C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984408 | |||||||
| chr9:32984453 | C | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+178G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984453 | |||||||
| chr9:32984460 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.770+171G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984460 | |||||||
| chr9:32984562 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.770+69T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984562 | |||||||
| chr9:32984584 | C | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.770+47G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 6/7 | chr9 | 32984584 | |||||||
| chr9:32984879 | A | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.544-22T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32984879 | |||||||
| chr9:32985275 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.544-418T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985275 | |||||||
| chr9:32985326 | G | GT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0038 others(19): Show |
37 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.544-470dupA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985326 | |||||||
| chr9:32985326 | G | GTT | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0125 others(5): Show |
10 | HG00423.hp2 HG00544.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-471_544-470dup others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985326 | |||||||
| chr9:32985326 | GT | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
203 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.544-470delA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985326 | |||||||
| chr9:32985326 | GTT | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0118 a0001c0001t0001g0126 others(2): Show |
6 | HG01496.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-471_544-470del others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985326 | |||||||
| chr9:32985326 | GTTT | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
35 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.544-472_544-470del others(3): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985326 | |||||||
| chr9:32985334 | T | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0054 others(4): Show |
8 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-477A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985334 | |||||||
| chr9:32985335 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
122 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.544-478A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985335 | |||||||
| chr9:32985356 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.544-499A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985356 | |||||||
| chr9:32985395 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.544-538A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985395 | |||||||
| chr9:32985622 | G | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0218 |
3 | HG02647.hp2 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+349C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985622 | |||||||
| chr9:32985647 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.543+324A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985647 | |||||||
| chr9:32985648 | A | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.543+323T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985648 | |||||||
| chr9:32985711 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.543+260T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985711 | |||||||
| chr9:32985913 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+58G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985913 | |||||||
| chr9:32985941 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.543+30A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985941 | |||||||
| chr9:32985941 | T | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.543+30A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 5/7 | chr9 | 32985941 | |||||||
| chr9:32986032 | TAAAAAAA others(17): Show |
T | 1 | a0001c0001t0002g0137 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.484-26_484-3delTGT others(21): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986032 | |||||||
| chr9:32986033 | AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0177 |
2 | HG01074.hp1 NA18972.hp2 |
splice_region_variant&intron_variant | LOW | c.484-25_484-4delGTT others(19): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986033 | |||||||
| chr9:32986034 | AAAAAAAA others(14): Show |
A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(57): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
splice_region_variant&intron_variant | LOW | c.484-25_484-5delGTT others(18): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986034 | |||||||
| chr9:32986035 | AAAAAAAA others(13): Show |
A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0001t0001g0145 others(4): Show |
8 | HG00544.hp1 HG02165.hp1 NA18612.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.484-25_484-6delGTT others(17): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986035 | |||||||
| chr9:32986038 | AAAAACAA others(10): Show |
A | 5 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-25_484-9delGTT others(14): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986038 | |||||||
| chr9:32986041 | A | AC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(3): Show |
12 | HG01433.hp2 HG01891.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.484-12_484-11insG | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986041 | |||||||
| chr9:32986042 | A | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
235 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.484-12T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986042 | |||||||
| chr9:32986043 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
259 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.484-13G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986043 | |||||||
| chr9:32986049 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.484-19T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986049 | |||||||
| chr9:32986055 | C | A | 2 | a0001c0001t0001g0058 a0001c0004t0005g0192 |
2 | HG02647.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.484-25G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986055 | |||||||
| chr9:32986056 | A | C | 2 | a0001c0001t0001g0058 a0001c0004t0005g0192 |
2 | HG02647.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.484-26T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986056 | |||||||
| chr9:32986059 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0199 |
2 | HG00642.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.484-29T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986059 | |||||||
| chr9:32986060 | A | C | 1 | a0001c0001t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.484-30T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986060 | |||||||
| chr9:32986062 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0127 |
3 | HG01884.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.484-32T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986062 | |||||||
| chr9:32986063 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.484-33T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986063 | |||||||
| chr9:32986229 | T | C | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-199A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986229 | |||||||
| chr9:32986250 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(66): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.484-220A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986250 | |||||||
| chr9:32986385 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.484-355G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986385 | |||||||
| chr9:32986407 | T | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(72): Show |
111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.484-377A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986407 | |||||||
| chr9:32986473 | A | C | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.484-443T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986473 | |||||||
| chr9:32986477 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.484-447C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986477 | |||||||
| chr9:32986528 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-498C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986528 | |||||||
| chr9:32986605 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.484-575G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986605 | |||||||
| chr9:32986646 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.484-616G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986646 | |||||||
| chr9:32986709 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.484-679G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986709 | |||||||
| chr9:32986955 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.483+589A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32986955 | |||||||
| chr9:32987015 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.483+529C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987015 | |||||||
| chr9:32987025 | C | A | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.483+519G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987025 | |||||||
| chr9:32987288 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0045 others(11): Show |
23 | HG01109.hp2 HG01168.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.483+256C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987288 | |||||||
| chr9:32987297 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.483+247A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987297 | |||||||
| chr9:32987312 | A | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+232T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987312 | |||||||
| chr9:32987338 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483+206G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987338 | |||||||
| chr9:32987420 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.483+124C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987420 | |||||||
| chr9:32987453 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.483+91C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987453 | |||||||
| chr9:32987476 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.483+68G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 4/7 | chr9 | 32987476 | |||||||
| chr9:32988048 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0107 a0001c0001t0001g0118 |
4 | NA18952.hp1 NA18961.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+35A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 3/7 | chr9 | 32988048 | |||||||
| chr9:32988175 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0140 a0001c0001t0001g0152 |
4 | HG00544.hp1 HG02165.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-46T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988175 | |||||||
| chr9:32988187 | C | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-58G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988187 | |||||||
| chr9:32988343 | C | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
37 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.134-214G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988343 | |||||||
| chr9:32988401 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134-272G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988401 | |||||||
| chr9:32988457 | G | A | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-328C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988457 | |||||||
| chr9:32988603 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.134-474G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988603 | |||||||
| chr9:32988685 | GGAAA | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0001c0001t0003g0225 others(1): Show |
4 | HG01361.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-560_134-557del others(4): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988685 | |||||||
| chr9:32988685 | GGAAAA | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(58): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.134-561_134-557del others(5): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988685 | |||||||
| chr9:32988685 | GGAAAAAA | G | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-563_134-557del others(7): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988685 | |||||||
| chr9:32988686 | GA | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
195 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.134-558delT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988686 | |||||||
| chr9:32988686 | GAA | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(20): Show |
35 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.134-559_134-558del others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988686 | |||||||
| chr9:32988686 | GAAAAAAA others(5): Show |
G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0006g0133 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-569_134-558del others(12): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988686 | |||||||
| chr9:32988686 | GAAAAAAA others(7): Show |
G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.134-571_134-558del others(14): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988686 | |||||||
| chr9:32988686 | GAAAAAAA others(8): Show |
G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0198 |
3 | NA18953.hp2 NA18965.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.134-572_134-558del others(15): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988686 | |||||||
| chr9:32988687 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(5): Show |
11 | HG02027.hp1 HG02056.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-558T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988687 | |||||||
| chr9:32988688 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(47): Show |
94 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.134-559T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988688 | |||||||
| chr9:32988689 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(19): Show |
34 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.134-560T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988689 | |||||||
| chr9:32988690 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-561T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988690 | |||||||
| chr9:32988716 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.134-587A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988716 | |||||||
| chr9:32988738 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.134-609C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988738 | |||||||
| chr9:32988936 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-807A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32988936 | |||||||
| chr9:32989006 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.133+753A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32989006 | |||||||
| chr9:32989375 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.133+384C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32989375 | |||||||
| chr9:32989396 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+363C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32989396 | |||||||
| chr9:32989528 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.133+231A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32989528 | |||||||
| chr9:32989550 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+209G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 2/7 | chr9 | 32989550 | |||||||
| chr9:32990003 | G | A | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-108C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990003 | |||||||
| chr9:32990134 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-4-239A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990134 | |||||||
| chr9:32990160 | CATTT | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0155 a0001c0001t0001g0156 |
4 | HG01496.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-269_-4-266delAA others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990160 | |||||||
| chr9:32990212 | C | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-317G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990212 | |||||||
| chr9:32990234 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(68): Show |
107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4-339T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990234 | |||||||
| chr9:32990249 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0069 others(6): Show |
11 | HG02818.hp2 HG03491.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4-354C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990249 | |||||||
| chr9:32990283 | C | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-388G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990283 | |||||||
| chr9:32990730 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-835A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990730 | |||||||
| chr9:32990834 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-939A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990834 | |||||||
| chr9:32990931 | T | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-1036A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990931 | |||||||
| chr9:32990948 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0006g0133 |
3 | HG02572.hp2 HG02895.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4-1053G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32990948 | |||||||
| chr9:32991029 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-4-1134G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991029 | |||||||
| chr9:32991105 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-4-1210A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991105 | |||||||
| chr9:32991278 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-4-1383G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991278 | |||||||
| chr9:32991422 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-4-1527C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991422 | |||||||
| chr9:32991447 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-4-1552G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991447 | |||||||
| chr9:32991670 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4-1775C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991670 | |||||||
| chr9:32991758 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-1863A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991758 | |||||||
| chr9:32991779 | GA | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(68): Show |
107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-4-1885delT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991779 | |||||||
| chr9:32991938 | C | A | 1 | a0001c0001t0003g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-4-2043G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991938 | |||||||
| chr9:32991992 | G | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-2097C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32991992 | |||||||
| chr9:32992168 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-4-2273C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992168 | |||||||
| chr9:32992196 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-2301T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992196 | |||||||
| chr9:32992518 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-4-2623C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992518 | |||||||
| chr9:32992583 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0095 |
2 | NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-4-2688C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992583 | |||||||
| chr9:32992665 | T | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-2770A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992665 | |||||||
| chr9:32992723 | G | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0107 others(4): Show |
11 | NA18940.hp2 NA18952.hp1 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.-4-2828C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992723 | |||||||
| chr9:32992768 | T | G | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-2873A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992768 | |||||||
| chr9:32992847 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-4-2952G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32992847 | |||||||
| chr9:32993183 | C | T | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-4-3288G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993183 | |||||||
| chr9:32993222 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-4-3327A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993222 | |||||||
| chr9:32993274 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-4-3379G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993274 | |||||||
| chr9:32993275 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-4-3380T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993275 | |||||||
| chr9:32993303 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-4-3408A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993303 | |||||||
| chr9:32993505 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-4-3610G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993505 | |||||||
| chr9:32993557 | G | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-4-3662C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993557 | |||||||
| chr9:32993719 | C | CT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-4-3825dupA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993719 | |||||||
| chr9:32993719 | CT | C | 10 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(7): Show |
10 | HG01109.hp2 HG01168.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4-3825delA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993719 | |||||||
| chr9:32993822 | A | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(79): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-4-3927T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993822 | |||||||
| chr9:32993885 | C | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-3990G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993885 | |||||||
| chr9:32993955 | G | GCGAT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
37 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4-4064_-4-4061dup others(4): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993955 | |||||||
| chr9:32993961 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-4-4066G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32993961 | |||||||
| chr9:32994026 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-4131T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994026 | |||||||
| chr9:32994301 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-4-4406C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994301 | |||||||
| chr9:32994369 | C | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-4474G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994369 | |||||||
| chr9:32994370 | T | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-4475A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994370 | |||||||
| chr9:32994502 | T | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-4-4607A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994502 | |||||||
| chr9:32994582 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-4-4687G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994582 | |||||||
| chr9:32994583 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-4-4688T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994583 | |||||||
| chr9:32994686 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-4-4791A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994686 | |||||||
| chr9:32994729 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-4-4834A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994729 | |||||||
| chr9:32994765 | A | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-4-4870T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994765 | |||||||
| chr9:32994780 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0212 |
7 | NA18973.hp1 NA18981.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-4885A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994780 | |||||||
| chr9:32994976 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-4-5081A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32994976 | |||||||
| chr9:32995112 | A | C | 1 | a0001c0001t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-4-5217T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995112 | |||||||
| chr9:32995281 | G | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-4-5386C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995281 | |||||||
| chr9:32995447 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(40): Show |
62 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-4-5552A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995447 | |||||||
| chr9:32995502 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0198 |
3 | NA18953.hp2 NA18965.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-4-5607A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995502 | |||||||
| chr9:32995714 | A | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0223 a0003c0003t0001g0222 others(1): Show |
4 | HG01256.hp1 HG02145.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-5819T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995714 | |||||||
| chr9:32995715 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-4-5820C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995715 | |||||||
| chr9:32995757 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-5+5810C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995757 | |||||||
| chr9:32995810 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-5+5757A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995810 | |||||||
| chr9:32995887 | C | CA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(27): Show |
47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-5+5679dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995887 | |||||||
| chr9:32995887 | C | CAA | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-5+5678_-5+5679dup others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995887 | |||||||
| chr9:32995930 | TCAGCAAC others(5): Show |
T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-5+5625_-5+5636del others(12): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995930 | |||||||
| chr9:32995938 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-5+5629A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995938 | |||||||
| chr9:32995995 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-5+5572G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995995 | |||||||
| chr9:32995998 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0087 |
3 | HG02083.hp1 HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-5+5569T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32995998 | |||||||
| chr9:32996033 | T | C | 1 | a0001c0001t0007g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-5+5534A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996033 | |||||||
| chr9:32996097 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+5470A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996097 | |||||||
| chr9:32996163 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0006g0133 |
3 | HG02572.hp2 HG02895.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-5+5404A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996163 | |||||||
| chr9:32996260 | T | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-5+5307A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996260 | |||||||
| chr9:32996278 | C | CT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.-5+5288dupA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996278 | |||||||
| chr9:32996372 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-5+5195G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996372 | |||||||
| chr9:32996542 | G | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG01192.hp2 HG02615.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+5025C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996542 | |||||||
| chr9:32996664 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-5+4903A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996664 | |||||||
| chr9:32996694 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+4873A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996694 | |||||||
| chr9:32996780 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-5+4787G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996780 | |||||||
| chr9:32996859 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0086 |
2 | HG01099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-5+4708C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32996859 | |||||||
| chr9:32997097 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0122 |
2 | NA18994.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-5+4470T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997097 | |||||||
| chr9:32997152 | T | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-5+4415A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997152 | |||||||
| chr9:32997159 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0108 |
4 | NA18961.hp2 NA18999.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+4408G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997159 | |||||||
| chr9:32997368 | C | CAG | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.-5+4198_-5+4199ins others(2): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997368 | |||||||
| chr9:32997379 | G | A | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+4188C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997379 | |||||||
| chr9:32997415 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0163 others(4): Show |
9 | HG00280.hp2 NA18941.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+4152C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997415 | |||||||
| chr9:32997457 | T | C | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+4110A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997457 | |||||||
| chr9:32997475 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-5+4092G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997475 | |||||||
| chr9:32997623 | G | GAAC | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-5+3941_-5+3943dup others(3): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997623 | |||||||
| chr9:32997664 | A | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG02280.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+3903T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997664 | |||||||
| chr9:32997830 | T | C | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG02717.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+3737A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32997830 | |||||||
| chr9:32998090 | A | G | 1 | a0001c0004t0005g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-5+3477T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998090 | |||||||
| chr9:32998239 | G | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(68): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-5+3328C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998239 | |||||||
| chr9:32998278 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-5+3289C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998278 | |||||||
| chr9:32998480 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-5+3087A>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998480 | |||||||
| chr9:32998699 | A | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0084 |
2 | NA18941.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-5+2868T>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998699 | |||||||
| chr9:32998714 | G | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(74): Show |
113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-5+2853C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998714 | |||||||
| chr9:32998858 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0130 |
8 | HG01891.hp2 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-5+2709T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998858 | |||||||
| chr9:32998890 | T | TA | 64 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(61): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.-5+2676dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32998890 | |||||||
| chr9:32999089 | C | T | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+2478G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999089 | |||||||
| chr9:32999125 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-5+2442T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999125 | |||||||
| chr9:32999126 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-5+2441G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999126 | |||||||
| chr9:32999308 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-5+2259C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999308 | |||||||
| chr9:32999421 | C | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(68): Show |
107 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-5+2146G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999421 | |||||||
| chr9:32999625 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-5+1942T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999625 | |||||||
| chr9:32999679 | A | G | 1 | a0001c0004t0001g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-5+1888T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999679 | |||||||
| chr9:32999779 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-5+1788A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999779 | |||||||
| chr9:32999831 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-5+1736G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999831 | |||||||
| chr9:32999926 | C | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+1641G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999926 | |||||||
| chr9:32999941 | C | CAGAG | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+1622_-5+1625dup others(4): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999941 | |||||||
| chr9:32999971 | T | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
39 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-5+1596A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 32999971 | |||||||
| chr9:33000010 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1557A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000010 | |||||||
| chr9:33000011 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1556T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000011 | |||||||
| chr9:33000013 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1554A>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000013 | |||||||
| chr9:33000014 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1553C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000014 | |||||||
| chr9:33000015 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1552C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000015 | |||||||
| chr9:33000017 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1550G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000017 | |||||||
| chr9:33000019 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1548C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000019 | |||||||
| chr9:33000021 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1546G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000021 | |||||||
| chr9:33000022 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1545C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000022 | |||||||
| chr9:33000025 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+1542C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000025 | |||||||
| chr9:33000369 | G | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
39 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-5+1198C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000369 | |||||||
| chr9:33000452 | C | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+1115G>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000452 | |||||||
| chr9:33000591 | T | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+976A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000591 | |||||||
| chr9:33000625 | C | CA | 54 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(51): Show |
86 | HG00544.hp2 HG00741.hp2 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.-5+941dupT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000625 | |||||||
| chr9:33000625 | C | CAA | 11 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0043 others(8): Show |
19 | HG00438.hp2 HG01361.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-5+940_-5+941dupTT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000625 | |||||||
| chr9:33000625 | CA | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
25 | HG00741.hp1 HG01192.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.-5+941delT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000625 | |||||||
| chr9:33000625 | CAA | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(58): Show |
104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-5+940_-5+941delTT | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000625 | |||||||
| chr9:33000625 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 |
3 | HG03041.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-5+932_-5+941delTT others(8): Show |
APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000625 | |||||||
| chr9:33000640 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+927T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000640 | |||||||
| chr9:33000643 | A | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-5+924T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000643 | |||||||
| chr9:33000726 | A | G | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+841T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000726 | |||||||
| chr9:33000844 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-5+723A>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000844 | |||||||
| chr9:33000845 | C | CT | 88 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-5+721dupA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000845 | |||||||
| chr9:33000845 | C | CTT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
15 | HG00621.hp2 HG01109.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5+720_-5+721dupAA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000845 | |||||||
| chr9:33000845 | C | T | 7 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0140 others(4): Show |
7 | HG00544.hp1 HG01106.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5+722G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000845 | |||||||
| chr9:33000883 | G | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+684C>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000883 | |||||||
| chr9:33000917 | A | G | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+650T>C | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33000917 | |||||||
| chr9:33001069 | A | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+498T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001069 | |||||||
| chr9:33001180 | CTG | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-5+385_-5+386delCA | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001180 | |||||||
| chr9:33001342 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-5+225C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001342 | |||||||
| chr9:33001415 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-5+152G>A | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001415 | |||||||
| chr9:33001441 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-5+126C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001441 | |||||||
| chr9:33001443 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
73 | HG00544.hp2 HG00741.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.-5+124C>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001443 | |||||||
| chr9:33001450 | G | C | 3 | a0001c0001t0001g0223 a0003c0003t0001g0222 a0003c0003t0001g0224 |
3 | HG01256.hp1 HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-5+117C>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001450 | |||||||
| chr9:33001451 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-5+116G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001451 | |||||||
| chr9:33001532 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-5+35T>G | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001532 | |||||||
| chr9:33001551 | C | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0226 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-5+16G>T | APTX | ENSG00000137074.20 | transcript | ENST00000379817.7 | protein_coding | 1/7 | chr9 | 33001551 |