Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 443 |
| ensemblid | ENSG00000108381.11 |
| hgncid | 756 |
| symbol | ASPA |
| name | aspartoacylase |
| refseq_nuc | NM_000049.4 |
| refseq_prot | NP_000040.1 |
| ensembl_nuc | ENST00000263080.3 |
| ensembl_prot | ENSP00000263080.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 3475997 |
| end | 3503405 |
| strand | + |
| ver | v1.2 |
| region | chr17:3475997-3503405 |
| region5000 | chr17:3470997-3508405 |
| regionname0 | ASPA_chr17_3475997_3503405 |
| regionname5000 | ASPA_chr17_3470997_3508405 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 313 | 446 | 93 | 84 | 201 | 16 | 50 | 157 | ASPA_chr17_3470997_3508405 | ASPA | MTSCH others(308): Show |
chr17 | 3470997 | 3508405 |
| a0002 | 0/0 | 313 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | MTSCH others(308): Show |
chr17 | 3470997 | 3508405 |
| a0003 | 0/0 | 313 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | MTSCH others(308): Show |
chr17 | 3470997 | 3508405 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 939 | 370 | 67 | 66 | 188 | 11 | 36 | ASPA_chr17_3470997_3508405 | ASPA | ATGAC others(934): Show |
chr17 | 3470997 | 3508405 | ||
| a0001c0002 | 0/0 | 939 | 69 | 26 | 13 | 11 | 5 | 14 | ASPA_chr17_3470997_3508405 | ASPA | ATGAC others(934): Show |
chr17 | 3470997 | 3508405 | ||
| a0001c0003 | 0/0 | 939 | 7 | 0 | 5 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | ATGAC others(934): Show |
chr17 | 3470997 | 3508405 | ||
| a0002c0004 | 0/0 | 939 | 3 | 3 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | ATGAC others(934): Show |
chr17 | 3470997 | 3508405 | ||
| a0003c0005 | 0/0 | 939 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | ATGAC others(934): Show |
chr17 | 3470997 | 3508405 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5428 | 120 | 1 | 20 | 92 | 0 | 7 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0002 | 0/0 | 5428 | 75 | 8 | 20 | 24 | 5 | 18 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0003 | 0/0 | 5417 | 48 | 1 | 4 | 41 | 0 | 2 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0004 | 0/1 | 5428 | 32 | 8 | 13 | 0 | 5 | 5 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0005 | 0/0 | 5430 | 3 | 1 | 1 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5425): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0006 | 0/0 | 5409 | 10 | 10 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5404): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0007 | 0/0 | 5429 | 4 | 1 | 1 | 0 | 1 | 1 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0008 | 0/0 | 5421 | 8 | 7 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5416): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0009 | 0/0 | 5426 | 7 | 0 | 0 | 7 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5421): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0010 | 0/0 | 5425 | 5 | 0 | 0 | 5 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5420): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0011 | 0/0 | 5422 | 4 | 2 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5417): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0012 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0013 | 0/0 | 5422 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5417): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0014 | 0/0 | 5429 | 3 | 3 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0015 | 0/0 | 5412 | 3 | 3 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5407): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0016 | 0/0 | 5429 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0018 | 0/0 | 5428 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0019 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0020 | 0/0 | 5428 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0021 | 0/0 | 5428 | 2 | 0 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0022 | 0/0 | 5419 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5414): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0023 | 1/0 | 5422 | 2 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5417): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0024 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0025 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5430): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0026 | 0/0 | 5426 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5421): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0027 | 0/0 | 5422 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5417): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0028 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5416): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0029 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0030 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0031 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0032 | 0/0 | 5427 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5422): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0034 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0035 | 0/0 | 5430 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5425): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0036 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0037 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0038 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0039 | 0/0 | 5429 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0040 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0041 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0042 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0043 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0044 | 0/0 | 5426 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5421): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0046 | 0/0 | 5417 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0047 | 0/0 | 5417 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0048 | 0/0 | 5417 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0049 | 0/0 | 5409 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5404): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0050 | 0/0 | 5409 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5404): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0051 | 0/0 | 5409 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5404): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0052 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0053 | 0/0 | 5423 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5418): Show |
chr17 | 3470997 | 3508405 |
| a0001c0001t0054 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0002 | 0/0 | 5428 | 8 | 2 | 2 | 0 | 1 | 3 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0003 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0004 | 0/0 | 5428 | 3 | 1 | 0 | 0 | 0 | 2 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0005 | 0/0 | 5430 | 23 | 4 | 2 | 10 | 2 | 5 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5425): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0006 | 0/0 | 5409 | 12 | 1 | 6 | 0 | 1 | 4 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5404): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0007 | 0/0 | 5429 | 14 | 10 | 3 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0008 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5416): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0013 | 0/0 | 5422 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5417): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0017 | 0/0 | 5430 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5425): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0019 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0033 | 0/0 | 5430 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5425): Show |
chr17 | 3470997 | 3508405 |
| a0001c0002t0045 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5412): Show |
chr17 | 3470997 | 3508405 |
| a0001c0003t0002 | 0/0 | 5428 | 7 | 0 | 5 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0002c0004t0004 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| a0002c0004t0007 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5424): Show |
chr17 | 3470997 | 3508405 |
| a0002c0004t0008 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5416): Show |
chr17 | 3470997 | 3508405 |
| a0003c0005t0002 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | AGAAC others(5423): Show |
chr17 | 3470997 | 3508405 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0004g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0006g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0008g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0010g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0011g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0012g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0014g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0015g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0015g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0016g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0016g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0019g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0020g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0020g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0021g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0022g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0023g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0023g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0024g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0025g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0026g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0027g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0028g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0029g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0030g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0031g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0034g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0035g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0036g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0037g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0038g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0039g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0040g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0041g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0042g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0043g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0044g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0046g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0047g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0048g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0049g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0050g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0051g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0052g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0053g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0001t0054g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0004g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0006g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0017g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0019g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0033g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0002t0045g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0002c0004t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0002c0004t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0002c0004t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| a0003c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00140 | hp2 | a0001 | c0002 | t0007 | g0014 | EUR | GBR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0256 | EUR | FIN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | FIN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00323 | hp2 | a0001 | c0002 | t0006 | g0015 | EUR | FIN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00597 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0063 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00642 | hp1 | a0001 | c0002 | t0006 | g0199 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0349 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01069 | hp2 | a0001 | c0002 | t0006 | g0191 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01074 | hp1 | a0001 | c0002 | t0007 | g0281 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01081 | hp1 | a0001 | c0001 | t0042 | g0101 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01106 | hp2 | a0001 | c0002 | t0007 | g0200 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0277 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01167 | hp1 | a0001 | c0001 | t0021 | g0031 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01167 | hp2 | a0001 | c0001 | t0011 | g0140 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01169 | hp2 | a0001 | c0001 | t0021 | g0031 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01192 | hp2 | a0001 | c0002 | t0006 | g0015 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0148 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0307 | AMR | PUR | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01255 | hp1 | a0001 | c0002 | t0006 | g0282 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01257 | hp2 | a0001 | c0002 | t0006 | g0112 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0111 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0314 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0231 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01433 | hp1 | a0001 | c0002 | t0006 | g0015 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0042 | EUR | IBS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0283 | EUR | IBS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0366 | EUR | IBS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01517 | hp2 | a0001 | c0002 | t0005 | g0042 | EUR | IBS | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0046 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0368 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01891 | hp1 | a0001 | c0002 | t0019 | g0370 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0078 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01975 | hp2 | a0001 | c0001 | t0054 | g0065 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0127 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0180 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02040 | hp2 | a0001 | c0001 | t0029 | g0033 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0014 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0319 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0210 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02155 | hp1 | a0001 | c0001 | t0035 | g0144 | EAS | CDX | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | CDX | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0375 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0016 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0325 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0300 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0046 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02451 | hp2 | a0002 | c0004 | t0008 | g0206 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02523 | hp1 | a0001 | c0002 | t0005 | g0237 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0369 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02602 | hp1 | a0001 | c0002 | t0006 | g0013 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0374 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0344 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0278 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0346 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0013 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02698 | hp1 | a0001 | c0002 | t0005 | g0163 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02717 | hp1 | a0001 | c0002 | t0008 | g0350 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02717 | hp2 | a0001 | c0001 | t0028 | g0367 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02735 | hp1 | a0001 | c0001 | t0038 | g0108 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02735 | hp2 | a0001 | c0001 | t0049 | g0059 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0221 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02809 | hp2 | a0001 | c0001 | t0051 | g0196 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0329 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02818 | hp2 | a0001 | c0001 | t0036 | g0336 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02886 | hp1 | a0001 | c0002 | t0007 | g0324 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02886 | hp2 | a0001 | c0001 | t0016 | g0353 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0170 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02895 | hp2 | a0001 | c0002 | t0017 | g0045 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02897 | hp1 | a0001 | c0002 | t0017 | g0045 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0203 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02922 | hp2 | a0001 | c0001 | t0052 | g0146 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0343 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02976 | hp1 | a0001 | c0002 | t0013 | g0145 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02976 | hp2 | a0001 | c0001 | t0053 | g0174 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03017 | hp1 | a0001 | c0002 | t0006 | g0291 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03017 | hp2 | a0001 | c0001 | t0039 | g0002 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0345 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03098 | hp1 | a0002 | c0004 | t0007 | g0328 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03130 | hp1 | a0001 | c0001 | t0037 | g0340 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0292 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0137 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0138 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0270 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0147 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0016 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03490 | hp2 | a0001 | c0002 | t0004 | g0040 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0166 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0040 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03516 | hp2 | a0001 | c0001 | t0027 | g0354 | AFR | ESN | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03540 | hp1 | a0001 | c0002 | t0005 | g0342 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0372 | AFR | GWD | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0186 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0352 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0313 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0183 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0363 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0311 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0245 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04184 | hp2 | a0001 | c0001 | t0007 | g0095 | SAS | BEB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04199 | hp2 | a0001 | c0002 | t0006 | g0013 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04204 | hp1 | a0001 | c0002 | t0005 | g0085 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04204 | hp2 | a0001 | c0002 | t0005 | g0198 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0216 | SAS | STU | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0326 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | CHB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18747 | hp2 | a0001 | c0001 | t0030 | g0004 | EAS | CHB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0339 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18906 | hp2 | a0001 | c0001 | t0050 | g0027 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18943 | hp1 | a0001 | c0001 | t0041 | g0020 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18943 | hp2 | a0001 | c0002 | t0005 | g0286 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18944 | hp2 | a0001 | c0001 | t0022 | g0089 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18949 | hp1 | a0001 | c0001 | t0047 | g0088 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18953 | hp2 | a0001 | c0002 | t0005 | g0096 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18956 | hp1 | a0001 | c0001 | t0009 | g0332 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0330 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18967 | hp1 | a0001 | c0001 | t0020 | g0356 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18972 | hp2 | a0001 | c0002 | t0005 | g0331 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18980 | hp1 | a0001 | c0001 | t0048 | g0297 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18982 | hp1 | a0001 | c0001 | t0046 | g0234 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0154 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18987 | hp1 | a0001 | c0002 | t0005 | g0019 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18988 | hp2 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18989 | hp1 | a0001 | c0001 | t0024 | g0106 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0262 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18999 | hp1 | a0001 | c0001 | t0009 | g0294 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19002 | hp2 | a0001 | c0001 | t0040 | g0361 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19003 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19005 | hp2 | a0001 | c0001 | t0020 | g0265 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19006 | hp1 | a0001 | c0002 | t0033 | g0238 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0338 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19030 | hp2 | a0001 | c0002 | t0045 | g0371 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0365 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19057 | hp1 | a0001 | c0001 | t0010 | g0258 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19058 | hp1 | a0001 | c0002 | t0005 | g0019 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19062 | hp2 | a0001 | c0001 | t0009 | g0204 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19064 | hp1 | a0001 | c0001 | t0044 | g0052 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19072 | hp2 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19077 | hp1 | a0001 | c0001 | t0022 | g0298 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19077 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19080 | hp1 | a0001 | c0001 | t0043 | g0224 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19084 | hp1 | a0003 | c0005 | t0002 | g0076 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | YRI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0169 | AFR | ASW | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0215 | AFR | ASW | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0164 | EUR | TSI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0117 | EUR | TSI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0184 | EUR | TSI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0192 | EUR | TSI | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | GIH | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | GIH | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0201 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0327 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02486 | hp2 | a0001 | c0001 | t0031 | g0103 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02559 | hp1 | a0001 | c0002 | t0007 | g0016 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0268 | AFR | ACB | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0341 | AFR | MSL | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG06807 | hp1 | a0002 | c0004 | t0004 | g0317 | AFR | USA | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | USA | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0373 | AFR | USA | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| NA21309 | hp2 | a0001 | c0001 | t0026 | g0360 | AFR | LWK | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0315 | REF | REF | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0023 | g0032 | REF | REF | ASPA_chr17_3470997_3508405 | ASPA | chr17 | 3470997 | 3508405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:3494418 | G | A | 1 | a0002 | 3 | HG02451.hp2 HG03098.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.703G>A | p.Glu235Lys | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/6 | 866/5422 | 703/942 | 235/313 | chr17 | 3494418 | |||
| chr17:3498978 | G | A | 1 | a0003 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.832G>A | p.Val278Met | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 995/5422 | 832/942 | 278/313 | chr17 | 3498978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:3494408 | C | T | 1 | a0001c0002 | 69 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(66): Show |
synonymous_variant | LOW | c.693C>T | p.Tyr231Tyr | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/6 | 856/5422 | 693/942 | 231/313 | chr17 | 3494408 | |||
| chr17:3498977 | C | T | 1 | a0001c0003 | 7 | HG00735.hp2 HG01358.hp2 HG02004.hp1 others(4): Show |
synonymous_variant | LOW | c.831C>T | p.Thr277Thr | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 994/5422 | 831/942 | 277/313 | chr17 | 3498977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:3476046 | A | G | 1 | a0001c0001t0054 | 1 | HG01975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/6 | 114 | chr17 | 3476046 | ||||||
| chr17:3476065 | G | A | 1 | a0001c0001t0024 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/6 | 95 | chr17 | 3476065 | ||||||
| chr17:3499091 | A | G | 1 | a0001c0001t0012 | 4 | HG02145.hp2 HG02280.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3 | chr17 | 3499091 | ||||||
| chr17:3499115 | C | T | 1 | a0001c0001t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 27 | chr17 | 3499115 | ||||||
| chr17:3499227 | C | A | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
3_prime_UTR_variant | MODIFIER | c.*139C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 139 | chr17 | 3499227 | ||||||
| chr17:3499447 | CTGTACT | C | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
3_prime_UTR_variant | MODIFIER | c.*367_*372delGTACTT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 367 | INFO_REALIGN_3_PRIME | chr17 | 3499447 | |||||
| chr17:3499524 | A | G | 1 | a0001c0001t0052 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 436 | chr17 | 3499524 | ||||||
| chr17:3499530 | ATGTGCTC others(12): Show |
A | 6 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0049 others(3): Show |
28 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*465delCTCACT others(13): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 447 | INFO_REALIGN_3_PRIME | chr17 | 3499530 | |||||
| chr17:3499646 | T | C | 1 | a0001c0001t0029 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 558 | chr17 | 3499646 | ||||||
| chr17:3500068 | C | CA | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
3_prime_UTR_variant | MODIFIER | c.*981dupA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 982 | INFO_REALIGN_3_PRIME | chr17 | 3500068 | |||||
| chr17:3500092 | C | G | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
3_prime_UTR_variant | MODIFIER | c.*1004C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1004 | chr17 | 3500092 | ||||||
| chr17:3500220 | G | A | 1 | a0001c0001t0016 | 2 | HG02886.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1132 | chr17 | 3500220 | ||||||
| chr17:3500339 | A | G | 1 | a0001c0001t0048 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1251 | chr17 | 3500339 | ||||||
| chr17:3500426 | T | G | 1 | a0001c0001t0030 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1338 | chr17 | 3500426 | ||||||
| chr17:3500504 | T | C | 1 | a0001c0001t0031 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1416T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1416 | chr17 | 3500504 | ||||||
| chr17:3500511 | T | TTTTTGTT others(5): Show |
1 | a0001c0001t0032 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1427_*1428insGTTT others(8): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1428 | INFO_REALIGN_3_PRIME | chr17 | 3500511 | |||||
| chr17:3500511 | T | TTTTTTG | 2 | a0001c0001t0011 a0001c0001t0022 |
6 | HG01109.hp2 HG01167.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1428_*1429insGTTT others(2): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1429 | INFO_REALIGN_3_PRIME | chr17 | 3500511 | |||||
| chr17:3500511 | T | TTTTTTGT others(6): Show |
48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(45): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*1428_*1429insGTTT others(9): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1429 | INFO_REALIGN_3_PRIME | chr17 | 3500511 | |||||
| chr17:3500643 | C | T | 1 | a0001c0001t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1555 | chr17 | 3500643 | ||||||
| chr17:3500706 | C | G | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
3_prime_UTR_variant | MODIFIER | c.*1618C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1618 | chr17 | 3500706 | ||||||
| chr17:3500733 | T | A | 14 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(11): Show |
58 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1645T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1645 | chr17 | 3500733 | ||||||
| chr17:3500747 | G | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(25): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*1659G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1659 | chr17 | 3500747 | ||||||
| chr17:3500755 | C | T | 2 | a0001c0001t0020 a0001c0001t0037 |
3 | HG03130.hp1 NA18967.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1667 | chr17 | 3500755 | ||||||
| chr17:3500795 | C | T | 3 | a0001c0001t0019 a0001c0001t0031 a0001c0002t0019 |
3 | HG01891.hp1 HG02486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1707C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1707 | chr17 | 3500795 | ||||||
| chr17:3500796 | G | A | 5 | a0001c0001t0006 a0001c0001t0049 a0001c0001t0050 others(2): Show |
25 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1708 | chr17 | 3500796 | ||||||
| chr17:3500940 | T | C | 1 | a0001c0001t0015 | 3 | HG02809.hp1 HG02897.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1852T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1852 | chr17 | 3500940 | ||||||
| chr17:3500950 | GA | G | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(32): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*1873delA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1873 | INFO_REALIGN_3_PRIME | chr17 | 3500950 | |||||
| chr17:3501029 | C | T | 6 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0049 others(3): Show |
28 | HG00323.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1941C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1941 | chr17 | 3501029 | ||||||
| chr17:3501030 | G | A | 3 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0037 |
6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1942G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1942 | chr17 | 3501030 | ||||||
| chr17:3501051 | G | A | 1 | a0001c0002t0017 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1963G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1963 | chr17 | 3501051 | ||||||
| chr17:3501052 | C | T | 4 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0043 others(1): Show |
11 | HG02040.hp1 HG02056.hp2 NA18944.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 1964 | chr17 | 3501052 | ||||||
| chr17:3501114 | C | T | 1 | a0001c0001t0050 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2026 | chr17 | 3501114 | ||||||
| chr17:3501188 | A | G | 1 | a0001c0001t0011 | 4 | HG01109.hp2 HG01167.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2100A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2100 | chr17 | 3501188 | ||||||
| chr17:3501373 | TG | T | 1 | a0001c0001t0015 | 3 | HG02809.hp1 HG02897.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2286delG | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2286 | chr17 | 3501373 | ||||||
| chr17:3501447 | G | A | 1 | a0001c0002t0033 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2359G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2359 | chr17 | 3501447 | ||||||
| chr17:3501669 | G | A | 1 | a0001c0001t0034 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2581G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2581 | chr17 | 3501669 | ||||||
| chr17:3501675 | G | A | 1 | a0001c0001t0049 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2587G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2587 | chr17 | 3501675 | ||||||
| chr17:3501863 | G | A | 7 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0019 others(4): Show |
42 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2775G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2775 | chr17 | 3501863 | ||||||
| chr17:3501950 | C | T | 1 | a0001c0001t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2862C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2862 | chr17 | 3501950 | ||||||
| chr17:3501952 | CA | C | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(43): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*2886delA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2886 | INFO_REALIGN_3_PRIME | chr17 | 3501952 | |||||
| chr17:3501952 | CAAA | C | 3 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0044 |
10 | HG02040.hp1 HG02056.hp2 NA18944.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2884_*2886delAAA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2884 | INFO_REALIGN_3_PRIME | chr17 | 3501952 | |||||
| chr17:3501956 | A | C | 1 | a0001c0001t0026 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2868A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2868 | chr17 | 3501956 | ||||||
| chr17:3501958 | A | C | 12 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0031 others(9): Show |
84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2870A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2870 | chr17 | 3501958 | ||||||
| chr17:3501959 | A | C | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(38): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*2871A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2871 | chr17 | 3501959 | ||||||
| chr17:3501960 | A | C | 1 | a0001c0001t0043 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2872A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2872 | chr17 | 3501960 | ||||||
| chr17:3501961 | A | C | 3 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0044 |
10 | HG02040.hp1 HG02056.hp2 NA18944.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2873A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2873 | chr17 | 3501961 | ||||||
| chr17:3501963 | A | C | 3 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0037 |
6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2875A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2875 | chr17 | 3501963 | ||||||
| chr17:3501965 | A | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(30): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2877A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2877 | chr17 | 3501965 | ||||||
| chr17:3501967 | A | C | 3 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0037 |
6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2879A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2879 | chr17 | 3501967 | ||||||
| chr17:3502065 | CTTG | C | 1 | a0001c0001t0010 | 5 | NA18960.hp1 NA18988.hp2 NA19010.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2983_*2985delGTT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 2983 | INFO_REALIGN_3_PRIME | chr17 | 3502065 | |||||
| chr17:3502224 | T | C | 1 | a0001c0001t0040 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3136T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3136 | chr17 | 3502224 | ||||||
| chr17:3502309 | C | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
3_prime_UTR_variant | MODIFIER | c.*3221C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3221 | chr17 | 3502309 | ||||||
| chr17:3502349 | T | C | 1 | a0001c0001t0027 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3261T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3261 | chr17 | 3502349 | ||||||
| chr17:3502522 | G | A | 3 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0037 |
6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3434G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3434 | chr17 | 3502522 | ||||||
| chr17:3502526 | C | T | 1 | a0001c0001t0047 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3438C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3438 | chr17 | 3502526 | ||||||
| chr17:3502834 | C | G | 1 | a0001c0001t0036 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3746C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3746 | chr17 | 3502834 | ||||||
| chr17:3502842 | G | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
431 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(428): Show |
3_prime_UTR_variant | MODIFIER | c.*3754G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3754 | chr17 | 3502842 | ||||||
| chr17:3502843 | C | A | 10 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0034 others(7): Show |
51 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3755C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3755 | chr17 | 3502843 | ||||||
| chr17:3502860 | G | C | 1 | a0001c0001t0026 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3772G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3772 | chr17 | 3502860 | ||||||
| chr17:3502895 | T | A | 10 | a0001c0001t0001 a0001c0001t0020 a0001c0001t0024 others(7): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*3807T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3807 | chr17 | 3502895 | ||||||
| chr17:3502962 | G | A | 1 | a0001c0001t0028 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3874G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3874 | chr17 | 3502962 | ||||||
| chr17:3503000 | C | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
3_prime_UTR_variant | MODIFIER | c.*3912C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 3912 | chr17 | 3503000 | ||||||
| chr17:3503150 | G | T | 1 | a0001c0001t0041 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4062G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 4062 | chr17 | 3503150 | ||||||
| chr17:3503170 | A | C | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*4082A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 4082 | chr17 | 3503170 | ||||||
| chr17:3503202 | G | GGAAT | 2 | a0001c0001t0015 a0001c0001t0026 |
4 | HG02809.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4139_*4142dupGAAT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 4143 | INFO_REALIGN_3_PRIME | chr17 | 3503202 | |||||
| chr17:3503231 | A | T | 1 | a0001c0001t0038 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4143A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 4143 | chr17 | 3503231 | ||||||
| chr17:3503319 | T | C | 2 | a0001c0001t0010 a0001c0001t0018 |
7 | NA18960.hp1 NA18988.hp2 NA19003.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4231T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 6/6 | 4231 | chr17 | 3503319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:3476521 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.236+126T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3476521 | |||||||
| chr17:3476548 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(111): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.236+153T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3476548 | |||||||
| chr17:3476692 | C | T | 1 | a0001c0001t0006g0375 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236+297C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3476692 | |||||||
| chr17:3477025 | G | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(27): Show |
34 | HG00558.hp2 HG01243.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+630G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477025 | |||||||
| chr17:3477090 | G | T | 1 | a0001c0001t0002g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.236+695G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477090 | |||||||
| chr17:3477161 | A | G | 1 | a0001c0001t0008g0374 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236+766A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477161 | |||||||
| chr17:3477166 | T | A | 6 | a0001c0001t0002g0172 a0001c0001t0008g0171 a0001c0001t0008g0173 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+771T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477166 | |||||||
| chr17:3477206 | C | T | 1 | a0001c0001t0019g0373 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.236+811C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477206 | |||||||
| chr17:3477219 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.236+824G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477219 | |||||||
| chr17:3477280 | C | T | 7 | a0001c0001t0004g0368 a0001c0001t0005g0369 a0001c0001t0006g0372 others(4): Show |
9 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+885C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477280 | |||||||
| chr17:3477545 | C | T | 1 | a0001c0001t0003g0135 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.236+1150C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477545 | |||||||
| chr17:3477554 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+1159G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477554 | |||||||
| chr17:3477582 | A | C | 2 | a0001c0001t0004g0366 a0001c0002t0006g0015 |
4 | HG00323.hp2 HG01192.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+1187A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477582 | |||||||
| chr17:3477743 | C | A | 1 | a0001c0001t0028g0367 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.236+1348C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477743 | |||||||
| chr17:3477920 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
14 | HG01346.hp1 HG01952.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+1525C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477920 | |||||||
| chr17:3477923 | C | G | 1 | a0001c0001t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236+1528C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3477923 | |||||||
| chr17:3478059 | C | A | 1 | a0001c0001t0003g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.236+1664C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478059 | |||||||
| chr17:3478084 | C | T | 1 | a0001c0001t0006g0365 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.236+1689C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478084 | |||||||
| chr17:3478102 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236+1707G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478102 | |||||||
| chr17:3478168 | G | A | 2 | a0001c0001t0003g0179 a0001c0001t0009g0180 |
2 | HG00423.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.236+1773G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478168 | |||||||
| chr17:3478171 | C | T | 1 | a0001c0001t0002g0364 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236+1776C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478171 | |||||||
| chr17:3478192 | A | AAT | 8 | a0001c0001t0002g0347 a0001c0001t0023g0343 a0001c0001t0025g0344 others(5): Show |
9 | HG00140.hp2 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+1798_236+1799i others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 3478192 | ||||||
| chr17:3478192 | A | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0047 others(47): Show |
57 | HG00558.hp2 HG00733.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.236+1797A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478192 | |||||||
| chr17:3478194 | A | AT | 7 | a0001c0001t0001g0276 a0001c0001t0002g0041 a0001c0001t0002g0275 others(4): Show |
11 | HG01952.hp2 HG02602.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+1799_236+1800i others(3): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478194 | |||||||
| chr17:3478194 | A | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(250): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.236+1799A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478194 | |||||||
| chr17:3478196 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0003g0181 a0001c0002t0005g0183 |
3 | HG02602.hp2 HG03831.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.236+1801T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478196 | |||||||
| chr17:3478277 | A | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(27): Show |
34 | HG00558.hp2 HG01243.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+1882A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478277 | |||||||
| chr17:3478494 | T | C | 3 | a0001c0001t0002g0348 a0001c0001t0011g0277 a0001c0001t0034g0278 |
3 | HG01109.hp2 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.236+2099T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478494 | |||||||
| chr17:3478563 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.236+2168G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478563 | |||||||
| chr17:3478713 | C | A | 6 | a0001c0001t0002g0172 a0001c0001t0008g0171 a0001c0001t0008g0173 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.236+2318C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478713 | |||||||
| chr17:3478713 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.236+2318C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478713 | |||||||
| chr17:3478827 | A | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(27): Show |
34 | HG00558.hp2 HG01243.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.236+2432A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478827 | |||||||
| chr17:3478848 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.236+2453T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478848 | |||||||
| chr17:3478945 | A | T | 7 | a0001c0001t0006g0139 a0001c0001t0008g0028 a0001c0001t0011g0027 others(4): Show |
8 | HG01167.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+2550A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3478945 | |||||||
| chr17:3479037 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.237-2566T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479037 | |||||||
| chr17:3479354 | C | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(62): Show |
78 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.237-2249C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479354 | |||||||
| chr17:3479497 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0044 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.237-2106G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479497 | |||||||
| chr17:3479691 | C | A | 1 | a0001c0002t0002g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237-1912C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479691 | |||||||
| chr17:3479752 | T | G | 3 | a0001c0001t0004g0318 a0001c0001t0006g0319 a0002c0004t0004g0317 |
3 | HG02055.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.237-1851T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479752 | |||||||
| chr17:3479810 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18957.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.237-1793A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479810 | |||||||
| chr17:3479903 | GA | G | 34 | a0001c0001t0001g0193 a0001c0001t0002g0188 a0001c0001t0002g0189 others(31): Show |
43 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.237-1692delA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 3479903 | ||||||
| chr17:3479938 | G | GGA | 4 | a0001c0001t0001g0320 a0001c0001t0002g0321 a0001c0001t0009g0204 others(1): Show |
4 | NA18955.hp1 NA18957.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-1661_237-1660d others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 3479938 | ||||||
| chr17:3479996 | A | G | 1 | a0001c0001t0003g0272 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.237-1607A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3479996 | |||||||
| chr17:3480046 | T | TAC | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(215): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.237-1556_237-1555i others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 3480046 | ||||||
| chr17:3480233 | A | G | 33 | a0001c0001t0001g0193 a0001c0001t0002g0188 a0001c0001t0002g0189 others(30): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-1370A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480233 | |||||||
| chr17:3480265 | T | G | 7 | a0001c0001t0006g0139 a0001c0001t0008g0028 a0001c0001t0011g0027 others(4): Show |
8 | HG01167.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-1338T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480265 | |||||||
| chr17:3480279 | C | T | 33 | a0001c0001t0001g0193 a0001c0001t0002g0188 a0001c0001t0002g0189 others(30): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.237-1324C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480279 | |||||||
| chr17:3480349 | C | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(185): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.237-1254C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480349 | |||||||
| chr17:3480351 | C | A | 1 | a0001c0001t0004g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.237-1252C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480351 | |||||||
| chr17:3480471 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.237-1132A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480471 | |||||||
| chr17:3480492 | ATAAGCCA others(3): Show |
A | 3 | a0001c0001t0002g0348 a0001c0001t0011g0277 a0001c0001t0034g0278 |
3 | HG01109.hp2 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.237-1108_237-1099d others(12): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 3480492 | ||||||
| chr17:3480706 | G | A | 1 | a0001c0002t0005g0342 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237-897G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480706 | |||||||
| chr17:3480880 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.237-723T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3480880 | |||||||
| chr17:3481059 | G | T | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.237-544G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3481059 | |||||||
| chr17:3481296 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(27): Show |
34 | HG00558.hp2 HG01243.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.237-307G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3481296 | |||||||
| chr17:3481376 | C | T | 3 | a0001c0001t0004g0318 a0001c0001t0006g0319 a0002c0004t0004g0317 |
3 | HG02055.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.237-227C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3481376 | |||||||
| chr17:3481407 | T | G | 2 | a0001c0001t0004g0285 a0001c0001t0008g0284 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.237-196T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 1/5 | chr17 | 3481407 | |||||||
| chr17:3481940 | G | C | 1 | a0001c0002t0005g0286 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.432+142G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3481940 | |||||||
| chr17:3481955 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(111): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.432+157A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3481955 | |||||||
| chr17:3482085 | A | T | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0044 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.432+287A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482085 | |||||||
| chr17:3482132 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.432+334A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482132 | |||||||
| chr17:3482251 | C | T | 1 | a0001c0001t0014g0270 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.432+453C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482251 | |||||||
| chr17:3482303 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432+505G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482303 | |||||||
| chr17:3482399 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.432+601A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482399 | |||||||
| chr17:3482477 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(141): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.432+679A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482477 | |||||||
| chr17:3482650 | G | C | 4 | a0001c0001t0004g0150 a0001c0001t0008g0148 a0001c0001t0012g0149 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-849G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482650 | |||||||
| chr17:3482768 | CT | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.433-720delT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr17 | 3482768 | ||||||
| chr17:3482789 | T | A | 2 | a0001c0001t0008g0374 a0001c0002t0008g0350 |
2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.433-710T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482789 | |||||||
| chr17:3482828 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.433-671T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482828 | |||||||
| chr17:3482832 | CA | C | 33 | a0001c0001t0001g0193 a0001c0001t0002g0188 a0001c0001t0002g0189 others(30): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.433-666delA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482832 | |||||||
| chr17:3482857 | G | A | 1 | a0001c0001t0009g0210 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.433-642G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482857 | |||||||
| chr17:3482868 | C | T | 5 | a0001c0001t0002g0348 a0001c0001t0011g0277 a0001c0001t0014g0270 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-631C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482868 | |||||||
| chr17:3482882 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(60): Show |
76 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.433-617C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482882 | |||||||
| chr17:3482931 | C | T | 7 | a0001c0001t0006g0139 a0001c0001t0008g0028 a0001c0001t0011g0027 others(4): Show |
8 | HG01167.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.433-568C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482931 | |||||||
| chr17:3482948 | A | G | 91 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(88): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.433-551A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482948 | |||||||
| chr17:3482981 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(27): Show |
34 | HG00558.hp2 HG01243.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.433-518C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3482981 | |||||||
| chr17:3483032 | T | A | 1 | a0001c0001t0049g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.433-467T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3483032 | |||||||
| chr17:3483198 | C | T | 1 | a0001c0002t0002g0117 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.433-301C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3483198 | |||||||
| chr17:3483264 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(147): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.433-235T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3483264 | |||||||
| chr17:3483412 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.433-87G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3483412 | |||||||
| chr17:3483432 | T | G | 1 | a0001c0001t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.433-67T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 2/5 | chr17 | 3483432 | |||||||
| chr17:3483639 | C | G | 4 | a0001c0001t0002g0178 a0001c0001t0004g0318 a0001c0001t0006g0319 others(1): Show |
4 | HG02055.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+47C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3483639 | |||||||
| chr17:3483681 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.526+89G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3483681 | |||||||
| chr17:3483721 | G | A | 9 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG00639.hp2 HG00741.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+129G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3483721 | |||||||
| chr17:3484060 | C | T | 27 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0323 others(24): Show |
30 | HG00140.hp2 HG00733.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.526+468C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484060 | |||||||
| chr17:3484183 | A | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(147): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.526+591A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484183 | |||||||
| chr17:3484351 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(147): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.526+759T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484351 | |||||||
| chr17:3484473 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(147): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.526+881G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484473 | |||||||
| chr17:3484605 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(182): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.526+1013C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484605 | |||||||
| chr17:3484693 | T | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(182): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.526+1101T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484693 | |||||||
| chr17:3484755 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.526+1163G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3484755 | |||||||
| chr17:3485022 | G | GT | 3 | a0001c0001t0002g0116 a0001c0001t0005g0068 a0001c0002t0002g0058 |
3 | HG01123.hp1 HG01168.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.526+1434dupT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3485022 | ||||||
| chr17:3485027 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(137): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.526+1435G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485027 | |||||||
| chr17:3485247 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.526+1655C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485247 | |||||||
| chr17:3485302 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(183): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.526+1710A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485302 | |||||||
| chr17:3485438 | C | T | 2 | a0001c0001t0004g0322 a0002c0004t0008g0206 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.526+1846C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485438 | |||||||
| chr17:3485462 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.526+1870G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485462 | |||||||
| chr17:3485482 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.526+1890C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485482 | |||||||
| chr17:3485517 | A | C | 1 | a0001c0001t0001g0048 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.526+1925A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485517 | |||||||
| chr17:3485623 | T | A | 1 | a0001c0001t0006g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+2031T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485623 | |||||||
| chr17:3485627 | T | C | 4 | a0001c0001t0002g0178 a0001c0001t0004g0318 a0001c0001t0006g0319 others(1): Show |
4 | HG02055.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+2035T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485627 | |||||||
| chr17:3485712 | T | A | 35 | a0001c0001t0001g0193 a0001c0001t0002g0188 a0001c0001t0002g0189 others(32): Show |
44 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.526+2120T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485712 | |||||||
| chr17:3485826 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.526+2234G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485826 | |||||||
| chr17:3485882 | AGAGAGCC others(5): Show |
A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | NA18945.hp1 NA18948.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+2292_526+2303d others(14): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3485882 | ||||||
| chr17:3485934 | C | CTT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(140): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.526+2356_526+2357d others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3485934 | ||||||
| chr17:3485934 | CT | C | 40 | a0001c0001t0001g0193 a0001c0001t0001g0218 a0001c0001t0001g0287 others(37): Show |
50 | HG00099.hp2 HG00423.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.526+2357delT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3485934 | ||||||
| chr17:3485944 | T | G | 1 | a0001c0001t0002g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.526+2352T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3485944 | |||||||
| chr17:3486066 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.526+2474G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486066 | |||||||
| chr17:3486255 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0003g0024 |
3 | NA18969.hp1 NA19006.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.526+2663G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486255 | |||||||
| chr17:3486358 | A | G | 1 | a0001c0002t0005g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.526+2766A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486358 | |||||||
| chr17:3486466 | G | A | 1 | a0001c0002t0013g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.527-2769G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486466 | |||||||
| chr17:3486533 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.527-2702A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486533 | |||||||
| chr17:3486608 | T | C | 1 | a0003c0005t0002g0076 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.527-2627T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486608 | |||||||
| chr17:3486714 | G | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(286): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.527-2521G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486714 | |||||||
| chr17:3486822 | C | T | 17 | a0001c0001t0002g0290 a0001c0001t0002g0310 a0001c0001t0002g0312 others(14): Show |
21 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-2413C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486822 | |||||||
| chr17:3486959 | A | T | 1 | a0001c0002t0007g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.527-2276A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486959 | |||||||
| chr17:3486962 | A | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(146): Show |
170 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.527-2273A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486962 | |||||||
| chr17:3486966 | T | C | 2 | a0001c0001t0004g0187 a0001c0001t0004g0273 |
2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.527-2269T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3486966 | |||||||
| chr17:3487008 | G | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0070 others(7): Show |
12 | NA18612.hp1 NA18940.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-2227G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487008 | |||||||
| chr17:3487073 | C | CGTGTGTG others(1): Show |
117 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.527-2156_527-2149d others(10): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3487073 | ||||||
| chr17:3487073 | C | CGTGTGTG others(3): Show |
33 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0128 others(30): Show |
37 | HG00558.hp2 HG01168.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.527-2158_527-2149d others(12): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 3487073 | ||||||
| chr17:3487099 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.527-2136G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487099 | |||||||
| chr17:3487312 | G | A | 1 | a0001c0001t0012g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.527-1923G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487312 | |||||||
| chr17:3487385 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(117): Show |
137 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.527-1850A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487385 | |||||||
| chr17:3487401 | C | T | 1 | a0001c0001t0002g0308 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.527-1834C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487401 | |||||||
| chr17:3487444 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.527-1791G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487444 | |||||||
| chr17:3487588 | A | C | 2 | a0001c0002t0002g0113 a0001c0002t0002g0117 |
2 | HG00642.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.527-1647A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487588 | |||||||
| chr17:3487628 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.527-1607T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487628 | |||||||
| chr17:3487820 | C | A | 1 | a0001c0001t0009g0330 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.527-1415C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3487820 | |||||||
| chr17:3488076 | G | A | 2 | a0001c0001t0009g0204 a0001c0001t0009g0205 |
2 | NA18957.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.527-1159G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488076 | |||||||
| chr17:3488156 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.527-1079T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488156 | |||||||
| chr17:3488180 | T | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
11 | NA18940.hp2 NA18954.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-1055T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488180 | |||||||
| chr17:3488358 | G | A | 1 | a0001c0002t0006g0291 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.527-877G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488358 | |||||||
| chr17:3488549 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG00323.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.527-686C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488549 | |||||||
| chr17:3488572 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(115): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.527-663G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488572 | |||||||
| chr17:3488656 | C | T | 1 | a0001c0002t0003g0268 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.527-579C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488656 | |||||||
| chr17:3488913 | A | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(28): Show |
35 | HG00558.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.527-322A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3488913 | |||||||
| chr17:3489028 | T | C | 6 | a0001c0001t0002g0172 a0001c0001t0008g0171 a0001c0001t0008g0173 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-207T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3489028 | |||||||
| chr17:3489058 | T | C | 4 | a0001c0001t0002g0178 a0001c0001t0004g0318 a0001c0001t0006g0319 others(1): Show |
4 | HG02055.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-177T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3489058 | |||||||
| chr17:3489105 | T | C | 1 | a0001c0002t0008g0350 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.527-130T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3489105 | |||||||
| chr17:3489169 | A | G | 4 | a0001c0001t0002g0178 a0001c0001t0004g0318 a0001c0001t0006g0319 others(1): Show |
4 | HG02055.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.527-66A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3489169 | |||||||
| chr17:3489212 | A | T | 1 | a0001c0002t0002g0325 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527-23A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 3/5 | chr17 | 3489212 | |||||||
| chr17:3489366 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.634+24T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489366 | |||||||
| chr17:3489569 | A | AAAAG | 47 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0152 others(44): Show |
52 | HG00558.hp2 HG01167.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.634+229_634+232dup others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3489569 | ||||||
| chr17:3489644 | A | C | 44 | a0001c0001t0001g0193 a0001c0001t0002g0172 a0001c0001t0002g0176 others(41): Show |
54 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.634+302A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489644 | |||||||
| chr17:3489708 | C | T | 1 | a0001c0001t0014g0329 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.634+366C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489708 | |||||||
| chr17:3489709 | G | A | 1 | a0001c0001t0015g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.634+367G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489709 | |||||||
| chr17:3489754 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.634+412T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489754 | |||||||
| chr17:3489774 | T | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0029 others(103): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.634+432T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489774 | |||||||
| chr17:3489792 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(211): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.634+450T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3489792 | |||||||
| chr17:3490011 | T | C | 11 | a0001c0001t0002g0172 a0001c0001t0004g0202 a0001c0001t0004g0368 others(8): Show |
11 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+669T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490011 | |||||||
| chr17:3490150 | A | G | 250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(247): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.634+808A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490150 | |||||||
| chr17:3490266 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(122): Show |
144 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(141): Show |
intron_variant | MODIFIER | c.634+924C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490266 | |||||||
| chr17:3490267 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.634+925G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490267 | |||||||
| chr17:3490305 | C | T | 1 | a0001c0001t0006g0341 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+963C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490305 | |||||||
| chr17:3490306 | A | ATTTATTT others(2): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0071 a0001c0001t0001g0153 others(3): Show |
9 | HG02071.hp1 NA18747.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+964_634+965ins others(9): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490306 | |||||||
| chr17:3490310 | T | C | 47 | a0001c0001t0001g0107 a0001c0001t0002g0122 a0001c0001t0002g0189 others(44): Show |
51 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.634+968T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490310 | |||||||
| chr17:3490487 | G | C | 1 | a0001c0001t0009g0210 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.634+1145G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490487 | |||||||
| chr17:3490536 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0182 a0001c0001t0001g0261 others(1): Show |
4 | NA18970.hp1 NA18989.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+1194C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490536 | |||||||
| chr17:3490537 | G | GTGC | 34 | a0001c0001t0001g0083 a0001c0001t0001g0218 a0001c0001t0002g0142 others(31): Show |
40 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.634+1196_634+1198d others(5): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3490537 | ||||||
| chr17:3490668 | T | C | 142 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0029 others(139): Show |
155 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.634+1326T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490668 | |||||||
| chr17:3490878 | T | G | 9 | a0001c0001t0002g0104 a0001c0001t0004g0105 a0001c0001t0004g0150 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+1536T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490878 | |||||||
| chr17:3490921 | A | G | 21 | a0001c0001t0002g0243 a0001c0001t0002g0348 a0001c0001t0003g0054 others(18): Show |
21 | HG00621.hp1 HG02109.hp1 HG02717.hp2 others(18): Show |
intron_variant | MODIFIER | c.634+1579A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490921 | |||||||
| chr17:3490941 | T | C | 12 | a0001c0001t0002g0244 a0001c0001t0005g0369 a0001c0001t0006g0319 others(9): Show |
12 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+1599T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490941 | |||||||
| chr17:3490952 | G | A | 1 | a0001c0001t0002g0352 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.634+1610G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3490952 | |||||||
| chr17:3491005 | C | A | 207 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0079 others(204): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.634+1663C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491005 | |||||||
| chr17:3491475 | G | A | 11 | a0001c0001t0001g0335 a0001c0001t0002g0190 a0001c0001t0002g0312 others(8): Show |
12 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+2133G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491475 | |||||||
| chr17:3491516 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.634+2174G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491516 | |||||||
| chr17:3491624 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.634+2282T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491624 | |||||||
| chr17:3491678 | G | A | 1 | a0001c0001t0053g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.634+2336G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491678 | |||||||
| chr17:3491697 | G | A | 1 | a0001c0001t0006g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.634+2355G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491697 | |||||||
| chr17:3491747 | A | G | 57 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0121 others(54): Show |
63 | HG00423.hp2 HG00544.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.634+2405A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491747 | |||||||
| chr17:3491750 | A | G | 2 | a0001c0001t0006g0167 a0001c0002t0005g0170 |
2 | HG02895.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.634+2408A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491750 | |||||||
| chr17:3491754 | A | G | 360 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(357): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.634+2412A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491754 | |||||||
| chr17:3491786 | A | C | 1 | a0001c0001t0002g0259 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.634+2444A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491786 | |||||||
| chr17:3491877 | C | CT | 25 | a0001c0001t0002g0244 a0001c0001t0002g0352 a0001c0001t0004g0285 others(22): Show |
26 | HG01074.hp1 HG01106.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.635-2455dupT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3491877 | ||||||
| chr17:3491877 | C | CTT | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.635-2456_635-2455d others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3491877 | ||||||
| chr17:3491877 | C | CTTT | 21 | a0001c0001t0001g0079 a0001c0001t0001g0093 a0001c0001t0001g0126 others(18): Show |
21 | HG00438.hp1 HG00673.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.635-2457_635-2455d others(5): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3491877 | ||||||
| chr17:3491877 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.635-2473C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491877 | |||||||
| chr17:3491909 | A | C | 4 | a0001c0001t0002g0244 a0001c0001t0015g0147 a0001c0001t0015g0221 others(1): Show |
4 | HG02615.hp2 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-2441A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3491909 | |||||||
| chr17:3492113 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.635-2237G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492113 | |||||||
| chr17:3492249 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(316): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.635-2101A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492249 | |||||||
| chr17:3492384 | TC | T | 11 | a0001c0001t0001g0086 a0001c0001t0003g0050 a0001c0001t0003g0051 others(8): Show |
11 | HG01358.hp2 HG02015.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-1964delC | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3492384 | ||||||
| chr17:3492434 | T | C | 2 | a0001c0001t0003g0057 a0001c0001t0048g0297 |
2 | NA18940.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.635-1916T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492434 | |||||||
| chr17:3492694 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.635-1656A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492694 | |||||||
| chr17:3492806 | A | G | 8 | a0001c0001t0005g0369 a0001c0001t0006g0319 a0001c0001t0007g0186 others(5): Show |
8 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-1544A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492806 | |||||||
| chr17:3492832 | G | A | 89 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0098 others(86): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.635-1518G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492832 | |||||||
| chr17:3492941 | C | T | 1 | a0001c0001t0004g0285 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.635-1409C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492941 | |||||||
| chr17:3492959 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.635-1391T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3492959 | |||||||
| chr17:3493004 | T | C | 1 | a0001c0001t0009g0330 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.635-1346T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493004 | |||||||
| chr17:3493072 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.635-1278G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493072 | |||||||
| chr17:3493103 | T | C | 89 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0098 others(86): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.635-1247T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493103 | |||||||
| chr17:3493240 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.635-1110G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493240 | |||||||
| chr17:3493247 | T | C | 56 | a0001c0001t0025g0344 a0001c0001t0035g0144 a0001c0002t0002g0058 others(53): Show |
66 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.635-1103T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493247 | |||||||
| chr17:3493422 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0246 |
2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.635-928G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493422 | |||||||
| chr17:3493486 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.635-864G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493486 | |||||||
| chr17:3493548 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.635-802G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493548 | |||||||
| chr17:3493560 | C | CA | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.635-767dupA | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3493560 | ||||||
| chr17:3493560 | C | CAA | 54 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0080 others(51): Show |
55 | HG00423.hp2 HG00558.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.635-768_635-767dup others(2): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3493560 | ||||||
| chr17:3493560 | C | CAAA | 6 | a0001c0001t0005g0369 a0001c0001t0006g0217 a0001c0001t0008g0327 others(3): Show |
7 | HG01074.hp1 HG01106.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-769_635-767dup others(3): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3493560 | ||||||
| chr17:3493600 | C | T | 54 | a0001c0002t0002g0058 a0001c0002t0002g0113 a0001c0002t0002g0117 others(51): Show |
64 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.635-750C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493600 | |||||||
| chr17:3493613 | A | G | 3 | a0001c0001t0014g0270 a0001c0001t0026g0360 a0001c0001t0028g0367 |
3 | HG02717.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.635-737A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493613 | |||||||
| chr17:3493809 | T | C | 1 | a0001c0002t0006g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.635-541T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493809 | |||||||
| chr17:3493880 | C | G | 46 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0121 others(43): Show |
51 | HG00423.hp2 HG00544.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.635-470C>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493880 | |||||||
| chr17:3493996 | T | A | 1 | a0001c0001t0002g0304 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.635-354T>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3493996 | |||||||
| chr17:3494008 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0002g0188 |
2 | HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.635-342C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3494008 | |||||||
| chr17:3494019 | T | G | 1 | a0001c0001t0002g0304 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.635-331T>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | chr17 | 3494019 | |||||||
| chr17:3494037 | AT | A | 328 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(325): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.635-297delT | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3494037 | ||||||
| chr17:3494037 | ATT | A | 36 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0121 others(33): Show |
41 | HG00423.hp2 HG00544.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.635-298_635-297del others(2): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | 3494037 | ||||||
| chr17:3494601 | C | T | 54 | a0001c0002t0002g0058 a0001c0002t0002g0113 a0001c0002t0002g0117 others(51): Show |
64 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.744+142C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3494601 | |||||||
| chr17:3494675 | G | A | 207 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0086 others(204): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.744+216G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3494675 | |||||||
| chr17:3494995 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.744+536T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3494995 | |||||||
| chr17:3495135 | G | A | 1 | a0001c0001t0007g0314 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.744+676G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495135 | |||||||
| chr17:3495247 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.744+788G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495247 | |||||||
| chr17:3495272 | C | A | 2 | a0001c0002t0008g0350 a0001c0002t0013g0145 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.744+813C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495272 | |||||||
| chr17:3495417 | A | T | 55 | a0001c0002t0002g0058 a0001c0002t0002g0113 a0001c0002t0002g0117 others(52): Show |
65 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.744+958A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495417 | |||||||
| chr17:3495517 | G | A | 2 | a0001c0002t0007g0200 a0001c0002t0007g0281 |
2 | HG01074.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.744+1058G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495517 | |||||||
| chr17:3495546 | GTTTGTTT others(5): Show |
G | 216 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0079 others(213): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.744+1115_744+1126d others(14): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr17 | 3495546 | ||||||
| chr17:3495600 | G | A | 1 | a0001c0001t0006g0319 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.744+1141G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495600 | |||||||
| chr17:3495694 | G | A | 6 | a0001c0001t0006g0197 a0001c0001t0006g0217 a0001c0001t0006g0341 others(3): Show |
6 | HG02809.hp2 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+1235G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495694 | |||||||
| chr17:3495730 | G | A | 35 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0121 others(32): Show |
40 | HG00423.hp2 HG00544.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.744+1271G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495730 | |||||||
| chr17:3495734 | A | G | 88 | a0001c0001t0001g0049 a0001c0001t0001g0079 a0001c0001t0001g0098 others(85): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.744+1275A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495734 | |||||||
| chr17:3495819 | G | C | 4 | a0001c0001t0014g0270 a0001c0001t0026g0360 a0001c0001t0028g0367 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+1360G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495819 | |||||||
| chr17:3495897 | CTG | C | 31 | a0001c0001t0001g0060 a0001c0001t0001g0086 a0001c0001t0001g0121 others(28): Show |
35 | HG00423.hp2 HG00544.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.744+1439_744+1440d others(4): Show |
ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495897 | |||||||
| chr17:3495926 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
196 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.744+1467T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495926 | |||||||
| chr17:3495936 | A | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
196 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.744+1477A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495936 | |||||||
| chr17:3495977 | T | C | 15 | a0001c0001t0002g0244 a0001c0001t0004g0285 a0001c0001t0004g0318 others(12): Show |
15 | HG02615.hp2 HG02630.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.744+1518T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3495977 | |||||||
| chr17:3496024 | G | A | 3 | a0001c0002t0005g0046 a0001c0002t0007g0046 a0001c0002t0008g0137 |
3 | HG01884.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.744+1565G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496024 | |||||||
| chr17:3496068 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
188 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.744+1609A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496068 | |||||||
| chr17:3496217 | T | C | 1 | a0001c0003t0002g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.744+1758T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496217 | |||||||
| chr17:3496260 | C | T | 1 | a0001c0001t0006g0319 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.744+1801C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496260 | |||||||
| chr17:3496305 | A | G | 1 | a0001c0001t0009g0210 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.744+1846A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496305 | |||||||
| chr17:3496355 | A | G | 9 | a0001c0001t0005g0369 a0001c0001t0007g0186 a0001c0001t0008g0284 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+1896A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496355 | |||||||
| chr17:3496401 | C | T | 42 | a0001c0001t0002g0017 a0001c0001t0005g0068 a0001c0001t0005g0110 others(39): Show |
49 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.744+1942C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496401 | |||||||
| chr17:3496500 | G | A | 1 | a0001c0001t0006g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744+2041G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496500 | |||||||
| chr17:3496727 | C | T | 8 | a0001c0001t0001g0060 a0001c0001t0001g0121 a0001c0001t0003g0012 others(5): Show |
11 | HG00544.hp1 NA18945.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.745-2164C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496727 | |||||||
| chr17:3496745 | C | T | 2 | a0001c0001t0003g0051 a0001c0001t0003g0099 |
2 | NA18959.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.745-2146C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496745 | |||||||
| chr17:3496789 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0002g0244 |
3 | HG02615.hp2 NA19005.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.745-2102A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496789 | |||||||
| chr17:3496792 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
189 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.745-2099A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496792 | |||||||
| chr17:3496792 | A | T | 2 | a0001c0001t0002g0244 a0001c0001t0006g0139 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.745-2099A>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496792 | |||||||
| chr17:3496794 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
173 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.745-2097C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496794 | |||||||
| chr17:3496795 | G | A | 2 | a0001c0001t0052g0146 a0001c0002t0013g0145 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.745-2096G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496795 | |||||||
| chr17:3496802 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
141 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.745-2089C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496802 | |||||||
| chr17:3496804 | C | A | 1 | a0001c0001t0008g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.745-2087C>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496804 | |||||||
| chr17:3496832 | C | T | 2 | a0001c0001t0008g0028 a0001c0001t0008g0148 |
3 | HG01243.hp1 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.745-2059C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496832 | |||||||
| chr17:3496838 | G | A | 4 | a0001c0001t0008g0028 a0001c0001t0008g0148 a0001c0002t0007g0200 others(1): Show |
5 | HG01074.hp1 HG01106.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-2053G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496838 | |||||||
| chr17:3496849 | G | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | NA18950.hp2 NA18968.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.745-2042G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496849 | |||||||
| chr17:3496870 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.745-2021T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496870 | |||||||
| chr17:3496945 | A | C | 4 | a0001c0001t0012g0149 a0001c0001t0012g0151 a0001c0001t0012g0175 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1946A>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496945 | |||||||
| chr17:3496959 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.745-1932G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3496959 | |||||||
| chr17:3497027 | C | T | 1 | a0001c0002t0017g0045 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.745-1864C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497027 | |||||||
| chr17:3497031 | A | G | 1 | a0001c0001t0002g0348 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.745-1860A>G | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497031 | |||||||
| chr17:3497092 | G | A | 1 | a0001c0001t0005g0369 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.745-1799G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497092 | |||||||
| chr17:3497094 | G | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0348 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.745-1797G>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497094 | |||||||
| chr17:3497398 | G | A | 10 | a0001c0001t0009g0180 a0001c0001t0009g0204 a0001c0001t0009g0205 others(7): Show |
10 | HG02040.hp1 HG02056.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.745-1493G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497398 | |||||||
| chr17:3497464 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0133 |
3 | NA18966.hp1 NA19007.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.745-1427G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497464 | |||||||
| chr17:3497706 | C | T | 49 | a0001c0001t0003g0012 a0001c0001t0003g0018 a0001c0001t0003g0024 others(46): Show |
54 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.745-1185C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497706 | |||||||
| chr17:3497746 | G | A | 3 | a0001c0001t0015g0147 a0001c0001t0015g0203 a0001c0001t0015g0221 |
3 | HG02809.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.745-1145G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497746 | |||||||
| chr17:3497942 | C | T | 126 | a0001c0001t0004g0006 a0001c0001t0004g0030 a0001c0001t0004g0064 others(123): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.745-949C>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3497942 | |||||||
| chr17:3498060 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.745-831T>C | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3498060 | |||||||
| chr17:3498166 | G | A | 1 | a0001c0001t0003g0091 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.745-725G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3498166 | |||||||
| chr17:3498216 | G | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0030 a0001c0001t0004g0064 others(33): Show |
41 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.745-675G>T | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3498216 | |||||||
| chr17:3498400 | G | A | 6 | a0001c0001t0014g0141 a0001c0001t0014g0270 a0001c0001t0014g0329 others(3): Show |
6 | HG02622.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-491G>A | ASPA | ENSG00000108381.11 | transcript | ENST00000263080.3 | protein_coding | 5/5 | chr17 | 3498400 |