Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5660 |
| ensemblid | ENSG00000197746.15 |
| hgncid | 9498 |
| symbol | PSAP |
| name | prosaposin |
| refseq_nuc | NM_002778.4 |
| refseq_prot | NP_002769.1 |
| ensembl_nuc | ENST00000394936.8 |
| ensembl_prot | ENSP00000378394.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 71816298 |
| end | 71851251 |
| strand | - |
| ver | v1.2 |
| region | chr10:71816298-71851251 |
| region5000 | chr10:71811298-71856251 |
| regionname0 | PSAP_chr10_71816298_71851251 |
| regionname5000 | PSAP_chr10_71811298_71856251 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 524 | 419 | 91 | 71 | 199 | 14 | 42 | 153 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| a0002 | 0/0 | 524 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| a0003 | 0/0 | 524 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| a0004 | 0/0 | 524 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| a0005 | 0/0 | 524 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| a0006 | 0/0 | 524 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | MYALF others(519): Show |
chr10 | 71811298 | 71856251 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1572 | 414 | 88 | 70 | 199 | 14 | 41 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0001c0006 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0001c0007 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0001c0009 | 0/0 | 1572 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0001c0010 | 0/0 | 1572 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0001c0011 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0002c0002 | 0/0 | 1572 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0003c0003 | 0/0 | 1572 | 3 | 3 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0004c0004 | 0/0 | 1572 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0005c0005 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 | ||
| a0006c0008 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | ATGTA others(1567): Show |
chr10 | 71811298 | 71856251 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2748 | 191 | 37 | 32 | 84 | 7 | 29 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0002 | 0/0 | 2748 | 141 | 42 | 26 | 64 | 2 | 7 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0003 | 0/0 | 2748 | 68 | 1 | 9 | 49 | 4 | 5 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0004 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0005 | 0/0 | 2748 | 4 | 2 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0006 | 0/0 | 2748 | 3 | 1 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0007 | 0/0 | 2748 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0009 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0010 | 0/0 | 2748 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0001t0011 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0006t0005 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0007t0001 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0009t0001 | 0/0 | 2748 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0010t0001 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0001c0011t0008 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0002c0002t0004 | 0/0 | 2748 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0003c0003t0002 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0003c0003t0004 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0004c0004t0002 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0005c0005t0001 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| a0006c0008t0002 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | GCATT others(2743): Show |
chr10 | 71811298 | 71856251 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0012 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0049 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0001g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0002 | 0/0 | 23 | 0 | 2 | 18 | 2 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0003 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0001 | 0/0 | 25 | 0 | 0 | 25 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0059 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0060 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0061 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0004g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0005g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0006t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0007t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0009t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0010t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0001c0011t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0002c0002t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0002c0002t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0002c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0003c0003t0002g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0003c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0004c0004t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0005c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| a0006c0008t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00280 | hp1 | a0001 | c0001 | t0010 | g0093 | EUR | FIN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0261 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0264 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01433 | hp2 | a0001 | c0010 | t0001 | g0096 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0233 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02004 | hp1 | a0004 | c0004 | t0002 | g0147 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0057 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0038 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0192 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0252 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02895 | hp1 | a0001 | c0011 | t0008 | g0095 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0039 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03130 | hp1 | a0005 | c0005 | t0001 | g0138 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0262 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0099 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0232 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | STU | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18522 | hp2 | a0002 | c0002 | t0004 | g0038 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0246 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18957 | hp2 | a0006 | c0008 | t0002 | g0091 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0057 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19043 | hp2 | a0001 | c0006 | t0005 | g0263 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20129 | hp2 | a0002 | c0002 | t0004 | g0039 | AFR | ASW | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0254 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | GIH | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20300 | hp1 | a0001 | c0007 | t0001 | g0065 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | LWK | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0229 | REF | REF | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | PSAP_chr10_71811298_71856251 | PSAP | chr10 | 71811298 | 71856251 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71818618 | T | C | 1 | a0005 | 1 | HG03130.hp1 | missense_variant&splice_region_variant | MODERATE | c.1538A>G | p.Asn513Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/14 | 1568/2748 | 1538/1575 | 513/524 | chr10 | 71818618 | |||
| chr10:71828039 | C | T | 1 | a0004 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.695G>A | p.Arg232His | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/14 | 725/2748 | 695/1575 | 232/524 | chr10 | 71828039 | |||
| chr10:71828883 | C | A | 1 | a0002 | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
missense_variant | MODERATE | c.570G>T | p.Gln190His | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/14 | 600/2748 | 570/1575 | 190/524 | chr10 | 71828883 | |||
| chr10:71828888 | G | A | 1 | a0006 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.565C>T | p.Pro189Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/14 | 595/2748 | 565/1575 | 189/524 | chr10 | 71828888 | |||
| chr10:71851206 | G | A | 1 | a0003 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.16C>T | p.Leu6Phe | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 46/2748 | 16/1575 | 6/524 | chr10 | 71851206 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71818704 | C | T | 1 | a0002c0002 | 5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
synonymous_variant | LOW | c.1452G>A | p.Ser484Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/14 | 1482/2748 | 1452/1575 | 484/524 | chr10 | 71818704 | |||
| chr10:71819082 | G | A | 1 | a0001c0006 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1380C>T | p.Pro460Pro | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/14 | 1410/2748 | 1380/1575 | 460/524 | chr10 | 71819082 | |||
| chr10:71819889 | G | A | 1 | a0001c0007 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1017C>T | p.Leu339Leu | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/14 | 1047/2748 | 1017/1575 | 339/524 | chr10 | 71819889 | |||
| chr10:71831165 | G | A | 1 | a0001c0009 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.336C>T | p.Ser112Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/14 | 366/2748 | 336/1575 | 112/524 | chr10 | 71831165 | |||
| chr10:71834426 | G | A | 1 | a0001c0011 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.120C>T | p.Ser40Ser | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/14 | 150/2748 | 120/1575 | 40/524 | chr10 | 71834426 | |||
| chr10:71834468 | G | A | 2 | a0001c0010 a0001c0011 |
2 | HG01433.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.78C>T | p.Thr26Thr | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/14 | 108/2748 | 78/1575 | 26/524 | chr10 | 71834468 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71816370 | T | C | 2 | a0001c0001t0009 a0001c0011t0008 |
2 | HG02895.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 1071 | chr10 | 71816370 | ||||||
| chr10:71816550 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(6): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*891G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 891 | chr10 | 71816550 | ||||||
| chr10:71816644 | T | C | 1 | a0001c0001t0010 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 797 | chr10 | 71816644 | ||||||
| chr10:71816666 | C | T | 3 | a0001c0001t0004 a0002c0002t0004 a0003c0003t0004 |
8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*775G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 775 | chr10 | 71816666 | ||||||
| chr10:71817319 | G | C | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 14/14 | 122 | chr10 | 71817319 | ||||||
| chr10:71851225 | G | A | 2 | a0001c0001t0003 a0001c0001t0006 |
71 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-4C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 4 | chr10 | 71851225 | ||||||
| chr10:71851231 | T | C | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0006t0005 |
7 | HG00639.hp1 HG00642.hp2 HG01123.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-10A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/14 | 10 | chr10 | 71851231 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:71817510 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(54): Show |
112 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1540-34C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817510 | |||||||
| chr10:71817747 | AC | A | 59 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(56): Show |
108 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1540-272delG | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817747 | |||||||
| chr10:71817754 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0196 a0001c0001t0001g0211 |
5 | NA18970.hp1 NA18984.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-278T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817754 | |||||||
| chr10:71817778 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1540-302C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817778 | |||||||
| chr10:71817795 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0205 a0001c0001t0002g0213 others(1): Show |
10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1540-319G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817795 | |||||||
| chr10:71817854 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1540-378A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817854 | |||||||
| chr10:71817869 | A | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(74): Show |
110 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1540-393T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71817869 | |||||||
| chr10:71818024 | T | C | 1 | a0001c0011t0008g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1540-548A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818024 | |||||||
| chr10:71818077 | T | C | 1 | a0001c0011t0008g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1539+540A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818077 | |||||||
| chr10:71818088 | G | A | 2 | a0001c0001t0001g0056 a0003c0003t0004g0232 |
3 | HG02922.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1539+529C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818088 | |||||||
| chr10:71818337 | T | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0086 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1539+280A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818337 | |||||||
| chr10:71818375 | C | CA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0054 others(4): Show |
12 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1539+241dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818375 | |||||||
| chr10:71818395 | T | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(51): Show |
108 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1539+222A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818395 | |||||||
| chr10:71818402 | A | T | 56 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(53): Show |
105 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.1539+215T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818402 | |||||||
| chr10:71818425 | T | G | 1 | a0003c0003t0002g0057 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1539+192A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 13/13 | chr10 | 71818425 | |||||||
| chr10:71818746 | G | A | 117 | a0001c0001t0001g0056 a0001c0001t0002g0002 a0001c0001t0002g0003 others(114): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1432-22C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818746 | |||||||
| chr10:71818753 | G | C | 2 | a0001c0001t0001g0056 a0001c0011t0008g0095 |
3 | HG02895.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1432-29C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818753 | |||||||
| chr10:71818773 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1432-49G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818773 | |||||||
| chr10:71818871 | C | T | 5 | a0001c0001t0004g0047 a0002c0002t0004g0038 a0002c0002t0004g0039 others(2): Show |
8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432-147G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818871 | |||||||
| chr10:71818915 | G | A | 61 | a0001c0001t0001g0056 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
111 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1431+116C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818915 | |||||||
| chr10:71818926 | C | T | 1 | a0001c0011t0008g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1431+105G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818926 | |||||||
| chr10:71818947 | AAGTCTC | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(74): Show |
110 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1431+78_1431+83del others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 12/13 | chr10 | 71818947 | |||||||
| chr10:71819125 | T | C | 119 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0001g0075 others(116): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1351-14A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 11/13 | chr10 | 71819125 | |||||||
| chr10:71819460 | C | T | 49 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0037 others(46): Show |
90 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(87): Show |
splice_region_variant&intron_variant | LOW | c.1350+5G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 11/13 | chr10 | 71819460 | |||||||
| chr10:71819640 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1193-18C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/13 | chr10 | 71819640 | |||||||
| chr10:71819648 | C | T | 49 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0037 others(46): Show |
90 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1193-26G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 10/13 | chr10 | 71819648 | |||||||
| chr10:71819921 | G | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0063 a0001c0001t0002g0064 others(4): Show |
9 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006-21C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71819921 | |||||||
| chr10:71819948 | G | C | 1 | a0001c0001t0003g0234 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1006-48C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71819948 | |||||||
| chr10:71820030 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0135 a0001c0001t0001g0144 |
5 | HG01167.hp2 HG02056.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-130T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820030 | |||||||
| chr10:71820030 | A | T | 3 | a0001c0001t0003g0061 a0001c0001t0003g0255 a0001c0001t0003g0259 |
4 | HG00140.hp1 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006-130T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820030 | |||||||
| chr10:71820085 | G | T | 1 | a0001c0001t0002g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1005+155C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820085 | |||||||
| chr10:71820111 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0116 a0001c0001t0001g0135 others(3): Show |
8 | HG01167.hp2 HG01433.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+129G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820111 | |||||||
| chr10:71820196 | G | A | 4 | a0001c0001t0004g0047 a0002c0002t0004g0038 a0002c0002t0004g0039 others(1): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+44C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820196 | |||||||
| chr10:71820198 | G | C | 1 | a0001c0006t0005g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1005+42C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820198 | |||||||
| chr10:71820222 | G | A | 58 | a0001c0001t0001g0071 a0001c0001t0002g0002 a0001c0001t0002g0003 others(55): Show |
113 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1005+18C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 9/13 | chr10 | 71820222 | |||||||
| chr10:71820432 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.910-97C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820432 | |||||||
| chr10:71820440 | A | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0168 a0001c0001t0001g0171 others(4): Show |
8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.910-105T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820440 | |||||||
| chr10:71820518 | C | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0100 a0001c0001t0001g0115 others(1): Show |
5 | HG00642.hp1 HG01081.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-183G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820518 | |||||||
| chr10:71820525 | C | T | 1 | a0001c0001t0003g0245 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.910-190G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820525 | |||||||
| chr10:71820640 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.910-305A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820640 | |||||||
| chr10:71820644 | C | T | 1 | a0001c0006t0005g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-309G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820644 | |||||||
| chr10:71820710 | G | GA | 118 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0002g0002 others(115): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.910-376dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820710 | |||||||
| chr10:71820720 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.910-385G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71820720 | |||||||
| chr10:71821011 | T | C | 4 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0003g0029 others(1): Show |
6 | HG00558.hp1 NA18940.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-676A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821011 | |||||||
| chr10:71821048 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.910-713C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821048 | |||||||
| chr10:71821115 | C | T | 2 | a0001c0001t0002g0030 a0003c0003t0002g0057 |
4 | HG02145.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+761G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821115 | |||||||
| chr10:71821319 | C | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(74): Show |
110 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.909+557G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821319 | |||||||
| chr10:71821417 | T | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0205 a0001c0001t0002g0213 others(1): Show |
10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+459A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821417 | |||||||
| chr10:71821420 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.909+456C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821420 | |||||||
| chr10:71821803 | A | T | 57 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(54): Show |
106 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.909+73T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821803 | |||||||
| chr10:71821844 | C | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
6 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+32G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 8/13 | chr10 | 71821844 | |||||||
| chr10:71822090 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.778-83G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822090 | |||||||
| chr10:71822126 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.778-119G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822126 | |||||||
| chr10:71822129 | CT | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0205 a0001c0001t0002g0213 others(1): Show |
10 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-123delA | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822129 | |||||||
| chr10:71822271 | C | G | 1 | a0001c0001t0001g0045 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.778-264G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822271 | |||||||
| chr10:71822276 | C | T | 2 | a0001c0001t0002g0030 a0003c0003t0002g0057 |
4 | HG02145.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-269G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822276 | |||||||
| chr10:71822277 | G | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0185 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-270C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822277 | |||||||
| chr10:71822286 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.778-279A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822286 | |||||||
| chr10:71822540 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01175.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.778-533A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822540 | |||||||
| chr10:71822684 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0200 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.778-677C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822684 | |||||||
| chr10:71822950 | A | AAAAT | 58 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0002g0002 others(55): Show |
114 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.778-947_778-944dup others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822950 | |||||||
| chr10:71822950 | AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0168 a0001c0001t0001g0171 others(4): Show |
8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-951_778-944del others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822950 | |||||||
| chr10:71822985 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.778-978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822985 | |||||||
| chr10:71822995 | T | A | 118 | a0001c0001t0001g0056 a0001c0001t0001g0071 a0001c0001t0002g0002 others(115): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.778-988A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71822995 | |||||||
| chr10:71823011 | G | GA | 5 | a0001c0001t0001g0107 a0001c0001t0002g0030 a0001c0001t0002g0112 others(2): Show |
7 | HG00597.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1005dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823011 | |||||||
| chr10:71823024 | G | T | 58 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(55): Show |
107 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.778-1017C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823024 | |||||||
| chr10:71823221 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-1214C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823221 | |||||||
| chr10:71823380 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.778-1373C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823380 | |||||||
| chr10:71823542 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0077 |
3 | NA18939.hp2 NA18950.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.778-1535A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823542 | |||||||
| chr10:71823615 | T | G | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-1608A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823615 | |||||||
| chr10:71823681 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.778-1674C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823681 | |||||||
| chr10:71823763 | G | C | 194 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(191): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.778-1756C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823763 | |||||||
| chr10:71823816 | C | CA | 87 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(84): Show |
124 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.778-1810dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823816 | |||||||
| chr10:71823844 | G | C | 1 | a0001c0001t0003g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.778-1837C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71823844 | |||||||
| chr10:71824142 | C | G | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.777+1695G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824142 | |||||||
| chr10:71824160 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1677C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824160 | |||||||
| chr10:71824191 | TG | T | 56 | a0001c0001t0001g0020 a0001c0001t0001g0116 a0001c0001t0001g0135 others(53): Show |
100 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.777+1645delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824191 | |||||||
| chr10:71824258 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.777+1579C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824258 | |||||||
| chr10:71824331 | G | C | 1 | a0001c0001t0003g0244 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.777+1506C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824331 | |||||||
| chr10:71824332 | G | C | 1 | a0001c0001t0002g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.777+1505C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824332 | |||||||
| chr10:71824358 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.777+1479C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824358 | |||||||
| chr10:71824488 | G | C | 38 | a0001c0001t0002g0022 a0001c0001t0002g0037 a0001c0001t0002g0077 others(35): Show |
74 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.777+1349C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824488 | |||||||
| chr10:71824498 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1339A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824498 | |||||||
| chr10:71824504 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0006g0246 |
2 | NA18943.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.777+1333A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824504 | |||||||
| chr10:71824513 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1324G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824513 | |||||||
| chr10:71824598 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+1239A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824598 | |||||||
| chr10:71824658 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+1179C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824658 | |||||||
| chr10:71824669 | T | C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.777+1168A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824669 | |||||||
| chr10:71824716 | A | C | 196 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(193): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.777+1121T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824716 | |||||||
| chr10:71824764 | T | C | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.777+1073A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824764 | |||||||
| chr10:71824826 | G | C | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+1011C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824826 | |||||||
| chr10:71824927 | G | C | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+910C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71824927 | |||||||
| chr10:71825032 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+805A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825032 | |||||||
| chr10:71825191 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0086 |
2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.777+646A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825191 | |||||||
| chr10:71825268 | C | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(198): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.777+569G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825268 | |||||||
| chr10:71825276 | A | G | 2 | a0001c0001t0001g0056 a0003c0003t0004g0232 |
3 | HG02922.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.777+561T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825276 | |||||||
| chr10:71825420 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0184 |
2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.777+417G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825420 | |||||||
| chr10:71825437 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.777+400G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825437 | |||||||
| chr10:71825567 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+270A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825567 | |||||||
| chr10:71825567 | TGGCTGGC others(7): Show |
T | 5 | a0001c0001t0002g0186 a0001c0001t0003g0059 a0001c0001t0003g0233 others(2): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+256_777+269del others(14): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825567 | |||||||
| chr10:71825580 | C | T | 1 | a0001c0007t0001g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.777+257G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825580 | |||||||
| chr10:71825655 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.777+182C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825655 | |||||||
| chr10:71825678 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.777+159C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825678 | |||||||
| chr10:71825734 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+103C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825734 | |||||||
| chr10:71825769 | A | G | 73 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0068 others(70): Show |
138 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.777+68T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 7/13 | chr10 | 71825769 | |||||||
| chr10:71826073 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0006g0246 |
2 | NA18943.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.721-180C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826073 | |||||||
| chr10:71826082 | A | C | 3 | a0001c0001t0001g0056 a0001c0001t0009g0167 a0001c0011t0008g0095 |
4 | HG02895.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-189T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826082 | |||||||
| chr10:71826180 | G | C | 47 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0037 others(44): Show |
87 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.721-287C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826180 | |||||||
| chr10:71826402 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.721-509T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826402 | |||||||
| chr10:71826561 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.721-668A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826561 | |||||||
| chr10:71826576 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0143 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.721-683T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826576 | |||||||
| chr10:71826743 | G | GA | 196 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(193): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.721-851dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826743 | |||||||
| chr10:71826782 | C | T | 1 | a0002c0002t0004g0038 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.721-889G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826782 | |||||||
| chr10:71826828 | A | G | 209 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(206): Show |
350 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.721-935T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826828 | |||||||
| chr10:71826959 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
7 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+1055C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71826959 | |||||||
| chr10:71827002 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+1012C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827002 | |||||||
| chr10:71827036 | C | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(122): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.720+978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827036 | |||||||
| chr10:71827044 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+970G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827044 | |||||||
| chr10:71827255 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0151 |
4 | HG03453.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+759G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827255 | |||||||
| chr10:71827315 | C | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0168 a0001c0001t0001g0171 others(4): Show |
8 | HG00621.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+699G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827315 | |||||||
| chr10:71827327 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.720+687T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827327 | |||||||
| chr10:71827405 | G | GA | 45 | a0001c0001t0002g0022 a0001c0001t0002g0030 a0001c0001t0002g0037 others(42): Show |
82 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.720+608dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827405 | |||||||
| chr10:71827405 | G | GAA | 75 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(72): Show |
107 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.720+607_720+608dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827405 | |||||||
| chr10:71827408 | A | AG | 4 | a0001c0001t0002g0007 a0001c0001t0002g0078 a0001c0001t0002g0082 others(1): Show |
8 | HG00735.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+605_720+606ins others(1): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827408 | |||||||
| chr10:71827418 | G | C | 1 | a0001c0001t0005g0062 | 2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.720+596C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827418 | |||||||
| chr10:71827455 | A | T | 38 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0002g0002 others(35): Show |
85 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.720+559T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827455 | |||||||
| chr10:71827619 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.720+395G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827619 | |||||||
| chr10:71827726 | C | CA | 10 | a0001c0001t0001g0075 a0001c0001t0001g0161 a0001c0001t0001g0216 others(7): Show |
10 | HG00639.hp1 HG01346.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+287dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827726 | |||||||
| chr10:71827726 | CA | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0201 a0001c0001t0001g0217 others(3): Show |
6 | HG01074.hp2 HG03490.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+287delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827726 | |||||||
| chr10:71827754 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.720+260T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827754 | |||||||
| chr10:71827785 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.720+229C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827785 | |||||||
| chr10:71827910 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.720+104A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827910 | |||||||
| chr10:71827923 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.720+91T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 6/13 | chr10 | 71827923 | |||||||
| chr10:71828167 | A | G | 1 | a0001c0001t0003g0242 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.577-10T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828167 | |||||||
| chr10:71828179 | T | A | 1 | a0001c0001t0002g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.577-22A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828179 | |||||||
| chr10:71828213 | C | T | 13 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0157 others(10): Show |
17 | HG00642.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.577-56G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828213 | |||||||
| chr10:71828310 | G | A | 1 | a0001c0006t0005g0263 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-153C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828310 | |||||||
| chr10:71828436 | G | A | 5 | a0001c0001t0004g0047 a0002c0002t0004g0038 a0002c0002t0004g0039 others(2): Show |
8 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.577-279C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828436 | |||||||
| chr10:71828542 | G | A | 46 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0037 others(43): Show |
86 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.576+335C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828542 | |||||||
| chr10:71828605 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.576+272T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828605 | |||||||
| chr10:71828662 | ATT | A | 7 | a0001c0001t0002g0010 a0001c0001t0002g0055 a0001c0001t0002g0220 others(4): Show |
13 | HG00558.hp2 HG02145.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.576+213_576+214del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828662 | |||||||
| chr10:71828717 | C | G | 4 | a0001c0001t0004g0047 a0002c0002t0004g0038 a0002c0002t0004g0039 others(1): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+160G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828717 | |||||||
| chr10:71828727 | C | T | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.576+150G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828727 | |||||||
| chr10:71828797 | A | C | 1 | a0001c0001t0002g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.576+80T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828797 | |||||||
| chr10:71828799 | G | A | 1 | a0001c0001t0002g0040 | 2 | NA18964.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.576+78C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 5/13 | chr10 | 71828799 | |||||||
| chr10:71829252 | G | A | 1 | a0001c0001t0003g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376-175C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829252 | |||||||
| chr10:71829486 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0002g0088 |
3 | HG04204.hp2 NA18948.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.376-409T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829486 | |||||||
| chr10:71829534 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.376-457T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829534 | |||||||
| chr10:71829541 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0075 |
4 | HG00099.hp1 HG02735.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.376-464T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829541 | |||||||
| chr10:71829565 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.376-488G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829565 | |||||||
| chr10:71829661 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0026 others(123): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.376-584A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829661 | |||||||
| chr10:71829678 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.376-601A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829678 | |||||||
| chr10:71829770 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0221 a0001c0001t0002g0010 others(6): Show |
15 | HG00558.hp2 HG02145.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.376-693C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829770 | |||||||
| chr10:71829774 | G | A | 1 | a0002c0002t0004g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.376-697C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829774 | |||||||
| chr10:71829896 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.376-819C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829896 | |||||||
| chr10:71829952 | G | A | 1 | a0001c0001t0003g0060 | 2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.376-875C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829952 | |||||||
| chr10:71829975 | C | T | 3 | a0001c0001t0001g0221 a0001c0001t0002g0055 a0001c0001t0002g0223 |
4 | HG00558.hp2 NA18747.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-898G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71829975 | |||||||
| chr10:71830038 | T | C | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-961A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830038 | |||||||
| chr10:71830096 | G | A | 10 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(7): Show |
15 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1019C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830096 | |||||||
| chr10:71830284 | C | T | 3 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+842G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830284 | |||||||
| chr10:71830294 | A | G | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.375+832T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830294 | |||||||
| chr10:71830364 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0196 a0001c0001t0001g0211 others(1): Show |
6 | NA18946.hp2 NA18970.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+762T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830364 | |||||||
| chr10:71830428 | A | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0180 |
2 | HG01175.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.375+698T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830428 | |||||||
| chr10:71830545 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.375+581C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830545 | |||||||
| chr10:71830591 | C | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
13 | HG02074.hp2 NA18612.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+535G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830591 | |||||||
| chr10:71830593 | C | A | 5 | a0001c0001t0001g0216 a0001c0001t0002g0030 a0001c0001t0002g0063 others(2): Show |
6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+533G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830593 | |||||||
| chr10:71830713 | C | T | 3 | a0001c0001t0007g0261 a0001c0001t0007g0262 a0001c0006t0005g0263 |
3 | HG00639.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.375+413G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830713 | |||||||
| chr10:71830762 | C | A | 3 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+364G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830762 | |||||||
| chr10:71830773 | A | C | 1 | a0001c0001t0002g0016 | 3 | NA18946.hp1 NA18959.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.375+353T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830773 | |||||||
| chr10:71830794 | AG | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0250 |
3 | HG00741.hp2 HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.375+331delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830794 | |||||||
| chr10:71830813 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.375+313A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830813 | |||||||
| chr10:71830824 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.375+302C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830824 | |||||||
| chr10:71830900 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(69): Show |
100 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.375+226G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830900 | |||||||
| chr10:71830918 | C | T | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+208G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830918 | |||||||
| chr10:71830919 | G | A | 6 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0108 others(3): Show |
6 | HG02074.hp2 NA18612.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+207C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830919 | |||||||
| chr10:71830921 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.375+205T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830921 | |||||||
| chr10:71830934 | C | A | 2 | a0001c0001t0004g0047 a0001c0001t0009g0167 |
3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.375+192G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71830934 | |||||||
| chr10:71831033 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.375+93G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 4/13 | chr10 | 71831033 | |||||||
| chr10:71831392 | T | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(86): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.250-141A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831392 | |||||||
| chr10:71831473 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0131 a0001c0001t0001g0149 others(1): Show |
5 | HG02040.hp1 NA19054.hp1 NA19080.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-222C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831473 | |||||||
| chr10:71831490 | T | G | 1 | a0001c0001t0003g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.250-239A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831490 | |||||||
| chr10:71831497 | A | T | 2 | a0001c0001t0004g0047 a0001c0001t0009g0167 |
3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.250-246T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831497 | |||||||
| chr10:71831520 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.250-269T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831520 | |||||||
| chr10:71831570 | G | A | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.249+276C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831570 | |||||||
| chr10:71831654 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01175.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.249+192T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831654 | |||||||
| chr10:71831665 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.249+181A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831665 | |||||||
| chr10:71831698 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.249+148T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831698 | |||||||
| chr10:71831773 | G | A | 13 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0101 others(10): Show |
17 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+73C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831773 | |||||||
| chr10:71831809 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.249+37G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831809 | |||||||
| chr10:71831821 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0154 others(1): Show |
4 | HG00408.hp1 NA18948.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+25T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 3/13 | chr10 | 71831821 | |||||||
| chr10:71831939 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.175-19C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71831939 | |||||||
| chr10:71832003 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0066 |
3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.175-83C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832003 | |||||||
| chr10:71832022 | G | T | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-102C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832022 | |||||||
| chr10:71832037 | G | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0056 others(27): Show |
40 | HG00639.hp1 HG00733.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.175-117C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832037 | |||||||
| chr10:71832060 | T | G | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-140A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832060 | |||||||
| chr10:71832072 | G | A | 72 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(69): Show |
100 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.175-152C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832072 | |||||||
| chr10:71832089 | G | A | 2 | a0001c0010t0001g0096 a0001c0011t0008g0095 |
2 | HG01433.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.175-169C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832089 | |||||||
| chr10:71832337 | C | T | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.175-417G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832337 | |||||||
| chr10:71832648 | T | C | 4 | a0001c0001t0001g0100 a0002c0002t0004g0038 a0002c0002t0004g0039 others(1): Show |
6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-728A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832648 | |||||||
| chr10:71832737 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.175-817T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832737 | |||||||
| chr10:71832758 | G | A | 1 | a0001c0001t0004g0047 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.175-838C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832758 | |||||||
| chr10:71832874 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175-954C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832874 | |||||||
| chr10:71832946 | G | C | 16 | a0001c0001t0001g0056 a0001c0001t0001g0217 a0001c0001t0001g0218 others(13): Show |
29 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.175-1026C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71832946 | |||||||
| chr10:71833016 | C | CAAAAAA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(27): Show |
46 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.175-1102_175-1097d others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
30 | HG00099.hp1 HG00609.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.175-1103_175-1097d others(9): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0177 a0001c0001t0001g0179 others(6): Show |
10 | HG00621.hp2 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.175-1104_175-1097d others(10): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(3): Show |
6 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1105_175-1097d others(11): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0161 |
3 | HG02258.hp1 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.175-1106_175-1097d others(12): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175-1107_175-1097d others(13): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833016 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.175-1108_175-1097d others(14): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833016 | |||||||
| chr10:71833027 | AAAAAC | A | 11 | a0001c0001t0001g0056 a0001c0001t0001g0182 a0001c0001t0001g0217 others(8): Show |
17 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-1112_175-1108d others(7): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833027 | |||||||
| chr10:71833028 | AAAAC | A | 16 | a0001c0001t0001g0221 a0001c0001t0002g0005 a0001c0001t0002g0010 others(13): Show |
25 | HG00558.hp2 HG00642.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-1112_175-1109d others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833028 | |||||||
| chr10:71833032 | C | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.175-1112G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833032 | |||||||
| chr10:71833033 | A | C | 33 | a0001c0001t0002g0094 a0001c0001t0003g0001 a0001c0001t0003g0014 others(30): Show |
69 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.175-1113T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833033 | |||||||
| chr10:71833039 | C | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(85): Show |
129 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.175-1119G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833039 | |||||||
| chr10:71833126 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.175-1206A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833126 | |||||||
| chr10:71833189 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.174+1183G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833189 | |||||||
| chr10:71833240 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.174+1132G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833240 | |||||||
| chr10:71833284 | C | A | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+1088G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833284 | |||||||
| chr10:71833434 | G | C | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+938C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833434 | |||||||
| chr10:71833501 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.174+871C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833501 | |||||||
| chr10:71833530 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+842A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833530 | |||||||
| chr10:71833596 | A | T | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.174+776T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833596 | |||||||
| chr10:71833621 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.174+751C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833621 | |||||||
| chr10:71833686 | T | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(99): Show |
149 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.174+686A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833686 | |||||||
| chr10:71833707 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.174+665T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833707 | |||||||
| chr10:71833760 | C | A | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(14): Show |
23 | HG00639.hp1 HG00733.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+612G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833760 | |||||||
| chr10:71833796 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0123 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.174+576A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833796 | |||||||
| chr10:71833935 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.174+437C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833935 | |||||||
| chr10:71833975 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.174+397G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71833975 | |||||||
| chr10:71834029 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.174+343G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834029 | |||||||
| chr10:71834038 | C | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+334G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834038 | |||||||
| chr10:71834057 | G | A | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.174+315C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834057 | |||||||
| chr10:71834071 | G | A | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00423.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+301C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834071 | |||||||
| chr10:71834156 | A | G | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.174+216T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834156 | |||||||
| chr10:71834208 | G | A | 16 | a0001c0001t0001g0056 a0001c0001t0001g0217 a0001c0001t0001g0218 others(13): Show |
29 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.174+164C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 2/13 | chr10 | 71834208 | |||||||
| chr10:71834522 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-17G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834522 | |||||||
| chr10:71834558 | G | A | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-53C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834558 | |||||||
| chr10:71834601 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(69): Show |
100 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.41-96G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834601 | |||||||
| chr10:71834674 | A | G | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-169T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834674 | |||||||
| chr10:71834702 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41-197T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834702 | |||||||
| chr10:71834742 | G | A | 130 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(127): Show |
185 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.41-237C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834742 | |||||||
| chr10:71834757 | T | C | 9 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(6): Show |
13 | HG00642.hp2 HG01243.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-252A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834757 | |||||||
| chr10:71834891 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.41-386T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834891 | |||||||
| chr10:71834894 | T | C | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-389A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834894 | |||||||
| chr10:71834940 | T | A | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-435A>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834940 | |||||||
| chr10:71834965 | G | A | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-460C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71834965 | |||||||
| chr10:71835021 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.41-516G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835021 | |||||||
| chr10:71835080 | C | CA | 4 | a0001c0001t0001g0053 a0001c0001t0001g0201 a0001c0001t0001g0209 others(1): Show |
5 | HG02896.hp2 NA18940.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-576dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835080 | |||||||
| chr10:71835134 | C | T | 89 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(86): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.41-629G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835134 | |||||||
| chr10:71835160 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0066 |
3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41-655A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835160 | |||||||
| chr10:71835208 | C | T | 24 | a0001c0001t0001g0092 a0001c0001t0002g0002 a0001c0001t0002g0003 others(21): Show |
67 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-703G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835208 | |||||||
| chr10:71835219 | A | AAAAT | 45 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0068 others(42): Show |
81 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.41-718_41-715dupAT others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | |||||||
| chr10:71835219 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 others(2): Show |
14 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-722_41-715dupAT others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | |||||||
| chr10:71835219 | AAAAT | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(81): Show |
117 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.41-718_41-715delAT others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | |||||||
| chr10:71835219 | AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0216 a0001c0001t0002g0030 a0001c0001t0002g0063 others(4): Show |
8 | HG01346.hp1 HG02145.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-722_41-715delAT others(6): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | |||||||
| chr10:71835219 | AAAATAAA others(5): Show |
A | 24 | a0001c0001t0001g0092 a0001c0001t0002g0002 a0001c0001t0002g0003 others(21): Show |
67 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-726_41-715delAT others(10): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835219 | |||||||
| chr10:71835253 | A | T | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-748T>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835253 | |||||||
| chr10:71835377 | C | T | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-872G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835377 | |||||||
| chr10:71835429 | G | A | 12 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(9): Show |
17 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-924C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835429 | |||||||
| chr10:71835464 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-959G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835464 | |||||||
| chr10:71835521 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.41-1016C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835521 | |||||||
| chr10:71835647 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-1142T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835647 | |||||||
| chr10:71835712 | A | G | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-1207T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835712 | |||||||
| chr10:71835719 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.41-1214A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835719 | |||||||
| chr10:71835728 | AG | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 others(1): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-1224delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835728 | |||||||
| chr10:71835821 | G | GA | 7 | a0001c0001t0001g0046 a0001c0001t0001g0217 a0001c0001t0002g0005 others(4): Show |
15 | HG01069.hp1 HG01074.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.41-1317dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | |||||||
| chr10:71835821 | G | GAA | 13 | a0001c0001t0001g0056 a0001c0001t0001g0218 a0001c0001t0001g0219 others(10): Show |
19 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-1318_41-1317dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | |||||||
| chr10:71835821 | GA | G | 19 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0102 others(16): Show |
22 | HG01070.hp1 HG01071.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.41-1317delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835821 | |||||||
| chr10:71835838 | AAC | A | 26 | a0001c0001t0001g0092 a0001c0001t0001g0176 a0001c0001t0002g0002 others(23): Show |
64 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.41-1335_41-1334del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835838 | |||||||
| chr10:71835839 | AC | A | 151 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(148): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.41-1335delG | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835839 | |||||||
| chr10:71835840 | C | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0056 others(46): Show |
67 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.41-1335G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835840 | |||||||
| chr10:71835844 | A | AAC | 10 | a0001c0001t0002g0021 a0001c0001t0002g0163 a0001c0001t0002g0164 others(7): Show |
14 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-1340_41-1339ins others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835844 | |||||||
| chr10:71835845 | C | A | 11 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(8): Show |
16 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-1340G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835845 | |||||||
| chr10:71835925 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.41-1420C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835925 | |||||||
| chr10:71835979 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.41-1474G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835979 | |||||||
| chr10:71835981 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(90): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.41-1476T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71835981 | |||||||
| chr10:71836066 | T | C | 174 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(171): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.41-1561A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836066 | |||||||
| chr10:71836118 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.41-1613G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836118 | |||||||
| chr10:71836148 | A | G | 1 | a0003c0003t0002g0057 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-1643T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836148 | |||||||
| chr10:71836273 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-1768G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836273 | |||||||
| chr10:71836371 | G | T | 1 | a0001c0001t0006g0257 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.41-1866C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836371 | |||||||
| chr10:71836385 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.41-1880C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836385 | |||||||
| chr10:71836607 | A | G | 42 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0097 others(39): Show |
79 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.41-2102T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836607 | |||||||
| chr10:71836877 | A | C | 1 | a0001c0010t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.41-2372T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71836877 | |||||||
| chr10:71837116 | G | A | 12 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0216 others(9): Show |
15 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-2611C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837116 | |||||||
| chr10:71837251 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41-2746G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837251 | |||||||
| chr10:71837283 | C | T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0017 a0001c0001t0002g0083 others(1): Show |
16 | HG00438.hp1 HG00544.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-2778G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837283 | |||||||
| chr10:71837420 | G | A | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-2915C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837420 | |||||||
| chr10:71837595 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-3090G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837595 | |||||||
| chr10:71837596 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-3091C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837596 | |||||||
| chr10:71837721 | G | A | 3 | a0002c0002t0004g0038 a0002c0002t0004g0039 a0002c0002t0004g0099 |
5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-3216C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837721 | |||||||
| chr10:71837759 | T | C | 1 | a0001c0001t0003g0249 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.41-3254A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837759 | |||||||
| chr10:71837896 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-3391G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71837896 | |||||||
| chr10:71838107 | G | C | 1 | a0001c0001t0002g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.41-3602C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838107 | |||||||
| chr10:71838196 | C | A | 2 | a0001c0001t0004g0047 a0001c0001t0009g0167 |
3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.41-3691G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838196 | |||||||
| chr10:71838203 | A | G | 89 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(86): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.41-3698T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838203 | |||||||
| chr10:71838208 | C | G | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-3703G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838208 | |||||||
| chr10:71838374 | C | G | 1 | a0001c0011t0008g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-3869G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838374 | |||||||
| chr10:71838434 | G | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(86): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.41-3929C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838434 | |||||||
| chr10:71838435 | C | CAT | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.41-3931_41-3930ins others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838435 | |||||||
| chr10:71838464 | G | A | 3 | a0001c0001t0002g0078 a0001c0001t0002g0082 a0001c0001t0002g0215 |
3 | HG02451.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41-3959C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838464 | |||||||
| chr10:71838614 | C | G | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41-4109G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838614 | |||||||
| chr10:71838982 | A | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-4477T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71838982 | |||||||
| chr10:71839132 | A | G | 195 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(192): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.41-4627T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839132 | |||||||
| chr10:71839147 | A | G | 64 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0092 others(61): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-4642T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839147 | |||||||
| chr10:71839168 | C | T | 12 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(9): Show |
18 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-4663G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839168 | |||||||
| chr10:71839178 | GGCAAATT others(2): Show |
G | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-4682_41-4674del others(9): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839178 | |||||||
| chr10:71839353 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(21): Show |
35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.41-4848G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839353 | |||||||
| chr10:71839396 | T | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-4891A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839396 | |||||||
| chr10:71839429 | A | G | 198 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(195): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.41-4924T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839429 | |||||||
| chr10:71839671 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.41-5166G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839671 | |||||||
| chr10:71839769 | G | A | 1 | a0001c0010t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.41-5264C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839769 | |||||||
| chr10:71839784 | G | A | 2 | a0003c0003t0002g0057 a0003c0003t0004g0232 |
3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-5279C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839784 | |||||||
| chr10:71839841 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.41-5336C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71839841 | |||||||
| chr10:71840141 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.41-5636A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840141 | |||||||
| chr10:71840148 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.41-5643C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840148 | |||||||
| chr10:71840211 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.41-5706C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840211 | |||||||
| chr10:71840339 | G | A | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-5834C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840339 | |||||||
| chr10:71840342 | C | T | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.41-5837G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840342 | |||||||
| chr10:71840343 | G | A | 6 | a0001c0001t0001g0070 a0001c0001t0002g0011 a0001c0001t0002g0069 others(3): Show |
9 | HG01258.hp2 HG01361.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-5838C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840343 | |||||||
| chr10:71840398 | G | A | 64 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0092 others(61): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.41-5893C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840398 | |||||||
| chr10:71840463 | T | C | 9 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0163 others(6): Show |
13 | HG00642.hp2 HG01243.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-5958A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840463 | |||||||
| chr10:71840559 | A | G | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-6054T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840559 | |||||||
| chr10:71840591 | T | C | 1 | a0001c0001t0004g0047 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.41-6086A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840591 | |||||||
| chr10:71840747 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(83): Show |
121 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.41-6242C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840747 | |||||||
| chr10:71840763 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.41-6258A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840763 | |||||||
| chr10:71840862 | C | A | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-6357G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840862 | |||||||
| chr10:71840888 | T | C | 12 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(9): Show |
18 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-6383A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840888 | |||||||
| chr10:71840893 | TG | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(21): Show |
35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.41-6389delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840893 | |||||||
| chr10:71840937 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-6432T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71840937 | |||||||
| chr10:71841045 | T | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-6540A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841045 | |||||||
| chr10:71841094 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0215 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.41-6589G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841094 | |||||||
| chr10:71841199 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.41-6694T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841199 | |||||||
| chr10:71841341 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(194): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.41-6836G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841341 | |||||||
| chr10:71841487 | C | T | 2 | a0003c0003t0002g0057 a0003c0003t0004g0232 |
3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.41-6982G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841487 | |||||||
| chr10:71841488 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(83): Show |
121 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.41-6983C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841488 | |||||||
| chr10:71841517 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-7012C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841517 | |||||||
| chr10:71841804 | G | A | 1 | a0001c0001t0002g0017 | 3 | NA19001.hp1 NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.41-7299C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841804 | |||||||
| chr10:71841862 | C | T | 13 | a0001c0001t0001g0056 a0001c0001t0001g0217 a0001c0001t0001g0218 others(10): Show |
20 | HG00423.hp1 HG00558.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-7357G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841862 | |||||||
| chr10:71841932 | C | T | 3 | a0001c0001t0001g0101 a0001c0010t0001g0096 a0001c0011t0008g0095 |
3 | HG01433.hp2 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.41-7427G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841932 | |||||||
| chr10:71841954 | C | T | 3 | a0002c0002t0004g0038 a0002c0002t0004g0039 a0002c0002t0004g0099 |
5 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-7449G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841954 | |||||||
| chr10:71841973 | T | G | 89 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(86): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.41-7468A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71841973 | |||||||
| chr10:71842000 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41-7495G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842000 | |||||||
| chr10:71842005 | T | TA | 66 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0092 others(63): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.41-7501dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842005 | |||||||
| chr10:71842005 | T | TAA | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-7502_41-7501dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842005 | |||||||
| chr10:71842195 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.41-7690G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842195 | |||||||
| chr10:71842254 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.41-7749A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842254 | |||||||
| chr10:71842434 | C | A | 1 | a0001c0001t0010g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.41-7929G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842434 | |||||||
| chr10:71842483 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(70): Show |
101 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.41-7978G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842483 | |||||||
| chr10:71842572 | C | G | 1 | a0001c0001t0004g0047 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.41-8067G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842572 | |||||||
| chr10:71842695 | T | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.41-8190A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842695 | |||||||
| chr10:71842794 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41-8289G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842794 | |||||||
| chr10:71842892 | A | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0044 others(15): Show |
26 | HG00099.hp2 HG01081.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.40+8290T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842892 | |||||||
| chr10:71842900 | C | T | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG00423.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+8282G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842900 | |||||||
| chr10:71842936 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.40+8246T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71842936 | |||||||
| chr10:71843015 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+8167C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843015 | |||||||
| chr10:71843038 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.40+8144G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843038 | |||||||
| chr10:71843056 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.40+8126G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843056 | |||||||
| chr10:71843125 | C | G | 196 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(193): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.40+8057G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843125 | |||||||
| chr10:71843177 | G | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(83): Show |
121 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.40+8005C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843177 | |||||||
| chr10:71843221 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0250 |
3 | HG00741.hp2 HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.40+7961C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843221 | |||||||
| chr10:71843304 | G | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(21): Show |
35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+7878C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843304 | |||||||
| chr10:71843331 | C | G | 2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.40+7851G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843331 | |||||||
| chr10:71843339 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.40+7843G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843339 | |||||||
| chr10:71843340 | A | G | 216 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(213): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.40+7842T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843340 | |||||||
| chr10:71843357 | C | T | 2 | a0001c0001t0003g0237 a0001c0001t0003g0252 |
2 | HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.40+7825G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843357 | |||||||
| chr10:71843392 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.40+7790G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843392 | |||||||
| chr10:71843425 | A | ACT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0010t0001g0096 others(4): Show |
9 | HG01433.hp2 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+7755_40+7756dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843425 | |||||||
| chr10:71843457 | C | CTA | 3 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+7723_40+7724dup others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843457 | |||||||
| chr10:71843548 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG00621.hp1 NA18961.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.40+7634A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843548 | |||||||
| chr10:71843583 | T | G | 1 | a0001c0001t0002g0098 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.40+7599A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843583 | |||||||
| chr10:71843713 | T | G | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+7469A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71843713 | |||||||
| chr10:71844172 | G | A | 2 | a0001c0001t0004g0047 a0001c0001t0009g0167 |
3 | HG02451.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.40+7010C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844172 | |||||||
| chr10:71844181 | T | C | 1 | a0001c0001t0011g0134 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.40+7001A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844181 | |||||||
| chr10:71844303 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.40+6879G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844303 | |||||||
| chr10:71844450 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.40+6732C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844450 | |||||||
| chr10:71844558 | C | T | 1 | a0003c0003t0004g0232 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.40+6624G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844558 | |||||||
| chr10:71844659 | C | G | 1 | a0001c0001t0003g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+6523G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844659 | |||||||
| chr10:71844680 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(194): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.40+6502G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844680 | |||||||
| chr10:71844696 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.40+6486A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844696 | |||||||
| chr10:71844763 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0066 |
3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.40+6419G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844763 | |||||||
| chr10:71844780 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(110): Show |
165 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.40+6402T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71844780 | |||||||
| chr10:71845080 | G | A | 1 | a0001c0001t0001g0056 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.40+6102C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845080 | |||||||
| chr10:71845160 | T | C | 1 | a0001c0001t0002g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40+6022A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845160 | |||||||
| chr10:71845209 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.40+5973T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845209 | |||||||
| chr10:71845300 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.40+5882C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845300 | |||||||
| chr10:71845326 | T | TGGC | 5 | a0001c0001t0001g0216 a0001c0001t0002g0030 a0001c0001t0002g0063 others(2): Show |
6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+5853_40+5855dup others(3): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845326 | |||||||
| chr10:71845383 | G | A | 35 | a0001c0001t0002g0094 a0001c0001t0003g0001 a0001c0001t0003g0014 others(32): Show |
71 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.40+5799C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845383 | |||||||
| chr10:71845529 | C | T | 1 | a0001c0010t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.40+5653G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845529 | |||||||
| chr10:71845569 | G | T | 1 | a0001c0001t0002g0040 | 2 | NA18964.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.40+5613C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845569 | |||||||
| chr10:71845636 | T | C | 12 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0216 others(9): Show |
15 | HG01346.hp1 HG01433.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+5546A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845636 | |||||||
| chr10:71845639 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.40+5543G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845639 | |||||||
| chr10:71845703 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+5479C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845703 | |||||||
| chr10:71845733 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.40+5449T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845733 | |||||||
| chr10:71845786 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.40+5396C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845786 | |||||||
| chr10:71845819 | T | C | 1 | a0001c0010t0001g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.40+5363A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71845819 | |||||||
| chr10:71846074 | T | C | 24 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(21): Show |
35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+5108A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846074 | |||||||
| chr10:71846096 | G | C | 216 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(213): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.40+5086C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846096 | |||||||
| chr10:71846099 | TACTA | T | 5 | a0001c0001t0001g0100 a0001c0001t0002g0175 a0002c0002t0004g0038 others(2): Show |
7 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+5079_40+5082del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846099 | |||||||
| chr10:71846169 | G | T | 179 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(176): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.40+5013C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846169 | |||||||
| chr10:71846425 | T | TA | 33 | a0001c0001t0001g0116 a0001c0001t0001g0145 a0001c0001t0001g0204 others(30): Show |
49 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.40+4756dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846425 | |||||||
| chr10:71846425 | TA | T | 12 | a0001c0001t0001g0050 a0001c0001t0001g0097 a0001c0001t0001g0102 others(9): Show |
13 | HG00642.hp1 HG01975.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+4756delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846425 | |||||||
| chr10:71846463 | G | A | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+4719C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846463 | |||||||
| chr10:71846468 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0002g0205 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.40+4714A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846468 | |||||||
| chr10:71846504 | C | A | 64 | a0001c0001t0001g0035 a0001c0001t0001g0084 a0001c0001t0001g0092 others(61): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.40+4678G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846504 | |||||||
| chr10:71846567 | A | G | 2 | a0003c0003t0002g0057 a0003c0003t0004g0232 |
3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+4615T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846567 | |||||||
| chr10:71846600 | C | A | 1 | a0003c0003t0002g0057 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+4582G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846600 | |||||||
| chr10:71846635 | G | A | 16 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0216 others(13): Show |
19 | HG00639.hp1 HG01123.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+4547C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846635 | |||||||
| chr10:71846656 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+4526G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846656 | |||||||
| chr10:71846731 | CA | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0070 others(8): Show |
16 | HG01496.hp1 HG01496.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+4450delT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | |||||||
| chr10:71846731 | CAA | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.40+4449_40+4450del others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | |||||||
| chr10:71846731 | CAAA | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(89): Show |
127 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.40+4448_40+4450del others(3): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | |||||||
| chr10:71846731 | CAAAA | C | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0217 others(9): Show |
19 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+4447_40+4450del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846731 | |||||||
| chr10:71846778 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.40+4404G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846778 | |||||||
| chr10:71846997 | A | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+4185T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71846997 | |||||||
| chr10:71847223 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(65): Show |
96 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.40+3959C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847223 | |||||||
| chr10:71847257 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.40+3925G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847257 | |||||||
| chr10:71847260 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.40+3922C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847260 | |||||||
| chr10:71847370 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.40+3812T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847370 | |||||||
| chr10:71847417 | G | A | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+3765C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847417 | |||||||
| chr10:71847453 | T | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.40+3729A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847453 | |||||||
| chr10:71847549 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0212 |
3 | HG00140.hp2 HG01192.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.40+3633T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847549 | |||||||
| chr10:71847568 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(112): Show |
168 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.40+3614G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847568 | |||||||
| chr10:71847605 | G | A | 4 | a0001c0001t0005g0260 a0001c0001t0007g0261 a0001c0001t0007g0262 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+3577C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847605 | |||||||
| chr10:71847612 | T | C | 4 | a0001c0001t0001g0100 a0002c0002t0004g0038 a0002c0002t0004g0039 others(1): Show |
6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+3570A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847612 | |||||||
| chr10:71847865 | T | G | 4 | a0001c0001t0001g0100 a0002c0002t0004g0038 a0002c0002t0004g0039 others(1): Show |
6 | HG02280.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+3317A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847865 | |||||||
| chr10:71847937 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.40+3245C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847937 | |||||||
| chr10:71847964 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40+3218G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847964 | |||||||
| chr10:71847997 | T | C | 24 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(21): Show |
35 | HG00642.hp2 HG00733.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.40+3185A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71847997 | |||||||
| chr10:71848011 | C | A | 5 | a0001c0001t0001g0216 a0001c0001t0002g0030 a0001c0001t0002g0063 others(2): Show |
6 | HG01346.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+3171G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848011 | |||||||
| chr10:71848103 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+3079G>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848103 | |||||||
| chr10:71848193 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0211 |
4 | NA18970.hp1 NA18984.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+2989C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848193 | |||||||
| chr10:71848315 | A | G | 3 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+2867T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848315 | |||||||
| chr10:71848343 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2839A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848343 | |||||||
| chr10:71848641 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG00423.hp1 HG01074.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.40+2541T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848641 | |||||||
| chr10:71848810 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.40+2372T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848810 | |||||||
| chr10:71848966 | A | G | 198 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(195): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.40+2216T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71848966 | |||||||
| chr10:71849244 | T | G | 1 | a0001c0001t0003g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.40+1938A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849244 | |||||||
| chr10:71849302 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(64): Show |
95 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.40+1880C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849302 | |||||||
| chr10:71849525 | CG | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1656delC | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849525 | |||||||
| chr10:71849534 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+1648C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849534 | |||||||
| chr10:71849562 | T | G | 1 | a0001c0001t0003g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.40+1620A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849562 | |||||||
| chr10:71849607 | A | G | 2 | a0003c0003t0002g0057 a0003c0003t0004g0232 |
3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+1575T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849607 | |||||||
| chr10:71849624 | AAAAC | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1554_40+1557del others(4): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849624 | |||||||
| chr10:71849646 | A | C | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+1536T>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849646 | |||||||
| chr10:71849658 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.40+1524C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849658 | |||||||
| chr10:71849660 | G | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
13 | HG02074.hp2 NA18612.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+1522C>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849660 | |||||||
| chr10:71849690 | T | C | 2 | a0003c0003t0002g0057 a0003c0003t0004g0232 |
3 | HG02145.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+1492A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849690 | |||||||
| chr10:71849771 | T | C | 5 | a0001c0001t0003g0061 a0001c0001t0003g0254 a0001c0001t0003g0255 others(2): Show |
6 | HG00140.hp1 HG01109.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+1411A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849771 | |||||||
| chr10:71849805 | A | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(194): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.40+1377T>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849805 | |||||||
| chr10:71849861 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.40+1321G>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849861 | |||||||
| chr10:71849903 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.40+1279G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71849903 | |||||||
| chr10:71850057 | G | GA | 101 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(98): Show |
147 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.40+1124dupT | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850057 | |||||||
| chr10:71850265 | GCTCT | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+913_40+916delAG others(2): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850265 | |||||||
| chr10:71850284 | T | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(14): Show |
23 | HG00642.hp1 HG00733.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.40+898A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850284 | |||||||
| chr10:71850298 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(92): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.40+884C>T | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850298 | |||||||
| chr10:71850362 | T | C | 1 | a0001c0001t0003g0258 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.40+820A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850362 | |||||||
| chr10:71850450 | T | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0213 a0001c0001t0002g0214 |
9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+732A>C | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850450 | |||||||
| chr10:71850479 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.40+703A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850479 | |||||||
| chr10:71850499 | T | C | 20 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0216 others(17): Show |
29 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.40+683A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850499 | |||||||
| chr10:71850580 | C | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
19 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.40+602G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850580 | |||||||
| chr10:71850837 | T | C | 1 | a0001c0001t0003g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.40+345A>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850837 | |||||||
| chr10:71850916 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.40+266G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850916 | |||||||
| chr10:71850982 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0066 |
3 | HG01069.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.40+200G>A | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71850982 | |||||||
| chr10:71851017 | C | CCCAGAGA others(3): Show |
5 | a0001c0001t0002g0030 a0001c0001t0002g0063 a0001c0001t0002g0064 others(2): Show |
7 | HG02145.hp1 HG02145.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.40+155_40+164dupCT others(8): Show |
PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71851017 | |||||||
| chr10:71851101 | G | C | 1 | a0001c0001t0002g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+81C>G | PSAP | ENSG00000197746.15 | transcript | ENST00000394936.8 | protein_coding | 1/13 | chr10 | 71851101 |