Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89958 |
| ensemblid | ENSG00000186193.9 |
| hgncid | 28055 |
| symbol | SAPCD2 |
| name | suppressor APC domain containing 2 |
| refseq_nuc | NM_178448.4 |
| refseq_prot | NP_848543.2 |
| ensembl_nuc | ENST00000409687.5 |
| ensembl_prot | ENSP00000386348.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 137062127 |
| end | 137070557 |
| strand | - |
| ver | v1.2 |
| region | chr9:137062127-137070557 |
| region5000 | chr9:137057127-137075557 |
| regionname0 | SAPCD2_chr9_137062127_137070557 |
| regionname5000 | SAPCD2_chr9_137057127_137075557 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 218 | 46 | 52 | 75 | 12 | 31 | 57 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| a0002 | 0/0 | 394 | 187 | 45 | 23 | 97 | 6 | 16 | 72 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| a0003 | 0/0 | 394 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| a0004 | 0/0 | 394 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| a0005 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| a0006 | 0/0 | 394 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | MAGAA others(389): Show |
chr9 | 137057127 | 137075557 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1182 | 216 | 45 | 51 | 75 | 12 | 31 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0001c0008 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0001c0011 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0002c0002 | 0/0 | 1182 | 183 | 44 | 21 | 96 | 6 | 16 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0002c0004 | 0/0 | 1182 | 2 | 1 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0002c0006 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0002c0007 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0003c0003 | 0/0 | 1182 | 5 | 5 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0004c0005 | 0/0 | 1182 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0005c0010 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 | ||
| a0006c0009 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | ATGGC others(1177): Show |
chr9 | 137057127 | 137075557 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3772 | 9 | 3 | 1 | 5 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0002 | 0/0 | 3814 | 84 | 1 | 24 | 48 | 3 | 8 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0003 | 0/0 | 3814 | 52 | 3 | 22 | 0 | 9 | 18 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0004 | 1/0 | 3814 | 21 | 6 | 1 | 8 | 0 | 5 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0005 | 0/0 | 3776 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3771): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0006 | 0/0 | 3814 | 9 | 9 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0007 | 0/0 | 3772 | 3 | 3 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0008 | 0/0 | 3814 | 6 | 0 | 0 | 6 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0009 | 0/0 | 3814 | 6 | 6 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0010 | 0/0 | 3814 | 5 | 0 | 0 | 5 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0011 | 0/0 | 3814 | 3 | 1 | 2 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0012 | 0/0 | 3814 | 3 | 3 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0014 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0016 | 0/0 | 3772 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0018 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0019 | 0/0 | 3814 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0022 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0026 | 0/1 | 3772 | 1 | 0 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0030 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0034 | 0/0 | 3772 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0035 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3798): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0036 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0001t0037 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0008t0002 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0001c0011t0021 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0001 | 0/0 | 3772 | 124 | 37 | 10 | 58 | 6 | 13 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0002 | 0/0 | 3814 | 9 | 0 | 1 | 8 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0003 | 0/0 | 3814 | 3 | 0 | 2 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0004 | 0/0 | 3814 | 7 | 0 | 0 | 7 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0005 | 0/0 | 3776 | 19 | 0 | 1 | 17 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3771): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0011 | 0/0 | 3814 | 2 | 0 | 2 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0013 | 0/0 | 3772 | 3 | 3 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0014 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0015 | 0/0 | 3776 | 3 | 0 | 3 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3771): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0017 | 0/0 | 3772 | 2 | 1 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0020 | 0/0 | 3772 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0023 | 0/0 | 3772 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0024 | 0/0 | 3772 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0025 | 0/0 | 3772 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0027 | 0/0 | 3772 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0028 | 0/0 | 3776 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3771): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0029 | 0/0 | 3772 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0031 | 0/0 | 3772 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0032 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0002t0033 | 0/0 | 3772 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0004t0001 | 0/0 | 3772 | 2 | 1 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0002c0006t0002 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0002c0007t0005 | 0/0 | 3776 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3771): Show |
chr9 | 137057127 | 137075557 |
| a0003c0003t0007 | 0/0 | 3772 | 5 | 5 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0004c0005t0001 | 0/0 | 3772 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3767): Show |
chr9 | 137057127 | 137075557 |
| a0005c0010t0018 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| a0006c0009t0003 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | GCTAT others(3809): Show |
chr9 | 137057127 | 137075557 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0002 | 0/0 | 46 | 0 | 12 | 30 | 2 | 2 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0004 | 0/0 | 19 | 0 | 5 | 11 | 0 | 3 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0007 | 0/0 | 7 | 1 | 4 | 0 | 1 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0003 | 0/0 | 36 | 2 | 19 | 0 | 6 | 9 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0008 | 0/0 | 7 | 0 | 0 | 0 | 2 | 5 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0011 | 0/0 | 6 | 2 | 0 | 3 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0008g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0009g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0010g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0012g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0014g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0016g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0019g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0022g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0026g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0030g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0034g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0035g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0036g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0001t0037g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0008t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0001c0011t0021g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0001 | 0/0 | 75 | 27 | 8 | 29 | 6 | 5 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0006 | 0/0 | 13 | 2 | 0 | 9 | 0 | 2 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0002g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0003g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0004g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0005g0005 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0011g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0015g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0017g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0020g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0024g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0025g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0027g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0028g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0029g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0031g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0032g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0002t0033g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0004t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0006t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0002c0007t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0003c0003t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0003c0003t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0003c0003t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0003c0003t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0004c0005t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0005c0010t0018g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| a0006c0009t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00423 | hp2 | a0002 | c0002 | t0005 | g0032 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00438 | hp1 | a0002 | c0007 | t0005 | g0071 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00438 | hp2 | a0002 | c0002 | t0005 | g0032 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00544 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00544 | hp2 | a0002 | c0002 | t0005 | g0054 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0028 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00673 | hp1 | a0002 | c0002 | t0031 | g0074 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00738 | hp1 | a0002 | c0002 | t0015 | g0019 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01081 | hp1 | a0002 | c0002 | t0032 | g0068 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01099 | hp2 | a0002 | c0002 | t0011 | g0078 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01192 | hp1 | a0002 | c0006 | t0002 | g0040 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01243 | hp1 | a0005 | c0010 | t0018 | g0141 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01243 | hp2 | a0002 | c0002 | t0011 | g0067 | AMR | PUR | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0030 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01261 | hp1 | a0002 | c0002 | t0017 | g0029 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0116 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01346 | hp2 | a0002 | c0002 | t0015 | g0019 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0120 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0041 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01928 | hp1 | a0002 | c0002 | t0005 | g0055 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01934 | hp2 | a0002 | c0002 | t0015 | g0019 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0028 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0077 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0030 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02148 | hp2 | a0001 | c0001 | t0030 | g0085 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02155 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | CDX | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02155 | hp2 | a0002 | c0002 | t0020 | g0058 | EAS | CDX | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02165 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | CDX | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02300 | hp1 | a0001 | c0008 | t0002 | g0091 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02572 | hp1 | a0002 | c0002 | t0013 | g0083 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0133 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02615 | hp1 | a0003 | c0003 | t0007 | g0138 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0035 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02896 | hp1 | a0003 | c0003 | t0007 | g0137 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02897 | hp1 | a0003 | c0003 | t0007 | g0039 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02922 | hp2 | a0003 | c0003 | t0007 | g0039 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02970 | hp1 | a0001 | c0001 | t0019 | g0129 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0112 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03098 | hp1 | a0002 | c0002 | t0017 | g0029 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0035 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03139 | hp2 | a0001 | c0001 | t0018 | g0135 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0099 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03453 | hp1 | a0001 | c0011 | t0021 | g0124 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03453 | hp2 | a0002 | c0002 | t0013 | g0059 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03486 | hp1 | a0002 | c0002 | t0023 | g0045 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03516 | hp2 | a0001 | c0001 | t0035 | g0132 | AFR | ESN | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0130 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0115 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0089 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03927 | hp2 | a0002 | c0002 | t0005 | g0005 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0011 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04184 | hp2 | a0006 | c0009 | t0003 | g0104 | SAS | BEB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04204 | hp1 | a0002 | c0002 | t0024 | g0060 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18522 | hp2 | a0002 | c0002 | t0033 | g0064 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18747 | hp2 | a0004 | c0005 | t0001 | g0036 | EAS | CHB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18906 | hp1 | a0001 | c0001 | t0036 | g0126 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18951 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18953 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18961 | hp2 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18964 | hp2 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18967 | hp2 | a0002 | c0002 | t0025 | g0073 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18969 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18969 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18973 | hp1 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18977 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18978 | hp1 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18981 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18982 | hp1 | a0002 | c0002 | t0029 | g0063 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18982 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18988 | hp2 | a0002 | c0002 | t0005 | g0072 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18993 | hp1 | a0004 | c0005 | t0001 | g0036 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18994 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19010 | hp1 | a0002 | c0002 | t0028 | g0062 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19011 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0100 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19060 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19066 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19070 | hp1 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0049 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19077 | hp2 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19084 | hp1 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19088 | hp2 | a0002 | c0002 | t0005 | g0005 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0108 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ASW | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | TSI | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20905 | hp1 | a0002 | c0002 | t0027 | g0061 | SAS | GIH | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | GIH | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02109 | hp1 | a0001 | c0001 | t0037 | g0142 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02486 | hp1 | a0001 | c0001 | t0034 | g0136 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02559 | hp1 | a0002 | c0002 | t0013 | g0056 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ACB | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03471 | hp1 | a0001 | c0001 | t0022 | g0098 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | USA | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| HG06807 | hp2 | a0003 | c0003 | t0007 | g0139 | AFR | USA | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | USA | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| NA21309 | hp2 | a0002 | c0002 | t0014 | g0080 | AFR | LWK | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0026 | g0103 | REF | REF | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0114 | REF | REF | SAPCD2_chr9_137057127_137075557 | SAPCD2 | chr9 | 137057127 | 137075557 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137065557 | G | A | 1 | a0003 | 5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.796C>T | p.Arg266Cys | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/6 | 893/3814 | 796/1185 | 266/394 | chr9 | 137065557 | |||
| chr9:137065596 | G | A | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.757C>T | p.Arg253Cys | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/6 | 854/3814 | 757/1185 | 253/394 | chr9 | 137065596 | |||
| chr9:137069995 | G | C | 2 | a0002 a0004 |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
missense_variant | MODERATE | c.466C>G | p.Arg156Gly | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 563/3814 | 466/1185 | 156/394 | chr9 | 137069995 | |||
| chr9:137069998 | C | T | 2 | a0002 a0004 |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
missense_variant | MODERATE | c.463G>A | p.Ala155Thr | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 560/3814 | 463/1185 | 155/394 | chr9 | 137069998 | |||
| chr9:137070067 | G | A | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.394C>T | p.Arg132Trp | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 491/3814 | 394/1185 | 132/394 | chr9 | 137070067 | |||
| chr9:137070411 | G | A | 1 | a0004 | 2 | NA18747.hp2 NA18993.hp1 |
missense_variant | MODERATE | c.50C>T | p.Pro17Leu | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 147/3814 | 50/1185 | 17/394 | chr9 | 137070411 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137064779 | G | A | 1 | a0002c0004 | 2 | HG01256.hp2 HG02145.hp2 |
synonymous_variant | LOW | c.1065C>T | p.Thr355Thr | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1162/3814 | 1065/1185 | 355/394 | chr9 | 137064779 | |||
| chr9:137065522 | G | A | 1 | a0001c0008 | 1 | HG02300.hp1 | splice_region_variant&synonymous_variant | LOW | c.831C>T | p.Ala277Ala | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/6 | 928/3814 | 831/1185 | 277/394 | chr9 | 137065522 | |||
| chr9:137066364 | C | T | 1 | a0002c0007 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.582G>A | p.Ala194Ala | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/6 | 679/3814 | 582/1185 | 194/394 | chr9 | 137066364 | |||
| chr9:137069897 | C | G | 1 | a0002c0006 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.564G>C | p.Ala188Ala | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 661/3814 | 564/1185 | 188/394 | chr9 | 137069897 | |||
| chr9:137070446 | G | A | 1 | a0001c0011 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.15C>T | p.Ala5Ala | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 112/3814 | 15/1185 | 5/394 | chr9 | 137070446 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137062299 | T | TTTTC | 5 | a0001c0001t0005 a0002c0002t0005 a0002c0002t0015 others(2): Show |
25 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2356_*2359dupGAAA | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 2359 | chr9 | 137062299 | ||||||
| chr9:137062502 | T | C | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0030 others(5): Show |
103 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2157A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 2157 | chr9 | 137062502 | ||||||
| chr9:137062611 | C | T | 1 | a0002c0002t0024 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2048G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 2048 | chr9 | 137062611 | ||||||
| chr9:137062612 | G | A | 1 | a0002c0002t0017 | 2 | HG01261.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2047C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 2047 | chr9 | 137062612 | ||||||
| chr9:137062662 | C | T | 1 | a0002c0002t0023 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1997G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1997 | chr9 | 137062662 | ||||||
| chr9:137062826 | C | T | 2 | a0001c0001t0019 a0001c0001t0022 |
3 | HG02970.hp1 HG03471.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1833G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1833 | chr9 | 137062826 | ||||||
| chr9:137062947 | A | G | 1 | a0001c0011t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1712T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1712 | chr9 | 137062947 | ||||||
| chr9:137062967 | C | T | 2 | a0001c0001t0034 a0002c0002t0013 |
4 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1692 | chr9 | 137062967 | ||||||
| chr9:137063217 | T | G | 1 | a0002c0002t0027 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1442 | chr9 | 137063217 | ||||||
| chr9:137063236 | G | A | 1 | a0001c0001t0010 | 5 | NA18965.hp2 NA18973.hp1 NA19004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1423C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1423 | chr9 | 137063236 | ||||||
| chr9:137063433 | C | T | 1 | a0001c0001t0030 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1226G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1226 | chr9 | 137063433 | ||||||
| chr9:137063467 | G | A | 1 | a0002c0002t0029 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1192 | chr9 | 137063467 | ||||||
| chr9:137063467 | G | C | 1 | a0002c0002t0028 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1192 | chr9 | 137063467 | ||||||
| chr9:137063489 | C | T | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0030 others(4): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1170G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1170 | chr9 | 137063489 | ||||||
| chr9:137063492 | ACACTGAC others(35): Show |
A | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(20): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1125_*1166delCGTG others(38): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1125 | chr9 | 137063492 | ||||||
| chr9:137063499 | CCCCGCAT others(34): Show |
C | 1 | a0002c0002t0004 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119_*1159delTCAG others(37): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1119 | chr9 | 137063499 | ||||||
| chr9:137063503 | G | A | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0030 others(4): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 1156 | chr9 | 137063503 | ||||||
| chr9:137063844 | T | C | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0030 others(4): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*815A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 815 | chr9 | 137063844 | ||||||
| chr9:137063864 | G | C | 1 | a0001c0001t0019 | 2 | HG02970.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*795C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 795 | chr9 | 137063864 | ||||||
| chr9:137063884 | G | A | 1 | a0002c0002t0031 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 775 | chr9 | 137063884 | ||||||
| chr9:137064035 | C | T | 1 | a0001c0001t0036 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 624 | chr9 | 137064035 | ||||||
| chr9:137064082 | C | A | 1 | a0002c0002t0032 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 577 | chr9 | 137064082 | ||||||
| chr9:137064088 | GTCCGACC others(4): Show |
G | 1 | a0001c0001t0035 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560_*570delTAGCGG others(5): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 560 | chr9 | 137064088 | ||||||
| chr9:137064125 | G | C | 5 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0035 others(2): Show |
14 | HG02451.hp2 HG02559.hp2 HG02630.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*534C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 534 | chr9 | 137064125 | ||||||
| chr9:137064131 | C | G | 3 | a0001c0001t0003 a0002c0002t0003 a0006c0009t0003 |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 528 | chr9 | 137064131 | ||||||
| chr9:137064193 | C | A | 2 | a0001c0001t0011 a0002c0002t0011 |
5 | HG01099.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*466G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 466 | chr9 | 137064193 | ||||||
| chr9:137064194 | G | A | 1 | a0002c0002t0033 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 465 | chr9 | 137064194 | ||||||
| chr9:137064203 | C | T | 3 | a0001c0001t0012 a0001c0001t0034 a0002c0002t0013 |
7 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*456G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 456 | chr9 | 137064203 | ||||||
| chr9:137064215 | G | A | 1 | a0002c0002t0015 | 3 | HG00738.hp1 HG01346.hp2 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 444 | chr9 | 137064215 | ||||||
| chr9:137064281 | A | G | 1 | a0002c0002t0020 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 378 | chr9 | 137064281 | ||||||
| chr9:137064354 | C | T | 2 | a0001c0001t0018 a0005c0010t0018 |
2 | HG01243.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*305G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 305 | chr9 | 137064354 | ||||||
| chr9:137064567 | T | A | 1 | a0001c0001t0008 | 6 | NA18939.hp2 NA18945.hp1 NA18953.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*92A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 6/6 | 92 | chr9 | 137064567 | ||||||
| chr9:137070465 | G | A | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(8): Show |
31 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 5 | chr9 | 137070465 | ||||||
| chr9:137070467 | C | T | 1 | a0001c0001t0016 | 2 | NA18978.hp1 NA19084.hp1 |
5_prime_UTR_variant | MODIFIER | c.-7G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | 7 | chr9 | 137070467 | ||||||
| chr9:137070484 | G | A | 1 | a0001c0001t0037 | 1 | HG02109.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/6 | chr9 | 137070484 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137064840 | C | G | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(19): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1056+23G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 5/5 | chr9 | 137064840 | |||||||
| chr9:137064852 | G | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0052 a0002c0002t0001g0075 |
8 | HG00408.hp1 HG00621.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1056+11C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 5/5 | chr9 | 137064852 | |||||||
| chr9:137065048 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.939+30G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 4/5 | chr9 | 137065048 | |||||||
| chr9:137065212 | T | C | 1 | a0002c0002t0001g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.832-27A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065212 | |||||||
| chr9:137065269 | GGCTCTCC others(6): Show |
G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-97_832-85delGA others(11): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065269 | |||||||
| chr9:137065283 | C | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-98G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065283 | |||||||
| chr9:137065284 | T | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-99A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065284 | |||||||
| chr9:137065287 | T | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-102A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065287 | |||||||
| chr9:137065290 | T | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-105A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065290 | |||||||
| chr9:137065292 | C | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-107G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065292 | |||||||
| chr9:137065297 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-112T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065297 | |||||||
| chr9:137065298 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-113C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065298 | |||||||
| chr9:137065302 | A | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-117T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065302 | |||||||
| chr9:137065303 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-118C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065303 | |||||||
| chr9:137065304 | A | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-119T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065304 | |||||||
| chr9:137065307 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-122C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065307 | |||||||
| chr9:137065308 | T | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-123A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065308 | |||||||
| chr9:137065315 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-130C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065315 | |||||||
| chr9:137065316 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-131C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065316 | |||||||
| chr9:137065318 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-133T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065318 | |||||||
| chr9:137065325 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-140T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065325 | |||||||
| chr9:137065328 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-143A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065328 | |||||||
| chr9:137065329 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-144C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065329 | |||||||
| chr9:137065333 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-148C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065333 | |||||||
| chr9:137065334 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-149C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065334 | |||||||
| chr9:137065337 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-152A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065337 | |||||||
| chr9:137065338 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-153C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065338 | |||||||
| chr9:137065340 | C | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-155G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065340 | |||||||
| chr9:137065343 | A | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-158T>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065343 | |||||||
| chr9:137065347 | A | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-162T>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065347 | |||||||
| chr9:137065351 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-166A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065351 | |||||||
| chr9:137065352 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-167T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065352 | |||||||
| chr9:137065353 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.832-168C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065353 | |||||||
| chr9:137065358 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+164A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065358 | |||||||
| chr9:137065363 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+159C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065363 | |||||||
| chr9:137065365 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+157C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065365 | |||||||
| chr9:137065366 | G | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+156C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065366 | |||||||
| chr9:137065370 | A | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+152T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065370 | |||||||
| chr9:137065373 | C | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+149G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065373 | |||||||
| chr9:137065374 | A | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+148T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065374 | |||||||
| chr9:137065381 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+141C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065381 | |||||||
| chr9:137065382 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+140T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065382 | |||||||
| chr9:137065383 | G | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+139C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065383 | |||||||
| chr9:137065385 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+137T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065385 | |||||||
| chr9:137065386 | A | T | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+136T>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065386 | |||||||
| chr9:137065401 | T | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(19): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.831+121A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065401 | |||||||
| chr9:137065401 | T | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+121A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065401 | |||||||
| chr9:137065402 | C | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+120G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065402 | |||||||
| chr9:137065405 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+117C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065405 | |||||||
| chr9:137065407 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+115C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065407 | |||||||
| chr9:137065411 | A | G | 1 | a0002c0002t0001g0048 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.831+111T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065411 | |||||||
| chr9:137065497 | C | T | 2 | a0001c0001t0006g0024 a0002c0002t0014g0080 |
4 | HG02451.hp2 HG03516.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+25G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 3/5 | chr9 | 137065497 | |||||||
| chr9:137065679 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.685-11A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065679 | |||||||
| chr9:137065725 | C | T | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(19): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.685-57G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065725 | |||||||
| chr9:137065726 | A | G | 113 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0087 others(110): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.685-58T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065726 | |||||||
| chr9:137065785 | G | A | 9 | a0001c0001t0006g0024 a0001c0001t0006g0125 a0001c0001t0006g0128 others(6): Show |
11 | HG02451.hp2 HG02630.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-117C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065785 | |||||||
| chr9:137065864 | C | G | 1 | a0002c0002t0001g0051 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.685-196G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065864 | |||||||
| chr9:137065867 | G | A | 1 | a0002c0002t0005g0032 | 2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.685-199C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065867 | |||||||
| chr9:137065970 | G | A | 1 | a0001c0001t0022g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.684+292C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137065970 | |||||||
| chr9:137066029 | C | T | 1 | a0002c0002t0013g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.684+233G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137066029 | |||||||
| chr9:137066188 | C | T | 64 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0087 others(61): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.684+74G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 2/5 | chr9 | 137066188 | |||||||
| chr9:137066442 | C | T | 11 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0022 others(8): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.572-68G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066442 | |||||||
| chr9:137066468 | G | A | 1 | a0002c0002t0011g0078 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.572-94C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066468 | |||||||
| chr9:137066475 | C | T | 1 | a0002c0002t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.572-101G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066475 | |||||||
| chr9:137066558 | T | A | 2 | a0002c0002t0001g0053 a0002c0002t0001g0065 |
2 | NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.572-184A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066558 | |||||||
| chr9:137066607 | C | T | 3 | a0001c0001t0006g0128 a0001c0001t0006g0131 a0001c0001t0035g0132 |
3 | HG02630.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.572-233G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066607 | |||||||
| chr9:137066617 | C | A | 13 | a0001c0001t0004g0011 a0001c0001t0004g0016 a0001c0001t0004g0089 others(10): Show |
28 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.572-243G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066617 | |||||||
| chr9:137066728 | A | C | 1 | a0002c0002t0005g0055 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.572-354T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066728 | |||||||
| chr9:137066729 | G | A | 2 | a0001c0001t0006g0128 a0001c0001t0035g0132 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.572-355C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066729 | |||||||
| chr9:137066730 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.572-356C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066730 | |||||||
| chr9:137066957 | G | A | 1 | a0001c0001t0019g0130 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.572-583C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066957 | |||||||
| chr9:137066961 | A | C | 1 | a0001c0001t0002g0093 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.572-587T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066961 | |||||||
| chr9:137066962 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.572-588C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137066962 | |||||||
| chr9:137067011 | T | C | 1 | a0001c0001t0014g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.572-637A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067011 | |||||||
| chr9:137067011 | T | G | 22 | a0001c0001t0003g0102 a0001c0001t0006g0024 a0001c0001t0006g0038 others(19): Show |
26 | HG01099.hp2 HG01243.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.572-637A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067011 | |||||||
| chr9:137067073 | C | T | 1 | a0002c0002t0005g0054 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.572-699G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067073 | |||||||
| chr9:137067089 | G | A | 22 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(19): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.572-715C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067089 | |||||||
| chr9:137067112 | C | T | 1 | a0001c0001t0006g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.572-738G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067112 | |||||||
| chr9:137067288 | C | T | 77 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0087 others(74): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.572-914G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067288 | |||||||
| chr9:137067355 | C | T | 4 | a0003c0003t0007g0039 a0003c0003t0007g0137 a0003c0003t0007g0138 others(1): Show |
5 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-981G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067355 | |||||||
| chr9:137067378 | G | A | 11 | a0001c0001t0004g0011 a0001c0001t0004g0016 a0001c0001t0004g0089 others(8): Show |
26 | HG00423.hp1 HG00558.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.572-1004C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067378 | |||||||
| chr9:137067470 | C | CA | 17 | a0001c0001t0002g0096 a0001c0001t0006g0024 a0001c0001t0006g0125 others(14): Show |
20 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.572-1097dupT | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067470 | |||||||
| chr9:137067470 | C | CAA | 5 | a0001c0001t0003g0102 a0001c0001t0006g0038 a0003c0003t0007g0039 others(2): Show |
7 | HG02559.hp2 HG02615.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.572-1098_572-1097d others(4): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067470 | |||||||
| chr9:137067541 | G | C | 1 | a0001c0001t0002g0088 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.572-1167C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067541 | |||||||
| chr9:137067542 | C | G | 1 | a0001c0001t0002g0088 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.572-1168G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067542 | |||||||
| chr9:137067543 | G | C | 72 | a0001c0001t0001g0087 a0001c0001t0001g0111 a0001c0001t0002g0101 others(69): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.572-1169C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067543 | |||||||
| chr9:137067571 | C | A | 1 | a0001c0001t0007g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.572-1197G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067571 | |||||||
| chr9:137067572 | A | G | 1 | a0001c0001t0007g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.572-1198T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067572 | |||||||
| chr9:137067635 | G | C | 1 | a0002c0002t0001g0070 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.572-1261C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067635 | |||||||
| chr9:137067644 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.572-1270A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067644 | |||||||
| chr9:137067683 | A | G | 1 | a0001c0011t0021g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.572-1309T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067683 | |||||||
| chr9:137067753 | C | T | 1 | a0001c0011t0021g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.572-1379G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067753 | |||||||
| chr9:137067774 | C | CA | 6 | a0001c0001t0004g0016 a0001c0001t0004g0089 a0001c0001t0004g0097 others(3): Show |
12 | HG02080.hp1 HG02155.hp1 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.572-1401dupT | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | C | CAA | 8 | a0001c0001t0003g0119 a0001c0001t0004g0121 a0001c0001t0006g0134 others(5): Show |
11 | HG00738.hp2 HG01099.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.572-1402_572-1401d others(4): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | C | CAAAAA | 8 | a0001c0001t0001g0090 a0001c0001t0002g0002 a0001c0001t0002g0007 others(5): Show |
62 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.572-1405_572-1401d others(7): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | C | CAAAAAA | 10 | a0001c0001t0001g0021 a0001c0001t0002g0004 a0001c0001t0002g0033 others(7): Show |
31 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.572-1406_572-1401d others(8): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | CA | C | 17 | a0001c0001t0001g0087 a0001c0001t0002g0105 a0001c0001t0003g0003 others(14): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.572-1401delT | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | CAA | C | 61 | a0001c0001t0001g0023 a0001c0001t0001g0111 a0001c0001t0002g0101 others(58): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.572-1402_572-1401d others(4): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | CAAA | C | 11 | a0001c0001t0006g0125 a0001c0001t0011g0109 a0001c0001t0014g0099 others(8): Show |
13 | HG02258.hp1 HG02698.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-1403_572-1401d others(5): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067774 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0022g0098 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.572-1412_572-1401d others(14): Show |
SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067774 | |||||||
| chr9:137067807 | C | T | 5 | a0002c0002t0001g0018 a0002c0002t0001g0047 a0002c0002t0001g0048 others(2): Show |
7 | NA18975.hp1 NA18980.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.572-1433G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067807 | |||||||
| chr9:137067808 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0033 |
9 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.572-1434C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067808 | |||||||
| chr9:137067812 | G | A | 1 | a0002c0002t0001g0082 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.572-1438C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067812 | |||||||
| chr9:137067844 | A | G | 2 | a0001c0001t0014g0099 a0001c0001t0022g0098 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.572-1470T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137067844 | |||||||
| chr9:137068130 | C | T | 1 | a0001c0011t0021g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.572-1756G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068130 | |||||||
| chr9:137068179 | G | A | 8 | a0001c0001t0034g0136 a0001c0001t0037g0142 a0002c0002t0013g0083 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+1711C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068179 | |||||||
| chr9:137068189 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.571+1701C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068189 | |||||||
| chr9:137068347 | T | G | 1 | a0002c0002t0001g0026 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.571+1543A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068347 | |||||||
| chr9:137068411 | G | C | 1 | a0001c0001t0003g0107 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.571+1479C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068411 | |||||||
| chr9:137068428 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.571+1462G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068428 | |||||||
| chr9:137068434 | C | T | 1 | a0001c0001t0012g0108 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.571+1456G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068434 | |||||||
| chr9:137068465 | C | T | 1 | a0001c0011t0021g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571+1425G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068465 | |||||||
| chr9:137068614 | T | C | 1 | a0003c0003t0007g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.571+1276A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068614 | |||||||
| chr9:137068639 | G | A | 20 | a0001c0001t0001g0021 a0001c0001t0001g0087 a0001c0001t0001g0090 others(17): Show |
97 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.571+1251C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068639 | |||||||
| chr9:137068920 | A | C | 4 | a0002c0002t0001g0013 a0002c0002t0001g0026 a0002c0002t0001g0044 others(1): Show |
8 | HG02109.hp2 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.571+970T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068920 | |||||||
| chr9:137068942 | C | T | 1 | a0002c0002t0001g0043 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.571+948G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068942 | |||||||
| chr9:137068988 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG01074.hp1 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.571+902C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137068988 | |||||||
| chr9:137069014 | G | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0087 a0001c0001t0001g0090 others(17): Show |
97 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.571+876C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069014 | |||||||
| chr9:137069166 | C | T | 1 | a0001c0001t0030g0085 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571+724G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069166 | |||||||
| chr9:137069182 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.571+708A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069182 | |||||||
| chr9:137069192 | C | T | 2 | a0001c0001t0006g0125 a0001c0001t0036g0126 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.571+698G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069192 | |||||||
| chr9:137069393 | G | GC | 8 | a0001c0001t0018g0135 a0001c0001t0034g0136 a0001c0001t0037g0142 others(5): Show |
9 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.571+496dupG | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069393 | |||||||
| chr9:137069483 | A | G | 57 | a0001c0001t0001g0021 a0001c0001t0001g0087 a0001c0001t0001g0090 others(54): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.571+407T>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069483 | |||||||
| chr9:137069531 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.571+359C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069531 | |||||||
| chr9:137069681 | C | G | 20 | a0001c0001t0001g0021 a0001c0001t0001g0087 a0001c0001t0001g0090 others(17): Show |
97 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.571+209G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069681 | |||||||
| chr9:137069693 | C | T | 1 | a0001c0001t0004g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.571+197G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069693 | |||||||
| chr9:137069781 | C | G | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+109G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069781 | |||||||
| chr9:137069783 | C | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+107G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069783 | |||||||
| chr9:137069786 | T | A | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+104A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069786 | |||||||
| chr9:137069787 | C | A | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+103G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069787 | |||||||
| chr9:137069794 | C | A | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+96G>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069794 | |||||||
| chr9:137069795 | T | G | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+95A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069795 | |||||||
| chr9:137069796 | T | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+94A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069796 | |||||||
| chr9:137069798 | T | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+92A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069798 | |||||||
| chr9:137069805 | T | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+85A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069805 | |||||||
| chr9:137069812 | G | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+78C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069812 | |||||||
| chr9:137069813 | C | G | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+77G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069813 | |||||||
| chr9:137069816 | C | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+74G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069816 | |||||||
| chr9:137069817 | A | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+73T>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069817 | |||||||
| chr9:137069818 | G | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+72C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069818 | |||||||
| chr9:137069820 | T | G | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+70A>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069820 | |||||||
| chr9:137069822 | T | A | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+68A>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069822 | |||||||
| chr9:137069823 | G | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+67C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069823 | |||||||
| chr9:137069826 | A | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+64T>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069826 | |||||||
| chr9:137069828 | T | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+62A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069828 | |||||||
| chr9:137069829 | G | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+61C>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069829 | |||||||
| chr9:137069834 | T | C | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+56A>G | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069834 | |||||||
| chr9:137069836 | C | G | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+54G>C | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069836 | |||||||
| chr9:137069838 | G | A | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+52C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069838 | |||||||
| chr9:137069838 | G | T | 20 | a0001c0001t0001g0021 a0001c0001t0001g0087 a0001c0001t0001g0090 others(17): Show |
97 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.571+52C>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069838 | |||||||
| chr9:137069841 | C | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+49G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069841 | |||||||
| chr9:137069846 | C | T | 1 | a0002c0002t0003g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.571+44G>A | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069846 | |||||||
| chr9:137069870 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571+20C>T | SAPCD2 | ENSG00000186193.9 | transcript | ENST00000409687.5 | protein_coding | 1/5 | chr9 | 137069870 |