Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5680 |
| ensemblid | ENSG00000243130.8 |
| hgncid | 9516 |
| symbol | PSG11 |
| name | pregnancy specific beta-1-glycoprotein 11 |
| refseq_nuc | NM_002785.3 |
| refseq_prot | NP_002776.3 |
| ensembl_nuc | ENST00000320078.12 |
| ensembl_prot | ENSP00000319140.7 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 43007656 |
| end | 43026469 |
| strand | - |
| ver | v1.2 |
| region | chr19:43007656-43026469 |
| region5000 | chr19:43002656-43031469 |
| regionname0 | PSG11_chr19_43007656_43026469 |
| regionname5000 | PSG11_chr19_43002656_43031469 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 335 | 198 | 49 | 28 | 93 | 11 | 17 | 73 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0002 | 0/0 | 335 | 78 | 4 | 11 | 59 | 0 | 4 | 46 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0003 | 0/1 | 335 | 45 | 12 | 15 | 1 | 4 | 12 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0004 | 1/0 | 335 | 36 | 3 | 18 | 1 | 3 | 10 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0005 | 0/0 | 335 | 21 | 3 | 1 | 15 | 0 | 2 | 11 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0006 | 0/0 | 335 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0007 | 0/0 | 335 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0008 | 0/0 | 335 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0009 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0010 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0011 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0012 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0013 | 0/0 | 335 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| a0014 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | MGPLS others(330): Show |
chr19 | 43002656 | 43031469 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1005 | 179 | 32 | 26 | 93 | 11 | 17 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0001c0006 | 0/0 | 1005 | 14 | 14 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0001c0008 | 0/0 | 1005 | 3 | 2 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0001c0011 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0001c0019 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0002c0002 | 0/0 | 1005 | 78 | 4 | 11 | 59 | 0 | 4 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0003c0003 | 0/1 | 1005 | 44 | 11 | 15 | 1 | 4 | 12 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0003c0018 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0004c0004 | 1/0 | 1005 | 36 | 3 | 18 | 1 | 3 | 10 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0005c0005 | 0/0 | 1005 | 21 | 3 | 1 | 15 | 0 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0006c0007 | 0/0 | 1005 | 13 | 13 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0007c0009 | 0/0 | 1005 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0008c0012 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0009c0015 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0010c0016 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0011c0014 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0012c0017 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0013c0010 | 0/0 | 1005 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 | ||
| a0014c0013 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | ATGGG others(1000): Show |
chr19 | 43002656 | 43031469 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1532 | 171 | 26 | 26 | 92 | 10 | 17 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0001c0001t0003 | 0/0 | 1532 | 2 | 0 | 0 | 1 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0001c0001t0006 | 0/0 | 1532 | 6 | 6 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0001c0006t0004 | 0/0 | 1536 | 13 | 13 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1531): Show |
chr19 | 43002656 | 43031469 |
| a0001c0006t0008 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1531): Show |
chr19 | 43002656 | 43031469 |
| a0001c0008t0004 | 0/0 | 1536 | 3 | 2 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1531): Show |
chr19 | 43002656 | 43031469 |
| a0001c0011t0001 | 0/0 | 1532 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0001c0019t0004 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1531): Show |
chr19 | 43002656 | 43031469 |
| a0002c0002t0001 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0002c0002t0003 | 0/0 | 1532 | 76 | 4 | 11 | 57 | 0 | 4 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0002c0002t0009 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0003c0003t0002 | 0/1 | 1532 | 44 | 11 | 15 | 1 | 4 | 12 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0003c0018t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0004c0004t0002 | 1/0 | 1532 | 36 | 3 | 18 | 1 | 3 | 10 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0005c0005t0001 | 0/0 | 1532 | 21 | 3 | 1 | 15 | 0 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0006c0007t0005 | 0/0 | 1532 | 10 | 10 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0006c0007t0007 | 0/0 | 1531 | 3 | 3 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1526): Show |
chr19 | 43002656 | 43031469 |
| a0007c0009t0002 | 0/0 | 1532 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0008c0012t0001 | 0/0 | 1532 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0009c0015t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0010c0016t0007 | 0/0 | 1531 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1526): Show |
chr19 | 43002656 | 43031469 |
| a0011c0014t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0012c0017t0005 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0013c0010t0001 | 0/0 | 1532 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| a0014c0013t0001 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | AGAAG others(1527): Show |
chr19 | 43002656 | 43031469 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 0 | 5 | 28 | 0 | 4 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 1 | 0 | 3 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 2 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0006t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0008t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0008t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0008t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0011t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0001c0019t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0002 | 0/0 | 29 | 0 | 1 | 26 | 0 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0005 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0002c0002t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0004 | 0/0 | 13 | 1 | 8 | 1 | 1 | 2 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0044 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0003c0018t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0003 | 1/0 | 13 | 1 | 6 | 0 | 0 | 5 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0004c0004t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0007 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0005c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0005g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0006c0007t0007g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0007c0009t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0007c0009t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0008c0012t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0009c0015t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0010c0016t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0011c0014t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0012c0017t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0013c0010t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| a0014c0013t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00099 | hp2 | a0004 | c0004 | t0002 | g0162 | EUR | GBR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0044 | EUR | GBR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0004 | EUR | GBR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00323 | hp1 | a0004 | c0004 | t0002 | g0180 | EUR | FIN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00323 | hp2 | a0004 | c0004 | t0002 | g0181 | EUR | FIN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00438 | hp1 | a0004 | c0004 | t0002 | g0021 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00544 | hp1 | a0005 | c0005 | t0001 | g0138 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00544 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00621 | hp1 | a0002 | c0002 | t0003 | g0200 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00639 | hp1 | a0001 | c0011 | t0001 | g0121 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00639 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0164 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00673 | hp1 | a0002 | c0002 | t0003 | g0214 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00733 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00735 | hp1 | a0004 | c0004 | t0002 | g0040 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00735 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00738 | hp1 | a0001 | c0008 | t0004 | g0053 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01070 | hp2 | a0004 | c0004 | t0002 | g0041 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01074 | hp1 | a0004 | c0004 | t0002 | g0166 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0043 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01106 | hp1 | a0004 | c0004 | t0002 | g0172 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01106 | hp2 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01109 | hp2 | a0004 | c0004 | t0002 | g0041 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01167 | hp1 | a0004 | c0004 | t0002 | g0191 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0163 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01175 | hp1 | a0004 | c0004 | t0002 | g0171 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0038 | AMR | PUR | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01255 | hp1 | a0004 | c0004 | t0002 | g0021 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01256 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01257 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01257 | hp2 | a0004 | c0004 | t0002 | g0046 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01258 | hp1 | a0004 | c0004 | t0002 | g0046 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01433 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0045 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0045 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0048 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01884 | hp2 | a0001 | c0006 | t0004 | g0146 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01891 | hp1 | a0006 | c0007 | t0005 | g0155 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01928 | hp1 | a0008 | c0012 | t0001 | g0082 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01934 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0186 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0047 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01993 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01993 | hp2 | a0004 | c0004 | t0002 | g0190 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02074 | hp1 | a0005 | c0005 | t0001 | g0141 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02074 | hp2 | a0005 | c0005 | t0001 | g0139 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02135 | hp1 | a0005 | c0005 | t0001 | g0143 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CDX | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0195 | EAS | CDX | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02257 | hp1 | a0009 | c0015 | t0001 | g0158 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02257 | hp2 | a0006 | c0007 | t0005 | g0012 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02273 | hp1 | a0004 | c0004 | t0002 | g0170 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02273 | hp2 | a0003 | c0003 | t0002 | g0004 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02280 | hp1 | a0001 | c0006 | t0004 | g0010 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02293 | hp2 | a0003 | c0003 | t0002 | g0182 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02300 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PEL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02451 | hp1 | a0006 | c0007 | t0005 | g0157 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02451 | hp2 | a0001 | c0006 | t0004 | g0151 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02523 | hp1 | a0002 | c0002 | t0003 | g0202 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0189 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02602 | hp1 | a0003 | c0003 | t0002 | g0043 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02615 | hp2 | a0001 | c0006 | t0004 | g0010 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02622 | hp1 | a0007 | c0009 | t0002 | g0193 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0196 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02630 | hp2 | a0003 | c0003 | t0002 | g0178 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02647 | hp1 | a0006 | c0007 | t0007 | g0020 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02683 | hp1 | a0005 | c0005 | t0001 | g0007 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0168 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02698 | hp2 | a0004 | c0004 | t0002 | g0175 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02717 | hp1 | a0001 | c0006 | t0004 | g0010 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02735 | hp1 | a0003 | c0003 | t0002 | g0047 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02738 | hp2 | a0004 | c0004 | t0002 | g0003 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02809 | hp1 | a0007 | c0009 | t0002 | g0192 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02809 | hp2 | a0006 | c0007 | t0007 | g0020 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02818 | hp2 | a0001 | c0008 | t0004 | g0052 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02886 | hp1 | a0006 | c0007 | t0005 | g0159 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02886 | hp2 | a0003 | c0003 | t0002 | g0187 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0049 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0134 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02896 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02897 | hp1 | a0003 | c0003 | t0002 | g0049 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02897 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02922 | hp1 | a0001 | c0006 | t0004 | g0010 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02922 | hp2 | a0006 | c0007 | t0005 | g0012 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02965 | hp2 | a0003 | c0018 | t0001 | g0114 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02970 | hp1 | a0005 | c0005 | t0001 | g0037 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02976 | hp2 | a0001 | c0006 | t0004 | g0010 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03041 | hp2 | a0001 | c0006 | t0008 | g0051 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03139 | hp1 | a0006 | c0007 | t0005 | g0019 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03195 | hp1 | a0001 | c0006 | t0004 | g0150 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03195 | hp2 | a0006 | c0007 | t0005 | g0019 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03225 | hp2 | a0010 | c0016 | t0007 | g0156 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03239 | hp1 | a0004 | c0004 | t0002 | g0021 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03239 | hp2 | a0004 | c0004 | t0002 | g0173 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03453 | hp1 | a0006 | c0007 | t0007 | g0020 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03453 | hp2 | a0005 | c0005 | t0001 | g0038 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03486 | hp2 | a0011 | c0014 | t0001 | g0160 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03491 | hp1 | a0004 | c0004 | t0002 | g0174 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03491 | hp2 | a0003 | c0003 | t0002 | g0004 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03492 | hp2 | a0003 | c0003 | t0002 | g0004 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03516 | hp1 | a0001 | c0006 | t0004 | g0149 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03516 | hp2 | a0012 | c0017 | t0005 | g0154 | AFR | ESN | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03540 | hp2 | a0006 | c0007 | t0005 | g0012 | AFR | GWD | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03579 | hp1 | a0001 | c0006 | t0004 | g0010 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03654 | hp1 | a0004 | c0004 | t0002 | g0003 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03654 | hp2 | a0004 | c0004 | t0002 | g0179 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03704 | hp1 | a0004 | c0004 | t0002 | g0003 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03710 | hp2 | a0004 | c0004 | t0002 | g0003 | SAS | PJL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03831 | hp1 | a0013 | c0010 | t0001 | g0136 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03831 | hp2 | a0003 | c0003 | t0002 | g0177 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03927 | hp1 | a0003 | c0003 | t0002 | g0185 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03927 | hp2 | a0003 | c0003 | t0002 | g0176 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0167 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0165 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04184 | hp2 | a0004 | c0004 | t0002 | g0003 | SAS | BEB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04199 | hp1 | a0002 | c0002 | t0003 | g0204 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04204 | hp1 | a0005 | c0005 | t0001 | g0144 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04228 | hp1 | a0003 | c0003 | t0002 | g0169 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0194 | SAS | STU | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CHB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18906 | hp1 | a0001 | c0006 | t0004 | g0147 | AFR | YRI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0207 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18948 | hp1 | a0014 | c0013 | t0001 | g0083 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18948 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18949 | hp1 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18949 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0209 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18963 | hp1 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18972 | hp1 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18973 | hp1 | a0002 | c0002 | t0003 | g0208 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18975 | hp2 | a0002 | c0002 | t0009 | g0197 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18983 | hp1 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18985 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18988 | hp2 | a0005 | c0005 | t0001 | g0142 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18991 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18993 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19001 | hp2 | a0005 | c0005 | t0001 | g0135 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19005 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19009 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0199 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19030 | hp2 | a0003 | c0003 | t0002 | g0048 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0188 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19054 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0024 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19060 | hp1 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19062 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19063 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19075 | hp1 | a0005 | c0005 | t0001 | g0145 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19076 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19083 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19084 | hp2 | a0005 | c0005 | t0001 | g0007 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19086 | hp2 | a0002 | c0002 | t0003 | g0198 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19240 | hp1 | a0001 | c0019 | t0004 | g0152 | AFR | YRI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA19240 | hp2 | a0006 | c0007 | t0005 | g0019 | AFR | YRI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20129 | hp1 | a0004 | c0004 | t0002 | g0040 | AFR | ASW | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | ASW | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | TSI | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0002 | SAS | GIH | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0183 | AMR | CLM | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02109 | hp1 | a0001 | c0006 | t0004 | g0148 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02486 | hp1 | a0006 | c0007 | t0005 | g0012 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0004 | AFR | ACB | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | MSL | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG06807 | hp1 | a0001 | c0008 | t0004 | g0054 | AFR | USA | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| HG06807 | hp2 | a0004 | c0004 | t0002 | g0003 | AFR | USA | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20300 | hp1 | a0005 | c0005 | t0001 | g0037 | AFR | USA | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA20300 | hp2 | a0001 | c0006 | t0004 | g0153 | AFR | USA | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| NA21309 | hp2 | a0004 | c0004 | t0002 | g0161 | AFR | LWK | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0044 | REF | REF | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0002 | g0003 | REF | REF | PSG11_chr19_43002656_43031469 | PSG11 | chr19 | 43002656 | 43031469 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43015118 | A | G | 2 | a0005 a0013 |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
missense_variant&splice_region_variant | MODERATE | c.962T>C | p.Ile321Thr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/6 | 1059/1532 | 962/1008 | 321/335 | chr19 | 43015118 | |||
| chr19:43015152 | C | T | 3 | a0006 a0010 a0012 |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
missense_variant | MODERATE | c.928G>A | p.Glu310Lys | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/6 | 1025/1532 | 928/1008 | 310/335 | chr19 | 43015152 | |||
| chr19:43015290 | T | C | 13 | a0001 a0002 a0003 others(10): Show |
363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
missense_variant | MODERATE | c.790A>G | p.Asn264Asp | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/6 | 887/1532 | 790/1008 | 264/335 | chr19 | 43015290 | |||
| chr19:43015293 | C | T | 1 | a0013 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.787G>A | p.Ala263Thr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/6 | 884/1532 | 787/1008 | 263/335 | chr19 | 43015293 | |||
| chr19:43018807 | A | C | 1 | a0014 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.672T>G | p.Ser224Arg | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/6 | 769/1532 | 672/1008 | 224/335 | chr19 | 43018807 | |||
| chr19:43018815 | A | T | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.664T>A | p.Ser222Thr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/6 | 761/1532 | 664/1008 | 222/335 | chr19 | 43018815 | |||
| chr19:43018821 | A | G | 1 | a0008 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.658T>C | p.Trp220Arg | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/6 | 755/1532 | 658/1008 | 220/335 | chr19 | 43018821 | |||
| chr19:43024732 | C | T | 1 | a0012 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.389G>A | p.Gly130Glu | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 486/1532 | 389/1008 | 130/335 | chr19 | 43024732 | |||
| chr19:43024741 | C | T | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.380G>A | p.Arg127Gln | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 477/1532 | 380/1008 | 127/335 | chr19 | 43024741 | |||
| chr19:43024772 | C | T | 1 | a0010 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.349G>A | p.Ala117Thr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 446/1532 | 349/1008 | 117/335 | chr19 | 43024772 | |||
| chr19:43024780 | C | T | 4 | a0005 a0009 a0011 others(1): Show |
24 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(21): Show |
missense_variant | MODERATE | c.341G>A | p.Arg114Gln | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 438/1532 | 341/1008 | 114/335 | chr19 | 43024780 | |||
| chr19:43024819 | A | G | 1 | a0007 | 2 | HG02622.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.302T>C | p.Val101Ala | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 399/1532 | 302/1008 | 101/335 | chr19 | 43024819 | |||
| chr19:43024874 | C | T | 6 | a0001 a0002 a0005 others(3): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
missense_variant | MODERATE | c.247G>A | p.Val83Ile | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 344/1532 | 247/1008 | 83/335 | chr19 | 43024874 | |||
| chr19:43026321 | G | C | 1 | a0002 | 78 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
missense_variant | MODERATE | c.52C>G | p.Leu18Val | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/6 | 149/1532 | 52/1008 | 18/335 | chr19 | 43026321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43015210 | C | T | 11 | a0001c0001 a0001c0006 a0001c0008 others(8): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
synonymous_variant | LOW | c.870G>A | p.Gln290Gln | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/6 | 967/1532 | 870/1008 | 290/335 | chr19 | 43015210 | |||
| chr19:43018869 | G | A | 1 | a0001c0019 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.610C>T | p.Leu204Leu | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/6 | 707/1532 | 610/1008 | 204/335 | chr19 | 43018869 | |||
| chr19:43018957 | C | T | 1 | a0001c0011 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.522G>A | p.Pro174Pro | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/6 | 619/1532 | 522/1008 | 174/335 | chr19 | 43018957 | |||
| chr19:43024773 | G | A | 2 | a0009c0015 a0011c0014 |
2 | HG02257.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.348C>T | p.Asp116Asp | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 445/1532 | 348/1008 | 116/335 | chr19 | 43024773 | |||
| chr19:43024782 | G | T | 2 | a0009c0015 a0011c0014 |
2 | HG02257.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.339C>A | p.Thr113Thr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 436/1532 | 339/1008 | 113/335 | chr19 | 43024782 | |||
| chr19:43024875 | A | G | 10 | a0001c0001 a0001c0006 a0001c0008 others(7): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
synonymous_variant | LOW | c.246T>C | p.Tyr82Tyr | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 343/1532 | 246/1008 | 82/335 | chr19 | 43024875 | |||
| chr19:43024983 | G | A | 3 | a0001c0006 a0001c0008 a0001c0019 |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
synonymous_variant | LOW | c.138C>T | p.Ser46Ser | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/6 | 235/1532 | 138/1008 | 46/335 | chr19 | 43024983 | |||
| chr19:43026340 | C | T | 1 | a0001c0008 | 3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.33G>A | p.Glu11Glu | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/6 | 130/1532 | 33/1008 | 11/335 | chr19 | 43026340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43007702 | T | C | 4 | a0001c0006t0004 a0001c0006t0008 a0001c0008t0004 others(1): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2296 | chr19 | 43007702 | ||||||
| chr19:43007729 | C | CAGAT | 4 | a0001c0006t0004 a0001c0006t0008 a0001c0008t0004 others(1): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*353_*354insATCT | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2268 | chr19 | 43007729 | ||||||
| chr19:43007742 | C | G | 4 | a0001c0006t0004 a0001c0006t0008 a0001c0008t0004 others(1): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2256 | chr19 | 43007742 | ||||||
| chr19:43007814 | G | A | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(15): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*269C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2184 | chr19 | 43007814 | ||||||
| chr19:43007825 | C | A | 3 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0009 |
79 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2173 | chr19 | 43007825 | ||||||
| chr19:43007835 | GC | G | 2 | a0006c0007t0007 a0010c0016t0007 |
4 | HG02647.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*247delG | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2162 | chr19 | 43007835 | ||||||
| chr19:43007843 | T | C | 1 | a0001c0001t0006 | 6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*240A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2155 | chr19 | 43007843 | ||||||
| chr19:43007918 | T | A | 1 | a0002c0002t0009 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2080 | chr19 | 43007918 | ||||||
| chr19:43007948 | C | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(19): Show |
318 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 6/6 | 2050 | chr19 | 43007948 | ||||||
| chr19:43026374 | A | G | 1 | a0001c0006t0008 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/6 | 2 | chr19 | 43026374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43008279 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.*41-237A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008279 | |||||||
| chr19:43008283 | T | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0101 |
2 | NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.*41-241A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008283 | |||||||
| chr19:43008314 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.*41-272G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008314 | |||||||
| chr19:43008337 | A | G | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*41-295T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008337 | |||||||
| chr19:43008610 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0131 |
5 | HG01123.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.*41-568A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008610 | |||||||
| chr19:43008765 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.*41-723C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008765 | |||||||
| chr19:43008931 | G | A | 7 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(4): Show |
12 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.*41-889C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008931 | |||||||
| chr19:43008931 | G | C | 1 | a0012c0017t0005g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*41-889C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008931 | |||||||
| chr19:43008978 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.*41-936A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43008978 | |||||||
| chr19:43009115 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(156): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.*40+843C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009115 | |||||||
| chr19:43009210 | T | C | 1 | a0001c0006t0004g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*40+748A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009210 | |||||||
| chr19:43009261 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.*40+697T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009261 | |||||||
| chr19:43009262 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.*40+696G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009262 | |||||||
| chr19:43009280 | G | A | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.*40+678C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009280 | |||||||
| chr19:43009282 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.*40+676C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009282 | |||||||
| chr19:43009424 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0081 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.*40+534C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009424 | |||||||
| chr19:43009470 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.*40+488C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009470 | |||||||
| chr19:43009507 | T | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(31): Show |
89 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.*40+451A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009507 | |||||||
| chr19:43009548 | T | C | 2 | a0004c0004t0002g0175 a0004c0004t0002g0179 |
2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.*40+410A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009548 | |||||||
| chr19:43009556 | A | T | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*40+402T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009556 | |||||||
| chr19:43009569 | G | A | 1 | a0001c0001t0006g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*40+389C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009569 | |||||||
| chr19:43009571 | T | C | 1 | a0001c0001t0006g0132 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*40+387A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009571 | |||||||
| chr19:43009584 | C | G | 1 | a0002c0002t0003g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*40+374G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009584 | |||||||
| chr19:43009618 | A | T | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*40+340T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009618 | |||||||
| chr19:43009651 | A | T | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*40+307T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009651 | |||||||
| chr19:43009654 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.*40+304C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009654 | |||||||
| chr19:43009669 | G | T | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*40+289C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009669 | |||||||
| chr19:43009670 | A | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0067 a0001c0001t0001g0093 |
4 | HG01891.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.*40+288T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009670 | |||||||
| chr19:43009770 | A | C | 1 | a0002c0002t0003g0207 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.*40+188T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009770 | |||||||
| chr19:43009829 | G | T | 1 | a0002c0002t0003g0205 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.*40+129C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009829 | |||||||
| chr19:43009865 | C | G | 1 | a0001c0001t0006g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40+93G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009865 | |||||||
| chr19:43009869 | G | T | 1 | a0001c0001t0006g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*40+89C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009869 | |||||||
| chr19:43009943 | A | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.*40+15T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009943 | |||||||
| chr19:43009949 | T | C | 1 | a0002c0002t0003g0210 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.*40+9A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 5/5 | chr19 | 43009949 | |||||||
| chr19:43010048 | T | C | 1 | a0002c0002t0003g0202 | 1 | HG02523.hp1 | splice_region_variant&intron_variant | LOW | c.965-7A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010048 | |||||||
| chr19:43010080 | T | C | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.965-39A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010080 | |||||||
| chr19:43010128 | A | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0213 |
8 | NA18948.hp2 NA18949.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-87T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010128 | |||||||
| chr19:43010209 | T | C | 2 | a0004c0004t0002g0046 a0004c0004t0002g0166 |
3 | HG01074.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.965-168A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010209 | |||||||
| chr19:43010292 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.965-251C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010292 | |||||||
| chr19:43010313 | T | A | 1 | a0001c0019t0004g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.965-272A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010313 | |||||||
| chr19:43010354 | G | T | 1 | a0003c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965-313C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010354 | |||||||
| chr19:43010367 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.965-326A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010367 | |||||||
| chr19:43010395 | A | T | 1 | a0002c0002t0003g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.965-354T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010395 | |||||||
| chr19:43010400 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.965-359C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010400 | |||||||
| chr19:43010425 | G | C | 1 | a0001c0006t0004g0147 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.965-384C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010425 | |||||||
| chr19:43010544 | C | G | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.965-503G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010544 | |||||||
| chr19:43010555 | G | T | 1 | a0003c0003t0002g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.965-514C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010555 | |||||||
| chr19:43010562 | G | A | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-521C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010562 | |||||||
| chr19:43010569 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.965-528C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010569 | |||||||
| chr19:43010573 | G | A | 7 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(4): Show |
12 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-532C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010573 | |||||||
| chr19:43010610 | T | A | 6 | a0004c0004t0002g0046 a0004c0004t0002g0166 a0004c0004t0002g0171 others(3): Show |
7 | HG00323.hp1 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-569A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010610 | |||||||
| chr19:43010693 | C | T | 8 | a0006c0007t0005g0012 a0006c0007t0005g0019 a0006c0007t0005g0155 others(5): Show |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.965-652G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010693 | |||||||
| chr19:43010694 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.965-653G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010694 | |||||||
| chr19:43010702 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18964.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.965-661G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010702 | |||||||
| chr19:43010760 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.965-719G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010760 | |||||||
| chr19:43010761 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.965-720C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010761 | |||||||
| chr19:43010804 | T | C | 1 | a0012c0017t0005g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.965-763A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010804 | |||||||
| chr19:43010890 | C | CAT | 12 | a0003c0003t0002g0044 a0003c0003t0002g0165 a0003c0003t0002g0183 others(9): Show |
17 | HG00140.hp1 HG01123.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.965-851_965-850dup others(2): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | C | CATAT | 4 | a0003c0003t0002g0189 a0006c0007t0005g0155 a0006c0007t0007g0020 others(1): Show |
6 | HG01891.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-853_965-850dup others(4): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | C | CATATATA others(3): Show |
1 | a0007c0009t0002g0193 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.965-859_965-850dup others(10): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | C | CATATATA others(9): Show |
1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.965-865_965-850dup others(16): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | CAT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(87): Show |
201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.965-851_965-850del others(2): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | CATAT | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(29): Show |
57 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.965-853_965-850del others(4): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010890 | CATATAT | C | 16 | a0001c0001t0001g0061 a0001c0001t0001g0125 a0001c0001t0006g0035 others(13): Show |
22 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.965-855_965-850del others(6): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010890 | |||||||
| chr19:43010905 | A | G | 1 | a0001c0006t0008g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.965-864T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010905 | |||||||
| chr19:43010939 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.965-898C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010939 | |||||||
| chr19:43010977 | A | C | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.965-936T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43010977 | |||||||
| chr19:43011002 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.965-961T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011002 | |||||||
| chr19:43011116 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(156): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.965-1075C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011116 | |||||||
| chr19:43011174 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.965-1133T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011174 | |||||||
| chr19:43011320 | G | C | 1 | a0003c0003t0002g0044 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.965-1279C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011320 | |||||||
| chr19:43011365 | C | T | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.965-1324G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011365 | |||||||
| chr19:43011701 | C | T | 1 | a0002c0002t0003g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.965-1660G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011701 | |||||||
| chr19:43011750 | G | A | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.965-1709C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011750 | |||||||
| chr19:43011750 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(74): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.965-1709C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011750 | |||||||
| chr19:43011754 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.965-1713C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011754 | |||||||
| chr19:43011756 | T | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(31): Show |
89 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.965-1715A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011756 | |||||||
| chr19:43011841 | T | C | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.965-1800A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011841 | |||||||
| chr19:43011903 | T | TA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(80): Show |
147 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.965-1863dupT | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011903 | |||||||
| chr19:43011932 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.965-1891G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011932 | |||||||
| chr19:43011947 | A | C | 6 | a0001c0001t0001g0122 a0001c0001t0006g0035 a0001c0001t0006g0132 others(3): Show |
7 | HG01243.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-1906T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011947 | |||||||
| chr19:43011976 | T | G | 1 | a0006c0007t0005g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.965-1935A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011976 | |||||||
| chr19:43011990 | C | T | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.965-1949G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43011990 | |||||||
| chr19:43012106 | T | C | 1 | a0003c0003t0002g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.965-2065A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012106 | |||||||
| chr19:43012177 | C | A | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.965-2136G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012177 | |||||||
| chr19:43012215 | A | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0011t0001g0121 |
5 | HG00639.hp1 HG01243.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-2174T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012215 | |||||||
| chr19:43012225 | C | T | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.965-2184G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012225 | |||||||
| chr19:43012269 | A | G | 1 | a0002c0002t0009g0197 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.965-2228T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012269 | |||||||
| chr19:43012319 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.965-2278T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012319 | |||||||
| chr19:43012356 | A | C | 2 | a0003c0003t0002g0049 a0003c0003t0002g0189 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.965-2315T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012356 | |||||||
| chr19:43012414 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(165): Show |
318 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.965-2373A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012414 | |||||||
| chr19:43012476 | A | T | 1 | a0001c0006t0004g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.965-2435T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012476 | |||||||
| chr19:43012561 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0131 |
5 | HG01123.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-2520T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012561 | |||||||
| chr19:43012574 | A | ATAAGTT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(143): Show |
279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.965-2534_965-2533i others(8): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012574 | |||||||
| chr19:43012583 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.964+2533C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012583 | |||||||
| chr19:43012639 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.964+2477T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012639 | |||||||
| chr19:43012652 | G | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(188): Show |
358 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.964+2464C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012652 | |||||||
| chr19:43012659 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.964+2457G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012659 | |||||||
| chr19:43012676 | T | C | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.964+2440A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012676 | |||||||
| chr19:43012775 | G | C | 2 | a0003c0003t0002g0049 a0003c0003t0002g0189 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.964+2341C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012775 | |||||||
| chr19:43012776 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.964+2340T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012776 | |||||||
| chr19:43012863 | G | C | 8 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(5): Show |
13 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+2253C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012863 | |||||||
| chr19:43012910 | G | C | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.964+2206C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012910 | |||||||
| chr19:43012958 | G | A | 2 | a0004c0004t0002g0175 a0004c0004t0002g0179 |
2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964+2158C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012958 | |||||||
| chr19:43012958 | G | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964+2158C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012958 | |||||||
| chr19:43012991 | T | C | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.964+2125A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43012991 | |||||||
| chr19:43013049 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.964+2067T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013049 | |||||||
| chr19:43013094 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.964+2022G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013094 | |||||||
| chr19:43013252 | C | T | 2 | a0001c0008t0004g0052 a0001c0008t0004g0053 |
2 | HG00738.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.964+1864G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013252 | |||||||
| chr19:43013312 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(74): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.964+1804T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013312 | |||||||
| chr19:43013511 | C | T | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.964+1605G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013511 | |||||||
| chr19:43013538 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.964+1578T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013538 | |||||||
| chr19:43013572 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(125): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.964+1544T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013572 | |||||||
| chr19:43013574 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(125): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.964+1542T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013574 | |||||||
| chr19:43013598 | T | C | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964+1518A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013598 | |||||||
| chr19:43013601 | C | A | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964+1515G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013601 | |||||||
| chr19:43013672 | T | A | 1 | a0001c0006t0004g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964+1444A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013672 | |||||||
| chr19:43013690 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.964+1426G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013690 | |||||||
| chr19:43013875 | C | A | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.964+1241G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013875 | |||||||
| chr19:43013907 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0116 |
3 | HG00280.hp2 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964+1209A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013907 | |||||||
| chr19:43013935 | A | C | 1 | a0005c0005t0001g0135 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.964+1181T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013935 | |||||||
| chr19:43013961 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.964+1155A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013961 | |||||||
| chr19:43013972 | A | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+1144T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013972 | |||||||
| chr19:43013976 | A | G | 1 | a0002c0002t0003g0202 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.964+1140T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013976 | |||||||
| chr19:43013991 | A | G | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.964+1125T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43013991 | |||||||
| chr19:43014101 | A | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+1015T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014101 | |||||||
| chr19:43014260 | T | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+856A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014260 | |||||||
| chr19:43014298 | T | C | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964+818A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014298 | |||||||
| chr19:43014394 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.964+722G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014394 | |||||||
| chr19:43014425 | A | G | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964+691T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014425 | |||||||
| chr19:43014459 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.964+657A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014459 | |||||||
| chr19:43014502 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0093 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.964+614G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014502 | |||||||
| chr19:43014688 | C | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+428G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014688 | |||||||
| chr19:43014713 | C | T | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+403G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014713 | |||||||
| chr19:43014790 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.964+326T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014790 | |||||||
| chr19:43014814 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.964+302G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014814 | |||||||
| chr19:43014869 | G | A | 4 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 others(1): Show |
4 | HG00738.hp1 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+247C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014869 | |||||||
| chr19:43014943 | A | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.964+173T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014943 | |||||||
| chr19:43014958 | C | G | 1 | a0004c0004t0002g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.964+158G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014958 | |||||||
| chr19:43014973 | G | A | 8 | a0006c0007t0005g0012 a0006c0007t0005g0019 a0006c0007t0005g0155 others(5): Show |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.964+143C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014973 | |||||||
| chr19:43014996 | G | A | 3 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 |
3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.964+120C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43014996 | |||||||
| chr19:43015109 | C | T | 4 | a0003c0003t0002g0165 a0003c0003t0002g0176 a0003c0003t0002g0184 others(1): Show |
4 | HG03669.hp1 HG03927.hp1 HG03927.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.964+7G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 4/5 | chr19 | 43015109 | |||||||
| chr19:43015421 | A | T | 1 | a0002c0002t0003g0201 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.710-51T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015421 | |||||||
| chr19:43015441 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02976.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.710-71C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015441 | |||||||
| chr19:43015551 | T | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-181A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015551 | |||||||
| chr19:43015583 | C | G | 1 | a0001c0006t0004g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.710-213G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015583 | |||||||
| chr19:43015621 | A | G | 1 | a0002c0002t0003g0022 | 3 | HG02723.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.710-251T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015621 | |||||||
| chr19:43015678 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.710-308C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015678 | |||||||
| chr19:43015720 | G | A | 1 | a0001c0006t0008g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.710-350C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015720 | |||||||
| chr19:43015732 | G | A | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.710-362C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015732 | |||||||
| chr19:43015739 | T | G | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.710-369A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015739 | |||||||
| chr19:43015783 | G | C | 1 | a0001c0006t0008g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.710-413C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015783 | |||||||
| chr19:43015817 | C | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.710-447G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015817 | |||||||
| chr19:43015838 | C | T | 1 | a0005c0005t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.710-468G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015838 | |||||||
| chr19:43015870 | G | C | 4 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 others(1): Show |
4 | HG00738.hp1 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-500C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015870 | |||||||
| chr19:43015926 | A | C | 1 | a0001c0008t0004g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.710-556T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43015926 | |||||||
| chr19:43016052 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(136): Show |
276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.710-682C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016052 | |||||||
| chr19:43016146 | C | T | 34 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(31): Show |
89 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.710-776G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016146 | |||||||
| chr19:43016169 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.710-799C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016169 | |||||||
| chr19:43016294 | A | G | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-924T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016294 | |||||||
| chr19:43016314 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-944G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016314 | |||||||
| chr19:43016322 | CT | C | 1 | a0001c0001t0001g0014 | 3 | NA18968.hp1 NA18973.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.710-953delA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016322 | |||||||
| chr19:43016324 | G | A | 1 | a0001c0001t0001g0014 | 3 | NA18968.hp1 NA18973.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.710-954C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016324 | |||||||
| chr19:43016328 | C | T | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.710-958G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016328 | |||||||
| chr19:43016345 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(125): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.710-975T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016345 | |||||||
| chr19:43016355 | G | C | 17 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(14): Show |
28 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-985C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016355 | |||||||
| chr19:43016358 | T | C | 1 | a0004c0004t0002g0179 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.710-988A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016358 | |||||||
| chr19:43016435 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.710-1065G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016435 | |||||||
| chr19:43016474 | A | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.710-1104T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016474 | |||||||
| chr19:43016485 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(152): Show |
293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.710-1115G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016485 | |||||||
| chr19:43016572 | C | G | 1 | a0004c0004t0002g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.710-1202G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016572 | |||||||
| chr19:43016577 | G | A | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.710-1207C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016577 | |||||||
| chr19:43016696 | G | A | 1 | a0005c0005t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.710-1326C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016696 | |||||||
| chr19:43016702 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(156): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.710-1332G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016702 | |||||||
| chr19:43016717 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0119 |
4 | NA18981.hp1 NA19001.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-1347T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016717 | |||||||
| chr19:43016724 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.710-1354C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016724 | |||||||
| chr19:43016747 | G | C | 1 | a0002c0002t0003g0207 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.710-1377C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016747 | |||||||
| chr19:43016813 | G | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-1443C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016813 | |||||||
| chr19:43016920 | T | A | 4 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 others(1): Show |
4 | HG00738.hp1 HG02818.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-1550A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016920 | |||||||
| chr19:43016928 | A | G | 2 | a0001c0001t0001g0066 a0003c0003t0002g0168 |
2 | HG02698.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.710-1558T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43016928 | |||||||
| chr19:43017032 | C | A | 1 | a0001c0001t0006g0035 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.710-1662G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017032 | |||||||
| chr19:43017042 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.710-1672T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017042 | |||||||
| chr19:43017044 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.710-1674C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017044 | |||||||
| chr19:43017080 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.709+1690C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017080 | |||||||
| chr19:43017171 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.709+1599C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017171 | |||||||
| chr19:43017177 | G | T | 1 | a0004c0004t0002g0046 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.709+1593C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017177 | |||||||
| chr19:43017246 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.709+1524T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017246 | |||||||
| chr19:43017365 | A | C | 1 | a0002c0002t0003g0050 | 2 | NA18952.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.709+1405T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017365 | |||||||
| chr19:43017383 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0086 |
2 | NA18984.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.709+1387G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017383 | |||||||
| chr19:43017426 | G | C | 2 | a0003c0003t0002g0044 a0003c0003t0002g0169 |
2 | HG00140.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.709+1344C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017426 | |||||||
| chr19:43017443 | C | T | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.709+1327G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017443 | |||||||
| chr19:43017444 | G | A | 3 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 |
3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.709+1326C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017444 | |||||||
| chr19:43017556 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0106 |
2 | NA18940.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.709+1214C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017556 | |||||||
| chr19:43017599 | T | A | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.709+1171A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017599 | |||||||
| chr19:43017621 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.709+1149T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017621 | |||||||
| chr19:43017641 | A | C | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.709+1129T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017641 | |||||||
| chr19:43017646 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.709+1124T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017646 | |||||||
| chr19:43017655 | G | T | 2 | a0001c0001t0001g0073 a0001c0006t0004g0149 |
2 | HG02735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.709+1115C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017655 | |||||||
| chr19:43017662 | A | G | 2 | a0001c0001t0001g0073 a0001c0006t0004g0149 |
2 | HG02735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.709+1108T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017662 | |||||||
| chr19:43017664 | T | G | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.709+1106A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017664 | |||||||
| chr19:43017739 | A | G | 1 | a0003c0003t0002g0045 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.709+1031T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017739 | |||||||
| chr19:43017747 | G | A | 1 | a0003c0003t0002g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.709+1023C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017747 | |||||||
| chr19:43017747 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02976.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.709+1023C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017747 | |||||||
| chr19:43017762 | A | T | 1 | a0003c0003t0002g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.709+1008T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017762 | |||||||
| chr19:43017769 | T | C | 1 | a0003c0003t0002g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.709+1001A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017769 | |||||||
| chr19:43017868 | T | C | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.709+902A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43017868 | |||||||
| chr19:43018026 | T | G | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.709+744A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018026 | |||||||
| chr19:43018088 | G | T | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.709+682C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018088 | |||||||
| chr19:43018143 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.709+627T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018143 | |||||||
| chr19:43018165 | T | C | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+605A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018165 | |||||||
| chr19:43018187 | C | T | 7 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(4): Show |
12 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.709+583G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018187 | |||||||
| chr19:43018215 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(154): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.709+555A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018215 | |||||||
| chr19:43018218 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.709+552C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018218 | |||||||
| chr19:43018252 | C | G | 1 | a0004c0004t0002g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.709+518G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018252 | |||||||
| chr19:43018252 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.709+518G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018252 | |||||||
| chr19:43018276 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.709+494T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018276 | |||||||
| chr19:43018357 | G | A | 1 | a0007c0009t0002g0193 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.709+413C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018357 | |||||||
| chr19:43018383 | A | C | 3 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 |
3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.709+387T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018383 | |||||||
| chr19:43018397 | T | C | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.709+373A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018397 | |||||||
| chr19:43018398 | G | A | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.709+372C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018398 | |||||||
| chr19:43018399 | A | C | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.709+371T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018399 | |||||||
| chr19:43018400 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.709+370G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018400 | |||||||
| chr19:43018555 | C | G | 1 | a0003c0003t0002g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.709+215G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018555 | |||||||
| chr19:43018592 | C | T | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+178G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018592 | |||||||
| chr19:43018594 | C | T | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+176G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018594 | |||||||
| chr19:43018598 | G | T | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+172C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018598 | |||||||
| chr19:43018602 | C | G | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+168G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018602 | |||||||
| chr19:43018612 | C | T | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+158G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018612 | |||||||
| chr19:43018618 | G | C | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+152C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018618 | |||||||
| chr19:43018626 | T | C | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+144A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018626 | |||||||
| chr19:43018635 | G | C | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+135C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018635 | |||||||
| chr19:43018663 | T | G | 1 | a0002c0002t0003g0208 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.709+107A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018663 | |||||||
| chr19:43018702 | A | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0129 |
3 | HG02717.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.709+68T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018702 | |||||||
| chr19:43018741 | T | C | 1 | a0001c0019t0004g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.709+29A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018741 | |||||||
| chr19:43018744 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+26G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018744 | |||||||
| chr19:43018759 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.709+11T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 3/5 | chr19 | 43018759 | |||||||
| chr19:43019077 | C | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-29G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019077 | |||||||
| chr19:43019203 | T | C | 2 | a0004c0004t0002g0040 a0004c0004t0002g0162 |
3 | HG00099.hp2 HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.431-155A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019203 | |||||||
| chr19:43019274 | T | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
33 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.431-226A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019274 | |||||||
| chr19:43019284 | C | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-236G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019284 | |||||||
| chr19:43019327 | G | C | 2 | a0004c0004t0002g0040 a0004c0004t0002g0162 |
3 | HG00099.hp2 HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.431-279C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019327 | |||||||
| chr19:43019348 | A | G | 4 | a0006c0007t0005g0012 a0006c0007t0005g0019 a0006c0007t0005g0155 others(1): Show |
9 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-300T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019348 | |||||||
| chr19:43019384 | G | C | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431-336C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019384 | |||||||
| chr19:43019467 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.431-419C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019467 | |||||||
| chr19:43019562 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.431-514C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019562 | |||||||
| chr19:43019621 | C | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG01891.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-573G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019621 | |||||||
| chr19:43019635 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.431-587C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019635 | |||||||
| chr19:43019653 | C | T | 1 | a0001c0019t0004g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-605G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019653 | |||||||
| chr19:43019663 | C | G | 2 | a0002c0002t0003g0200 a0005c0005t0001g0142 |
2 | HG00621.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.431-615G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019663 | |||||||
| chr19:43019732 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-684G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019732 | |||||||
| chr19:43019740 | A | G | 10 | a0005c0005t0001g0007 a0005c0005t0001g0135 a0005c0005t0001g0138 others(7): Show |
18 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.431-692T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019740 | |||||||
| chr19:43019749 | C | A | 1 | a0001c0006t0004g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-701G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019749 | |||||||
| chr19:43019754 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.431-706T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019754 | |||||||
| chr19:43019829 | A | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-781T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019829 | |||||||
| chr19:43019845 | A | G | 1 | a0001c0006t0004g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.431-797T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019845 | |||||||
| chr19:43019863 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.431-815C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019863 | |||||||
| chr19:43019889 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.431-841T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019889 | |||||||
| chr19:43019991 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(172): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.431-943C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43019991 | |||||||
| chr19:43020000 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.431-952G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020000 | |||||||
| chr19:43020001 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(172): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.431-953G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020001 | |||||||
| chr19:43020066 | G | A | 1 | a0001c0006t0004g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.431-1018C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020066 | |||||||
| chr19:43020117 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.431-1069C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020117 | |||||||
| chr19:43020146 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0131 |
5 | HG01123.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-1098C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020146 | |||||||
| chr19:43020153 | T | A | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.431-1105A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020153 | |||||||
| chr19:43020165 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-1117G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020165 | |||||||
| chr19:43020174 | A | C | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-1126T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020174 | |||||||
| chr19:43020225 | A | C | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-1177T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020225 | |||||||
| chr19:43020277 | C | T | 2 | a0001c0006t0004g0150 a0001c0006t0004g0151 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.431-1229G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020277 | |||||||
| chr19:43020374 | A | G | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431-1326T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020374 | |||||||
| chr19:43020422 | A | T | 1 | a0001c0019t0004g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-1374T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020422 | |||||||
| chr19:43020474 | T | G | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-1426A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020474 | |||||||
| chr19:43020522 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.431-1474T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020522 | |||||||
| chr19:43020603 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.431-1555G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020603 | |||||||
| chr19:43020616 | T | G | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-1568A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020616 | |||||||
| chr19:43020626 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.431-1578T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020626 | |||||||
| chr19:43020638 | A | G | 8 | a0005c0005t0001g0007 a0005c0005t0001g0135 a0005c0005t0001g0138 others(5): Show |
16 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.431-1590T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020638 | |||||||
| chr19:43020646 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(154): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.431-1598T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020646 | |||||||
| chr19:43020678 | T | G | 1 | a0006c0007t0005g0019 | 3 | HG03139.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.431-1630A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020678 | |||||||
| chr19:43020687 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-1639G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020687 | |||||||
| chr19:43020738 | A | G | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-1690T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020738 | |||||||
| chr19:43020752 | A | G | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1704T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020752 | |||||||
| chr19:43020815 | T | C | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1767A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020815 | |||||||
| chr19:43020835 | C | CAG | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1789_431-1788d others(4): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020835 | |||||||
| chr19:43020874 | G | C | 1 | a0004c0004t0002g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.431-1826C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020874 | |||||||
| chr19:43020895 | G | C | 2 | a0001c0001t0006g0133 a0004c0004t0002g0181 |
2 | HG00323.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.431-1847C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43020895 | |||||||
| chr19:43021027 | C | G | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.431-1979G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021027 | |||||||
| chr19:43021053 | A | G | 2 | a0004c0004t0002g0170 a0004c0004t0002g0190 |
2 | HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.431-2005T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021053 | |||||||
| chr19:43021076 | C | T | 1 | a0001c0001t0006g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.431-2028G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021076 | |||||||
| chr19:43021085 | A | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0130 |
4 | HG01123.hp1 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-2037T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021085 | |||||||
| chr19:43021085 | A | G | 1 | a0001c0006t0008g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.431-2037T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021085 | |||||||
| chr19:43021088 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(172): Show |
327 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.431-2040T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021088 | |||||||
| chr19:43021283 | C | T | 1 | a0003c0003t0002g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.431-2235G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021283 | |||||||
| chr19:43021316 | T | C | 1 | a0001c0006t0004g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.431-2268A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021316 | |||||||
| chr19:43021328 | C | T | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.431-2280G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021328 | |||||||
| chr19:43021409 | T | G | 5 | a0003c0003t0002g0004 a0003c0003t0002g0163 a0003c0003t0002g0164 others(2): Show |
17 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.431-2361A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021409 | |||||||
| chr19:43021527 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.431-2479T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021527 | |||||||
| chr19:43021550 | A | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-2502T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021550 | |||||||
| chr19:43021651 | A | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-2603T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021651 | |||||||
| chr19:43021652 | A | G | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-2604T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021652 | |||||||
| chr19:43021771 | G | T | 3 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 |
3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.431-2723C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021771 | |||||||
| chr19:43021785 | T | A | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.431-2737A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021785 | |||||||
| chr19:43021926 | A | G | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430+2765T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021926 | |||||||
| chr19:43021967 | C | T | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+2724G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021967 | |||||||
| chr19:43021969 | C | T | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430+2722G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43021969 | |||||||
| chr19:43022034 | G | A | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.430+2657C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022034 | |||||||
| chr19:43022074 | A | G | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.430+2617T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022074 | |||||||
| chr19:43022115 | A | G | 1 | a0005c0005t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.430+2576T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022115 | |||||||
| chr19:43022248 | A | T | 1 | a0004c0004t0002g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.430+2443T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022248 | |||||||
| chr19:43022260 | C | T | 6 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(3): Show |
11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+2431G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022260 | |||||||
| chr19:43022349 | C | A | 8 | a0006c0007t0005g0012 a0006c0007t0005g0019 a0006c0007t0005g0155 others(5): Show |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+2342G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022349 | |||||||
| chr19:43022499 | T | C | 3 | a0001c0008t0004g0052 a0001c0008t0004g0053 a0001c0008t0004g0054 |
3 | HG00738.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.430+2192A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022499 | |||||||
| chr19:43022579 | A | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.430+2112T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022579 | |||||||
| chr19:43022608 | T | G | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.430+2083A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022608 | |||||||
| chr19:43022620 | G | A | 3 | a0003c0003t0002g0165 a0003c0003t0002g0184 a0003c0003t0002g0185 |
3 | HG03669.hp1 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.430+2071C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022620 | |||||||
| chr19:43022652 | G | T | 6 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(3): Show |
11 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+2039C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022652 | |||||||
| chr19:43022676 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.430+2015G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022676 | |||||||
| chr19:43022775 | A | T | 2 | a0001c0006t0004g0150 a0001c0006t0004g0151 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.430+1916T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022775 | |||||||
| chr19:43022784 | C | T | 1 | a0001c0006t0004g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430+1907G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022784 | |||||||
| chr19:43022799 | C | T | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1892G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022799 | |||||||
| chr19:43022870 | G | C | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430+1821C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022870 | |||||||
| chr19:43022871 | C | T | 9 | a0002c0002t0003g0199 a0006c0007t0005g0012 a0006c0007t0005g0019 others(6): Show |
16 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.430+1820G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022871 | |||||||
| chr19:43022872 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.430+1819C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022872 | |||||||
| chr19:43022882 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(163): Show |
316 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.430+1809A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022882 | |||||||
| chr19:43022883 | A | T | 1 | a0002c0002t0003g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.430+1808T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022883 | |||||||
| chr19:43022894 | C | A | 1 | a0002c0002t0003g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.430+1797G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022894 | |||||||
| chr19:43022895 | C | G | 1 | a0002c0002t0003g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.430+1796G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022895 | |||||||
| chr19:43022897 | A | G | 1 | a0002c0002t0003g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.430+1794T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022897 | |||||||
| chr19:43022897 | A | T | 1 | a0003c0003t0002g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.430+1794T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43022897 | |||||||
| chr19:43023018 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.430+1673C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023018 | |||||||
| chr19:43023051 | G | A | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+1640C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023051 | |||||||
| chr19:43023061 | C | T | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1630G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023061 | |||||||
| chr19:43023111 | C | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0006g0035 others(4): Show |
8 | HG02109.hp2 HG02135.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1580G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023111 | |||||||
| chr19:43023111 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(135): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.430+1580G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023111 | |||||||
| chr19:43023111 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+1580G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023111 | |||||||
| chr19:43023136 | CTTCAGAG others(10): Show |
C | 1 | a0004c0004t0002g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.430+1538_430+1554d others(19): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023136 | |||||||
| chr19:43023146 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.430+1545T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023146 | |||||||
| chr19:43023160 | G | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.430+1531C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023160 | |||||||
| chr19:43023170 | G | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.430+1521C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023170 | |||||||
| chr19:43023195 | A | G | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+1496T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023195 | |||||||
| chr19:43023203 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(143): Show |
282 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.430+1488G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023203 | |||||||
| chr19:43023237 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.430+1454T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023237 | |||||||
| chr19:43023257 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
301 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.430+1434A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023257 | |||||||
| chr19:43023261 | G | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(42): Show |
106 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.430+1430C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023261 | |||||||
| chr19:43023411 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.430+1280G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023411 | |||||||
| chr19:43023431 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.430+1260T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023431 | |||||||
| chr19:43023457 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02976.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.430+1234C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023457 | |||||||
| chr19:43023500 | T | A | 1 | a0002c0002t0003g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430+1191A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023500 | |||||||
| chr19:43023513 | A | G | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+1178T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023513 | |||||||
| chr19:43023518 | G | C | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1173C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023518 | |||||||
| chr19:43023521 | G | T | 1 | a0002c0002t0003g0198 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.430+1170C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023521 | |||||||
| chr19:43023594 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.430+1097C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023594 | |||||||
| chr19:43023612 | G | T | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1079C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023612 | |||||||
| chr19:43023631 | C | G | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430+1060G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023631 | |||||||
| chr19:43023708 | A | C | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+983T>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023708 | |||||||
| chr19:43023787 | A | G | 5 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(2): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+904T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023787 | |||||||
| chr19:43023796 | G | A | 1 | a0001c0006t0004g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+895C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023796 | |||||||
| chr19:43023901 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.430+790T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023901 | |||||||
| chr19:43023923 | C | T | 34 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(31): Show |
89 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.430+768G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023923 | |||||||
| chr19:43023926 | C | T | 1 | a0001c0006t0004g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430+765G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023926 | |||||||
| chr19:43023946 | G | A | 1 | a0003c0003t0002g0186 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.430+745C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023946 | |||||||
| chr19:43023973 | C | G | 1 | a0002c0002t0009g0197 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.430+718G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43023973 | |||||||
| chr19:43024025 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
11 | HG00099.hp1 HG00733.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+666A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024025 | |||||||
| chr19:43024035 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.430+656A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024035 | |||||||
| chr19:43024056 | C | T | 1 | a0005c0005t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.430+635G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024056 | |||||||
| chr19:43024062 | A | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430+629T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024062 | |||||||
| chr19:43024072 | C | T | 8 | a0006c0007t0005g0012 a0006c0007t0005g0019 a0006c0007t0005g0155 others(5): Show |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+619G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024072 | |||||||
| chr19:43024146 | G | A | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+545C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024146 | |||||||
| chr19:43024204 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+487A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024204 | |||||||
| chr19:43024208 | G | A | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.430+483C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024208 | |||||||
| chr19:43024220 | C | G | 2 | a0003c0003t0002g0042 a0005c0005t0001g0037 |
4 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+471G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024220 | |||||||
| chr19:43024241 | C | G | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+450G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024241 | |||||||
| chr19:43024276 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(74): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.430+415T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024276 | |||||||
| chr19:43024327 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02976.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.430+364G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024327 | |||||||
| chr19:43024418 | T | A | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430+273A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024418 | |||||||
| chr19:43024504 | G | A | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.430+187C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024504 | |||||||
| chr19:43024531 | T | G | 3 | a0001c0001t0001g0028 a0007c0009t0002g0192 a0007c0009t0002g0193 |
4 | HG02622.hp1 HG02809.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+160A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024531 | |||||||
| chr19:43024540 | C | G | 1 | a0001c0006t0004g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+151G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024540 | |||||||
| chr19:43024577 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(156): Show |
302 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.430+114A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024577 | |||||||
| chr19:43024595 | G | A | 12 | a0005c0005t0001g0007 a0005c0005t0001g0037 a0005c0005t0001g0038 others(9): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.430+96C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024595 | |||||||
| chr19:43024618 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(71): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.430+73A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 2/5 | chr19 | 43024618 | |||||||
| chr19:43025079 | G | A | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.65-23C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025079 | |||||||
| chr19:43025080 | T | A | 28 | a0001c0001t0003g0056 a0002c0002t0003g0002 a0002c0002t0003g0005 others(25): Show |
78 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.65-24A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025080 | |||||||
| chr19:43025087 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.65-31A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025087 | |||||||
| chr19:43025103 | G | A | 1 | a0001c0001t0006g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.65-47C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025103 | |||||||
| chr19:43025114 | T | G | 1 | a0001c0006t0004g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.65-58A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025114 | |||||||
| chr19:43025127 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-71G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025127 | |||||||
| chr19:43025160 | G | GAC | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(100): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.65-106_65-105dupGT | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025160 | |||||||
| chr19:43025160 | G | GACAC | 47 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(44): Show |
104 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.65-108_65-105dupGT others(2): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025160 | |||||||
| chr19:43025160 | G | GACACAC | 9 | a0001c0001t0003g0056 a0001c0006t0004g0010 a0001c0006t0004g0146 others(6): Show |
16 | HG00438.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-110_65-105dupGT others(4): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025160 | |||||||
| chr19:43025193 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0057 a0001c0001t0001g0105 others(2): Show |
7 | NA18940.hp1 NA18941.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-137T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025193 | |||||||
| chr19:43025216 | G | T | 1 | a0009c0015t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.65-160C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025216 | |||||||
| chr19:43025228 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.65-172T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025228 | |||||||
| chr19:43025311 | C | A | 2 | a0003c0003t0002g0049 a0003c0003t0002g0189 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.65-255G>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025311 | |||||||
| chr19:43025350 | T | G | 1 | a0001c0006t0004g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.65-294A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025350 | |||||||
| chr19:43025358 | T | C | 5 | a0001c0001t0006g0035 a0001c0001t0006g0132 a0001c0001t0006g0133 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-302A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025358 | |||||||
| chr19:43025373 | G | C | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.65-317C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025373 | |||||||
| chr19:43025452 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.65-396A>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025452 | |||||||
| chr19:43025524 | A | T | 1 | a0005c0005t0001g0139 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.65-468T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025524 | |||||||
| chr19:43025543 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(165): Show |
318 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.65-487T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025543 | |||||||
| chr19:43025544 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.65-488A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025544 | |||||||
| chr19:43025559 | C | T | 1 | a0002c0002t0003g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.65-503G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025559 | |||||||
| chr19:43025581 | T | C | 15 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0140 others(12): Show |
26 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-525A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025581 | |||||||
| chr19:43025638 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0011t0001g0121 |
5 | HG00639.hp1 HG01243.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-582G>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025638 | |||||||
| chr19:43025640 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0011t0001g0121 |
5 | HG00639.hp1 HG01243.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-584C>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025640 | |||||||
| chr19:43025643 | C | T | 7 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(4): Show |
12 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-587G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025643 | |||||||
| chr19:43025646 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.65-590C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025646 | |||||||
| chr19:43025655 | GT | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(132): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.65-600delA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025655 | |||||||
| chr19:43025668 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-612A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025668 | |||||||
| chr19:43025690 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.64+619T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025690 | |||||||
| chr19:43025691 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.64+618A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025691 | |||||||
| chr19:43025714 | G | GCT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.64+594_64+595insAG | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025714 | |||||||
| chr19:43025716 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.64+593A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025716 | |||||||
| chr19:43025729 | T | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0004c0004t0002g0161 |
3 | HG02976.hp1 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64+580A>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025729 | |||||||
| chr19:43025731 | G | A | 1 | a0004c0004t0002g0190 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.64+578C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025731 | |||||||
| chr19:43025803 | A | G | 1 | a0001c0006t0008g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64+506T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025803 | |||||||
| chr19:43025852 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(153): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.64+457C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025852 | |||||||
| chr19:43025916 | C | CT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(88): Show |
191 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.64+392dupA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025916 | |||||||
| chr19:43025916 | CT | C | 6 | a0001c0006t0004g0010 a0001c0006t0004g0147 a0001c0006t0004g0148 others(3): Show |
11 | HG01167.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+392delA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025916 | |||||||
| chr19:43025916 | CTTTTTTT others(20): Show |
C | 2 | a0001c0006t0004g0153 a0006c0007t0005g0159 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.64+366_64+392delAA others(25): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025916 | |||||||
| chr19:43025931 | TTTC | T | 6 | a0001c0006t0004g0150 a0001c0006t0004g0151 a0001c0008t0004g0052 others(3): Show |
6 | HG00738.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+375_64+377delGA others(1): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025931 | |||||||
| chr19:43025931 | TTTCTC | T | 11 | a0001c0001t0001g0036 a0001c0001t0001g0140 a0005c0005t0001g0007 others(8): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+373_64+377delGA others(3): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025931 | |||||||
| chr19:43025933 | TC | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0125 others(4): Show |
10 | HG01168.hp2 HG02004.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+375delG | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025933 | |||||||
| chr19:43025934 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
35 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.64+375G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025934 | |||||||
| chr19:43025935 | T | C | 1 | a0002c0002t0003g0005 | 10 | HG00642.hp2 HG01255.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+374A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025935 | |||||||
| chr19:43025936 | C | CT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
6 | HG01123.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+372dupA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025936 | |||||||
| chr19:43025936 | C | T | 1 | a0002c0002t0003g0005 | 10 | HG00642.hp2 HG01255.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+373G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025936 | |||||||
| chr19:43025936 | CT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(101): Show |
202 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.64+372delA | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025936 | |||||||
| chr19:43025937 | T | C | 1 | a0002c0002t0003g0005 | 10 | HG00642.hp2 HG01255.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+372A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025937 | |||||||
| chr19:43025937 | T | TC | 16 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
30 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+371_64+372insG | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025937 | |||||||
| chr19:43025937 | T | TTTTTTTT others(12): Show |
1 | a0003c0018t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64+371_64+372insGA others(17): Show |
PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025937 | |||||||
| chr19:43025938 | T | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0123 others(14): Show |
21 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.64+371A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025938 | |||||||
| chr19:43025939 | T | C | 1 | a0001c0001t0006g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+370A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025939 | |||||||
| chr19:43025940 | T | C | 11 | a0001c0001t0001g0036 a0001c0001t0001g0140 a0005c0005t0001g0007 others(8): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+369A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025940 | |||||||
| chr19:43025941 | T | C | 2 | a0001c0001t0006g0137 a0005c0005t0001g0145 |
2 | NA19075.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64+368A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025941 | |||||||
| chr19:43025942 | T | C | 11 | a0001c0001t0001g0036 a0001c0001t0001g0140 a0005c0005t0001g0007 others(8): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+367A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025942 | |||||||
| chr19:43025943 | T | C | 1 | a0005c0005t0001g0145 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.64+366A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025943 | |||||||
| chr19:43025973 | G | A | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+336C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025973 | |||||||
| chr19:43025992 | C | T | 2 | a0004c0004t0002g0040 a0004c0004t0002g0162 |
3 | HG00099.hp2 HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.64+317G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43025992 | |||||||
| chr19:43026074 | T | C | 2 | a0007c0009t0002g0192 a0007c0009t0002g0193 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.64+235A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026074 | |||||||
| chr19:43026151 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64+158A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026151 | |||||||
| chr19:43026152 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64+157C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026152 | |||||||
| chr19:43026172 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(133): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.64+137T>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026172 | |||||||
| chr19:43026176 | C | T | 13 | a0001c0006t0004g0010 a0001c0006t0004g0146 a0001c0006t0004g0147 others(10): Show |
18 | HG00738.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+133G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026176 | |||||||
| chr19:43026177 | G | A | 2 | a0001c0001t0001g0039 a0002c0002t0003g0214 |
3 | HG00673.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.64+132C>T | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026177 | |||||||
| chr19:43026182 | C | T | 1 | a0004c0004t0002g0021 | 3 | HG00438.hp1 HG01255.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.64+127G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026182 | |||||||
| chr19:43026189 | C | T | 1 | a0002c0002t0003g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64+120G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026189 | |||||||
| chr19:43026204 | A | G | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+105T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026204 | |||||||
| chr19:43026211 | C | T | 1 | a0004c0004t0002g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+98G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026211 | |||||||
| chr19:43026217 | T | C | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+92A>G | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026217 | |||||||
| chr19:43026227 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.64+82T>C | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026227 | |||||||
| chr19:43026237 | G | T | 1 | a0011c0014t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+72C>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026237 | |||||||
| chr19:43026238 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(164): Show |
317 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.64+71G>A | PSG11 | ENSG00000243130.8 | transcript | ENST00000320078.12 | protein_coding | 1/5 | chr19 | 43026238 |