Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5281 |
| ensemblid | ENSG00000151665.13 |
| hgncid | 8962 |
| symbol | PIGF |
| name | phosphatidylinositol glycan anchor biosynthesis class F |
| refseq_nuc | NM_002643.4 |
| refseq_prot | NP_002634.1 |
| ensembl_nuc | ENST00000281382.11 |
| ensembl_prot | ENSP00000281382.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 46580937 |
| end | 46617041 |
| strand | - |
| ver | v1.2 |
| region | chr2:46580937-46617041 |
| region5000 | chr2:46575937-46622041 |
| regionname0 | PIGF_chr2_46580937_46617041 |
| regionname5000 | PIGF_chr2_46575937_46622041 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 219 | 360 | 92 | 74 | 130 | 16 | 46 | 98 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| a0002 | 0/0 | 219 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| a0003 | 0/0 | 219 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| a0004 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| a0005 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| a0006 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | MKDND others(214): Show |
chr2 | 46575937 | 46622041 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 657 | 300 | 90 | 49 | 109 | 14 | 36 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0001c0002 | 0/0 | 657 | 60 | 2 | 25 | 21 | 2 | 10 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0002c0003 | 0/0 | 657 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0003c0004 | 0/0 | 657 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0004c0005 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0005c0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 | ||
| a0006c0007 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | ATGAA others(652): Show |
chr2 | 46575937 | 46622041 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1294 | 287 | 89 | 42 | 108 | 12 | 34 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0001t0002 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1287): Show |
chr2 | 46575937 | 46622041 |
| a0001c0001t0003 | 0/0 | 1294 | 9 | 0 | 6 | 0 | 2 | 1 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0001t0004 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0001t0005 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0001t0006 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0002t0001 | 0/0 | 1294 | 7 | 0 | 2 | 2 | 0 | 3 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0001c0002t0002 | 0/0 | 1292 | 53 | 2 | 23 | 19 | 2 | 7 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1287): Show |
chr2 | 46575937 | 46622041 |
| a0002c0003t0001 | 0/0 | 1294 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0003c0004t0003 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0004c0005t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0005c0006t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| a0006c0007t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | CTGGG others(1289): Show |
chr2 | 46575937 | 46622041 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 31 | 1 | 4 | 24 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0003 | 0/0 | 12 | 2 | 2 | 7 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0006 | 1/0 | 5 | 1 | 3 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0002 | 0/0 | 19 | 0 | 10 | 7 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0002c0003t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0003c0004t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0004c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0005c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| a0006c0007t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0050 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01074 | hp2 | a0003 | c0004 | t0003 | g0210 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03225 | hp1 | a0005 | c0006 | t0001 | g0089 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03516 | hp2 | a0006 | c0007 | t0001 | g0144 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0226 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | ASW | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0077 | EUR | TSI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | GIH | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02559 | hp1 | a0004 | c0005 | t0001 | g0136 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46612295 | T | C | 1 | a0003 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.370A>G | p.Thr124Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 463/1294 | 370/660 | 124/219 | chr2 | 46612295 | |||
| chr2:46612304 | T | C | 1 | a0004 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.361A>G | p.Thr121Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 454/1294 | 361/660 | 121/219 | chr2 | 46612304 | |||
| chr2:46612318 | G | A | 1 | a0005 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.347C>T | p.Ala116Val | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 440/1294 | 347/660 | 116/219 | chr2 | 46612318 | |||
| chr2:46614938 | T | C | 1 | a0006 | 1 | HG03516.hp2 | missense_variant&splice_region_variant | MODERATE | c.227A>G | p.Lys76Arg | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/6 | 320/1294 | 227/660 | 76/219 | chr2 | 46614938 | |||
| chr2:46614980 | A | G | 1 | a0002 | 2 | HG01167.hp2 HG02280.hp2 |
missense_variant | MODERATE | c.185T>C | p.Val62Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/6 | 278/1294 | 185/660 | 62/219 | chr2 | 46614980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46612338 | T | C | 1 | a0001c0002 | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
synonymous_variant | LOW | c.327A>G | p.Ala109Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 420/1294 | 327/660 | 109/219 | chr2 | 46612338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46581029 | C | T | 2 | a0001c0001t0003 a0003c0004t0003 |
10 | HG00741.hp2 HG01074.hp1 HG01074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*449G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 449 | chr2 | 46581029 | ||||||
| chr2:46581104 | GGA | G | 2 | a0001c0001t0002 a0001c0002t0002 |
54 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*372_*373delTC | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 372 | chr2 | 46581104 | ||||||
| chr2:46581164 | A | G | 1 | a0001c0001t0004 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 314 | chr2 | 46581164 | ||||||
| chr2:46581428 | T | G | 1 | a0001c0001t0005 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*50A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 50 | chr2 | 46581428 | ||||||
| chr2:46617032 | G | C | 1 | a0001c0001t0006 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/6 | 1868 | chr2 | 46617032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46581663 | A | G | 13 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-72T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46581663 | |||||||
| chr2:46581907 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-316G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46581907 | |||||||
| chr2:46582102 | T | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(56): Show |
74 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.547-511A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582102 | |||||||
| chr2:46582232 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-641C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582232 | |||||||
| chr2:46582263 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.547-672T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582263 | |||||||
| chr2:46582418 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-827A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582418 | |||||||
| chr2:46582482 | T | C | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(60): Show |
78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.547-891A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582482 | |||||||
| chr2:46582833 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.547-1242G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582833 | |||||||
| chr2:46582845 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0200 |
2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.547-1254A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582845 | |||||||
| chr2:46583765 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0119 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.547-2174C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46583765 | |||||||
| chr2:46584976 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547-3385G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46584976 | |||||||
| chr2:46585088 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.547-3497T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585088 | |||||||
| chr2:46585199 | A | G | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(66): Show |
88 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.547-3608T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585199 | |||||||
| chr2:46585239 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.547-3648T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585239 | |||||||
| chr2:46585279 | G | A | 11 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
11 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-3688C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585279 | |||||||
| chr2:46585303 | G | GT | 3 | a0001c0001t0001g0025 a0001c0001t0001g0138 a0001c0001t0001g0209 |
5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-3713dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585303 | |||||||
| chr2:46585592 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0194 |
2 | NA19076.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.547-4001C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585592 | |||||||
| chr2:46585864 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.547-4273G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585864 | |||||||
| chr2:46585898 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0139 others(2): Show |
8 | HG00597.hp2 HG03490.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-4307G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585898 | |||||||
| chr2:46586034 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-4443T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586034 | |||||||
| chr2:46586155 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.547-4564G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586155 | |||||||
| chr2:46586164 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-4573G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586164 | |||||||
| chr2:46586229 | C | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0109 |
2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.547-4638G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586229 | |||||||
| chr2:46586320 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0149 a0001c0001t0001g0170 others(2): Show |
8 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-4729G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586320 | |||||||
| chr2:46586416 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.547-4825T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586416 | |||||||
| chr2:46586459 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0191 |
2 | HG00438.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.547-4868A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586459 | |||||||
| chr2:46586473 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.547-4882T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586473 | |||||||
| chr2:46586929 | C | T | 2 | a0001c0002t0002g0076 a0001c0002t0002g0077 |
2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.547-5338G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586929 | |||||||
| chr2:46587005 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.547-5414G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587005 | |||||||
| chr2:46587240 | C | T | 1 | a0001c0002t0002g0065 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+5235G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587240 | |||||||
| chr2:46587241 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.546+5234C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587241 | |||||||
| chr2:46587439 | GA | G | 45 | a0001c0001t0001g0018 a0001c0001t0001g0081 a0001c0001t0001g0083 others(42): Show |
71 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.546+5035delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587439 | |||||||
| chr2:46587498 | T | A | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(63): Show |
83 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.546+4977A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587498 | |||||||
| chr2:46587649 | A | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0139 others(2): Show |
8 | HG00597.hp2 HG03490.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+4826T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587649 | |||||||
| chr2:46587756 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.546+4719T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587756 | |||||||
| chr2:46587866 | A | C | 1 | a0001c0002t0002g0064 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.546+4609T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587866 | |||||||
| chr2:46588085 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+4390C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588085 | |||||||
| chr2:46588156 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.546+4319C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588156 | |||||||
| chr2:46588341 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+4134G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588341 | |||||||
| chr2:46588452 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0224 |
4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+4023C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588452 | |||||||
| chr2:46588515 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.546+3960G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588515 | |||||||
| chr2:46588590 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0001c0001t0001g0205 others(1): Show |
7 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+3885G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588590 | |||||||
| chr2:46588604 | G | A | 1 | a0001c0002t0002g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+3871C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588604 | |||||||
| chr2:46588822 | T | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(56): Show |
74 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.546+3653A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588822 | |||||||
| chr2:46588989 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.546+3486T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588989 | |||||||
| chr2:46589103 | A | C | 122 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+3372T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589103 | |||||||
| chr2:46589319 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.546+3156C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589319 | |||||||
| chr2:46589326 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0095 |
4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+3149G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589326 | |||||||
| chr2:46589392 | A | C | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(57): Show |
75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.546+3083T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589392 | |||||||
| chr2:46589513 | T | C | 12 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+2962A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589513 | |||||||
| chr2:46589611 | C | T | 1 | a0001c0002t0002g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.546+2864G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589611 | |||||||
| chr2:46589988 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+2487G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589988 | |||||||
| chr2:46590370 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.546+2105A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590370 | |||||||
| chr2:46590505 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(170): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.546+1970A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590505 | |||||||
| chr2:46590632 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0138 a0001c0001t0001g0209 |
5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+1843T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590632 | |||||||
| chr2:46590852 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0138 a0001c0001t0001g0209 |
5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+1623T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590852 | |||||||
| chr2:46590921 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.546+1554C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590921 | |||||||
| chr2:46590946 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.546+1529A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590946 | |||||||
| chr2:46591052 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.546+1423A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591052 | |||||||
| chr2:46591095 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.546+1380T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591095 | |||||||
| chr2:46591199 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(50): Show |
64 | HG00140.hp1 HG00140.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.546+1276G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591199 | |||||||
| chr2:46591200 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1275C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591200 | |||||||
| chr2:46591362 | G | C | 1 | a0003c0004t0003g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.546+1113C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591362 | |||||||
| chr2:46591393 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.546+1082A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591393 | |||||||
| chr2:46591395 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.546+1080G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591395 | |||||||
| chr2:46591397 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.546+1078A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591397 | |||||||
| chr2:46591414 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.546+1061C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591414 | |||||||
| chr2:46591447 | C | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.546+1028G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591447 | |||||||
| chr2:46591612 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0200 |
2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.546+863A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591612 | |||||||
| chr2:46591644 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+831C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591644 | |||||||
| chr2:46591664 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
8 | HG00597.hp2 HG01928.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+811A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591664 | |||||||
| chr2:46591811 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0200 |
2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.546+664C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591811 | |||||||
| chr2:46591841 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.546+634A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591841 | |||||||
| chr2:46591853 | C | T | 33 | a0001c0001t0002g0154 a0001c0002t0001g0056 a0001c0002t0001g0066 others(30): Show |
57 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.546+622G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591853 | |||||||
| chr2:46591876 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.546+599A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591876 | |||||||
| chr2:46591882 | G | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.546+593C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591882 | |||||||
| chr2:46591911 | C | G | 1 | a0001c0001t0003g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.546+564G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591911 | |||||||
| chr2:46592095 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0097 |
3 | HG01884.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.546+380A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592095 | |||||||
| chr2:46592291 | C | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(60): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.546+184G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592291 | |||||||
| chr2:46592352 | A | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0225 |
2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.546+123T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592352 | |||||||
| chr2:46592665 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.438-82T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592665 | |||||||
| chr2:46592676 | A | G | 112 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(109): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.438-93T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592676 | |||||||
| chr2:46592704 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.438-121G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592704 | |||||||
| chr2:46592911 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-328G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592911 | |||||||
| chr2:46593085 | A | G | 10 | a0001c0001t0001g0028 a0001c0001t0001g0096 a0001c0001t0001g0098 others(7): Show |
11 | HG01255.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-502T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593085 | |||||||
| chr2:46593097 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.438-514A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593097 | |||||||
| chr2:46593134 | C | CT | 65 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0037 others(62): Show |
94 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.438-552dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593134 | |||||||
| chr2:46593311 | T | G | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0086 others(3): Show |
6 | HG01884.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.438-728A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593311 | |||||||
| chr2:46593426 | C | T | 1 | a0001c0002t0002g0030 | 2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.438-843G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593426 | |||||||
| chr2:46593446 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.438-863A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593446 | |||||||
| chr2:46593547 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02976.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.438-964G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593547 | |||||||
| chr2:46593567 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-984T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593567 | |||||||
| chr2:46593663 | G | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
82 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-1080C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593663 | |||||||
| chr2:46593664 | T | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
82 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-1081A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593664 | |||||||
| chr2:46593706 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438-1123T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593706 | |||||||
| chr2:46593771 | C | T | 11 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(8): Show |
11 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-1188G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593771 | |||||||
| chr2:46593800 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.438-1217A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593800 | |||||||
| chr2:46593840 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.438-1257A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593840 | |||||||
| chr2:46593847 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.438-1264G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593847 | |||||||
| chr2:46593929 | A | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-1346T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593929 | |||||||
| chr2:46594114 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.438-1531C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594114 | |||||||
| chr2:46594156 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.438-1573T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594156 | |||||||
| chr2:46594308 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-1725C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594308 | |||||||
| chr2:46594438 | GA | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-1856delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594438 | |||||||
| chr2:46594501 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0028 others(40): Show |
51 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.438-1918C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594501 | |||||||
| chr2:46594536 | AT | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(130): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.438-1954delA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594536 | |||||||
| chr2:46594536 | ATT | A | 31 | a0001c0001t0002g0154 a0001c0002t0001g0056 a0001c0002t0001g0066 others(28): Show |
55 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.438-1955_438-1954d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594536 | |||||||
| chr2:46594565 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0003g0032 a0001c0001t0003g0172 others(1): Show |
5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.438-1982G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594565 | |||||||
| chr2:46594604 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.438-2021G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594604 | |||||||
| chr2:46594755 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.438-2172G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594755 | |||||||
| chr2:46594772 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00544.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.438-2189C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594772 | |||||||
| chr2:46594840 | G | GT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(85): Show |
157 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.438-2258dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594840 | |||||||
| chr2:46594848 | T | TG | 7 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
8 | HG00408.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.438-2266_438-2265i others(3): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594848 | |||||||
| chr2:46594848 | T | TTG | 8 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0091 others(5): Show |
11 | HG00597.hp2 HG02293.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-2266_438-2265i others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594848 | |||||||
| chr2:46594849 | T | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0224 |
5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-2266A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594849 | |||||||
| chr2:46595188 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | HG01261.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.438-2605G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595188 | |||||||
| chr2:46595341 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-2758G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595341 | |||||||
| chr2:46595527 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.438-2944A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595527 | |||||||
| chr2:46595893 | C | G | 67 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(64): Show |
84 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.438-3310G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595893 | |||||||
| chr2:46596000 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.438-3417C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596000 | |||||||
| chr2:46596168 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.438-3585C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596168 | |||||||
| chr2:46596192 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-3609C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596192 | |||||||
| chr2:46596199 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.438-3616G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596199 | |||||||
| chr2:46596212 | C | CA | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
80 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(77): Show |
intron_variant | MODIFIER | c.438-3630dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596212 | |||||||
| chr2:46596283 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.438-3700C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596283 | |||||||
| chr2:46596325 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.438-3742A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596325 | |||||||
| chr2:46596327 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-3744C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596327 | |||||||
| chr2:46596364 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0001c0001t0001g0205 others(1): Show |
7 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-3781G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596364 | |||||||
| chr2:46596379 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.438-3796G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596379 | |||||||
| chr2:46596485 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0224 |
5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-3902A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596485 | |||||||
| chr2:46596527 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-3944T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596527 | |||||||
| chr2:46596690 | G | C | 1 | a0001c0002t0002g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.438-4107C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596690 | |||||||
| chr2:46596853 | G | A | 55 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
82 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-4270C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596853 | |||||||
| chr2:46596951 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.438-4368A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596951 | |||||||
| chr2:46596981 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.438-4398G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596981 | |||||||
| chr2:46597079 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0208 |
3 | HG01243.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.438-4496G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597079 | |||||||
| chr2:46597134 | G | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.438-4551C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597134 | |||||||
| chr2:46597239 | T | TAAAA | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.438-4657_438-4656i others(6): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597239 | |||||||
| chr2:46597419 | G | GT | 4 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0209 others(1): Show |
6 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.438-4837dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597419 | |||||||
| chr2:46597443 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-4860G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597443 | |||||||
| chr2:46597465 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.438-4882A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597465 | |||||||
| chr2:46597475 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.438-4892G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597475 | |||||||
| chr2:46597674 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.438-5091T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597674 | |||||||
| chr2:46597691 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.438-5108G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597691 | |||||||
| chr2:46597704 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0224 |
5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-5121C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597704 | |||||||
| chr2:46597724 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-5141A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597724 | |||||||
| chr2:46597742 | A | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(100): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.438-5159T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597742 | |||||||
| chr2:46597808 | G | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0139 others(3): Show |
9 | HG00597.hp2 HG03490.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.438-5225C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597808 | |||||||
| chr2:46597941 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.438-5358A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597941 | |||||||
| chr2:46598029 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.438-5446A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598029 | |||||||
| chr2:46598192 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0113 |
3 | HG00140.hp2 HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.438-5609G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598192 | |||||||
| chr2:46598198 | G | C | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.438-5615C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598198 | |||||||
| chr2:46598442 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(65): Show |
85 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.438-5859T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598442 | |||||||
| chr2:46598529 | A | AT | 13 | a0001c0001t0001g0047 a0001c0001t0001g0149 a0001c0001t0001g0158 others(10): Show |
13 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.438-5947dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATT | 47 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0042 others(44): Show |
74 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.438-5948_438-5947d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTT | 7 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0090 others(4): Show |
9 | HG01106.hp2 HG01884.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5949_438-5947d others(5): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(4): Show |
7 | a0001c0001t0001g0092 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG02818.hp1 HG02970.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-5957_438-5947d others(13): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(5): Show |
17 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0046 others(14): Show |
21 | HG00140.hp2 HG01192.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.438-5958_438-5947d others(14): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(6): Show |
14 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0045 others(11): Show |
18 | HG00140.hp1 HG01099.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.438-5959_438-5947d others(15): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(7): Show |
10 | a0001c0001t0001g0027 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
11 | HG01884.hp2 HG01891.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-5960_438-5947d others(16): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0108 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-5961_438-5947d others(17): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(14): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0123 |
4 | HG02615.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-5967_438-5947d others(23): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0122 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.438-5968_438-5947d others(24): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438-5947_438-5946i others(30): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598529 | ATTTTTTT | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0095 others(2): Show |
9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5953_438-5947d others(9): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | |||||||
| chr2:46598569 | G | GT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0095 others(2): Show |
9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5987dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598569 | |||||||
| chr2:46598683 | G | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(63): Show |
83 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.438-6100C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598683 | |||||||
| chr2:46598831 | A | G | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(63): Show |
83 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.438-6248T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598831 | |||||||
| chr2:46598844 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-6261A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598844 | |||||||
| chr2:46598887 | A | C | 57 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
84 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.438-6304T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598887 | |||||||
| chr2:46598920 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0224 |
5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-6337C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598920 | |||||||
| chr2:46598999 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0139 others(3): Show |
9 | HG00597.hp2 HG03490.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.438-6416G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598999 | |||||||
| chr2:46599242 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.438-6659T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599242 | |||||||
| chr2:46599328 | G | T | 1 | a0001c0001t0004g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438-6745C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599328 | |||||||
| chr2:46599432 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0145 a0001c0001t0001g0209 |
5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.438-6849G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599432 | |||||||
| chr2:46599434 | T | C | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.438-6851A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599434 | |||||||
| chr2:46599468 | T | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0095 others(2): Show |
9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-6885A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599468 | |||||||
| chr2:46599657 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-7074C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599657 | |||||||
| chr2:46599750 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0200 |
2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.438-7167A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599750 | |||||||
| chr2:46599899 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.438-7316G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599899 | |||||||
| chr2:46599936 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-7353A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599936 | |||||||
| chr2:46599979 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-7396A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599979 | |||||||
| chr2:46600160 | C | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0028 others(27): Show |
38 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.438-7577G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600160 | |||||||
| chr2:46600236 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-7653C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600236 | |||||||
| chr2:46600354 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0005g0180 |
2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.438-7771T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600354 | |||||||
| chr2:46600479 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0138 |
4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-7896A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600479 | |||||||
| chr2:46600561 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.438-7978T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600561 | |||||||
| chr2:46600576 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-7993G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600576 | |||||||
| chr2:46600755 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.438-8172A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600755 | |||||||
| chr2:46600841 | C | T | 1 | a0003c0004t0003g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.438-8258G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600841 | |||||||
| chr2:46600938 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438-8355G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600938 | |||||||
| chr2:46601038 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.438-8455G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601038 | |||||||
| chr2:46601500 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-8917C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601500 | |||||||
| chr2:46601655 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.438-9072G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601655 | |||||||
| chr2:46601952 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.438-9369T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601952 | |||||||
| chr2:46601985 | G | A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(51): Show |
81 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.438-9402C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601985 | |||||||
| chr2:46601992 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-9409A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601992 | |||||||
| chr2:46602036 | GA | G | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.438-9454delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602036 | |||||||
| chr2:46602060 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-9477T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602060 | |||||||
| chr2:46602284 | T | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
11 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-9701A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602284 | |||||||
| chr2:46602348 | T | G | 125 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(122): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.438-9765A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602348 | |||||||
| chr2:46602416 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+9812T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602416 | |||||||
| chr2:46602679 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+9549C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602679 | |||||||
| chr2:46602790 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.437+9438C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602790 | |||||||
| chr2:46603032 | A | G | 1 | a0001c0002t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437+9196T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603032 | |||||||
| chr2:46603045 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG00738.hp2 HG00741.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+9183T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603045 | |||||||
| chr2:46603370 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0209 |
4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+8858A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603370 | |||||||
| chr2:46603500 | T | TA | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+8727dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603500 | |||||||
| chr2:46603501 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.437+8727T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603501 | |||||||
| chr2:46603519 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+8709G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603519 | |||||||
| chr2:46603522 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.437+8706A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603522 | |||||||
| chr2:46603655 | C | T | 34 | a0001c0001t0002g0154 a0001c0002t0001g0066 a0001c0002t0001g0067 others(31): Show |
58 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.437+8573G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603655 | |||||||
| chr2:46603721 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.437+8507C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603721 | |||||||
| chr2:46603923 | C | A | 36 | a0001c0001t0002g0154 a0001c0002t0001g0056 a0001c0002t0001g0066 others(33): Show |
60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+8305G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603923 | |||||||
| chr2:46604021 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+8207G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604021 | |||||||
| chr2:46604339 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.437+7889G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604339 | |||||||
| chr2:46604346 | A | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+7882T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604346 | |||||||
| chr2:46604361 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0006c0007t0001g0144 |
3 | HG02451.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.437+7867G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604361 | |||||||
| chr2:46604414 | T | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+7814A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604414 | |||||||
| chr2:46604855 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.437+7373C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604855 | |||||||
| chr2:46604927 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.437+7301A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604927 | |||||||
| chr2:46605121 | G | T | 1 | a0001c0001t0003g0167 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.437+7107C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605121 | |||||||
| chr2:46605301 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.437+6927C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605301 | |||||||
| chr2:46605384 | T | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0138 |
4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+6844A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605384 | |||||||
| chr2:46605463 | C | T | 126 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.437+6765G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605463 | |||||||
| chr2:46605581 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.437+6647C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605581 | |||||||
| chr2:46605745 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.437+6483G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605745 | |||||||
| chr2:46605808 | G | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0095 others(2): Show |
9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.437+6420C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605808 | |||||||
| chr2:46606011 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.437+6217T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606011 | |||||||
| chr2:46606129 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0211 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.437+6099C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606129 | |||||||
| chr2:46606614 | A | C | 4 | a0001c0001t0001g0174 a0001c0001t0003g0032 a0001c0001t0003g0172 others(1): Show |
5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+5614T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606614 | |||||||
| chr2:46606701 | T | G | 65 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+5527A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606701 | |||||||
| chr2:46606897 | C | G | 36 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0154 others(33): Show |
60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+5331G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606897 | |||||||
| chr2:46607014 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG00639.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.437+5214T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607014 | |||||||
| chr2:46607071 | A | G | 2 | a0001c0002t0002g0021 a0001c0002t0002g0030 |
5 | HG02071.hp1 NA18965.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+5157T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607071 | |||||||
| chr2:46607074 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0205 a0001c0001t0001g0214 |
3 | HG02630.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.437+5154A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607074 | |||||||
| chr2:46607090 | G | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(64): Show |
84 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.437+5138C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607090 | |||||||
| chr2:46607099 | T | C | 1 | a0001c0002t0002g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.437+5129A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607099 | |||||||
| chr2:46607126 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0138 |
4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+5102G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607126 | |||||||
| chr2:46607163 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0095 |
4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+5065A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607163 | |||||||
| chr2:46607209 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+5019G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607209 | |||||||
| chr2:46607310 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0097 |
3 | HG01884.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.437+4918T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607310 | |||||||
| chr2:46607494 | C | T | 1 | a0001c0002t0002g0059 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.437+4734G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607494 | |||||||
| chr2:46607505 | T | G | 1 | a0001c0001t0006g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.437+4723A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607505 | |||||||
| chr2:46607533 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.437+4695A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607533 | |||||||
| chr2:46607655 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437+4573A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607655 | |||||||
| chr2:46607737 | C | G | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.437+4491G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607737 | |||||||
| chr2:46607826 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+4402G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607826 | |||||||
| chr2:46608021 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.437+4207A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608021 | |||||||
| chr2:46608035 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.437+4193C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608035 | |||||||
| chr2:46608140 | C | A | 1 | a0001c0002t0002g0052 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.437+4088G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608140 | |||||||
| chr2:46608243 | G | A | 1 | a0001c0002t0002g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.437+3985C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608243 | |||||||
| chr2:46608328 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.437+3900T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608328 | |||||||
| chr2:46608363 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.437+3865G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608363 | |||||||
| chr2:46608497 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0003g0032 a0001c0001t0003g0172 others(1): Show |
5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+3731G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608497 | |||||||
| chr2:46608613 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+3615T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608613 | |||||||
| chr2:46608830 | T | C | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.437+3398A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608830 | |||||||
| chr2:46608858 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.437+3370T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608858 | |||||||
| chr2:46608860 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437+3368A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608860 | |||||||
| chr2:46608888 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0224 |
2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.437+3340T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608888 | |||||||
| chr2:46609077 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+3151C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609077 | |||||||
| chr2:46609109 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0048 |
5 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+3119T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609109 | |||||||
| chr2:46609136 | G | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
8 | HG00642.hp2 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.437+3092C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609136 | |||||||
| chr2:46609153 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+3075C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609153 | |||||||
| chr2:46609162 | T | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.437+3066A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609162 | |||||||
| chr2:46609207 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.437+3021G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609207 | |||||||
| chr2:46609208 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.437+3020C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609208 | |||||||
| chr2:46609272 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2956A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609272 | |||||||
| chr2:46609275 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437+2953G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609275 | |||||||
| chr2:46609300 | A | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.437+2928T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609300 | |||||||
| chr2:46609363 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+2865A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609363 | |||||||
| chr2:46609403 | A | T | 36 | a0001c0002t0001g0056 a0001c0002t0001g0066 a0001c0002t0001g0067 others(33): Show |
60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+2825T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609403 | |||||||
| chr2:46609449 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2779A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609449 | |||||||
| chr2:46609614 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+2614G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609614 | |||||||
| chr2:46609629 | G | A | 1 | a0006c0007t0001g0144 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.437+2599C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609629 | |||||||
| chr2:46609737 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+2491C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609737 | |||||||
| chr2:46609767 | A | G | 57 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
84 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.437+2461T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609767 | |||||||
| chr2:46609903 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2325A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609903 | |||||||
| chr2:46609936 | C | T | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(60): Show |
78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.437+2292G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609936 | |||||||
| chr2:46609939 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(61): Show |
79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+2289G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609939 | |||||||
| chr2:46610361 | C | T | 1 | a0001c0002t0002g0030 | 2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.437+1867G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610361 | |||||||
| chr2:46610371 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.437+1857A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610371 | |||||||
| chr2:46610480 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+1748A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610480 | |||||||
| chr2:46610518 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+1710T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610518 | |||||||
| chr2:46610526 | C | CT | 57 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0042 others(54): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.437+1701dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610526 | |||||||
| chr2:46610526 | C | CTT | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(63): Show |
81 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.437+1700_437+1701d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610526 | |||||||
| chr2:46610543 | T | TC | 3 | a0001c0002t0002g0076 a0001c0002t0002g0077 a0001c0002t0002g0078 |
3 | HG02698.hp1 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.437+1684_437+1685i others(3): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610543 | |||||||
| chr2:46610619 | T | G | 1 | a0001c0001t0001g0023 | 3 | NA18957.hp2 NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.437+1609A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610619 | |||||||
| chr2:46610620 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+1608G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610620 | |||||||
| chr2:46610710 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(26): Show |
70 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.437+1518T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610710 | |||||||
| chr2:46610744 | G | A | 1 | a0001c0001t0001g0007 | 5 | HG02056.hp1 NA18943.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+1484C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610744 | |||||||
| chr2:46610776 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0095 |
4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1452G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610776 | |||||||
| chr2:46610839 | C | G | 1 | a0001c0001t0001g0011 | 4 | NA18956.hp2 NA19003.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1389G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610839 | |||||||
| chr2:46610866 | T | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(51): Show |
65 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.437+1362A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610866 | |||||||
| chr2:46610963 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.437+1265G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610963 | |||||||
| chr2:46610990 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+1238C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610990 | |||||||
| chr2:46610991 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+1237G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610991 | |||||||
| chr2:46611071 | A | G | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1157T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611071 | |||||||
| chr2:46611108 | C | G | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(121): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.437+1120G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611108 | |||||||
| chr2:46611183 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.437+1045A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611183 | |||||||
| chr2:46611278 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+950C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611278 | |||||||
| chr2:46611291 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0090 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.437+937G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611291 | |||||||
| chr2:46611367 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+861G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611367 | |||||||
| chr2:46611433 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.437+795C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611433 | |||||||
| chr2:46611462 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0207 |
3 | HG03704.hp2 HG03927.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.437+766C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611462 | |||||||
| chr2:46611469 | C | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(57): Show |
75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.437+759G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611469 | |||||||
| chr2:46611470 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437+758C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611470 | |||||||
| chr2:46611482 | C | CA | 53 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(50): Show |
80 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+745dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611482 | |||||||
| chr2:46611517 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437+711C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611517 | |||||||
| chr2:46611719 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.437+509G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611719 | |||||||
| chr2:46611720 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+508C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611720 | |||||||
| chr2:46611793 | T | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.437+435A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611793 | |||||||
| chr2:46611819 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437+409C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611819 | |||||||
| chr2:46611962 | CT | C | 50 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(47): Show |
74 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.437+265delA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611962 | |||||||
| chr2:46612069 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.437+159A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46612069 | |||||||
| chr2:46612348 | GA | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
9 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.321-5delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612348 | |||||||
| chr2:46612542 | C | T | 36 | a0001c0002t0001g0056 a0001c0002t0001g0066 a0001c0002t0001g0067 others(33): Show |
60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.321-198G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612542 | |||||||
| chr2:46612642 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.321-298A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612642 | |||||||
| chr2:46612660 | GTC | G | 56 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(53): Show |
83 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.321-318_321-317del others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612660 | |||||||
| chr2:46612811 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.321-467C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612811 | |||||||
| chr2:46612874 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.321-530A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612874 | |||||||
| chr2:46612896 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321-552A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612896 | |||||||
| chr2:46612905 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0141 |
5 | NA18942.hp1 NA18953.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.321-561G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612905 | |||||||
| chr2:46613043 | A | AAT | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0080 others(10): Show |
13 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.320+649_320+650dup others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | |||||||
| chr2:46613043 | A | AATAT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
9 | HG00597.hp2 HG02040.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+647_320+650dup others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | |||||||
| chr2:46613043 | A | AATATAT | 33 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0002t0001g0056 others(30): Show |
57 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.320+645_320+650dup others(6): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | |||||||
| chr2:46613043 | A | AATATATA others(1): Show |
3 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0001c0002t0002g0054 |
3 | HG02683.hp1 HG02738.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.320+643_320+650dup others(8): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | |||||||
| chr2:46613043 | A | AATATATA others(3): Show |
1 | a0001c0002t0002g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.320+641_320+650dup others(10): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | |||||||
| chr2:46613055 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.320+639A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613055 | |||||||
| chr2:46613090 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.320+604C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613090 | |||||||
| chr2:46613182 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.320+512A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613182 | |||||||
| chr2:46613413 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+281A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613413 | |||||||
| chr2:46613541 | T | A | 56 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0080 others(53): Show |
83 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.320+153A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613541 | |||||||
| chr2:46613589 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0048 |
5 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+105A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613589 | |||||||
| chr2:46613596 | T | C | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(57): Show |
75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.320+98A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613596 | |||||||
| chr2:46613956 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.229-171G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46613956 | |||||||
| chr2:46613997 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG01081.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.229-212G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46613997 | |||||||
| chr2:46614017 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-232C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614017 | |||||||
| chr2:46614022 | A | C | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(60): Show |
78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.229-237T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614022 | |||||||
| chr2:46614058 | A | G | 1 | a0001c0002t0002g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229-273T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614058 | |||||||
| chr2:46614305 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.229-520T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614305 | |||||||
| chr2:46614339 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-554T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614339 | |||||||
| chr2:46614445 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0091 others(3): Show |
9 | HG00597.hp2 HG02572.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+492C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614445 | |||||||
| chr2:46614505 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0142 others(1): Show |
8 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.228+432C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614505 | |||||||
| chr2:46614715 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.228+222G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614715 | |||||||
| chr2:46614722 | G | T | 48 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(45): Show |
72 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.228+215C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614722 | |||||||
| chr2:46614756 | A | T | 1 | a0001c0002t0002g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.228+181T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614756 | |||||||
| chr2:46615271 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-21-86T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615271 | |||||||
| chr2:46615324 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-139G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615324 | |||||||
| chr2:46615417 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21-232A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615417 | |||||||
| chr2:46615586 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-21-401A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615586 | |||||||
| chr2:46615864 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18982.hp2 NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-21-679C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615864 | |||||||
| chr2:46615914 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-729G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615914 | |||||||
| chr2:46615932 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-747C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615932 | |||||||
| chr2:46615950 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-765A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615950 | |||||||
| chr2:46615959 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-21-774A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615959 | |||||||
| chr2:46615968 | C | G | 1 | a0001c0002t0002g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-21-783G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615968 | |||||||
| chr2:46616049 | ACG | A | 120 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(117): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-21-866_-21-865del others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616049 | |||||||
| chr2:46616102 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-22+868C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616102 | |||||||
| chr2:46616259 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+711A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616259 | |||||||
| chr2:46616325 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-22+645A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616325 | |||||||
| chr2:46616367 | A | T | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22+603T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616367 | |||||||
| chr2:46616411 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+559A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616411 | |||||||
| chr2:46616440 | T | C | 2 | a0001c0002t0002g0021 a0001c0002t0002g0030 |
5 | HG02071.hp1 NA18965.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+530A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616440 | |||||||
| chr2:46616467 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-22+503G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616467 | |||||||
| chr2:46616492 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-22+478T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616492 | |||||||
| chr2:46616526 | C | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
9 | HG00735.hp2 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+444G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616526 | |||||||
| chr2:46616617 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+353T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616617 | |||||||
| chr2:46616676 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+294C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616676 | |||||||
| chr2:46616781 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22+189G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616781 | |||||||
| chr2:46616919 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-22+51C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616919 |