Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5738 |
| ensemblid | ENSG00000134247.10 |
| hgncid | 9601 |
| symbol | PTGFRN |
| name | prostaglandin F2 receptor inhibitor |
| refseq_nuc | NM_020440.4 |
| refseq_prot | NP_065173.2 |
| ensembl_nuc | ENST00000393203.3 |
| ensembl_prot | ENSP00000376899.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 116909916 |
| end | 116990353 |
| strand | + |
| ver | v1.2 |
| region | chr1:116909916-116990353 |
| region5000 | chr1:116904916-116995353 |
| regionname0 | PTGFRN_chr1_116909916_116990353 |
| regionname5000 | PTGFRN_chr1_116904916_116995353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 879 | 118 | 50 | 22 | 29 | 5 | 12 | 24 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0002 | 0/1 | 879 | 90 | 8 | 26 | 39 | 6 | 10 | 26 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0003 | 0/0 | 879 | 45 | 0 | 3 | 38 | 0 | 4 | 28 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0004 | 1/0 | 879 | 33 | 8 | 3 | 16 | 5 | 0 | 12 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0005 | 0/0 | 879 | 11 | 9 | 0 | 1 | 0 | 1 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0006 | 0/0 | 879 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0007 | 0/0 | 879 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0008 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0009 | 0/0 | 879 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0010 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0011 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| a0012 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | MGRLA others(874): Show |
chr1 | 116904916 | 116995353 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2637 | 106 | 40 | 21 | 29 | 5 | 11 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0006 | 0/0 | 2637 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0008 | 0/0 | 2637 | 3 | 2 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0011 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0017 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0018 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0001c0020 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0002c0002 | 0/1 | 2637 | 89 | 7 | 26 | 39 | 6 | 10 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0002c0019 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0003c0003 | 0/0 | 2637 | 45 | 0 | 3 | 38 | 0 | 4 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0004c0004 | 1/0 | 2637 | 30 | 8 | 3 | 16 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0004c0009 | 0/0 | 2637 | 3 | 0 | 0 | 0 | 3 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0005c0005 | 0/0 | 2637 | 11 | 9 | 0 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0006c0007 | 0/0 | 2637 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0006c0012 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0006c0022 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0007c0010 | 0/0 | 2637 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0007c0013 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0008c0023 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0009c0015 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0010c0014 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0011c0021 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 | ||
| a0012c0016 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | ATGGG others(2632): Show |
chr1 | 116904916 | 116995353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6314 | 82 | 27 | 16 | 28 | 4 | 7 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0005 | 0/0 | 6315 | 6 | 3 | 1 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0007 | 0/0 | 6312 | 5 | 0 | 3 | 0 | 1 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0012 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0014 | 0/0 | 6312 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0016 | 0/0 | 6312 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0018 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0019 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0020 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0037 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0001c0001t0038 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0001c0006t0009 | 0/0 | 6309 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6304): Show |
chr1 | 116904916 | 116995353 |
| a0001c0006t0023 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6304): Show |
chr1 | 116904916 | 116995353 |
| a0001c0008t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0001c0008t0021 | 0/0 | 6314 | 2 | 1 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0011t0001 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0017t0001 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0001c0018t0029 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0001c0020t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0002 | 0/0 | 6312 | 3 | 1 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0003 | 0/0 | 6313 | 39 | 1 | 11 | 18 | 3 | 6 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0004 | 0/0 | 6312 | 26 | 3 | 7 | 11 | 3 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0006 | 0/0 | 6313 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0008 | 0/1 | 6312 | 4 | 0 | 2 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0015 | 0/0 | 6314 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0017 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0022 | 0/0 | 6313 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0024 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0025 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0039 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0040 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0002c0002t0041 | 0/0 | 6315 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0002c0019t0030 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0003c0003t0002 | 0/0 | 6312 | 40 | 0 | 2 | 36 | 0 | 2 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0003c0003t0010 | 0/0 | 6313 | 3 | 0 | 1 | 1 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0003c0003t0026 | 0/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0003c0003t0027 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0001 | 1/0 | 6314 | 24 | 6 | 3 | 12 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0005 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0028 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0032 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0034 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0004c0004t0035 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0004c0009t0001 | 0/0 | 6314 | 2 | 0 | 0 | 0 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0004c0009t0031 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0005c0005t0001 | 0/0 | 6314 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0005c0005t0002 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0005c0005t0003 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0005c0005t0004 | 0/0 | 6312 | 6 | 6 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0005c0005t0015 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0006c0007t0001 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0006c0007t0005 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0006c0007t0012 | 0/0 | 6313 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0006c0012t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0006c0012t0018 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0006c0022t0011 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0007c0010t0013 | 0/0 | 6314 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0007c0013t0002 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0007c0013t0017 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6308): Show |
chr1 | 116904916 | 116995353 |
| a0008c0023t0033 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0009c0015t0001 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6309): Show |
chr1 | 116904916 | 116995353 |
| a0010c0014t0004 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| a0011c0021t0036 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6310): Show |
chr1 | 116904916 | 116995353 |
| a0012c0016t0002 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | CCCTT others(6307): Show |
chr1 | 116904916 | 116995353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0007g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0014g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0016g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0019g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0020g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0037g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0001t0038g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0006t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0006t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0006t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0006t0023g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0008t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0008t0021g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0008t0021g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0011t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0017t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0018t0029g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0001c0020t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0008g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0008g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0008g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0017g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0022g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0022g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0025g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0039g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0040g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0002t0041g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0002c0019t0030g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0010g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0010g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0026g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0003c0003t0027g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0028g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0032g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0034g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0004t0035g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0009t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0004c0009t0031g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0005c0005t0015g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0007t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0007t0012g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0012t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0012t0018g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0006c0022t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0007c0010t0013g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0007c0010t0013g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0007c0010t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0007c0013t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0007c0013t0017g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0008c0023t0033g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0009c0015t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0010c0014t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0011c0021t0036g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| a0012c0016t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0003 | g0001 | EUR | GBR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00280 | hp1 | a0002 | c0002 | t0004 | g0041 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0117 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00408 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0124 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00438 | hp2 | a0004 | c0004 | t0032 | g0255 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00558 | hp1 | a0002 | c0002 | t0004 | g0068 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00558 | hp2 | a0003 | c0003 | t0002 | g0098 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00597 | hp1 | a0002 | c0002 | t0004 | g0103 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0045 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00621 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0078 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | CHS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00733 | hp2 | a0002 | c0002 | t0008 | g0109 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00735 | hp2 | a0002 | c0002 | t0017 | g0179 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0248 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0029 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01099 | hp1 | a0002 | c0002 | t0008 | g0110 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01099 | hp2 | a0002 | c0002 | t0041 | g0121 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0207 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0017 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01109 | hp1 | a0003 | c0003 | t0010 | g0074 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01109 | hp2 | a0001 | c0001 | t0038 | g0198 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01169 | hp1 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01169 | hp2 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0062 | AMR | PUR | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0061 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01258 | hp2 | a0002 | c0002 | t0039 | g0022 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0021 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01346 | hp1 | a0002 | c0002 | t0003 | g0039 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0129 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01433 | hp2 | a0001 | c0008 | t0021 | g0199 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0018 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0059 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01515 | hp2 | a0004 | c0009 | t0001 | g0011 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01516 | hp1 | a0004 | c0004 | t0001 | g0250 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01516 | hp2 | a0002 | c0002 | t0004 | g0064 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01517 | hp1 | a0004 | c0004 | t0001 | g0251 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01517 | hp2 | a0004 | c0009 | t0001 | g0011 | EUR | IBS | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01884 | hp1 | a0002 | c0002 | t0004 | g0065 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01891 | hp1 | a0007 | c0013 | t0017 | g0283 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01928 | hp1 | a0003 | c0003 | t0002 | g0171 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01928 | hp2 | a0002 | c0002 | t0022 | g0020 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01934 | hp1 | a0002 | c0002 | t0004 | g0178 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01934 | hp2 | a0002 | c0002 | t0006 | g0139 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0009 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0083 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01952 | hp1 | a0002 | c0002 | t0022 | g0019 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01952 | hp2 | a0002 | c0002 | t0004 | g0249 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0172 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG01978 | hp2 | a0002 | c0002 | t0004 | g0180 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02015 | hp1 | a0002 | c0002 | t0015 | g0173 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02015 | hp2 | a0004 | c0004 | t0001 | g0241 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02027 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02027 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02071 | hp2 | a0004 | c0004 | t0001 | g0235 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02132 | hp1 | a0004 | c0004 | t0001 | g0256 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02145 | hp1 | a0007 | c0010 | t0013 | g0286 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02145 | hp2 | a0004 | c0004 | t0028 | g0112 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0257 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0080 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0143 | EAS | CDX | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02257 | hp1 | a0008 | c0023 | t0033 | g0281 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02273 | hp1 | a0004 | c0004 | t0001 | g0262 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02273 | hp2 | a0002 | c0002 | t0004 | g0009 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02293 | hp1 | a0004 | c0004 | t0001 | g0261 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0084 | AMR | PEL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0292 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0218 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0196 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02622 | hp1 | a0005 | c0005 | t0004 | g0232 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02622 | hp2 | a0001 | c0008 | t0011 | g0233 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02630 | hp1 | a0007 | c0010 | t0013 | g0284 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02698 | hp2 | a0003 | c0003 | t0010 | g0092 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02717 | hp2 | a0001 | c0008 | t0021 | g0044 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02723 | hp2 | a0002 | c0019 | t0030 | g0270 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02735 | hp1 | a0009 | c0015 | t0001 | g0140 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02735 | hp2 | a0005 | c0005 | t0003 | g0252 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02809 | hp1 | a0010 | c0014 | t0004 | g0114 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02809 | hp2 | a0006 | c0007 | t0001 | g0282 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02818 | hp2 | a0006 | c0012 | t0011 | g0266 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02886 | hp2 | a0005 | c0005 | t0004 | g0210 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02895 | hp2 | a0001 | c0001 | t0020 | g0201 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02896 | hp1 | a0006 | c0007 | t0012 | g0015 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02896 | hp2 | a0004 | c0004 | t0001 | g0219 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02897 | hp1 | a0006 | c0007 | t0012 | g0015 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0289 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02965 | hp2 | a0001 | c0006 | t0009 | g0212 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02970 | hp1 | a0005 | c0005 | t0004 | g0215 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0269 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02976 | hp2 | a0004 | c0004 | t0034 | g0223 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03041 | hp1 | a0001 | c0001 | t0019 | g0148 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0200 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0279 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03139 | hp1 | a0001 | c0006 | t0009 | g0211 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03139 | hp2 | a0005 | c0005 | t0001 | g0217 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03195 | hp1 | a0006 | c0012 | t0018 | g0267 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03195 | hp2 | a0001 | c0011 | t0001 | g0013 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0263 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03225 | hp2 | a0001 | c0006 | t0023 | g0214 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0023 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03486 | hp1 | a0005 | c0005 | t0002 | g0272 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03486 | hp2 | a0011 | c0021 | t0036 | g0287 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03516 | hp1 | a0004 | c0004 | t0001 | g0221 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03540 | hp1 | a0007 | c0013 | t0002 | g0268 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03540 | hp2 | a0006 | c0022 | t0011 | g0265 | AFR | GWD | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03579 | hp1 | a0005 | c0005 | t0004 | g0222 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0253 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03654 | hp2 | a0001 | c0001 | t0016 | g0228 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0160 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03669 | hp2 | a0001 | c0001 | t0016 | g0229 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03688 | hp1 | a0003 | c0003 | t0026 | g0116 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0115 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0060 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0186 | SAS | PJL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03831 | hp1 | a0001 | c0017 | t0001 | g0048 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0123 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03942 | hp2 | a0002 | c0002 | t0008 | g0108 | SAS | BEB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0107 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0089 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0102 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0130 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18612 | hp2 | a0002 | c0002 | t0004 | g0067 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18747 | hp1 | a0003 | c0003 | t0002 | g0087 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18906 | hp1 | a0005 | c0005 | t0001 | g0220 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18906 | hp2 | a0006 | c0007 | t0005 | g0280 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18939 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18944 | hp2 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18947 | hp2 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18950 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18951 | hp2 | a0004 | c0004 | t0001 | g0237 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18956 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18957 | hp1 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18957 | hp2 | a0002 | c0002 | t0006 | g0170 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0086 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18963 | hp1 | a0004 | c0004 | t0005 | g0238 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18964 | hp1 | a0003 | c0003 | t0027 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18968 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18968 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18973 | hp1 | a0004 | c0004 | t0001 | g0244 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18974 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18977 | hp1 | a0002 | c0002 | t0006 | g0104 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18978 | hp2 | a0002 | c0002 | t0006 | g0132 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18982 | hp2 | a0002 | c0002 | t0025 | g0106 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18985 | hp1 | a0004 | c0004 | t0001 | g0264 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18985 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0051 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0054 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19000 | hp2 | a0002 | c0002 | t0004 | g0096 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19001 | hp1 | a0004 | c0004 | t0005 | g0259 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19002 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19004 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0099 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19030 | hp1 | a0005 | c0005 | t0004 | g0216 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19043 | hp1 | a0001 | c0001 | t0037 | g0273 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0224 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0077 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19058 | hp1 | a0005 | c0005 | t0015 | g0242 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19060 | hp1 | a0004 | c0004 | t0001 | g0239 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19062 | hp2 | a0002 | c0002 | t0006 | g0105 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19063 | hp2 | a0003 | c0003 | t0002 | g0050 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19065 | hp1 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19065 | hp2 | a0002 | c0002 | t0006 | g0033 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19066 | hp2 | a0003 | c0003 | t0002 | g0128 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19074 | hp2 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19077 | hp1 | a0003 | c0003 | t0002 | g0245 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19080 | hp1 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19080 | hp2 | a0002 | c0002 | t0015 | g0024 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0094 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19083 | hp1 | a0003 | c0003 | t0010 | g0097 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19083 | hp2 | a0004 | c0004 | t0001 | g0254 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19085 | hp2 | a0012 | c0016 | t0002 | g0049 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0125 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19091 | hp2 | a0004 | c0004 | t0035 | g0247 | EAS | JPT | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19240 | hp1 | a0001 | c0011 | t0001 | g0013 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA19240 | hp2 | a0007 | c0010 | t0013 | g0285 | AFR | YRI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20129 | hp2 | a0002 | c0002 | t0024 | g0066 | AFR | ASW | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0113 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20805 | hp1 | a0004 | c0009 | t0031 | g0147 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20805 | hp2 | a0002 | c0002 | t0003 | g0136 | EUR | TSI | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20905 | hp2 | a0002 | c0002 | t0040 | g0141 | SAS | GIH | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02109 | hp2 | a0001 | c0006 | t0009 | g0213 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03471 | hp1 | a0005 | c0005 | t0004 | g0209 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| HG06807 | hp2 | a0002 | c0002 | t0004 | g0260 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20300 | hp1 | a0004 | c0004 | t0001 | g0271 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0119 | AFR | USA | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA21309 | hp1 | a0001 | c0018 | t0029 | g0040 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| NA21309 | hp2 | a0001 | c0020 | t0001 | g0187 | AFR | LWK | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0008 | g0174 | REF | REF | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0090 | REF | REF | PTGFRN_chr1_116904916_116995353 | PTGFRN | chr1 | 116904916 | 116995353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116910247 | C | G | 4 | a0006 a0007 a0008 others(1): Show |
14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
missense_variant | MODERATE | c.44C>G | p.Ser15Trp | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/9 | 332/6314 | 44/2640 | 15/879 | chr1 | 116910247 | |||
| chr1:116944717 | C | A | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.457C>A | p.Pro153Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 745/6314 | 457/2640 | 153/879 | chr1 | 116944717 | |||
| chr1:116945089 | T | A | 8 | a0001 a0002 a0003 others(5): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
missense_variant | MODERATE | c.829T>A | p.Ser277Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 1117/6314 | 829/2640 | 277/879 | chr1 | 116945089 | |||
| chr1:116949339 | G | C | 1 | a0009 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.980G>C | p.Gly327Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/9 | 1268/6314 | 980/2640 | 327/879 | chr1 | 116949339 | |||
| chr1:116961318 | G | A | 2 | a0003 a0012 |
46 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(43): Show |
missense_variant | MODERATE | c.1289G>A | p.Arg430Gln | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1577/6314 | 1289/2640 | 430/879 | chr1 | 116961318 | |||
| chr1:116961399 | A | G | 1 | a0012 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1370A>G | p.Asn457Ser | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1658/6314 | 1370/2640 | 457/879 | chr1 | 116961399 | |||
| chr1:116984919 | A | G | 1 | a0010 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2407A>G | p.Thr803Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/9 | 2695/6314 | 2407/2640 | 803/879 | chr1 | 116984919 | |||
| chr1:116986836 | G | A | 6 | a0002 a0003 a0005 others(3): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
missense_variant | MODERATE | c.2509G>A | p.Val837Ile | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2797/6314 | 2509/2640 | 837/879 | chr1 | 116986836 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116941959 | C | T | 1 | a0001c0011 | 2 | HG03195.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.294C>T | p.Ala98Ala | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/9 | 582/6314 | 294/2640 | 98/879 | chr1 | 116941959 | |||
| chr1:116944722 | G | A | 3 | a0001c0006 a0006c0012 a0006c0022 |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.462G>A | p.Pro154Pro | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 750/6314 | 462/2640 | 154/879 | chr1 | 116944722 | |||
| chr1:116944770 | C | T | 1 | a0004c0009 | 3 | HG01515.hp2 HG01517.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.510C>T | p.Thr170Thr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 798/6314 | 510/2640 | 170/879 | chr1 | 116944770 | |||
| chr1:116945088 | A | G | 18 | a0001c0001 a0001c0006 a0001c0008 others(15): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
synonymous_variant | LOW | c.828A>G | p.Pro276Pro | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/9 | 1116/6314 | 828/2640 | 276/879 | chr1 | 116945088 | |||
| chr1:116949502 | A | G | 1 | a0007c0010 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1143A>G | p.Gly381Gly | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/9 | 1431/6314 | 1143/2640 | 381/879 | chr1 | 116949502 | |||
| chr1:116961571 | C | T | 3 | a0001c0008 a0006c0022 a0011c0021 |
5 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
synonymous_variant | LOW | c.1542C>T | p.Tyr514Tyr | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/9 | 1830/6314 | 1542/2640 | 514/879 | chr1 | 116961571 | |||
| chr1:116967053 | C | T | 1 | a0001c0020 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1782C>T | p.Gly594Gly | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2070/6314 | 1782/2640 | 594/879 | chr1 | 116967053 | |||
| chr1:116967110 | G | T | 1 | a0002c0019 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1839G>T | p.Val613Val | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2127/6314 | 1839/2640 | 613/879 | chr1 | 116967110 | |||
| chr1:116967311 | G | A | 1 | a0002c0019 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2040G>A | p.Glu680Glu | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/9 | 2328/6314 | 2040/2640 | 680/879 | chr1 | 116967311 | |||
| chr1:116984822 | C | T | 1 | a0001c0011 | 2 | HG03195.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.2310C>T | p.Arg770Arg | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/9 | 2598/6314 | 2310/2640 | 770/879 | chr1 | 116984822 | |||
| chr1:116986829 | G | T | 1 | a0001c0018 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2502G>T | p.Leu834Leu | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2790/6314 | 2502/2640 | 834/879 | chr1 | 116986829 | |||
| chr1:116986856 | C | T | 1 | a0001c0017 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2529C>T | p.Ile843Ile | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2817/6314 | 2529/2640 | 843/879 | chr1 | 116986856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116910138 | AGAG | A | 2 | a0001c0006t0009 a0001c0006t0023 |
4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-51delGAG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/9 | 51 | INFO_REALIGN_3_PRIME | chr1 | 116910138 | |||||
| chr1:116987237 | A | AT | 9 | a0002c0002t0003 a0002c0002t0006 a0002c0002t0015 others(6): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*278dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 279 | INFO_REALIGN_3_PRIME | chr1 | 116987237 | |||||
| chr1:116987343 | A | G | 3 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0038 |
9 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 376 | chr1 | 116987343 | ||||||
| chr1:116987367 | C | T | 1 | a0001c0006t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 400 | chr1 | 116987367 | ||||||
| chr1:116987460 | C | T | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 493 | chr1 | 116987460 | ||||||
| chr1:116987571 | C | CT | 5 | a0001c0001t0005 a0001c0001t0037 a0004c0004t0005 others(2): Show |
11 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*623dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 624 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | |||||
| chr1:116987571 | CT | C | 14 | a0001c0001t0012 a0001c0001t0018 a0001c0008t0011 others(11): Show |
18 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*623delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 623 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | |||||
| chr1:116987571 | CTT | C | 26 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0016 others(23): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*622_*623delTT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 622 | INFO_REALIGN_3_PRIME | chr1 | 116987571 | |||||
| chr1:116987631 | T | C | 1 | a0002c0002t0022 | 2 | HG01928.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*664T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 664 | chr1 | 116987631 | ||||||
| chr1:116987651 | A | G | 49 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(46): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 684 | chr1 | 116987651 | ||||||
| chr1:116987855 | G | A | 48 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(45): Show |
182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 888 | chr1 | 116987855 | ||||||
| chr1:116987885 | C | T | 44 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(41): Show |
175 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*918C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 918 | chr1 | 116987885 | ||||||
| chr1:116987889 | C | T | 48 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(45): Show |
182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 922 | chr1 | 116987889 | ||||||
| chr1:116987942 | A | G | 1 | a0002c0019t0030 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*975A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 975 | chr1 | 116987942 | ||||||
| chr1:116987965 | T | C | 3 | a0001c0006t0009 a0001c0006t0023 a0004c0004t0034 |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*998T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 998 | chr1 | 116987965 | ||||||
| chr1:116987999 | A | G | 10 | a0002c0002t0003 a0002c0002t0006 a0002c0002t0015 others(7): Show |
55 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1032A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1032 | chr1 | 116987999 | ||||||
| chr1:116988040 | C | A | 1 | a0004c0009t0031 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1073 | chr1 | 116988040 | ||||||
| chr1:116988081 | G | A | 1 | a0004c0004t0032 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1114 | chr1 | 116988081 | ||||||
| chr1:116988105 | T | C | 1 | a0002c0002t0024 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1138 | chr1 | 116988105 | ||||||
| chr1:116988179 | A | G | 2 | a0001c0001t0020 a0008c0023t0033 |
3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1212 | chr1 | 116988179 | ||||||
| chr1:116988418 | C | T | 1 | a0001c0001t0038 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1451 | chr1 | 116988418 | ||||||
| chr1:116988500 | A | G | 4 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0016 others(1): Show |
11 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1533A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1533 | chr1 | 116988500 | ||||||
| chr1:116988705 | C | T | 1 | a0001c0001t0019 | 2 | HG02615.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1738 | chr1 | 116988705 | ||||||
| chr1:116988811 | C | G | 1 | a0002c0019t0030 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1844C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1844 | chr1 | 116988811 | ||||||
| chr1:116988813 | C | T | 1 | a0001c0001t0016 | 2 | HG03654.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 1846 | chr1 | 116988813 | ||||||
| chr1:116988998 | G | A | 31 | a0001c0001t0016 a0001c0006t0009 a0001c0006t0023 others(28): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2031G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2031 | chr1 | 116988998 | ||||||
| chr1:116988999 | A | G | 9 | a0002c0002t0002 a0003c0003t0002 a0003c0003t0010 others(6): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2032A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2032 | chr1 | 116988999 | ||||||
| chr1:116989005 | A | G | 4 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0016 others(1): Show |
11 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2038A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2038 | chr1 | 116989005 | ||||||
| chr1:116989191 | T | C | 49 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0014 others(46): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2224T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2224 | chr1 | 116989191 | ||||||
| chr1:116989289 | A | G | 32 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0020 others(29): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2322A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2322 | chr1 | 116989289 | ||||||
| chr1:116989409 | T | C | 1 | a0011c0021t0036 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2442T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2442 | chr1 | 116989409 | ||||||
| chr1:116989533 | C | T | 1 | a0007c0010t0013 | 3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2566C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2566 | chr1 | 116989533 | ||||||
| chr1:116989534 | G | A | 1 | a0002c0002t0039 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2567 | chr1 | 116989534 | ||||||
| chr1:116989669 | A | G | 19 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0018 others(16): Show |
68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2702A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2702 | chr1 | 116989669 | ||||||
| chr1:116989690 | T | G | 1 | a0002c0002t0025 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2723T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2723 | chr1 | 116989690 | ||||||
| chr1:116989750 | G | T | 27 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0018 others(24): Show |
111 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2783G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2783 | chr1 | 116989750 | ||||||
| chr1:116989755 | A | T | 1 | a0002c0002t0006 | 6 | HG01934.hp2 NA18957.hp2 NA18977.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2788A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2788 | chr1 | 116989755 | ||||||
| chr1:116989887 | C | A | 3 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0038 |
9 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2920C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2920 | chr1 | 116989887 | ||||||
| chr1:116989897 | C | G | 1 | a0002c0002t0008 | 3 | HG00733.hp2 HG01099.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2930C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2930 | chr1 | 116989897 | ||||||
| chr1:116989912 | C | T | 1 | a0004c0004t0028 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2945 | chr1 | 116989912 | ||||||
| chr1:116989927 | C | T | 1 | a0002c0002t0040 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2960C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 2960 | chr1 | 116989927 | ||||||
| chr1:116990168 | C | T | 32 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0018 others(29): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3201C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3201 | chr1 | 116990168 | ||||||
| chr1:116990176 | C | G | 15 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0018 others(12): Show |
63 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3209C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3209 | chr1 | 116990176 | ||||||
| chr1:116990193 | A | G | 1 | a0003c0003t0027 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3226A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3226 | chr1 | 116990193 | ||||||
| chr1:116990207 | A | G | 1 | a0003c0003t0026 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3240A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3240 | chr1 | 116990207 | ||||||
| chr1:116990269 | T | C | 11 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0020 others(8): Show |
23 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3302T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 9/9 | 3302 | chr1 | 116990269 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116910638 | G | C | 7 | a0002c0002t0003g0016 a0002c0002t0003g0017 a0002c0002t0003g0018 others(4): Show |
7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+386G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910638 | |||||||
| chr1:116910668 | C | T | 5 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+416C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910668 | |||||||
| chr1:116910720 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.49+468G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910720 | |||||||
| chr1:116910911 | A | G | 71 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(68): Show |
78 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+659A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116910911 | |||||||
| chr1:116911063 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.49+811C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911063 | |||||||
| chr1:116911080 | A | G | 9 | a0006c0007t0001g0282 a0006c0007t0005g0280 a0006c0007t0012g0015 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+828A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911080 | |||||||
| chr1:116911133 | G | A | 39 | a0001c0001t0001g0227 a0001c0001t0001g0230 a0001c0001t0001g0231 others(36): Show |
41 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.49+881G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911133 | |||||||
| chr1:116911165 | C | G | 58 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(55): Show |
64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+913C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911165 | |||||||
| chr1:116911173 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.49+921C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911173 | |||||||
| chr1:116911321 | C | T | 16 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(13): Show |
16 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+1069C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911321 | |||||||
| chr1:116911402 | A | G | 13 | a0006c0007t0001g0282 a0006c0007t0005g0280 a0006c0007t0012g0015 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1150A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911402 | |||||||
| chr1:116911403 | T | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(68): Show |
78 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+1151T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911403 | |||||||
| chr1:116911407 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(55): Show |
64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1155T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911407 | |||||||
| chr1:116911478 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49+1226C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911478 | |||||||
| chr1:116911502 | C | T | 1 | a0004c0004t0001g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.49+1250C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911502 | |||||||
| chr1:116911508 | C | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+1256C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911508 | |||||||
| chr1:116911590 | T | G | 1 | a0002c0002t0003g0023 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+1338T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911590 | |||||||
| chr1:116911686 | A | G | 13 | a0006c0007t0001g0282 a0006c0007t0005g0280 a0006c0007t0012g0015 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1434A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911686 | |||||||
| chr1:116911717 | A | C | 9 | a0006c0007t0001g0282 a0006c0007t0005g0280 a0006c0007t0012g0015 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1465A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911717 | |||||||
| chr1:116911803 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 |
4 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1551C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911803 | |||||||
| chr1:116911866 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(55): Show |
64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1614C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911866 | |||||||
| chr1:116911948 | G | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(55): Show |
64 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1696G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116911948 | |||||||
| chr1:116912190 | C | T | 1 | a0002c0002t0004g0207 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49+1938C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912190 | |||||||
| chr1:116912296 | A | G | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.49+2044A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912296 | |||||||
| chr1:116912367 | G | A | 1 | a0002c0002t0015g0024 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.49+2115G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912367 | |||||||
| chr1:116912431 | A | G | 9 | a0006c0007t0001g0282 a0006c0007t0005g0280 a0006c0007t0012g0015 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+2179A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912431 | |||||||
| chr1:116912472 | C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+2220C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912472 | |||||||
| chr1:116912499 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG01192.hp2 HG01358.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+2247C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912499 | |||||||
| chr1:116912820 | C | T | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0199 |
3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+2568C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912820 | |||||||
| chr1:116912866 | G | C | 1 | a0001c0001t0001g0025 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.49+2614G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912866 | |||||||
| chr1:116912927 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0274 a0001c0001t0001g0275 others(10): Show |
17 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.49+2675C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912927 | |||||||
| chr1:116912931 | C | T | 44 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0234 others(41): Show |
46 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.49+2679C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116912931 | |||||||
| chr1:116913214 | A | C | 1 | a0001c0001t0038g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.49+2962A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913214 | |||||||
| chr1:116913379 | C | T | 1 | a0001c0001t0007g0012 | 2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.49+3127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913379 | |||||||
| chr1:116913413 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.49+3161G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913413 | |||||||
| chr1:116913588 | A | G | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+3336A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913588 | |||||||
| chr1:116913778 | A | G | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0199 |
3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+3526A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913778 | |||||||
| chr1:116913805 | A | G | 16 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(13): Show |
16 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+3553A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913805 | |||||||
| chr1:116913822 | G | C | 15 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(12): Show |
15 | HG02109.hp2 HG02615.hp1 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+3570G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913822 | |||||||
| chr1:116913884 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0002c0002t0003g0027 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+3632G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116913884 | |||||||
| chr1:116914003 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0037g0273 a0004c0004t0001g0271 others(1): Show |
6 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+3751T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914003 | |||||||
| chr1:116914217 | C | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0005g0193 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3965C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914217 | |||||||
| chr1:116914309 | G | A | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.49+4057G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914309 | |||||||
| chr1:116914314 | A | G | 19 | a0001c0001t0001g0005 a0001c0001t0037g0273 a0001c0006t0009g0211 others(16): Show |
21 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.49+4062A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914314 | |||||||
| chr1:116914331 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
7 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+4079C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914331 | |||||||
| chr1:116914393 | G | C | 3 | a0006c0012t0011g0266 a0006c0012t0018g0267 a0006c0022t0011g0265 |
3 | HG02818.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.49+4141G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914393 | |||||||
| chr1:116914505 | C | G | 2 | a0004c0004t0001g0261 a0004c0004t0001g0262 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.49+4253C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914505 | |||||||
| chr1:116914800 | A | G | 1 | a0002c0002t0004g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.49+4548A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914800 | |||||||
| chr1:116914822 | T | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49+4570T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116914822 | |||||||
| chr1:116914856 | TC | T | 25 | a0001c0001t0001g0026 a0001c0001t0001g0175 a0001c0001t0001g0181 others(22): Show |
26 | HG00621.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.49+4606delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116914856 | ||||||
| chr1:116915029 | T | G | 1 | a0002c0002t0004g0207 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49+4777T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915029 | |||||||
| chr1:116915164 | T | G | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.49+4912T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915164 | |||||||
| chr1:116915242 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(83): Show |
93 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(90): Show |
intron_variant | MODIFIER | c.49+4990G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915242 | |||||||
| chr1:116915477 | T | A | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+5225T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915477 | |||||||
| chr1:116915670 | C | G | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0199 |
3 | HG01433.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+5418C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915670 | |||||||
| chr1:116915753 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(86): Show |
96 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(93): Show |
intron_variant | MODIFIER | c.49+5501G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915753 | |||||||
| chr1:116915862 | T | A | 5 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+5610T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915862 | |||||||
| chr1:116915937 | G | T | 2 | a0004c0004t0001g0261 a0004c0004t0001g0262 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.49+5685G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116915937 | |||||||
| chr1:116916077 | C | T | 1 | a0002c0002t0015g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.49+5825C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916077 | |||||||
| chr1:116916108 | T | C | 25 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(22): Show |
27 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+5856T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916108 | |||||||
| chr1:116916184 | A | G | 6 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5932A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916184 | |||||||
| chr1:116916553 | G | T | 2 | a0003c0003t0002g0171 a0003c0003t0002g0172 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.49+6301G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916553 | |||||||
| chr1:116916610 | G | A | 2 | a0001c0001t0001g0175 a0001c0008t0021g0199 |
2 | HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.49+6358G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916610 | |||||||
| chr1:116916664 | G | A | 1 | a0002c0002t0003g0023 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+6412G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916664 | |||||||
| chr1:116916766 | G | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+6514G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916766 | |||||||
| chr1:116916769 | A | C | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.49+6517A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916769 | |||||||
| chr1:116916977 | G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+6725G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116916977 | |||||||
| chr1:116917154 | A | G | 1 | a0002c0002t0006g0170 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.49+6902A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917154 | |||||||
| chr1:116917213 | T | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(58): Show |
66 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.49+6961T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917213 | |||||||
| chr1:116917289 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49+7037G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917289 | |||||||
| chr1:116917309 | AAC | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(58): Show |
66 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.49+7059_49+7060del others(2): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116917309 | ||||||
| chr1:116917662 | C | G | 82 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0028 others(79): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.49+7410C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917662 | |||||||
| chr1:116917794 | T | C | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+7542T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917794 | |||||||
| chr1:116917832 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(4): Show |
9 | HG02109.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+7580G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917832 | |||||||
| chr1:116917902 | C | T | 12 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(9): Show |
13 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+7650C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917902 | |||||||
| chr1:116917961 | C | T | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+7709C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116917961 | |||||||
| chr1:116918121 | A | G | 11 | a0004c0004t0001g0218 a0004c0004t0001g0219 a0004c0004t0001g0221 others(8): Show |
11 | HG02615.hp1 HG02809.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+7869A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918121 | |||||||
| chr1:116918165 | G | C | 1 | a0002c0002t0004g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49+7913G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918165 | |||||||
| chr1:116918278 | T | C | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+8026T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918278 | |||||||
| chr1:116918312 | T | C | 40 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0194 others(37): Show |
43 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+8060T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918312 | |||||||
| chr1:116918476 | A | G | 4 | a0001c0006t0023g0214 a0006c0012t0011g0266 a0006c0012t0018g0267 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+8224A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918476 | |||||||
| chr1:116918483 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0005g0291 a0004c0004t0001g0289 |
3 | HG01891.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.49+8231G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918483 | |||||||
| chr1:116918568 | A | G | 6 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+8316A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918568 | |||||||
| chr1:116918653 | G | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+8401G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918653 | |||||||
| chr1:116918720 | A | C | 1 | a0002c0002t0004g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.49+8468A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918720 | |||||||
| chr1:116918978 | T | C | 12 | a0004c0004t0001g0218 a0004c0004t0001g0219 a0004c0004t0001g0221 others(9): Show |
12 | HG02615.hp1 HG02809.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+8726T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116918978 | |||||||
| chr1:116919291 | G | A | 15 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+9039G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919291 | |||||||
| chr1:116919313 | A | G | 2 | a0001c0001t0020g0200 a0001c0001t0020g0201 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+9061A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919313 | |||||||
| chr1:116919392 | G | A | 1 | a0002c0002t0004g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.49+9140G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919392 | |||||||
| chr1:116919417 | A | T | 3 | a0001c0001t0037g0273 a0004c0004t0001g0271 a0005c0005t0002g0272 |
3 | HG03486.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.49+9165A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919417 | |||||||
| chr1:116919428 | G | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9176G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919428 | |||||||
| chr1:116919460 | C | T | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0044 others(1): Show |
4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+9208C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919460 | |||||||
| chr1:116919484 | A | G | 2 | a0004c0004t0001g0004 a0004c0004t0005g0259 |
4 | NA18990.hp1 NA19001.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+9232A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919484 | |||||||
| chr1:116919491 | T | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9239T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919491 | |||||||
| chr1:116919496 | G | C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9244G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919496 | |||||||
| chr1:116919530 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9278C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919530 | |||||||
| chr1:116919856 | T | G | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+9604T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919856 | |||||||
| chr1:116919920 | C | T | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0044 others(1): Show |
4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+9668C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116919920 | |||||||
| chr1:116920026 | C | G | 15 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+9774C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920026 | |||||||
| chr1:116920069 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9817C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920069 | |||||||
| chr1:116920178 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+9926C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920178 | |||||||
| chr1:116920319 | T | C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10067T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920319 | |||||||
| chr1:116920518 | C | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(64): Show |
72 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.49+10266C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920518 | |||||||
| chr1:116920532 | C | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10280C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920532 | |||||||
| chr1:116920596 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10344A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920596 | |||||||
| chr1:116920706 | C | T | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.49+10454C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920706 | |||||||
| chr1:116920731 | C | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+10479C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920731 | |||||||
| chr1:116920894 | G | A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0031 others(51): Show |
59 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+10642G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920894 | |||||||
| chr1:116920915 | T | C | 156 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0025 others(153): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.49+10663T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116920915 | |||||||
| chr1:116921093 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0230 others(90): Show |
100 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(97): Show |
intron_variant | MODIFIER | c.49+10841T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921093 | |||||||
| chr1:116921228 | G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+10976G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921228 | |||||||
| chr1:116921260 | G | A | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.49+11008G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921260 | |||||||
| chr1:116921273 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(71): Show |
79 | HG00280.hp2 HG00438.hp2 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.49+11021A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921273 | |||||||
| chr1:116921275 | C | T | 7 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+11023C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921275 | |||||||
| chr1:116921550 | A | C | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49+11298A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921550 | |||||||
| chr1:116921630 | C | CTT | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+11390_49+11391d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116921630 | ||||||
| chr1:116921676 | C | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49+11424C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921676 | |||||||
| chr1:116921797 | G | A | 5 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+11545G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921797 | |||||||
| chr1:116921840 | A | G | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+11588A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921840 | |||||||
| chr1:116921915 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+11663C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116921915 | |||||||
| chr1:116922106 | A | G | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+11854A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922106 | |||||||
| chr1:116922125 | C | T | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+11873C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922125 | |||||||
| chr1:116922147 | C | T | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+11895C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922147 | |||||||
| chr1:116922291 | A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+12039A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922291 | |||||||
| chr1:116922578 | G | A | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12326G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922578 | |||||||
| chr1:116922630 | T | C | 15 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
16 | HG01433.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+12378T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922630 | |||||||
| chr1:116922709 | G | A | 1 | a0002c0002t0004g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.49+12457G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922709 | |||||||
| chr1:116922921 | T | C | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.49+12669T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922921 | |||||||
| chr1:116922926 | T | G | 1 | a0002c0002t0004g0047 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.49+12674T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116922926 | |||||||
| chr1:116923094 | T | C | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+12842T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923094 | |||||||
| chr1:116923097 | G | C | 1 | a0001c0017t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.49+12845G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923097 | |||||||
| chr1:116923143 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+12891A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923143 | |||||||
| chr1:116923200 | T | C | 1 | a0012c0016t0002g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.49+12948T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923200 | |||||||
| chr1:116923211 | A | G | 1 | a0003c0003t0002g0172 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.49+12959A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923211 | |||||||
| chr1:116923240 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+12988G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923240 | |||||||
| chr1:116923263 | G | A | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0044 others(1): Show |
4 | HG01433.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+13011G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923263 | |||||||
| chr1:116923281 | C | T | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+13029C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923281 | |||||||
| chr1:116923282 | A | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(89): Show |
99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.49+13030A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923282 | |||||||
| chr1:116923315 | A | G | 1 | a0002c0002t0003g0111 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.49+13063A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923315 | |||||||
| chr1:116923390 | T | A | 4 | a0003c0003t0002g0002 a0003c0003t0002g0050 a0003c0003t0002g0051 others(1): Show |
5 | NA18939.hp2 NA18964.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13138T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923390 | |||||||
| chr1:116923428 | T | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13176T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923428 | |||||||
| chr1:116923484 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0208 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.49+13232T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923484 | |||||||
| chr1:116923531 | T | C | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13279T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923531 | |||||||
| chr1:116923580 | G | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+13328G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923580 | |||||||
| chr1:116923621 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13369G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923621 | |||||||
| chr1:116923718 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+13466G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923718 | |||||||
| chr1:116923930 | A | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49+13678A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116923930 | |||||||
| chr1:116924054 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.49+13802T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924054 | |||||||
| chr1:116924143 | A | AT | 8 | a0001c0001t0001g0168 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
8 | HG00741.hp1 HG02965.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+13913dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | ||||||
| chr1:116924143 | A | ATT | 9 | a0001c0001t0001g0230 a0001c0001t0001g0275 a0001c0001t0001g0276 others(6): Show |
11 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+13912_49+13913d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | ||||||
| chr1:116924143 | AT | A | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0226 others(12): Show |
15 | HG00099.hp2 HG00323.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+13913delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | ||||||
| chr1:116924143 | ATT | A | 30 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0018g0269 others(27): Show |
30 | HG00438.hp2 HG02109.hp2 HG02273.hp1 others(27): Show |
intron_variant | MODIFIER | c.49+13912_49+13913d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | ||||||
| chr1:116924143 | ATTT | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0236 a0001c0001t0001g0243 others(31): Show |
39 | HG01069.hp1 HG01516.hp1 HG01517.hp1 others(36): Show |
intron_variant | MODIFIER | c.49+13911_49+13913d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924143 | ||||||
| chr1:116924184 | T | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+13932T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924184 | |||||||
| chr1:116924233 | C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+13981C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924233 | |||||||
| chr1:116924303 | CACCCG | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14052_49+14056d others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924303 | |||||||
| chr1:116924387 | T | TA | 5 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+14136dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116924387 | ||||||
| chr1:116924551 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(89): Show |
99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.49+14299G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924551 | |||||||
| chr1:116924624 | T | C | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.49+14372T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924624 | |||||||
| chr1:116924636 | C | T | 4 | a0002c0002t0003g0107 a0002c0002t0008g0108 a0002c0002t0008g0109 others(1): Show |
4 | HG00733.hp2 HG01099.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+14384C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924636 | |||||||
| chr1:116924704 | T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+14452T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116924704 | |||||||
| chr1:116925068 | G | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14816G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925068 | |||||||
| chr1:116925069 | A | T | 1 | a0004c0004t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.49+14817A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925069 | |||||||
| chr1:116925156 | AG | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0008t0011g0233 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+14905delG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925156 | |||||||
| chr1:116925212 | G | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.49+14960G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925212 | |||||||
| chr1:116925435 | G | GA | 72 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(69): Show |
77 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.49+15193dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116925435 | ||||||
| chr1:116925759 | A | C | 1 | a0009c0015t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.49+15507A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925759 | |||||||
| chr1:116925954 | G | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+15702G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925954 | |||||||
| chr1:116925995 | T | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-15720T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116925995 | |||||||
| chr1:116926063 | C | T | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-15652C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926063 | |||||||
| chr1:116926064 | AG | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15649delG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116926064 | ||||||
| chr1:116926073 | GTGT | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15636_50-15634d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116926073 | ||||||
| chr1:116926130 | G | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0236 a0001c0001t0001g0243 others(35): Show |
43 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-15585G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926130 | |||||||
| chr1:116926145 | G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.50-15570G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926145 | |||||||
| chr1:116926202 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.50-15513A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926202 | |||||||
| chr1:116926284 | G | C | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-15431G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926284 | |||||||
| chr1:116926286 | G | C | 7 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-15429G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926286 | |||||||
| chr1:116926361 | C | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15354C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926361 | |||||||
| chr1:116926418 | C | A | 1 | a0004c0004t0001g0235 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-15297C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926418 | |||||||
| chr1:116926686 | G | A | 6 | a0001c0001t0001g0058 a0002c0002t0003g0169 a0003c0003t0002g0054 others(3): Show |
6 | NA18951.hp1 NA18964.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-15029G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926686 | |||||||
| chr1:116926700 | T | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-15015T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926700 | |||||||
| chr1:116926740 | C | G | 2 | a0001c0001t0001g0194 a0002c0002t0001g0195 |
2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.50-14975C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926740 | |||||||
| chr1:116926779 | C | G | 27 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0037g0273 others(24): Show |
27 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-14936C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926779 | |||||||
| chr1:116926891 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(70): Show |
78 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-14824A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116926891 | |||||||
| chr1:116927015 | C | T | 92 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(89): Show |
99 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(96): Show |
intron_variant | MODIFIER | c.50-14700C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927015 | |||||||
| chr1:116927113 | C | T | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-14602C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927113 | |||||||
| chr1:116927159 | C | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(74): Show |
82 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(79): Show |
intron_variant | MODIFIER | c.50-14556C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927159 | |||||||
| chr1:116927167 | A | G | 1 | a0002c0002t0025g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.50-14548A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927167 | |||||||
| chr1:116927254 | A | G | 1 | a0001c0006t0023g0214 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-14461A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927254 | |||||||
| chr1:116927401 | A | G | 7 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0005g0291 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-14314A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927401 | |||||||
| chr1:116927469 | G | A | 1 | a0002c0002t0003g0111 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.50-14246G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927469 | |||||||
| chr1:116927525 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(9): Show |
14 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.50-14179_50-14171d others(11): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | ||||||
| chr1:116927525 | C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0231 a0001c0001t0001g0277 a0001c0001t0001g0278 others(29): Show |
32 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-14180_50-14171d others(12): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | ||||||
| chr1:116927525 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0234 a0001c0001t0037g0273 a0004c0004t0001g0221 others(2): Show |
5 | HG02486.hp2 HG03486.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-14181_50-14171d others(13): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | ||||||
| chr1:116927525 | CT | C | 6 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0008t0021g0044 others(3): Show |
6 | HG01433.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-14171delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | ||||||
| chr1:116927525 | CTT | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0236 a0001c0001t0001g0243 others(34): Show |
42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-14172_50-14171d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116927525 | ||||||
| chr1:116927543 | T | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0236 a0001c0001t0001g0243 others(34): Show |
42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-14172T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927543 | |||||||
| chr1:116927598 | A | G | 3 | a0001c0001t0037g0273 a0004c0004t0001g0271 a0005c0005t0002g0272 |
3 | HG03486.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.50-14117A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927598 | |||||||
| chr1:116927690 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0234 others(72): Show |
80 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.50-14025T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927690 | |||||||
| chr1:116927872 | T | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0236 a0001c0001t0001g0243 others(34): Show |
42 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.50-13843T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927872 | |||||||
| chr1:116927988 | G | A | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.50-13727G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927988 | |||||||
| chr1:116927990 | A | T | 13 | a0004c0004t0001g0218 a0004c0004t0001g0219 a0004c0004t0001g0221 others(10): Show |
13 | HG02145.hp2 HG02615.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-13725A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116927990 | |||||||
| chr1:116928207 | G | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-13508G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928207 | |||||||
| chr1:116928223 | G | C | 1 | a0004c0009t0031g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.50-13492G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928223 | |||||||
| chr1:116928228 | C | A | 10 | a0001c0001t0037g0273 a0001c0006t0009g0211 a0001c0006t0009g0212 others(7): Show |
10 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-13487C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928228 | |||||||
| chr1:116928266 | A | G | 4 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13449A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928266 | |||||||
| chr1:116928285 | C | T | 4 | a0001c0001t0001g0278 a0001c0001t0014g0014 a0001c0001t0014g0279 others(1): Show |
5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13430C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928285 | |||||||
| chr1:116928332 | C | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0236 others(46): Show |
55 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-13383C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928332 | |||||||
| chr1:116928336 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.50-13379T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928336 | |||||||
| chr1:116928472 | T | C | 39 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0290 others(36): Show |
39 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-13243T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928472 | |||||||
| chr1:116928631 | G | A | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13084G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928631 | |||||||
| chr1:116928642 | C | CA | 6 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(3): Show |
7 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-13073_50-13072i others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928642 | |||||||
| chr1:116928805 | T | G | 1 | a0001c0011t0001g0013 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12910T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928805 | |||||||
| chr1:116928887 | C | T | 38 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0290 others(35): Show |
38 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.50-12828C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116928887 | |||||||
| chr1:116929292 | C | T | 4 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0008t0011g0233 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-12423C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929292 | |||||||
| chr1:116929334 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-12381A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929334 | |||||||
| chr1:116929353 | C | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-12362C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929353 | |||||||
| chr1:116929404 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50-12311C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929404 | |||||||
| chr1:116929427 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0236 others(51): Show |
61 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.50-12288G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929427 | |||||||
| chr1:116929503 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.50-12212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929503 | |||||||
| chr1:116929532 | C | T | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.50-12183C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929532 | |||||||
| chr1:116929641 | A | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-12074A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929641 | |||||||
| chr1:116929796 | G | C | 1 | a0001c0001t0038g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-11919G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929796 | |||||||
| chr1:116929906 | C | G | 6 | a0001c0001t0001g0230 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
7 | HG02280.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-11809C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929906 | |||||||
| chr1:116929939 | C | T | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-11776C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116929939 | |||||||
| chr1:116930080 | T | G | 1 | a0002c0002t0025g0106 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.50-11635T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930080 | |||||||
| chr1:116930081 | A | G | 41 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0290 others(38): Show |
41 | HG01433.hp2 HG01891.hp2 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-11634A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930081 | |||||||
| chr1:116930193 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0243 others(51): Show |
58 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.50-11522A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930193 | |||||||
| chr1:116930284 | T | C | 32 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0231 others(29): Show |
32 | HG01433.hp2 HG01891.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-11431T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930284 | |||||||
| chr1:116930342 | A | G | 2 | a0001c0001t0001g0146 a0002c0002t0003g0039 |
2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.50-11373A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930342 | |||||||
| chr1:116930377 | A | G | 128 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0028 others(125): Show |
137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.50-11338A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930377 | |||||||
| chr1:116930457 | C | T | 1 | a0002c0002t0006g0139 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.50-11258C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930457 | |||||||
| chr1:116930663 | C | T | 2 | a0001c0001t0037g0273 a0007c0010t0013g0284 |
2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.50-11052C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930663 | |||||||
| chr1:116930714 | C | G | 1 | a0002c0002t0015g0024 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.50-11001C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930714 | |||||||
| chr1:116930719 | A | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0293 a0001c0008t0011g0233 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-10996A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930719 | |||||||
| chr1:116930797 | G | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
68 | HG00735.hp1 HG00741.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.50-10918G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930797 | |||||||
| chr1:116930813 | GC | G | 3 | a0006c0012t0011g0266 a0006c0012t0018g0267 a0006c0022t0011g0265 |
3 | HG02818.hp2 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.50-10900delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116930813 | ||||||
| chr1:116930826 | G | A | 2 | a0001c0001t0001g0028 a0002c0002t0003g0029 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.50-10889G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930826 | |||||||
| chr1:116930841 | C | G | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.50-10874C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930841 | |||||||
| chr1:116930966 | A | G | 43 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0156 others(40): Show |
46 | HG00099.hp2 HG00735.hp1 HG01433.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-10749A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116930966 | |||||||
| chr1:116931130 | A | G | 1 | a0003c0003t0010g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.50-10585A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931130 | |||||||
| chr1:116931133 | C | T | 1 | a0003c0003t0002g0091 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.50-10582C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931133 | |||||||
| chr1:116931218 | G | A | 292 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(289): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.50-10497G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931218 | |||||||
| chr1:116931403 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.50-10312C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931403 | |||||||
| chr1:116931496 | C | CT | 8 | a0001c0001t0001g0293 a0001c0001t0012g0292 a0001c0001t0016g0228 others(5): Show |
8 | HG02145.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-10204dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116931496 | ||||||
| chr1:116931496 | CTTT | C | 55 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(52): Show |
57 | HG00438.hp2 HG01071.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.50-10206_50-10204d others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116931496 | ||||||
| chr1:116931524 | C | T | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10191C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931524 | |||||||
| chr1:116931541 | C | T | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10174C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931541 | |||||||
| chr1:116931588 | C | T | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931588 | |||||||
| chr1:116931607 | T | G | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-10108T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931607 | |||||||
| chr1:116931775 | A | G | 199 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.50-9940A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931775 | |||||||
| chr1:116931849 | G | A | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-9866G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931849 | |||||||
| chr1:116931986 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0278 a0001c0001t0014g0014 others(5): Show |
12 | HG01515.hp2 HG01517.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-9729C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116931986 | |||||||
| chr1:116932185 | G | C | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-9530G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932185 | |||||||
| chr1:116932254 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9461G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932254 | |||||||
| chr1:116932321 | A | G | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-9394A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932321 | |||||||
| chr1:116932334 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9381G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932334 | |||||||
| chr1:116932344 | G | A | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-9371G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932344 | |||||||
| chr1:116932358 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9357G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932358 | |||||||
| chr1:116932392 | G | A | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-9323G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932392 | |||||||
| chr1:116932535 | C | T | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9180C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932535 | |||||||
| chr1:116932553 | A | G | 190 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.50-9162A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932553 | |||||||
| chr1:116932619 | C | A | 1 | a0003c0003t0002g0069 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.50-9096C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932619 | |||||||
| chr1:116932624 | A | AT | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9089dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116932624 | ||||||
| chr1:116932636 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-9079G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932636 | |||||||
| chr1:116932839 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-8876G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932839 | |||||||
| chr1:116932943 | T | A | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-8772T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116932943 | |||||||
| chr1:116933093 | A | G | 190 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.50-8622A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933093 | |||||||
| chr1:116933170 | A | G | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(233): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.50-8545A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933170 | |||||||
| chr1:116933360 | G | T | 236 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(233): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.50-8355G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933360 | |||||||
| chr1:116933371 | C | A | 1 | a0001c0001t0001g0025 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.50-8344C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933371 | |||||||
| chr1:116933619 | G | T | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-8096G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933619 | |||||||
| chr1:116933822 | T | G | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7893T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933822 | |||||||
| chr1:116933844 | A | G | 184 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.50-7871A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116933844 | |||||||
| chr1:116934200 | C | G | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7515C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934200 | |||||||
| chr1:116934224 | C | T | 7 | a0001c0001t0016g0228 a0001c0001t0016g0229 a0001c0001t0018g0269 others(4): Show |
7 | HG02145.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-7491C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934224 | |||||||
| chr1:116934486 | C | G | 45 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0006t0009g0211 others(42): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-7229C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934486 | |||||||
| chr1:116934619 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7096G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934619 | |||||||
| chr1:116934630 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934630 | |||||||
| chr1:116934674 | A | G | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.50-7041A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934674 | |||||||
| chr1:116934675 | T | C | 1 | a0003c0003t0002g0158 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.50-7040T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934675 | |||||||
| chr1:116934679 | CT | C | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-7034delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116934679 | ||||||
| chr1:116934764 | G | T | 184 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(181): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.50-6951G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934764 | |||||||
| chr1:116934852 | A | G | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6863A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934852 | |||||||
| chr1:116934950 | A | G | 251 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(248): Show |
262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.50-6765A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116934950 | |||||||
| chr1:116935198 | G | C | 251 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(248): Show |
262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.50-6517G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935198 | |||||||
| chr1:116935248 | G | A | 10 | a0001c0001t0001g0293 a0001c0001t0012g0292 a0001c0001t0016g0228 others(7): Show |
10 | HG02145.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-6467G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935248 | |||||||
| chr1:116935423 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.50-6292T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935423 | |||||||
| chr1:116935484 | G | A | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6231G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935484 | |||||||
| chr1:116935662 | T | C | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-6053T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935662 | |||||||
| chr1:116935735 | G | A | 2 | a0004c0004t0001g0224 a0008c0023t0033g0281 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.50-5980G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935735 | |||||||
| chr1:116935860 | T | C | 1 | a0002c0002t0004g0249 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.50-5855T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935860 | |||||||
| chr1:116935954 | G | A | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-5761G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935954 | |||||||
| chr1:116935961 | T | A | 1 | a0005c0005t0004g0210 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.50-5754T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116935961 | |||||||
| chr1:116936242 | TAAC | T | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-5470_50-5468del others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 116936242 | ||||||
| chr1:116936359 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0230 others(8): Show |
12 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-5356T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936359 | |||||||
| chr1:116936571 | T | C | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-5144T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936571 | |||||||
| chr1:116936623 | C | T | 45 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0006t0009g0211 others(42): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-5092C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936623 | |||||||
| chr1:116936669 | A | G | 1 | a0004c0004t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.50-5046A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936669 | |||||||
| chr1:116936749 | C | T | 57 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0001g0243 others(54): Show |
59 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.50-4966C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936749 | |||||||
| chr1:116936871 | G | A | 1 | a0002c0002t0004g0249 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.50-4844G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936871 | |||||||
| chr1:116936953 | T | C | 45 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0006t0009g0211 others(42): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-4762T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936953 | |||||||
| chr1:116936958 | G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-4757G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116936958 | |||||||
| chr1:116937072 | A | C | 1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-4643A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937072 | |||||||
| chr1:116937130 | T | C | 264 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(261): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.50-4585T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937130 | |||||||
| chr1:116937541 | G | T | 45 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0006t0009g0211 others(42): Show |
47 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-4174G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937541 | |||||||
| chr1:116937658 | G | T | 1 | a0002c0002t0006g0105 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-4057G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937658 | |||||||
| chr1:116937694 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0278 others(21): Show |
29 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.50-4021G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937694 | |||||||
| chr1:116937703 | C | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-4012C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116937703 | |||||||
| chr1:116938079 | A | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3636A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938079 | |||||||
| chr1:116938268 | A | G | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(246): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.50-3447A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938268 | |||||||
| chr1:116938371 | A | T | 9 | a0002c0002t0004g0003 a0002c0002t0004g0009 a0002c0002t0004g0047 others(6): Show |
12 | HG00558.hp1 HG00597.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-3344A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938371 | |||||||
| chr1:116938673 | C | T | 1 | a0001c0001t0016g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.50-3042C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938673 | |||||||
| chr1:116938700 | A | G | 1 | a0001c0006t0009g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.50-3015A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938700 | |||||||
| chr1:116938743 | G | C | 4 | a0001c0008t0021g0044 a0001c0008t0021g0199 a0004c0004t0001g0224 others(1): Show |
4 | HG01433.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-2972G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938743 | |||||||
| chr1:116938763 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50-2952T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938763 | |||||||
| chr1:116938833 | A | G | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-2882A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116938833 | |||||||
| chr1:116939040 | G | A | 1 | a0005c0005t0004g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-2675G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939040 | |||||||
| chr1:116939124 | C | T | 1 | a0002c0002t0003g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.50-2591C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939124 | |||||||
| chr1:116939185 | C | T | 2 | a0003c0003t0002g0088 a0003c0003t0002g0177 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.50-2530C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939185 | |||||||
| chr1:116939200 | A | G | 1 | a0007c0010t0013g0284 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-2515A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939200 | |||||||
| chr1:116939204 | C | T | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.50-2511C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939204 | |||||||
| chr1:116939462 | T | C | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(245): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.50-2253T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939462 | |||||||
| chr1:116939973 | A | G | 2 | a0003c0003t0002g0086 a0003c0003t0002g0087 |
2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.50-1742A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939973 | |||||||
| chr1:116939974 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.50-1741A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116939974 | |||||||
| chr1:116940001 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-1714T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940001 | |||||||
| chr1:116940143 | C | T | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-1572C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940143 | |||||||
| chr1:116940181 | A | C | 3 | a0001c0001t0001g0293 a0001c0001t0012g0292 a0001c0001t0037g0273 |
3 | HG02572.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.50-1534A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940181 | |||||||
| chr1:116940192 | C | T | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-1523C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940192 | |||||||
| chr1:116940196 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0227 a0001c0001t0001g0231 others(27): Show |
35 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-1519A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940196 | |||||||
| chr1:116940279 | C | T | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-1436C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940279 | |||||||
| chr1:116940447 | T | C | 2 | a0002c0019t0030g0270 a0011c0021t0036g0287 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.50-1268T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940447 | |||||||
| chr1:116940491 | C | G | 8 | a0001c0008t0021g0044 a0001c0008t0021g0199 a0004c0004t0001g0224 others(5): Show |
8 | HG01433.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1224C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940491 | |||||||
| chr1:116940651 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0278 a0001c0001t0014g0014 others(4): Show |
11 | HG01515.hp2 HG01517.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-1064C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940651 | |||||||
| chr1:116940739 | G | A | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.50-976G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116940739 | |||||||
| chr1:116941583 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.50-132A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 1/8 | chr1 | 116941583 | |||||||
| chr1:116942215 | T | G | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.418+132T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116942215 | |||||||
| chr1:116942364 | G | C | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.418+281G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116942364 | |||||||
| chr1:116943096 | A | G | 2 | a0004c0004t0001g0004 a0004c0004t0005g0259 |
4 | NA18990.hp1 NA19001.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+1013A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943096 | |||||||
| chr1:116943203 | A | G | 1 | a0002c0002t0004g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.418+1120A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943203 | |||||||
| chr1:116943276 | A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.418+1193A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943276 | |||||||
| chr1:116943298 | A | T | 2 | a0002c0019t0030g0270 a0011c0021t0036g0287 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.418+1215A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943298 | |||||||
| chr1:116943347 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0093 a0001c0001t0001g0157 others(45): Show |
56 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+1264G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943347 | |||||||
| chr1:116943563 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0278 a0001c0001t0014g0014 others(1): Show |
7 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-1116G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943563 | |||||||
| chr1:116943732 | G | A | 6 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(3): Show |
7 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-947G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943732 | |||||||
| chr1:116943828 | G | A | 190 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0025 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.419-851G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943828 | |||||||
| chr1:116943840 | A | T | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.419-839A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943840 | |||||||
| chr1:116943934 | C | T | 1 | a0002c0002t0024g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.419-745C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116943934 | |||||||
| chr1:116944197 | C | T | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.419-482C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944197 | |||||||
| chr1:116944477 | G | T | 27 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0018t0029g0040 others(24): Show |
30 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.419-202G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944477 | |||||||
| chr1:116944521 | A | G | 4 | a0001c0001t0012g0292 a0001c0001t0018g0269 a0001c0001t0037g0273 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-158A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944521 | |||||||
| chr1:116944543 | G | A | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0234 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.419-136G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944543 | |||||||
| chr1:116944648 | G | A | 94 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0036 others(91): Show |
98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.419-31G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 2/8 | chr1 | 116944648 | |||||||
| chr1:116945262 | G | A | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(187): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.832+170G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945262 | |||||||
| chr1:116945484 | C | T | 2 | a0002c0002t0008g0109 a0002c0002t0008g0110 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.832+392C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945484 | |||||||
| chr1:116945569 | C | T | 1 | a0002c0002t0022g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.832+477C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945569 | |||||||
| chr1:116945744 | C | CT | 10 | a0001c0001t0001g0208 a0001c0001t0001g0234 a0001c0008t0011g0233 others(7): Show |
10 | HG01243.hp1 HG01433.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.832+669dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 116945744 | ||||||
| chr1:116945744 | CT | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0043 others(42): Show |
49 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.832+669delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 116945744 | ||||||
| chr1:116945778 | A | G | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.832+686A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945778 | |||||||
| chr1:116945861 | T | G | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.832+769T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945861 | |||||||
| chr1:116945877 | A | G | 9 | a0001c0001t0001g0276 a0001c0001t0012g0292 a0001c0001t0016g0228 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+785A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116945877 | |||||||
| chr1:116946133 | C | T | 1 | a0007c0010t0013g0284 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.832+1041C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946133 | |||||||
| chr1:116946142 | A | T | 1 | a0002c0002t0008g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.832+1050A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946142 | |||||||
| chr1:116946442 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.832+1350G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946442 | |||||||
| chr1:116946794 | G | A | 1 | a0003c0003t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.832+1702G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116946794 | |||||||
| chr1:116947275 | C | T | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.833-1917C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947275 | |||||||
| chr1:116947577 | T | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0208 a0001c0001t0001g0293 |
3 | HG01243.hp1 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.833-1615T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947577 | |||||||
| chr1:116947638 | C | T | 4 | a0005c0005t0004g0210 a0005c0005t0004g0215 a0005c0005t0004g0216 others(1): Show |
4 | HG02886.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-1554C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947638 | |||||||
| chr1:116947639 | G | T | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(240): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.833-1553G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116947639 | |||||||
| chr1:116948009 | C | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-1183C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948009 | |||||||
| chr1:116948038 | C | T | 52 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0234 others(49): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.833-1154C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948038 | |||||||
| chr1:116948071 | C | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.833-1121C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948071 | |||||||
| chr1:116948195 | G | A | 6 | a0001c0001t0001g0234 a0001c0008t0011g0233 a0001c0008t0021g0044 others(3): Show |
6 | HG01433.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-997G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948195 | |||||||
| chr1:116948366 | C | G | 2 | a0004c0004t0001g0224 a0008c0023t0033g0281 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.833-826C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948366 | |||||||
| chr1:116948501 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0028 others(90): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.833-691A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948501 | |||||||
| chr1:116948520 | A | G | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.833-672A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948520 | |||||||
| chr1:116948628 | C | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-564C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948628 | |||||||
| chr1:116948746 | T | G | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.833-446T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948746 | |||||||
| chr1:116948842 | T | C | 3 | a0001c0001t0012g0292 a0001c0001t0037g0273 a0006c0007t0012g0015 |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-350T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948842 | |||||||
| chr1:116948967 | T | C | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(189): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.833-225T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116948967 | |||||||
| chr1:116949015 | G | A | 1 | a0006c0007t0001g0282 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.833-177G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 3/8 | chr1 | 116949015 | |||||||
| chr1:116949807 | A | G | 6 | a0001c0001t0001g0234 a0001c0008t0011g0233 a0001c0008t0021g0044 others(3): Show |
6 | HG01433.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1213+235A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116949807 | |||||||
| chr1:116949942 | G | A | 4 | a0004c0004t0001g0004 a0004c0004t0001g0254 a0004c0004t0001g0264 others(1): Show |
6 | NA18985.hp1 NA18990.hp1 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+370G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116949942 | |||||||
| chr1:116950002 | A | AT | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+440dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116950002 | ||||||
| chr1:116950130 | T | C | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+558T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950130 | |||||||
| chr1:116950217 | C | A | 2 | a0001c0001t0001g0031 a0002c0002t0003g0030 |
2 | NA18947.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1213+645C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950217 | |||||||
| chr1:116950390 | T | C | 30 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(27): Show |
33 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1213+818T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950390 | |||||||
| chr1:116950430 | CT | C | 50 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(47): Show |
55 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1213+859delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950430 | |||||||
| chr1:116950453 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1213+881G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950453 | |||||||
| chr1:116950547 | T | C | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+975T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950547 | |||||||
| chr1:116950585 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0006t0009g0211 others(5): Show |
9 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1213+1013T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950585 | |||||||
| chr1:116950630 | A | G | 5 | a0003c0003t0002g0080 a0003c0003t0002g0088 a0003c0003t0002g0143 others(2): Show |
5 | HG02155.hp2 HG02165.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213+1058A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950630 | |||||||
| chr1:116950741 | C | T | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1213+1169C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950741 | |||||||
| chr1:116950787 | C | A | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+1215C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950787 | |||||||
| chr1:116950809 | C | T | 18 | a0002c0002t0001g0195 a0003c0003t0002g0076 a0003c0003t0002g0077 others(15): Show |
18 | HG00558.hp2 HG00673.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1213+1237C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116950809 | |||||||
| chr1:116951109 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1213+1537G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951109 | |||||||
| chr1:116951120 | T | G | 4 | a0001c0008t0011g0233 a0006c0022t0011g0265 a0007c0013t0002g0268 others(1): Show |
4 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213+1548T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951120 | |||||||
| chr1:116951189 | G | A | 30 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(27): Show |
33 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1213+1617G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951189 | |||||||
| chr1:116951266 | A | G | 7 | a0002c0002t0003g0016 a0002c0002t0003g0017 a0002c0002t0003g0018 others(4): Show |
7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+1694A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951266 | |||||||
| chr1:116951524 | T | A | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+1952T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951524 | |||||||
| chr1:116951627 | A | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1213+2055A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951627 | |||||||
| chr1:116951657 | G | A | 29 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(26): Show |
32 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1213+2085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951657 | |||||||
| chr1:116951677 | CT | C | 5 | a0001c0001t0001g0276 a0004c0009t0001g0011 a0004c0009t0031g0147 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+2106delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951677 | |||||||
| chr1:116951699 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1213+2127C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951699 | |||||||
| chr1:116951725 | A | G | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1213+2153A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951725 | |||||||
| chr1:116951901 | T | C | 1 | a0004c0004t0032g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1213+2329T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951901 | |||||||
| chr1:116951953 | C | T | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+2381C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116951953 | |||||||
| chr1:116952049 | G | A | 1 | a0007c0013t0017g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213+2477G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952049 | |||||||
| chr1:116952198 | T | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(145): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1213+2626T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952198 | |||||||
| chr1:116952282 | T | C | 1 | a0001c0006t0009g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1213+2710T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952282 | |||||||
| chr1:116952474 | A | G | 1 | a0004c0004t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1213+2902A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952474 | |||||||
| chr1:116952479 | T | C | 1 | a0003c0003t0002g0184 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1213+2907T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952479 | |||||||
| chr1:116952588 | ATTATAT | A | 102 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(99): Show |
109 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1213+3019_1213+302 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116952588 | ||||||
| chr1:116952710 | C | T | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+3138C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952710 | |||||||
| chr1:116952762 | A | G | 2 | a0001c0001t0001g0166 a0002c0002t0002g0165 |
2 | HG02071.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1213+3190A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952762 | |||||||
| chr1:116952802 | C | G | 1 | a0002c0002t0003g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1213+3230C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116952802 | |||||||
| chr1:116953081 | A | T | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1213+3509A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953081 | |||||||
| chr1:116953399 | G | A | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(146): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1213+3827G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953399 | |||||||
| chr1:116953550 | C | G | 29 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(26): Show |
32 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1213+3978C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953550 | |||||||
| chr1:116953775 | T | C | 292 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(289): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1213+4203T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953775 | |||||||
| chr1:116953847 | A | G | 251 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1213+4275A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953847 | |||||||
| chr1:116953853 | C | CT | 48 | a0002c0002t0003g0018 a0002c0002t0008g0108 a0003c0003t0002g0002 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1213+4298dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116953853 | ||||||
| chr1:116953883 | C | T | 7 | a0002c0002t0003g0016 a0002c0002t0003g0017 a0002c0002t0003g0018 others(4): Show |
7 | HG01106.hp2 HG01255.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+4311C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953883 | |||||||
| chr1:116953892 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1213+4320G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953892 | |||||||
| chr1:116953955 | C | A | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1213+4383C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116953955 | |||||||
| chr1:116954119 | A | G | 5 | a0001c0001t0012g0292 a0001c0001t0016g0228 a0001c0001t0016g0229 others(2): Show |
6 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213+4547A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954119 | |||||||
| chr1:116954123 | G | C | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1213+4551G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954123 | |||||||
| chr1:116954298 | C | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1213+4726C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954298 | |||||||
| chr1:116954557 | G | A | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1213+4985G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954557 | |||||||
| chr1:116954721 | A | G | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1213+5149A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954721 | |||||||
| chr1:116954767 | C | CT | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(147): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1213+5197dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116954767 | ||||||
| chr1:116954857 | T | C | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213+5285T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954857 | |||||||
| chr1:116954881 | A | G | 1 | a0003c0003t0002g0079 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1213+5309A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116954881 | |||||||
| chr1:116955788 | C | T | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(146): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1214-5455C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955788 | |||||||
| chr1:116955800 | C | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1214-5443C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955800 | |||||||
| chr1:116955880 | A | G | 11 | a0002c0002t0001g0195 a0004c0004t0001g0271 a0004c0004t0001g0289 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1214-5363A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955880 | |||||||
| chr1:116955964 | G | A | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(146): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1214-5279G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116955964 | |||||||
| chr1:116956158 | G | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1214-5085G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956158 | |||||||
| chr1:116956167 | G | A | 2 | a0001c0001t0001g0258 a0002c0002t0003g0248 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1214-5076G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956167 | |||||||
| chr1:116956333 | G | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-4910G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956333 | |||||||
| chr1:116956421 | C | T | 2 | a0003c0003t0002g0171 a0003c0003t0002g0172 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1214-4822C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956421 | |||||||
| chr1:116956532 | C | T | 1 | a0002c0002t0003g0017 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1214-4711C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956532 | |||||||
| chr1:116956544 | G | A | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1214-4699G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956544 | |||||||
| chr1:116956570 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1214-4673G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956570 | |||||||
| chr1:116956575 | A | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0144 a0001c0001t0001g0152 others(5): Show |
8 | NA18944.hp1 NA18950.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1214-4668A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956575 | |||||||
| chr1:116956615 | G | T | 6 | a0001c0001t0016g0228 a0001c0001t0016g0229 a0001c0008t0011g0233 others(3): Show |
6 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-4628G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956615 | |||||||
| chr1:116956616 | G | T | 6 | a0001c0001t0016g0228 a0001c0001t0016g0229 a0001c0008t0011g0233 others(3): Show |
6 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-4627G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956616 | |||||||
| chr1:116956637 | C | T | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-4606C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956637 | |||||||
| chr1:116956681 | G | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-4562G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956681 | |||||||
| chr1:116956926 | A | T | 46 | a0001c0001t0001g0276 a0003c0003t0002g0002 a0003c0003t0002g0007 others(43): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1214-4317A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116956926 | |||||||
| chr1:116956955 | C | CA | 4 | a0001c0008t0011g0233 a0006c0022t0011g0265 a0007c0013t0002g0268 others(1): Show |
4 | HG02622.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-4287dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116956955 | ||||||
| chr1:116957026 | A | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0157 others(29): Show |
35 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1214-4217A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957026 | |||||||
| chr1:116957104 | ACT | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(244): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1214-4118_1214-411 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957104 | ||||||
| chr1:116957104 | ACTCTCT | A | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0004c0004t0001g0241 |
3 | HG02015.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1214-4122_1214-411 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957104 | ||||||
| chr1:116957106 | T | A | 5 | a0001c0008t0021g0044 a0001c0008t0021g0199 a0007c0010t0013g0284 others(2): Show |
5 | HG01433.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1214-4137T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957106 | |||||||
| chr1:116957151 | C | CTG | 57 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(54): Show |
61 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1214-4068_1214-406 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | ||||||
| chr1:116957151 | CTG | C | 6 | a0001c0001t0005g0038 a0001c0001t0014g0014 a0001c0001t0014g0279 others(3): Show |
7 | HG01884.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1214-4068_1214-406 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | ||||||
| chr1:116957151 | CTGTGTG | C | 6 | a0001c0001t0001g0127 a0001c0001t0001g0163 a0001c0008t0011g0233 others(3): Show |
6 | HG00639.hp1 HG02622.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1214-4072_1214-406 others(10): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 116957151 | ||||||
| chr1:116957222 | C | T | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1214-4021C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957222 | |||||||
| chr1:116957248 | C | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-3995C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957248 | |||||||
| chr1:116957249 | G | A | 1 | a0001c0006t0009g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1214-3994G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957249 | |||||||
| chr1:116957355 | G | A | 2 | a0003c0003t0002g0088 a0003c0003t0002g0177 |
2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1214-3888G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957355 | |||||||
| chr1:116957492 | T | A | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-3751T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957492 | |||||||
| chr1:116957494 | A | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0042 others(8): Show |
12 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1214-3749A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957494 | |||||||
| chr1:116957613 | A | G | 53 | a0001c0001t0001g0276 a0001c0001t0012g0292 a0001c0001t0037g0273 others(50): Show |
56 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1214-3630A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957613 | |||||||
| chr1:116957715 | G | A | 1 | a0003c0003t0026g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1214-3528G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957715 | |||||||
| chr1:116957808 | T | C | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1214-3435T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957808 | |||||||
| chr1:116957864 | G | A | 45 | a0003c0003t0002g0002 a0003c0003t0002g0007 a0003c0003t0002g0045 others(42): Show |
47 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1214-3379G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957864 | |||||||
| chr1:116957921 | G | T | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-3322G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957921 | |||||||
| chr1:116957929 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1214-3314G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116957929 | |||||||
| chr1:116958142 | G | A | 31 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0018t0029g0040 others(28): Show |
34 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1214-3101G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958142 | |||||||
| chr1:116958693 | T | G | 12 | a0002c0002t0001g0195 a0002c0002t0002g0263 a0004c0004t0001g0271 others(9): Show |
12 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1214-2550T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958693 | |||||||
| chr1:116958788 | C | A | 78 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0018t0029g0040 others(75): Show |
83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1214-2455C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116958788 | |||||||
| chr1:116959046 | C | G | 2 | a0001c0001t0018g0269 a0004c0004t0028g0112 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1214-2197C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959046 | |||||||
| chr1:116959228 | C | A | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-2015C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959228 | |||||||
| chr1:116959266 | G | A | 1 | a0002c0002t0003g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1214-1977G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959266 | |||||||
| chr1:116959330 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1214-1913A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959330 | |||||||
| chr1:116959521 | C | T | 1 | a0001c0001t0016g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1214-1722C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959521 | |||||||
| chr1:116959561 | T | C | 1 | a0003c0003t0002g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1214-1682T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959561 | |||||||
| chr1:116959732 | G | A | 1 | a0002c0002t0004g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1214-1511G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959732 | |||||||
| chr1:116959745 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1214-1498G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959745 | |||||||
| chr1:116959938 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1214-1305A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959938 | |||||||
| chr1:116959999 | T | C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0131 a0001c0001t0001g0183 others(3): Show |
6 | HG00621.hp1 NA18747.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-1244T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116959999 | |||||||
| chr1:116960001 | T | A | 1 | a0011c0021t0036g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1214-1242T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960001 | |||||||
| chr1:116960137 | A | G | 3 | a0001c0008t0011g0233 a0006c0022t0011g0265 a0011c0021t0036g0287 |
3 | HG02622.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1214-1106A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960137 | |||||||
| chr1:116960144 | A | G | 3 | a0001c0008t0021g0044 a0001c0008t0021g0199 a0007c0013t0017g0283 |
3 | HG01433.hp2 HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-1099A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960144 | |||||||
| chr1:116960223 | T | C | 1 | a0010c0014t0004g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1214-1020T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960223 | |||||||
| chr1:116960393 | A | G | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1214-850A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960393 | |||||||
| chr1:116960473 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0279 |
3 | HG01884.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1214-770G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960473 | |||||||
| chr1:116960553 | G | A | 1 | a0001c0001t0020g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1214-690G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960553 | |||||||
| chr1:116960569 | C | G | 7 | a0001c0001t0018g0269 a0001c0008t0011g0233 a0001c0008t0021g0044 others(4): Show |
7 | HG01433.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-674C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960569 | |||||||
| chr1:116960676 | C | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1214-567C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960676 | |||||||
| chr1:116960814 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1214-429G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960814 | |||||||
| chr1:116960825 | C | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1214-418C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960825 | |||||||
| chr1:116960900 | G | C | 5 | a0001c0008t0011g0233 a0001c0008t0021g0044 a0001c0008t0021g0199 others(2): Show |
5 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214-343G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116960900 | |||||||
| chr1:116961048 | C | T | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-195C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116961048 | |||||||
| chr1:116961096 | T | C | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1214-147T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 4/8 | chr1 | 116961096 | |||||||
| chr1:116961808 | C | T | 1 | a0003c0003t0002g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1639+140C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116961808 | |||||||
| chr1:116961982 | C | T | 1 | a0002c0002t0015g0173 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1639+314C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116961982 | |||||||
| chr1:116962250 | G | A | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+582G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962250 | |||||||
| chr1:116962272 | C | G | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+604C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962272 | |||||||
| chr1:116962466 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1639+798A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962466 | |||||||
| chr1:116962641 | T | A | 1 | a0003c0003t0002g0051 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1639+973T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962641 | |||||||
| chr1:116962690 | C | T | 87 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(84): Show |
92 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1639+1022C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962690 | |||||||
| chr1:116962691 | C | T | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1639+1023C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962691 | |||||||
| chr1:116962695 | C | G | 1 | a0002c0002t0002g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1639+1027C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962695 | |||||||
| chr1:116962826 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1639+1158T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962826 | |||||||
| chr1:116962888 | C | T | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+1220C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962888 | |||||||
| chr1:116962889 | G | A | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1639+1221G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962889 | |||||||
| chr1:116962933 | C | G | 1 | a0003c0003t0002g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1639+1265C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116962933 | |||||||
| chr1:116963036 | G | GCTTC | 3 | a0002c0002t0003g0137 a0002c0002t0003g0169 a0002c0002t0006g0105 |
3 | NA19062.hp1 NA19062.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1639+1374_1639+137 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116963036 | ||||||
| chr1:116963049 | C | T | 4 | a0001c0008t0011g0233 a0001c0008t0021g0044 a0001c0008t0021g0199 others(1): Show |
4 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+1381C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963049 | |||||||
| chr1:116963116 | C | T | 5 | a0001c0008t0011g0233 a0001c0008t0021g0044 a0001c0008t0021g0199 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1639+1448C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963116 | |||||||
| chr1:116963210 | C | T | 5 | a0001c0001t0012g0292 a0001c0001t0018g0269 a0001c0001t0037g0273 others(2): Show |
6 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639+1542C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963210 | |||||||
| chr1:116963290 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0208 others(3): Show |
6 | HG01243.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639+1622C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963290 | |||||||
| chr1:116963564 | A | T | 46 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(43): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1639+1896A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963564 | |||||||
| chr1:116963579 | G | A | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1639+1911G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963579 | |||||||
| chr1:116963619 | G | A | 1 | a0002c0002t0006g0132 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1639+1951G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963619 | |||||||
| chr1:116963689 | C | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1639+2021C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963689 | |||||||
| chr1:116963732 | C | T | 4 | a0001c0008t0011g0233 a0001c0008t0021g0044 a0001c0008t0021g0199 others(1): Show |
4 | HG01433.hp2 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+2064C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963732 | |||||||
| chr1:116963774 | A | AT | 40 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1639+2121dupT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116963774 | ||||||
| chr1:116963924 | A | G | 1 | a0002c0002t0004g0094 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1639+2256A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116963924 | |||||||
| chr1:116964000 | G | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0058 others(27): Show |
32 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1639+2332G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964000 | |||||||
| chr1:116964018 | G | A | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1639+2350G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964018 | |||||||
| chr1:116964076 | G | GAC | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+2408_1639+240 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964076 | |||||||
| chr1:116964079 | G | C | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1639+2411G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964079 | |||||||
| chr1:116964079 | G | GC | 80 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(77): Show |
83 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639+2418dupC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116964079 | ||||||
| chr1:116964079 | G | GCC | 40 | a0001c0001t0001g0093 a0001c0001t0001g0276 a0001c0001t0018g0269 others(37): Show |
43 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1639+2417_1639+241 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116964079 | ||||||
| chr1:116964084 | C | CG | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639+2416_1639+241 others(5): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964084 | |||||||
| chr1:116964110 | C | G | 46 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(43): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1639+2442C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964110 | |||||||
| chr1:116964188 | C | T | 1 | a0004c0004t0001g0219 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1639+2520C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964188 | |||||||
| chr1:116964230 | C | T | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639+2562C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964230 | |||||||
| chr1:116964231 | T | G | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1639+2563T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964231 | |||||||
| chr1:116964270 | T | A | 27 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0081 others(24): Show |
27 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1639+2602T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964270 | |||||||
| chr1:116964395 | G | A | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1640-2516G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964395 | |||||||
| chr1:116964542 | T | A | 12 | a0002c0002t0001g0195 a0004c0004t0001g0271 a0005c0005t0001g0217 others(9): Show |
12 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1640-2369T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964542 | |||||||
| chr1:116964548 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1640-2363A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964548 | |||||||
| chr1:116964582 | T | C | 1 | a0004c0004t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1640-2329T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964582 | |||||||
| chr1:116964599 | A | G | 45 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(42): Show |
49 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1640-2312A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964599 | |||||||
| chr1:116964780 | T | C | 54 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0227 others(51): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1640-2131T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964780 | |||||||
| chr1:116964893 | T | C | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640-2018T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116964893 | |||||||
| chr1:116965013 | C | T | 1 | a0002c0002t0003g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1640-1898C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965013 | |||||||
| chr1:116965043 | C | G | 37 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(34): Show |
40 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1640-1868C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965043 | |||||||
| chr1:116965171 | C | T | 13 | a0002c0002t0001g0195 a0004c0004t0001g0271 a0004c0004t0028g0112 others(10): Show |
13 | HG01891.hp1 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1640-1740C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965171 | |||||||
| chr1:116965226 | A | G | 7 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(4): Show |
8 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640-1685A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965226 | |||||||
| chr1:116965258 | G | A | 7 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(4): Show |
8 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1640-1653G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965258 | |||||||
| chr1:116965379 | G | A | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1640-1532G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965379 | |||||||
| chr1:116965524 | A | G | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1640-1387A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965524 | |||||||
| chr1:116965548 | T | C | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1640-1363T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965548 | |||||||
| chr1:116965564 | A | C | 46 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0276 others(43): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1640-1347A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965564 | |||||||
| chr1:116965623 | TC | T | 50 | a0001c0001t0001g0031 a0001c0001t0001g0134 a0001c0001t0001g0166 others(47): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1640-1285delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 116965623 | ||||||
| chr1:116965682 | C | T | 53 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(50): Show |
56 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1640-1229C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965682 | |||||||
| chr1:116965852 | G | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | HG01192.hp2 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-1059G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116965852 | |||||||
| chr1:116966499 | A | G | 32 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0018t0029g0040 others(29): Show |
35 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1640-412A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966499 | |||||||
| chr1:116966548 | C | T | 7 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1640-363C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966548 | |||||||
| chr1:116966760 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1640-151T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966760 | |||||||
| chr1:116966789 | G | A | 2 | a0003c0003t0002g0057 a0007c0013t0017g0283 |
2 | HG01891.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1640-122G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 5/8 | chr1 | 116966789 | |||||||
| chr1:116967359 | G | A | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+29G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967359 | |||||||
| chr1:116967365 | C | T | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+35C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967365 | |||||||
| chr1:116967439 | C | T | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+109C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967439 | |||||||
| chr1:116967714 | GC | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0236 |
3 | HG00408.hp2 HG02083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2059+385delC | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967714 | |||||||
| chr1:116967895 | G | A | 64 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(61): Show |
68 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.2059+565G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116967895 | |||||||
| chr1:116968182 | G | A | 122 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0227 others(119): Show |
129 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.2059+852G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968182 | |||||||
| chr1:116968283 | A | AG | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+953_2059+954i others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968283 | |||||||
| chr1:116968355 | A | C | 5 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(2): Show |
6 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059+1025A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968355 | |||||||
| chr1:116968387 | A | G | 1 | a0003c0003t0002g0099 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2059+1057A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968387 | |||||||
| chr1:116968573 | T | G | 1 | a0005c0005t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2059+1243T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968573 | |||||||
| chr1:116968639 | A | G | 1 | a0004c0004t0001g0240 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2059+1309A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968639 | |||||||
| chr1:116968819 | C | G | 2 | a0001c0001t0001g0234 a0001c0001t0005g0193 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2059+1489C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968819 | |||||||
| chr1:116968861 | A | C | 40 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(37): Show |
43 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2059+1531A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968861 | |||||||
| chr1:116968992 | T | C | 1 | a0004c0004t0001g0261 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2059+1662T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116968992 | |||||||
| chr1:116969036 | G | C | 123 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0227 others(120): Show |
130 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2059+1706G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969036 | |||||||
| chr1:116969120 | GTT | G | 37 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0020g0200 others(34): Show |
40 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2059+1803_2059+180 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116969120 | ||||||
| chr1:116969159 | A | G | 108 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0001g0227 others(105): Show |
115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2059+1829A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969159 | |||||||
| chr1:116969182 | T | C | 67 | a0001c0001t0001g0227 a0001c0001t0001g0276 a0001c0001t0007g0012 others(64): Show |
71 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2059+1852T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969182 | |||||||
| chr1:116969218 | T | C | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+1888T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969218 | |||||||
| chr1:116969274 | G | A | 5 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(2): Show |
6 | HG00280.hp2 HG00741.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059+1944G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969274 | |||||||
| chr1:116969322 | T | C | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2059+1992T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969322 | |||||||
| chr1:116969508 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0230 a0001c0001t0001g0277 |
3 | HG02280.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2059+2178A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969508 | |||||||
| chr1:116969570 | A | G | 41 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(38): Show |
44 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.2059+2240A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969570 | |||||||
| chr1:116969612 | C | T | 9 | a0002c0002t0004g0003 a0002c0002t0004g0009 a0002c0002t0004g0047 others(6): Show |
12 | HG00558.hp1 HG00597.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.2059+2282C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969612 | |||||||
| chr1:116969679 | A | G | 2 | a0001c0008t0011g0233 a0006c0022t0011g0265 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2059+2349A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969679 | |||||||
| chr1:116969752 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+2422G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969752 | |||||||
| chr1:116969860 | A | T | 2 | a0003c0003t0002g0071 a0003c0003t0002g0072 |
2 | NA18950.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2059+2530A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969860 | |||||||
| chr1:116969883 | T | C | 45 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0012g0292 others(42): Show |
49 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2059+2553T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969883 | |||||||
| chr1:116969924 | G | C | 40 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0001t0018g0269 others(37): Show |
43 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.2059+2594G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116969924 | |||||||
| chr1:116970165 | CT | C | 3 | a0001c0001t0001g0031 a0001c0001t0005g0185 a0002c0002t0003g0123 |
3 | HG01261.hp1 HG03831.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2059+2837delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116970165 | ||||||
| chr1:116970165 | CTT | C | 48 | a0001c0001t0001g0028 a0001c0001t0001g0134 a0001c0001t0001g0166 others(45): Show |
52 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.2059+2836_2059+283 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970165 | |||||||
| chr1:116970179 | T | C | 3 | a0001c0001t0005g0038 a0001c0001t0019g0148 a0001c0001t0019g0196 |
3 | HG02615.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2059+2849T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970179 | |||||||
| chr1:116970304 | T | A | 1 | a0003c0003t0002g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2059+2974T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970304 | |||||||
| chr1:116970364 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2059+3034A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970364 | |||||||
| chr1:116970379 | G | T | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+3049G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970379 | |||||||
| chr1:116970537 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2059+3207T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970537 | |||||||
| chr1:116970639 | G | T | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2059+3309G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970639 | |||||||
| chr1:116970816 | G | A | 11 | a0002c0002t0001g0195 a0004c0004t0001g0271 a0005c0005t0001g0217 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2060-3400G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970816 | |||||||
| chr1:116970830 | C | G | 79 | a0001c0001t0001g0227 a0001c0001t0001g0276 a0001c0001t0007g0012 others(76): Show |
83 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.2060-3386C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970830 | |||||||
| chr1:116970998 | A | T | 2 | a0002c0002t0003g0039 a0002c0002t0003g0136 |
2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2060-3218A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116970998 | |||||||
| chr1:116971198 | T | TA | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG01358.hp1 HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2060-3017dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116971198 | ||||||
| chr1:116971281 | C | T | 4 | a0002c0002t0004g0003 a0002c0002t0004g0094 a0002c0002t0004g0095 others(1): Show |
6 | NA18974.hp2 NA18985.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.2060-2935C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971281 | |||||||
| chr1:116971282 | T | TTAGCCAT others(17): Show |
1 | a0001c0001t0018g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2060-2913_2060-291 others(28): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116971282 | ||||||
| chr1:116971363 | T | G | 31 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0001c0018t0029g0040 others(28): Show |
34 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2060-2853T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971363 | |||||||
| chr1:116971426 | A | G | 47 | a0003c0003t0002g0002 a0003c0003t0002g0007 a0003c0003t0002g0045 others(44): Show |
49 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.2060-2790A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971426 | |||||||
| chr1:116971500 | C | G | 2 | a0001c0001t0001g0234 a0001c0001t0005g0193 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2060-2716C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971500 | |||||||
| chr1:116971712 | A | G | 85 | a0001c0001t0001g0025 a0001c0001t0001g0081 a0001c0001t0001g0100 others(82): Show |
89 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2060-2504A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971712 | |||||||
| chr1:116971936 | G | A | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2060-2280G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971936 | |||||||
| chr1:116971998 | C | T | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2060-2218C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116971998 | |||||||
| chr1:116972053 | G | A | 23 | a0001c0001t0001g0157 a0001c0001t0012g0292 a0001c0001t0016g0228 others(20): Show |
24 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2060-2163G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972053 | |||||||
| chr1:116972058 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2060-2158C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972058 | |||||||
| chr1:116972102 | C | T | 1 | a0002c0002t0006g0132 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2060-2114C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972102 | |||||||
| chr1:116972161 | A | G | 4 | a0002c0019t0030g0270 a0007c0010t0013g0284 a0007c0010t0013g0285 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2060-2055A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972161 | |||||||
| chr1:116972310 | G | A | 2 | a0001c0001t0037g0273 a0011c0021t0036g0287 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2060-1906G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972310 | |||||||
| chr1:116972493 | A | G | 122 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(119): Show |
130 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2060-1723A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972493 | |||||||
| chr1:116972662 | C | A | 45 | a0002c0002t0002g0118 a0003c0003t0002g0002 a0003c0003t0002g0007 others(42): Show |
47 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.2060-1554C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972662 | |||||||
| chr1:116972678 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2060-1538C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972678 | |||||||
| chr1:116972694 | G | A | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2060-1522G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972694 | |||||||
| chr1:116972902 | G | T | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2060-1314G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972902 | |||||||
| chr1:116972986 | C | T | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2060-1230C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116972986 | |||||||
| chr1:116973026 | C | A | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2060-1190C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973026 | |||||||
| chr1:116973044 | A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2060-1172A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973044 | |||||||
| chr1:116973052 | G | C | 1 | a0006c0012t0018g0267 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2060-1164G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973052 | |||||||
| chr1:116973104 | G | T | 2 | a0001c0001t0001g0234 a0001c0001t0005g0193 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2060-1112G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973104 | |||||||
| chr1:116973135 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2060-1081C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973135 | |||||||
| chr1:116973309 | A | T | 1 | a0002c0002t0002g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2060-907A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973309 | |||||||
| chr1:116973488 | C | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2060-728C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973488 | |||||||
| chr1:116973535 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2060-681G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973535 | |||||||
| chr1:116973581 | C | G | 26 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(23): Show |
29 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.2060-635C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973581 | |||||||
| chr1:116973581 | C | T | 1 | a0002c0002t0008g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2060-635C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973581 | |||||||
| chr1:116973604 | CA | C | 71 | a0001c0001t0001g0152 a0001c0001t0005g0038 a0001c0001t0007g0012 others(68): Show |
75 | HG00438.hp1 HG00597.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.2060-593delA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116973604 | ||||||
| chr1:116973604 | CAA | C | 44 | a0001c0001t0012g0292 a0001c0018t0029g0040 a0002c0002t0001g0195 others(41): Show |
48 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2060-594_2060-593d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 116973604 | ||||||
| chr1:116973719 | A | G | 33 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(30): Show |
36 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.2060-497A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973719 | |||||||
| chr1:116973882 | C | G | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2060-334C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 6/8 | chr1 | 116973882 | |||||||
| chr1:116974386 | C | T | 1 | a0002c0002t0003g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2167+63C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974386 | |||||||
| chr1:116974387 | G | A | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2167+64G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974387 | |||||||
| chr1:116974387 | G | T | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2167+64G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974387 | |||||||
| chr1:116974479 | T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2167+156T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974479 | |||||||
| chr1:116974491 | G | A | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+168G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974491 | |||||||
| chr1:116974510 | C | T | 2 | a0001c0001t0037g0273 a0011c0021t0036g0287 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2167+187C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974510 | |||||||
| chr1:116974657 | C | T | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167+334C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974657 | |||||||
| chr1:116974740 | G | A | 1 | a0002c0002t0003g0083 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2167+417G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974740 | |||||||
| chr1:116974798 | C | T | 1 | a0002c0002t0003g0027 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2167+475C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974798 | |||||||
| chr1:116974901 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0163 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2167+578G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974901 | |||||||
| chr1:116974904 | C | T | 3 | a0001c0008t0011g0233 a0006c0012t0011g0266 a0006c0022t0011g0265 |
3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2167+581C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974904 | |||||||
| chr1:116974916 | C | T | 1 | a0002c0002t0004g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2167+593C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974916 | |||||||
| chr1:116974938 | C | T | 1 | a0006c0012t0018g0267 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2167+615C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974938 | |||||||
| chr1:116974945 | C | T | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+622C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116974945 | |||||||
| chr1:116975013 | G | A | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+690G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975013 | |||||||
| chr1:116975047 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2167+724G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975047 | |||||||
| chr1:116975076 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2167+753T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975076 | |||||||
| chr1:116975087 | T | C | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+764T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975087 | |||||||
| chr1:116975118 | C | T | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+795C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975118 | |||||||
| chr1:116975186 | C | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+863C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975186 | |||||||
| chr1:116975211 | A | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2167+888A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975211 | |||||||
| chr1:116975296 | G | A | 2 | a0004c0004t0001g0237 a0004c0004t0001g0244 |
2 | NA18951.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2167+973G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975296 | |||||||
| chr1:116975411 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2167+1088C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975411 | |||||||
| chr1:116975553 | T | A | 1 | a0004c0004t0001g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2167+1230T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975553 | |||||||
| chr1:116975636 | A | G | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2167+1313A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975636 | |||||||
| chr1:116975755 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+1432C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975755 | |||||||
| chr1:116975777 | A | G | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0018t0029g0040 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1454A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116975777 | |||||||
| chr1:116976027 | A | G | 1 | a0003c0003t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2167+1704A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976027 | |||||||
| chr1:116976057 | T | C | 4 | a0002c0019t0030g0270 a0007c0010t0013g0284 a0007c0010t0013g0285 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1734T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976057 | |||||||
| chr1:116976139 | C | T | 20 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(17): Show |
22 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2167+1816C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976139 | |||||||
| chr1:116976154 | G | A | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0008c0023t0033g0281 |
3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2167+1831G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976154 | |||||||
| chr1:116976187 | G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2167+1864G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976187 | |||||||
| chr1:116976374 | G | A | 8 | a0002c0002t0001g0195 a0005c0005t0001g0217 a0005c0005t0001g0220 others(5): Show |
8 | HG02622.hp1 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2167+2051G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976374 | |||||||
| chr1:116976491 | C | G | 1 | a0003c0003t0002g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167+2168C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976491 | |||||||
| chr1:116976544 | C | A | 5 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(2): Show |
6 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167+2221C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976544 | |||||||
| chr1:116976608 | A | G | 1 | a0001c0001t0037g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2167+2285A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976608 | |||||||
| chr1:116976769 | A | G | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2167+2446A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116976769 | |||||||
| chr1:116977120 | CAAAG | C | 48 | a0002c0002t0002g0118 a0002c0002t0002g0263 a0003c0003t0002g0002 others(45): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2167+2800_2167+280 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116977120 | ||||||
| chr1:116977125 | A | G | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2167+2802A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977125 | |||||||
| chr1:116977186 | A | G | 1 | a0002c0002t0003g0169 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2167+2863A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977186 | |||||||
| chr1:116977195 | C | T | 1 | a0001c0008t0011g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2167+2872C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977195 | |||||||
| chr1:116977197 | A | G | 1 | a0001c0001t0005g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2167+2874A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977197 | |||||||
| chr1:116977252 | A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2167+2929A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977252 | |||||||
| chr1:116977432 | A | C | 123 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(120): Show |
131 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.2167+3109A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977432 | |||||||
| chr1:116977596 | C | A | 24 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(21): Show |
26 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.2167+3273C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977596 | |||||||
| chr1:116977610 | C | T | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+3287C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977610 | |||||||
| chr1:116977626 | G | A | 3 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0008c0023t0033g0281 |
3 | HG02257.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2167+3303G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977626 | |||||||
| chr1:116977794 | A | T | 1 | a0002c0002t0041g0121 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2167+3471A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116977794 | |||||||
| chr1:116978019 | A | G | 2 | a0004c0004t0001g0250 a0004c0004t0001g0251 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2167+3696A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978019 | |||||||
| chr1:116978043 | C | T | 30 | a0002c0002t0004g0003 a0002c0002t0004g0009 a0002c0002t0004g0041 others(27): Show |
33 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2167+3720C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978043 | |||||||
| chr1:116978064 | A | G | 1 | a0003c0003t0002g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2167+3741A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978064 | |||||||
| chr1:116978325 | G | C | 95 | a0001c0001t0018g0269 a0001c0001t0020g0200 a0001c0001t0020g0201 others(92): Show |
100 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.2167+4002G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978325 | |||||||
| chr1:116978494 | TCCAGCAG others(21): Show |
T | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+4173_2167+420 others(32): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116978494 | ||||||
| chr1:116978514 | C | G | 27 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(24): Show |
30 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2167+4191C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978514 | |||||||
| chr1:116978535 | G | A | 25 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(22): Show |
28 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2167+4212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978535 | |||||||
| chr1:116978577 | T | C | 1 | a0004c0004t0034g0223 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2167+4254T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978577 | |||||||
| chr1:116978641 | A | G | 2 | a0001c0008t0021g0044 a0001c0008t0021g0199 |
2 | HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2167+4318A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978641 | |||||||
| chr1:116978772 | A | G | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167+4449A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978772 | |||||||
| chr1:116978815 | G | A | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0018t0029g0040 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+4492G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978815 | |||||||
| chr1:116978853 | T | G | 124 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(121): Show |
132 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.2167+4530T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978853 | |||||||
| chr1:116978909 | A | G | 119 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(116): Show |
127 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.2167+4586A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116978909 | |||||||
| chr1:116979079 | GACAA | G | 3 | a0003c0003t0002g0075 a0003c0003t0002g0080 a0003c0003t0002g0143 |
3 | HG02155.hp2 HG02165.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.2167+4760_2167+476 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116979079 | ||||||
| chr1:116979102 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2167+4779A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979102 | |||||||
| chr1:116979120 | G | A | 118 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(115): Show |
126 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2167+4797G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979120 | |||||||
| chr1:116979124 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0100 |
2 | HG00408.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.2167+4801C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979124 | |||||||
| chr1:116979175 | A | T | 1 | a0001c0020t0001g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2167+4852A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979175 | |||||||
| chr1:116979260 | A | G | 8 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(5): Show |
10 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2167+4937A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979260 | |||||||
| chr1:116979275 | C | T | 3 | a0002c0002t0004g0178 a0002c0002t0004g0180 a0002c0002t0017g0179 |
3 | HG00735.hp2 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2167+4952C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979275 | |||||||
| chr1:116979276 | A | G | 3 | a0002c0002t0004g0178 a0002c0002t0004g0180 a0002c0002t0017g0179 |
3 | HG00735.hp2 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.2167+4953A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979276 | |||||||
| chr1:116979307 | A | G | 1 | a0004c0004t0001g0271 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2167+4984A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979307 | |||||||
| chr1:116979316 | A | G | 124 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(121): Show |
132 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.2167+4993A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979316 | |||||||
| chr1:116979690 | C | T | 116 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(113): Show |
123 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.2168-4990C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979690 | |||||||
| chr1:116979743 | T | C | 1 | a0001c0001t0020g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2168-4937T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979743 | |||||||
| chr1:116979787 | G | A | 124 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(121): Show |
132 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.2168-4893G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979787 | |||||||
| chr1:116979846 | G | T | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2168-4834G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116979846 | |||||||
| chr1:116979880 | TTAAAC | T | 4 | a0001c0001t0016g0228 a0001c0001t0016g0229 a0003c0003t0002g0171 others(1): Show |
4 | HG01928.hp1 HG01978.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-4795_2168-479 others(9): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116979880 | ||||||
| chr1:116980021 | G | GAAGA | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4657_2168-465 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116980021 | ||||||
| chr1:116980025 | A | AAAAC | 113 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(110): Show |
121 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.2168-4652_2168-464 others(8): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116980025 | ||||||
| chr1:116980025 | A | C | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4655A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980025 | |||||||
| chr1:116980114 | C | T | 48 | a0002c0002t0002g0118 a0002c0002t0002g0263 a0003c0003t0002g0002 others(45): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2168-4566C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980114 | |||||||
| chr1:116980120 | T | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4560T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980120 | |||||||
| chr1:116980155 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4525C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980155 | |||||||
| chr1:116980159 | A | G | 5 | a0001c0006t0009g0211 a0001c0006t0009g0212 a0001c0006t0009g0213 others(2): Show |
5 | HG02109.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-4521A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980159 | |||||||
| chr1:116980162 | C | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4518C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980162 | |||||||
| chr1:116980163 | A | G | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4517A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980163 | |||||||
| chr1:116980165 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4515C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980165 | |||||||
| chr1:116980171 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0230 others(7): Show |
11 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2168-4509C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980171 | |||||||
| chr1:116980243 | G | A | 2 | a0003c0003t0002g0007 a0003c0003t0002g0073 |
3 | NA18956.hp2 NA18963.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2168-4437G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980243 | |||||||
| chr1:116980379 | A | G | 114 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(111): Show |
122 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2168-4301A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980379 | |||||||
| chr1:116980537 | G | A | 2 | a0003c0003t0002g0054 a0003c0003t0002g0055 |
2 | NA18951.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2168-4143G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980537 | |||||||
| chr1:116980573 | G | C | 2 | a0001c0001t0037g0273 a0011c0021t0036g0287 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2168-4107G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980573 | |||||||
| chr1:116980711 | C | T | 49 | a0002c0002t0002g0118 a0002c0002t0002g0263 a0003c0003t0002g0002 others(46): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2168-3969C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980711 | |||||||
| chr1:116980736 | A | C | 1 | a0007c0013t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2168-3944A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980736 | |||||||
| chr1:116980850 | A | G | 5 | a0002c0019t0030g0270 a0004c0004t0028g0112 a0007c0010t0013g0284 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-3830A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980850 | |||||||
| chr1:116980876 | G | A | 113 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(110): Show |
121 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2168-3804G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116980876 | |||||||
| chr1:116981107 | T | C | 4 | a0001c0001t0018g0269 a0001c0008t0021g0044 a0001c0008t0021g0199 others(1): Show |
4 | HG01433.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2168-3573T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981107 | |||||||
| chr1:116981186 | C | CATT | 6 | a0001c0001t0001g0162 a0001c0001t0001g0288 a0004c0004t0001g0237 others(3): Show |
6 | HG02015.hp2 NA18939.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2168-3492_2168-349 others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116981186 | ||||||
| chr1:116981270 | A | G | 2 | a0001c0001t0020g0200 a0001c0001t0020g0201 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2168-3410A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981270 | |||||||
| chr1:116981400 | T | G | 116 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(113): Show |
124 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.2168-3280T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981400 | |||||||
| chr1:116981560 | G | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0230 a0001c0001t0001g0274 others(3): Show |
7 | HG02280.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2168-3120G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981560 | |||||||
| chr1:116981601 | C | A | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0018t0029g0040 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-3079C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981601 | |||||||
| chr1:116981623 | T | G | 1 | a0002c0019t0030g0270 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2168-3057T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981623 | |||||||
| chr1:116981641 | A | T | 1 | a0003c0003t0002g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2168-3039A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981641 | |||||||
| chr1:116981775 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2168-2905C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981775 | |||||||
| chr1:116981850 | C | A | 1 | a0005c0005t0002g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2168-2830C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981850 | |||||||
| chr1:116981975 | C | T | 40 | a0002c0002t0001g0195 a0002c0002t0004g0003 a0002c0002t0004g0009 others(37): Show |
43 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2168-2705C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116981975 | |||||||
| chr1:116982005 | A | C | 1 | a0001c0001t0007g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2168-2675A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982005 | |||||||
| chr1:116982011 | G | C | 1 | a0002c0002t0006g0033 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2168-2669G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982011 | |||||||
| chr1:116982033 | C | T | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2168-2647C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982033 | |||||||
| chr1:116982045 | T | C | 3 | a0001c0008t0011g0233 a0006c0012t0011g0266 a0006c0022t0011g0265 |
3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2168-2635T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982045 | |||||||
| chr1:116982112 | C | T | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0018t0029g0040 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-2568C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982112 | |||||||
| chr1:116982113 | G | A | 4 | a0001c0001t0012g0292 a0001c0001t0016g0228 a0001c0001t0016g0229 others(1): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-2567G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982113 | |||||||
| chr1:116982451 | A | G | 4 | a0003c0003t0002g0002 a0003c0003t0002g0050 a0003c0003t0002g0051 others(1): Show |
5 | NA18939.hp2 NA18964.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2168-2229A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982451 | |||||||
| chr1:116982577 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0005g0010 |
3 | HG02698.hp1 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2168-2103G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982577 | |||||||
| chr1:116982614 | C | A | 1 | a0004c0009t0001g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2168-2066C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982614 | |||||||
| chr1:116982670 | A | T | 4 | a0002c0019t0030g0270 a0007c0010t0013g0284 a0007c0010t0013g0285 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-2010A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982670 | |||||||
| chr1:116982694 | C | T | 3 | a0002c0002t0003g0023 a0002c0002t0003g0119 a0005c0005t0003g0252 |
3 | HG02735.hp2 HG03239.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2168-1986C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982694 | |||||||
| chr1:116982703 | C | G | 1 | a0003c0003t0002g0078 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2168-1977C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982703 | |||||||
| chr1:116982784 | G | T | 2 | a0001c0001t0018g0269 a0006c0012t0018g0267 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2168-1896G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982784 | |||||||
| chr1:116982796 | A | G | 1 | a0003c0003t0002g0054 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2168-1884A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982796 | |||||||
| chr1:116982836 | C | A | 113 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(110): Show |
121 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2168-1844C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982836 | |||||||
| chr1:116982887 | G | A | 4 | a0002c0019t0030g0270 a0007c0010t0013g0284 a0007c0010t0013g0285 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-1793G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982887 | |||||||
| chr1:116982906 | A | G | 2 | a0001c0001t0018g0269 a0006c0012t0018g0267 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2168-1774A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982906 | |||||||
| chr1:116982935 | A | C | 4 | a0002c0019t0030g0270 a0007c0010t0013g0284 a0007c0010t0013g0285 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2168-1745A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116982935 | |||||||
| chr1:116983158 | G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2168-1522G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983158 | |||||||
| chr1:116983188 | C | T | 38 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0017 others(35): Show |
41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-1492C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983188 | |||||||
| chr1:116983189 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2168-1491G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983189 | |||||||
| chr1:116983240 | G | T | 2 | a0001c0001t0037g0273 a0011c0021t0036g0287 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2168-1440G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983240 | |||||||
| chr1:116983433 | A | G | 38 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0017 others(35): Show |
41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-1247A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983433 | |||||||
| chr1:116983498 | C | CA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0197 others(5): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2168-1158dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | ||||||
| chr1:116983498 | CA | C | 17 | a0001c0001t0001g0144 a0001c0001t0037g0273 a0001c0006t0009g0211 others(14): Show |
17 | HG01069.hp1 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2168-1158delA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | ||||||
| chr1:116983498 | CAA | C | 56 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(53): Show |
62 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2168-1159_2168-115 others(6): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | ||||||
| chr1:116983498 | CAAA | C | 85 | a0002c0002t0001g0195 a0002c0002t0002g0118 a0002c0002t0002g0165 others(82): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2168-1160_2168-115 others(7): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | ||||||
| chr1:116983498 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | HG00099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2168-1170_2168-115 others(17): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 116983498 | ||||||
| chr1:116983585 | G | C | 49 | a0002c0002t0002g0118 a0002c0002t0002g0165 a0002c0002t0002g0263 others(46): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.2168-1095G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983585 | |||||||
| chr1:116983638 | T | A | 11 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(8): Show |
14 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2168-1042T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983638 | |||||||
| chr1:116983789 | T | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-891T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983789 | |||||||
| chr1:116983790 | C | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-890C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983790 | |||||||
| chr1:116983795 | G | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-885G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983795 | |||||||
| chr1:116983797 | G | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-883G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983797 | |||||||
| chr1:116983798 | G | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-882G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983798 | |||||||
| chr1:116983802 | T | G | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-878T>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983802 | |||||||
| chr1:116983803 | A | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-877A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983803 | |||||||
| chr1:116983808 | A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-872A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983808 | |||||||
| chr1:116983809 | A | T | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-871A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983809 | |||||||
| chr1:116983828 | C | A | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-852C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983828 | |||||||
| chr1:116983829 | T | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-851T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983829 | |||||||
| chr1:116983855 | C | T | 1 | a0003c0003t0010g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2168-825C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983855 | |||||||
| chr1:116983868 | A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-812A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983868 | |||||||
| chr1:116983898 | A | C | 1 | a0003c0003t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2168-782A>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116983898 | |||||||
| chr1:116984135 | C | A | 1 | a0001c0001t0001g0005 | 3 | HG02109.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2168-545C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984135 | |||||||
| chr1:116984145 | A | G | 1 | a0001c0018t0029g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2168-535A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984145 | |||||||
| chr1:116984179 | G | A | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2168-501G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984179 | |||||||
| chr1:116984283 | G | C | 167 | a0001c0001t0001g0227 a0001c0001t0007g0012 a0001c0001t0007g0059 others(164): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2168-397G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984283 | |||||||
| chr1:116984477 | A | T | 38 | a0002c0002t0003g0001 a0002c0002t0003g0016 a0002c0002t0003g0017 others(35): Show |
41 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2168-203A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984477 | |||||||
| chr1:116984508 | A | G | 2 | a0001c0001t0016g0228 a0001c0001t0016g0229 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2168-172A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984508 | |||||||
| chr1:116984530 | A | T | 44 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(41): Show |
46 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2168-150A>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984530 | |||||||
| chr1:116984574 | G | A | 11 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(8): Show |
14 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2168-106G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984574 | |||||||
| chr1:116984605 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2168-75C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984605 | |||||||
| chr1:116984626 | A | G | 1 | a0002c0002t0003g0135 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2168-54A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 7/8 | chr1 | 116984626 | |||||||
| chr1:116985023 | GTCT | G | 115 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(112): Show |
123 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.2473+46_2473+48del others(3): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985023 | ||||||
| chr1:116985079 | A | G | 1 | a0002c0002t0004g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2473+94A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985079 | |||||||
| chr1:116985094 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2473+109G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985094 | |||||||
| chr1:116985117 | G | T | 1 | a0004c0004t0028g0112 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2473+132G>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985117 | |||||||
| chr1:116985470 | G | A | 2 | a0001c0001t0037g0273 a0011c0021t0036g0287 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2473+485G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985470 | |||||||
| chr1:116985473 | C | T | 2 | a0001c0001t0012g0292 a0006c0007t0012g0015 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2473+488C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985473 | |||||||
| chr1:116985555 | C | A | 152 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(149): Show |
162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2473+570C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985555 | |||||||
| chr1:116985617 | A | G | 40 | a0002c0002t0001g0195 a0002c0002t0004g0003 a0002c0002t0004g0009 others(37): Show |
43 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2473+632A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985617 | |||||||
| chr1:116985657 | G | A | 89 | a0002c0002t0001g0195 a0002c0002t0002g0118 a0002c0002t0002g0165 others(86): Show |
94 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2473+672G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985657 | |||||||
| chr1:116985703 | A | G | 2 | a0001c0001t0018g0269 a0006c0012t0018g0267 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2473+718A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985703 | |||||||
| chr1:116985707 | C | CA | 25 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(22): Show |
28 | HG00741.hp2 HG01069.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.2473+736dupA | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985707 | ||||||
| chr1:116985707 | C | CAA | 50 | a0002c0002t0003g0001 a0002c0002t0003g0008 a0002c0002t0003g0016 others(47): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.2473+735_2473+736d others(4): Show |
PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985707 | ||||||
| chr1:116985722 | G | A | 89 | a0002c0002t0001g0195 a0002c0002t0002g0118 a0002c0002t0002g0165 others(86): Show |
94 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2473+737G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985722 | |||||||
| chr1:116985744 | G | A | 50 | a0002c0002t0003g0001 a0002c0002t0003g0008 a0002c0002t0003g0016 others(47): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.2473+759G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985744 | |||||||
| chr1:116985818 | C | G | 3 | a0001c0008t0011g0233 a0006c0012t0011g0266 a0006c0022t0011g0265 |
3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2473+833C>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985818 | |||||||
| chr1:116985885 | CT | C | 4 | a0001c0001t0012g0292 a0001c0001t0016g0228 a0001c0001t0016g0229 others(1): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2473+902delT | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116985885 | ||||||
| chr1:116985888 | G | C | 1 | a0008c0023t0033g0281 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2473+903G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985888 | |||||||
| chr1:116985889 | G | A | 3 | a0001c0008t0011g0233 a0006c0012t0011g0266 a0006c0022t0011g0265 |
3 | HG02622.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2473+904G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985889 | |||||||
| chr1:116985909 | C | A | 1 | a0003c0003t0002g0057 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2474-892C>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985909 | |||||||
| chr1:116985994 | A | G | 165 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(162): Show |
177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2474-807A>G | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116985994 | |||||||
| chr1:116986024 | G | C | 4 | a0001c0001t0020g0200 a0001c0001t0020g0201 a0001c0018t0029g0040 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2474-777G>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986024 | |||||||
| chr1:116986071 | T | C | 2 | a0001c0001t0018g0269 a0006c0012t0018g0267 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2474-730T>C | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986071 | |||||||
| chr1:116986188 | T | TG | 165 | a0001c0001t0007g0012 a0001c0001t0007g0059 a0001c0001t0007g0060 others(162): Show |
177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2474-610dupG | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 116986188 | ||||||
| chr1:116986554 | C | T | 3 | a0007c0010t0013g0284 a0007c0010t0013g0285 a0007c0010t0013g0286 |
3 | HG02145.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2474-247C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986554 | |||||||
| chr1:116986589 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2474-212G>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986589 | |||||||
| chr1:116986600 | T | A | 2 | a0002c0002t0003g0102 a0002c0002t0003g0186 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2474-201T>A | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986600 | |||||||
| chr1:116986757 | C | T | 1 | a0006c0007t0012g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2474-44C>T | PTGFRN | ENSG00000134247.10 | transcript | ENST00000393203.3 | protein_coding | 8/8 | chr1 | 116986757 |