Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5228 |
| ensemblid | ENSG00000119630.14 |
| hgncid | 8893 |
| symbol | PGF |
| name | placental growth factor |
| refseq_nuc | NM_002632.6 |
| refseq_prot | NP_002623.2 |
| ensembl_nuc | ENST00000555567.6 |
| ensembl_prot | ENSP00000451040.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74941834 |
| end | 74955597 |
| strand | - |
| ver | v1.2 |
| region | chr14:74941834-74955597 |
| region5000 | chr14:74936834-74960597 |
| regionname0 | PGF_chr14_74941834_74955597 |
| regionname5000 | PGF_chr14_74936834_74960597 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 510 | 406 | 96 | 74 | 178 | 16 | 40 | PGF_chr14_74936834_74960597 | PGF | ATGCC others(505): Show |
chr14 | 74936834 | 74960597 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1741 | 259 | 25 | 53 | 146 | 14 | 20 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0002 | 0/0 | 1740 | 57 | 1 | 11 | 28 | 2 | 15 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0003 | 0/0 | 1740 | 33 | 26 | 4 | 0 | 0 | 3 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0004 | 0/0 | 1740 | 17 | 14 | 2 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0005 | 0/0 | 1740 | 8 | 8 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0006 | 0/0 | 1740 | 7 | 7 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0007 | 0/0 | 1740 | 6 | 6 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0008 | 1/0 | 1740 | 4 | 1 | 1 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0009 | 0/0 | 1740 | 2 | 0 | 1 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0010 | 0/0 | 1740 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0011 | 0/0 | 1741 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0012 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0013 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0014 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0015 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0016 | 0/0 | 1741 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0017 | 0/0 | 1741 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0018 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1735): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0019 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| a0001c0001t0020 | 0/0 | 1741 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | AGAAG others(1736): Show |
chr14 | 74936834 | 74960597 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 56 | 1 | 5 | 43 | 2 | 5 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0002 | 0/0 | 48 | 7 | 8 | 25 | 4 | 4 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0003 | 0/0 | 17 | 2 | 8 | 1 | 4 | 2 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0004 | 0/0 | 13 | 0 | 0 | 10 | 0 | 3 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0005 | 0/0 | 11 | 0 | 5 | 0 | 2 | 4 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0006 | 0/0 | 10 | 5 | 3 | 0 | 0 | 2 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0005g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0005g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0007g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0007g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0008g0025 | 1/0 | 3 | 0 | 1 | 0 | 0 | 1 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0010g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0011g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0016g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0017g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0018g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0019g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| a0001c0001t0020g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01081 | hp2 | a0001 | c0001 | t0018 | g0055 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01346 | hp1 | a0001 | c0001 | t0008 | g0025 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01981 | hp1 | a0001 | c0001 | t0020 | g0155 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0075 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0037 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02273 | hp1 | a0001 | c0001 | t0009 | g0072 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0025 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0050 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02895 | hp2 | a0001 | c0001 | t0019 | g0061 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02897 | hp2 | a0001 | c0001 | t0015 | g0131 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0050 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18954 | hp1 | a0001 | c0001 | t0009 | g0121 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18975 | hp1 | a0001 | c0001 | t0017 | g0111 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19005 | hp2 | a0001 | c0001 | t0016 | g0145 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | YRI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0037 | AFR | ASW | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | GIH | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | GIH | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0053 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | MSL | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | USA | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| HG06807 | hp2 | a0001 | c0001 | t0014 | g0138 | AFR | USA | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | USA | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0096 | REF | REF | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0025 | REF | REF | PGF_chr14_74936834_74960597 | PGF | chr14 | 74936834 | 74960597 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74941960 | C | T | 2 | a0001c0001t0005 a0001c0001t0007 |
14 | HG02451.hp1 HG02886.hp2 HG02922.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*746G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 746 | chr14 | 74941960 | ||||||
| chr14:74942064 | G | C | 3 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0015 |
4 | HG02273.hp1 HG02897.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*642C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 642 | chr14 | 74942064 | ||||||
| chr14:74942064 | G | T | 2 | a0001c0001t0002 a0001c0001t0013 |
58 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*642C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 642 | chr14 | 74942064 | ||||||
| chr14:74942086 | T | C | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(3): Show |
101 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*620A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 620 | chr14 | 74942086 | ||||||
| chr14:74942109 | G | A | 1 | a0001c0001t0016 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 597 | chr14 | 74942109 | ||||||
| chr14:74942144 | G | A | 1 | a0001c0001t0017 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 562 | chr14 | 74942144 | ||||||
| chr14:74942305 | C | CT | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*400dupA | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 400 | chr14 | 74942305 | ||||||
| chr14:74942340 | T | A | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 366 | chr14 | 74942340 | ||||||
| chr14:74942467 | T | C | 2 | a0001c0001t0006 a0001c0001t0018 |
8 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*239A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 239 | chr14 | 74942467 | ||||||
| chr14:74942519 | T | A | 2 | a0001c0001t0006 a0001c0001t0018 |
8 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*187A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 187 | chr14 | 74942519 | ||||||
| chr14:74942580 | C | T | 2 | a0001c0001t0004 a0001c0001t0010 |
19 | HG01109.hp1 HG01496.hp2 HG02717.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*126G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 126 | chr14 | 74942580 | ||||||
| chr14:74942602 | G | T | 1 | a0001c0001t0009 | 2 | HG02273.hp1 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*104C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 104 | chr14 | 74942602 | ||||||
| chr14:74942629 | C | T | 1 | a0001c0001t0013 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 77 | chr14 | 74942629 | ||||||
| chr14:74942638 | T | C | 2 | a0001c0001t0011 a0001c0001t0012 |
3 | HG02055.hp2 HG02486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 68 | chr14 | 74942638 | ||||||
| chr14:74942700 | G | A | 1 | a0001c0001t0019 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 7/7 | 6 | chr14 | 74942700 | ||||||
| chr14:74955468 | G | A | 1 | a0001c0001t0020 | 1 | HG01981.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-226C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/7 | chr14 | 74955468 | |||||||
| chr14:74955472 | C | T | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 |
16 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-230G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/7 | 230 | chr14 | 74955472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74942772 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.486-39G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74942772 | |||||||
| chr14:74942878 | T | C | 4 | a0001c0001t0006g0015 a0001c0001t0006g0033 a0001c0001t0006g0054 others(1): Show |
8 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-145A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74942878 | |||||||
| chr14:74942901 | G | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0022 a0001c0001t0007g0059 |
9 | HG02451.hp1 HG02922.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-168C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74942901 | |||||||
| chr14:74942979 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.486-246A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74942979 | |||||||
| chr14:74943115 | C | T | 1 | a0001c0001t0019g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.486-382G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943115 | |||||||
| chr14:74943168 | C | T | 4 | a0001c0001t0004g0023 a0001c0001t0004g0060 a0001c0001t0004g0100 others(1): Show |
6 | HG01109.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-435G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943168 | |||||||
| chr14:74943184 | T | C | 4 | a0001c0001t0006g0015 a0001c0001t0006g0033 a0001c0001t0006g0054 others(1): Show |
8 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-451A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943184 | |||||||
| chr14:74943191 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486-458A>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943191 | |||||||
| chr14:74943473 | T | C | 3 | a0001c0001t0009g0072 a0001c0001t0009g0121 a0001c0001t0014g0138 |
3 | HG02273.hp1 HG06807.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.486-740A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943473 | |||||||
| chr14:74943820 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.486-1087G>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943820 | |||||||
| chr14:74943947 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.486-1214A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943947 | |||||||
| chr14:74943996 | T | C | 7 | a0001c0001t0003g0147 a0001c0001t0004g0023 a0001c0001t0004g0032 others(4): Show |
12 | HG02622.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-1263A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74943996 | |||||||
| chr14:74944081 | A | AT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.486-1349dupA | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944081 | |||||||
| chr14:74944081 | A | ATT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0040 others(6): Show |
19 | NA18747.hp1 NA18955.hp1 NA18977.hp1 others(16): Show |
intron_variant | MODIFIER | c.486-1350_486-1349d others(4): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944081 | |||||||
| chr14:74944109 | C | CT | 25 | a0001c0001t0001g0077 a0001c0001t0001g0122 a0001c0001t0003g0006 others(22): Show |
47 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.486-1377dupA | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944109 | |||||||
| chr14:74944126 | A | G | 2 | a0001c0001t0007g0024 a0001c0001t0007g0038 |
5 | HG02886.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1393T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944126 | |||||||
| chr14:74944172 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.486-1439C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944172 | |||||||
| chr14:74944174 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.486-1441G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944174 | |||||||
| chr14:74944185 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
7 | HG00323.hp1 HG01934.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-1452A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944185 | |||||||
| chr14:74944195 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.486-1462G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944195 | |||||||
| chr14:74944248 | A | G | 4 | a0001c0001t0003g0147 a0001c0001t0004g0014 a0001c0001t0004g0032 others(1): Show |
10 | HG01496.hp2 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-1515T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944248 | |||||||
| chr14:74944252 | A | C | 1 | a0001c0001t0006g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486-1519T>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944252 | |||||||
| chr14:74944252 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0003g0147 a0001c0001t0004g0014 others(2): Show |
11 | HG01106.hp1 HG01496.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-1519T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944252 | |||||||
| chr14:74944259 | C | T | 1 | a0001c0001t0001g0040 | 2 | NA19003.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.486-1526G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944259 | |||||||
| chr14:74944288 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.486-1555G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944288 | |||||||
| chr14:74944292 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.486-1559A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944292 | |||||||
| chr14:74944303 | C | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0018 others(35): Show |
80 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.486-1570G>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944303 | |||||||
| chr14:74944304 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.486-1571T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944304 | |||||||
| chr14:74944317 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.486-1584A>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944317 | |||||||
| chr14:74944318 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.486-1585C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944318 | |||||||
| chr14:74944332 | A | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0084 others(1): Show |
6 | HG00323.hp2 HG00738.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-1599T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944332 | |||||||
| chr14:74944340 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.486-1607C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944340 | |||||||
| chr14:74944349 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.486-1616C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944349 | |||||||
| chr14:74944353 | T | C | 2 | a0001c0001t0002g0080 a0001c0001t0018g0055 |
2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.486-1620A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944353 | |||||||
| chr14:74944354 | G | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0076 others(22): Show |
46 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.486-1621C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944354 | |||||||
| chr14:74944361 | A | C | 1 | a0001c0001t0002g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.486-1628T>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944361 | |||||||
| chr14:74944381 | T | C | 1 | a0001c0001t0019g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.486-1648A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944381 | |||||||
| chr14:74944389 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0040 others(1): Show |
12 | NA18747.hp1 NA18955.hp1 NA18981.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-1656T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944389 | |||||||
| chr14:74944392 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.486-1659C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944392 | |||||||
| chr14:74944455 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.486-1722C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944455 | |||||||
| chr14:74944602 | G | A | 1 | a0001c0001t0017g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.485+1611C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944602 | |||||||
| chr14:74944745 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.485+1468T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944745 | |||||||
| chr14:74944879 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.485+1334A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944879 | |||||||
| chr14:74944920 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.485+1293A>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944920 | |||||||
| chr14:74944922 | CT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.485+1290delA | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944922 | |||||||
| chr14:74944987 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.485+1226A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74944987 | |||||||
| chr14:74945105 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.485+1108C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945105 | |||||||
| chr14:74945109 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.485+1104A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945109 | |||||||
| chr14:74945112 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.485+1101C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945112 | |||||||
| chr14:74945154 | C | G | 2 | a0001c0001t0007g0024 a0001c0001t0007g0038 |
5 | HG02886.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1059G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945154 | |||||||
| chr14:74945249 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.485+964C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945249 | |||||||
| chr14:74945319 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.485+894G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945319 | |||||||
| chr14:74945324 | AACTCGGG others(45): Show |
A | 1 | a0001c0001t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.485+837_485+888del others(52): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945324 | |||||||
| chr14:74945331 | G | A | 1 | a0001c0001t0003g0034 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485+882C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945331 | |||||||
| chr14:74945367 | T | C | 7 | a0001c0001t0003g0147 a0001c0001t0003g0149 a0001c0001t0004g0032 others(4): Show |
10 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+846A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945367 | |||||||
| chr14:74945395 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.485+818C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945395 | |||||||
| chr14:74945416 | G | A | 1 | a0001c0001t0001g0051 | 2 | NA18998.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.485+797C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945416 | |||||||
| chr14:74945466 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.485+747G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945466 | |||||||
| chr14:74945567 | TTGAC | T | 3 | a0001c0001t0011g0037 a0001c0001t0012g0053 a0001c0001t0018g0055 |
4 | HG01081.hp2 HG02055.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+642_485+645del others(4): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945567 | |||||||
| chr14:74945574 | T | C | 3 | a0001c0001t0003g0147 a0001c0001t0004g0032 a0001c0001t0019g0061 |
5 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+639A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945574 | |||||||
| chr14:74945611 | C | G | 1 | a0001c0001t0005g0012 | 5 | HG02451.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+602G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945611 | |||||||
| chr14:74945723 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.485+490G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945723 | |||||||
| chr14:74945799 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.485+414G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 6/6 | chr14 | 74945799 | |||||||
| chr14:74946308 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0005g0012 a0001c0001t0005g0022 |
11 | HG02451.hp1 HG02559.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.423-33A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 5/6 | chr14 | 74946308 | |||||||
| chr14:74946610 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0151 |
3 | HG00408.hp1 HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.393-202G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74946610 | |||||||
| chr14:74947124 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.393-716C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947124 | |||||||
| chr14:74947591 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0005g0012 a0001c0001t0005g0022 |
11 | HG02451.hp1 HG02559.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.392+916T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947591 | |||||||
| chr14:74947765 | T | C | 1 | a0001c0001t0012g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.392+742A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947765 | |||||||
| chr14:74947916 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.392+591A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947916 | |||||||
| chr14:74947985 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0006g0015 |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.392+522G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947985 | |||||||
| chr14:74947986 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0086 a0001c0001t0001g0113 others(1): Show |
6 | NA18968.hp1 NA18982.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.392+521C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74947986 | |||||||
| chr14:74948114 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.392+393G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948114 | |||||||
| chr14:74948122 | C | A | 1 | a0001c0001t0001g0045 | 2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.392+385G>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948122 | |||||||
| chr14:74948158 | C | T | 1 | a0001c0001t0018g0055 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.392+349G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948158 | |||||||
| chr14:74948174 | G | A | 1 | a0001c0001t0002g0019 | 4 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+333C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948174 | |||||||
| chr14:74948217 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0003g0062 a0001c0001t0003g0153 |
3 | HG02572.hp2 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.392+290G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948217 | |||||||
| chr14:74948227 | C | T | 2 | a0001c0001t0003g0020 a0001c0001t0003g0144 |
5 | HG01168.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.392+280G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948227 | |||||||
| chr14:74948491 | G | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.392+16C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 4/6 | chr14 | 74948491 | |||||||
| chr14:74948627 | C | T | 4 | a0001c0001t0001g0056 a0001c0001t0002g0141 a0001c0001t0004g0057 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-44G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74948627 | |||||||
| chr14:74948636 | G | T | 6 | a0001c0001t0001g0029 a0001c0001t0005g0012 a0001c0001t0005g0022 others(3): Show |
18 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.316-53C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74948636 | |||||||
| chr14:74948670 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.316-87C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74948670 | |||||||
| chr14:74948700 | AGGCCCTC others(4): Show |
A | 1 | a0001c0001t0001g0087 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.316-128_316-118del others(11): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74948700 | |||||||
| chr14:74948734 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.316-151C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74948734 | |||||||
| chr14:74949023 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.315+334C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74949023 | |||||||
| chr14:74949166 | CTGGTGGG others(5): Show |
C | 1 | a0001c0001t0003g0071 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.315+179_315+190del others(12): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74949166 | |||||||
| chr14:74949202 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.315+155C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74949202 | |||||||
| chr14:74949223 | C | T | 1 | a0001c0001t0006g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.315+134G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74949223 | |||||||
| chr14:74949297 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(32): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.315+60G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 3/6 | chr14 | 74949297 | |||||||
| chr14:74949752 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.119-199C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74949752 | |||||||
| chr14:74949808 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.119-255C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74949808 | |||||||
| chr14:74949838 | T | C | 1 | a0001c0001t0004g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.119-285A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74949838 | |||||||
| chr14:74949855 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0002g0141 a0001c0001t0004g0057 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-302T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74949855 | |||||||
| chr14:74950018 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.119-465A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950018 | |||||||
| chr14:74950081 | C | T | 19 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0058 others(16): Show |
36 | HG01081.hp2 HG01496.hp2 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.119-528G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950081 | |||||||
| chr14:74950149 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0005g0012 a0001c0001t0005g0022 others(4): Show |
19 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.119-596G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950149 | |||||||
| chr14:74950163 | C | CAGCT | 2 | a0001c0001t0003g0147 a0001c0001t0004g0032 |
4 | HG02622.hp2 HG02723.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-614_119-611dup others(4): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950163 | |||||||
| chr14:74950225 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.119-672G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950225 | |||||||
| chr14:74950512 | T | C | 3 | a0001c0001t0003g0062 a0001c0001t0003g0147 a0001c0001t0004g0032 |
5 | HG02622.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-959A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950512 | |||||||
| chr14:74950554 | G | A | 3 | a0001c0001t0006g0015 a0001c0001t0006g0033 a0001c0001t0006g0054 |
7 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-1001C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950554 | |||||||
| chr14:74950579 | A | T | 1 | a0001c0001t0003g0034 | 2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.119-1026T>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950579 | |||||||
| chr14:74950652 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1099C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950652 | |||||||
| chr14:74950658 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1105C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950658 | |||||||
| chr14:74950659 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1106C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950659 | |||||||
| chr14:74950663 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1110C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950663 | |||||||
| chr14:74950673 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1120G>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950673 | |||||||
| chr14:74950685 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1132C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950685 | |||||||
| chr14:74950699 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1146C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950699 | |||||||
| chr14:74950701 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1148A>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950701 | |||||||
| chr14:74950702 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1149C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950702 | |||||||
| chr14:74950705 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1152T>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950705 | |||||||
| chr14:74950711 | GAAGGTTG others(3): Show |
G | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1168_119-1159d others(12): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950711 | |||||||
| chr14:74950730 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1177A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950730 | |||||||
| chr14:74950739 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.119-1186A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950739 | |||||||
| chr14:74950832 | C | G | 2 | a0001c0001t0004g0014 a0001c0001t0004g0092 |
6 | HG02965.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-1279G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74950832 | |||||||
| chr14:74951132 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.119-1579A>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951132 | |||||||
| chr14:74951164 | GCTGCTCC others(3): Show |
G | 1 | a0001c0001t0001g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.119-1621_119-1612d others(12): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951164 | |||||||
| chr14:74951231 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.119-1678C>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951231 | |||||||
| chr14:74951288 | C | T | 6 | a0001c0001t0005g0012 a0001c0001t0005g0022 a0001c0001t0006g0015 others(3): Show |
16 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.119-1735G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951288 | |||||||
| chr14:74951370 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.119-1817C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951370 | |||||||
| chr14:74951446 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0137 |
4 | HG00741.hp1 HG01175.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-1893C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951446 | |||||||
| chr14:74951491 | T | C | 1 | a0001c0001t0007g0024 | 3 | HG02886.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.119-1938A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951491 | |||||||
| chr14:74951517 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0004g0057 a0001c0001t0018g0055 |
3 | HG01081.hp2 HG01496.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.119-1964A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951517 | |||||||
| chr14:74951547 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.119-1994G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951547 | |||||||
| chr14:74951664 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.119-2111C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951664 | |||||||
| chr14:74951714 | C | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(35): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.119-2161G>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951714 | |||||||
| chr14:74951765 | T | C | 23 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0064 others(20): Show |
40 | HG01081.hp2 HG01109.hp1 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.118+2139A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951765 | |||||||
| chr14:74951984 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.118+1920G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74951984 | |||||||
| chr14:74952004 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118+1900G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952004 | |||||||
| chr14:74952120 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.118+1784C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952120 | |||||||
| chr14:74952180 | G | C | 9 | a0001c0001t0003g0062 a0001c0001t0003g0147 a0001c0001t0004g0032 others(6): Show |
21 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.118+1724C>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952180 | |||||||
| chr14:74952189 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0002g0141 a0001c0001t0004g0057 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+1715C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952189 | |||||||
| chr14:74952425 | C | T | 6 | a0001c0001t0005g0012 a0001c0001t0005g0022 a0001c0001t0006g0015 others(3): Show |
16 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+1479G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952425 | |||||||
| chr14:74952449 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.118+1455A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952449 | |||||||
| chr14:74952615 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.118+1289C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952615 | |||||||
| chr14:74952674 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118+1230C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952674 | |||||||
| chr14:74952741 | A | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
73 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.118+1163T>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952741 | |||||||
| chr14:74952808 | G | A | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0143 others(1): Show |
10 | HG01168.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+1096C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952808 | |||||||
| chr14:74952936 | C | CAAAAAGG others(4): Show |
1 | a0001c0001t0003g0071 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.118+957_118+967dup others(11): Show |
PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74952936 | |||||||
| chr14:74953039 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.118+865C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953039 | |||||||
| chr14:74953046 | G | A | 1 | a0001c0001t0016g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.118+858C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953046 | |||||||
| chr14:74953146 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118+758G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953146 | |||||||
| chr14:74953225 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.118+679G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953225 | |||||||
| chr14:74953243 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.118+661C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953243 | |||||||
| chr14:74953419 | G | A | 8 | a0001c0001t0003g0147 a0001c0001t0004g0032 a0001c0001t0005g0012 others(5): Show |
20 | HG02109.hp2 HG02145.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.118+485C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953419 | |||||||
| chr14:74953744 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.118+160T>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953744 | |||||||
| chr14:74953745 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.118+159A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953745 | |||||||
| chr14:74953867 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118+37A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 2/6 | chr14 | 74953867 | |||||||
| chr14:74954126 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.76-180A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954126 | |||||||
| chr14:74954138 | C | G | 8 | a0001c0001t0001g0058 a0001c0001t0003g0034 a0001c0001t0003g0062 others(5): Show |
13 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-192G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954138 | |||||||
| chr14:74954254 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.76-308C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954254 | |||||||
| chr14:74954427 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.76-481A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954427 | |||||||
| chr14:74954474 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG01433.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.76-528C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954474 | |||||||
| chr14:74954705 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0004g0023 a0001c0001t0004g0060 others(2): Show |
7 | HG01109.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+463G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954705 | |||||||
| chr14:74954732 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0003g0034 a0001c0001t0004g0023 others(4): Show |
12 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+436G>A | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954732 | |||||||
| chr14:74954816 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.75+352A>G | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74954816 | |||||||
| chr14:74955118 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.75+50C>T | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74955118 | |||||||
| chr14:74955142 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0004g0057 a0001c0001t0018g0055 |
3 | HG01081.hp2 HG01496.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75+26G>C | PGF | ENSG00000119630.14 | transcript | ENST00000555567.6 | protein_coding | 1/6 | chr14 | 74955142 |