| geneid | 81608 |
|---|---|
| ensemblid | ENSG00000145216.17 |
| hgncid | 19124 |
| symbol | FIP1L1 |
| name | factor interacting with PAPOLA and CPSF1 |
| refseq_nuc | NM_030917.4 |
| refseq_prot | NP_112179.2 |
| ensembl_nuc | ENST00000337488.11 |
| ensembl_prot | ENSP00000336752.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 53377641 |
| end | 53460862 |
| strand | + |
| ver | v1.2 |
| region | chr4:53377641-53460862 |
| region5000 | chr4:53372641-53465862 |
| regionname0 | FIP1L1_chr4_53377641_53460862 |
| regionname5000 | FIP1L1_chr4_53372641_53465862 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 594 | 392 | 86 | 66 | 178 | 14 | 46 | 134 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1785 | 392 | 86 | 66 | 178 | 14 | 46 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1608 | 107 | 11 | 28 | 51 | 7 | 10 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0002 | 0/0 | 1612 | 77 | 26 | 2 | 33 | 0 | 16 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0003 | 1/1 | 1612 | 68 | 7 | 11 | 38 | 1 | 9 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0004 | 0/0 | 1608 | 60 | 10 | 15 | 28 | 4 | 3 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0005 | 0/0 | 1608 | 46 | 8 | 6 | 24 | 2 | 6 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0006 | 0/0 | 1608 | 15 | 13 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0007 | 0/0 | 1612 | 4 | 0 | 0 | 2 | 0 | 2 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0008 | 0/0 | 1608 | 3 | 3 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0009 | 0/0 | 1608 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0010 | 0/0 | 1612 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0011 | 0/0 | 1612 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0012 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0013 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0014 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0015 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0016 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0017 | 0/0 | 1612 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0018 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| t0019 | 0/0 | 1612 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1785 | 392 | 86 | 66 | 178 | 14 | 46 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3392 | 107 | 11 | 28 | 51 | 7 | 10 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0002 | 0/0 | 3396 | 77 | 26 | 2 | 33 | 0 | 16 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0003 | 1/1 | 3396 | 68 | 7 | 11 | 38 | 1 | 9 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0004 | 0/0 | 3392 | 60 | 10 | 15 | 28 | 4 | 3 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0005 | 0/0 | 3392 | 46 | 8 | 6 | 24 | 2 | 6 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0006 | 0/0 | 3392 | 15 | 13 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0007 | 0/0 | 3396 | 4 | 0 | 0 | 2 | 0 | 2 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0008 | 0/0 | 3392 | 3 | 3 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0009 | 0/0 | 3392 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0010 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0011 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0012 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0013 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0014 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0015 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0016 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0017 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0018 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| a0001c0001t0019 | 0/0 | 3396 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | copy fasta | chr4 | 53372641 | 53465862 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0003g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0008g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0010g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0011g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0017g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| a0001c0001t0019g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0121 | EUR | GBR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0196 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | FIN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00642 | hp2 | a0001 | c0001 | t0019 | g0366 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0136 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0255 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01243 | hp2 | a0001 | c0001 | t0018 | g0215 | AMR | PUR | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | CLM | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0138 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0031 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02015 | hp2 | a0001 | c0001 | t0017 | g0026 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0373 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | CDX | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0292 | AMR | PEL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0357 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0347 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0237 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0368 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0132 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0369 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0252 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0367 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0371 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0370 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0365 | AFR | ESN | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0071 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0374 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0235 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0345 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0375 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0122 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0133 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0120 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0338 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | BEB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0358 | SAS | STU | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0364 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0377 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0376 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0378 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0372 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0379 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19089 | hp1 | a0001 | c0001 | t0014 | g0289 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0226 | AFR | ASW | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ASW | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0220 | EUR | TSI | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0340 | SAS | GIH | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | MSL | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | USA | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | LWK | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0014 | REF | REF | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0021 | REF | REF | FIP1L1_chr4_53372641_53465862 | FIP1L1 | chr4 | 53372641 | 53465862 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:53377658
|
C | T | 1 | a0001c0001t0019 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 181 | chr4 | 53377658 | |||||
| chr4:53377662
|
C | T | 1 | a0001c0001t0018 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-177C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 177 | chr4 | 53377662 | |||||
| chr4:53377738
|
T | C | 11 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | 239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
5_prime_UTR_variant | MODIFIER | c.-101T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/18 | 101 | chr4 | 53377738 | |||||
| chr4:53459823
|
T | C | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 374 | chr4 | 53459823 | |||||
| chr4:53459921
|
T | C | 2 | a0001c0001t0010a0001c0001t0011 | 2 | HG02055.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 472 | chr4 | 53459921 | |||||
| chr4:53459987
|
C | T | 1 | a0001c0001t0011 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 538 | chr4 | 53459987 | |||||
| chr4:53460048
|
A | G | 1 | a0001c0001t0014 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 599 | chr4 | 53460048 | |||||
| chr4:53460054
|
T | C | 1 | a0001c0001t0016 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 605 | chr4 | 53460054 | |||||
| chr4:53460055
|
AAATT | A | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*619delATTA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 616 | INFO_REALIGN_3_PRIME | chr4 | 53460055 | ||||
| chr4:53460150
|
G | C | 1 | a0001c0001t0012 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 701 | chr4 | 53460150 | |||||
| chr4:53460228
|
C | CAGTT | 1 | a0001c0001t0007 | 4 | HG02683.hp2 HG03704.hp1 NA18963.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*781_*784dupGTTA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 785 | INFO_REALIGN_3_PRIME | chr4 | 53460228 | ||||
| chr4:53460228
|
C | T | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(2): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*779C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 779 | chr4 | 53460228 | |||||
| chr4:53460247
|
A | G | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 798 | chr4 | 53460247 | |||||
| chr4:53460357
|
CAAAT | C | 2 | a0001c0001t0006a0001c0001t0016 | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*911_*914delATAA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 911 | INFO_REALIGN_3_PRIME | chr4 | 53460357 | ||||
| chr4:53460377
|
A | G | 1 | a0001c0001t0013 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 928 | chr4 | 53460377 | |||||
| chr4:53460383
|
A | T | 1 | a0001c0001t0005 | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*934A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 934 | chr4 | 53460383 | |||||
| chr4:53460624
|
A | AAATC | 4 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(1): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1177_*1180dupATCA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1181 | INFO_REALIGN_3_PRIME | chr4 | 53460624 | ||||
| chr4:53460630
|
T | A | 1 | a0001c0001t0017 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1181T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1181 | chr4 | 53460630 | |||||
| chr4:53460757
|
G | C | 2 | a0001c0001t0008a0001c0001t0015 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1308G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 18/18 | 1308 | chr4 | 53460757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:53377935
|
C | A | 1 | a0001c0001t0005g0012 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85+12C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377935 | ||||||
| chr4:53377935
|
C | T | 4 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0003g0378others(1): Show | 4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+12C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377935 | ||||||
| chr4:53377936
|
C | A | 1 | a0001c0001t0005g0012 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85+13C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53377936 | ||||||
| chr4:53378007
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85+84G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378007 | ||||||
| chr4:53378060
|
G | C | 1 | a0001c0001t0003g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+137G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378060 | ||||||
| chr4:53378109
|
C | T | 1 | a0001c0001t0003g0375 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.85+186C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378109 | ||||||
| chr4:53378154
|
C | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(231): Show | 239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.85+231C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378154 | ||||||
| chr4:53378156
|
G | T | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.85+233G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378156 | ||||||
| chr4:53378251
|
C | G | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.85+328C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378251 | ||||||
| chr4:53378268
|
G | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+345G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378268 | ||||||
| chr4:53378271
|
G | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.85+348G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378271 | ||||||
| chr4:53378299
|
C | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.85+376C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378299 | ||||||
| chr4:53378534
|
G | C | 1 | a0001c0001t0002g0299 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86-539G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378534 | ||||||
| chr4:53378752
|
T | C | 1 | a0001c0001t0006g0004 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.86-321T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378752 | ||||||
| chr4:53378841
|
G | A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.86-232G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378841 | ||||||
| chr4:53378842
|
A | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.86-231A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378842 | ||||||
| chr4:53378862
|
T | TA | 81 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(78): Show | 83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.86-202dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 53378862 | |||||
| chr4:53378894
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.86-179A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 1/17 | chr4 | 53378894 | ||||||
| chr4:53379309
|
A | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.170+45A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379309 | ||||||
| chr4:53379332
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.170+68A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379332 | ||||||
| chr4:53379379
|
A | G | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+115A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379379 | ||||||
| chr4:53379516
|
T | G | 1 | a0001c0001t0005g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.170+252T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379516 | ||||||
| chr4:53379582
|
T | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+318T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379582 | ||||||
| chr4:53379608
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+344A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379608 | ||||||
| chr4:53379802
|
G | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+538G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53379802 | ||||||
| chr4:53380177
|
G | A | 7 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(4): Show | 8 | NA18941.hp2 NA18956.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.170+913G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380177 | ||||||
| chr4:53380177
|
GTGAAT | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.170+914_170+918del others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380177 | ||||||
| chr4:53380267
|
G | T | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.170+1003G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380267 | ||||||
| chr4:53380405
|
T | A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.170+1141T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380405 | ||||||
| chr4:53380479
|
G | T | 1 | a0001c0001t0001g0297 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.170+1215G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380479 | ||||||
| chr4:53380570
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170+1306C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380570 | ||||||
| chr4:53380582
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.170+1318G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380582 | ||||||
| chr4:53380656
|
C | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01358.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.170+1392C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380656 | ||||||
| chr4:53380758
|
A | G | 2 | a0001c0001t0002g0364a0001c0001t0002g0365 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.170+1494A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380758 | ||||||
| chr4:53380789
|
T | G | 2 | a0001c0001t0002g0364a0001c0001t0002g0365 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.171-1489T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380789 | ||||||
| chr4:53380974
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.171-1304C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380974 | ||||||
| chr4:53380975
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.171-1303G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53380975 | ||||||
| chr4:53381417
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.171-861T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381417 | ||||||
| chr4:53381615
|
C | G | 3 | a0001c0001t0002g0361a0001c0001t0002g0362a0001c0001t0002g0363 | 3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.171-663C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381615 | ||||||
| chr4:53381676
|
T | A | 1 | a0001c0001t0019g0366 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.171-602T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381676 | ||||||
| chr4:53381753
|
C | CTTTT | 37 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(34): Show | 41 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.171-504_171-501dup others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTT | 20 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307others(17): Show | 21 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.171-505_171-501dup others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTT | 62 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0309others(59): Show | 64 | HG00597.hp2 HG00642.hp2 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.171-506_171-501dup others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT | 8 | a0001c0001t0002g0299a0001c0001t0002g0355a0001c0001t0002g0356others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.171-507_171-501dup others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0301 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.171-510_171-501dup others(10): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0365a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.171-511_171-501dup others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0001g0204a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01255.hp2 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-512_171-501dup others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0150a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG02145.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-513_171-501dup others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(7): Show |
19 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0216others(16): Show | 19 | HG00280.hp2 HG00597.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.171-514_171-501dup others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(8): Show |
27 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.171-515_171-501dup others(15): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(9): Show |
22 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(19): Show | 22 | HG00558.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.171-516_171-501dup others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0274a0001c0001t0001g0280a0001c0001t0001g0281others(10): Show | 14 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.171-517_171-501dup others(17): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(11): Show |
7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG01071.hp1 HG01433.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-518_171-501dup others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0291 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.171-519_171-501dup others(19): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.171-520_171-501dup others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.171-524_171-501dup others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.171-501_171-500ins others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
CT | C | 57 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(54): Show | 58 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.171-501delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0190a0001c0001t0005g0191 | 2 | NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.171-511_171-501del others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381753
|
CTTTTTTT others(5): Show |
C | 42 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0151others(39): Show | 44 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.171-512_171-501del others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381753 | |||||
| chr4:53381815
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.171-463A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53381815 | ||||||
| chr4:53381929
|
AT | A | 79 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(76): Show | 81 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.171-336delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53381929 | |||||
| chr4:53382109
|
C | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.171-169C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382109 | ||||||
| chr4:53382146
|
A | AT | 3 | a0001c0001t0005g0227a0001c0001t0005g0253a0001c0001t0005g0273 | 3 | HG02132.hp1 NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.171-128dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 53382146 | |||||
| chr4:53382233
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-45C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382233 | ||||||
| chr4:53382239
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.171-39G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382239 | ||||||
| chr4:53382251
|
A | G | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.171-27A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 3/17 | chr4 | 53382251 | ||||||
| chr4:53382531
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.228+196A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382531 | ||||||
| chr4:53382565
|
G | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 15 | HG01346.hp1 HG01952.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.228+230G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382565 | ||||||
| chr4:53382863
|
T | G | 1 | a0001c0001t0004g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.228+528T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382863 | ||||||
| chr4:53382869
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.228+534T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382869 | ||||||
| chr4:53382873
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.228+538G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382873 | ||||||
| chr4:53382924
|
A | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.228+589A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53382924 | ||||||
| chr4:53383018
|
G | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(154): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.228+683G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383018 | ||||||
| chr4:53383018
|
GT | G | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.228+694delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 53383018 | |||||
| chr4:53383066
|
A | G | 1 | a0001c0001t0006g0074 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.229-707A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383066 | ||||||
| chr4:53383068
|
T | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.229-705T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383068 | ||||||
| chr4:53383106
|
T | C | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(73): Show | 78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.229-667T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383106 | ||||||
| chr4:53383308
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.229-465T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383308 | ||||||
| chr4:53383421
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.229-352G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383421 | ||||||
| chr4:53383470
|
T | C | 1 | a0001c0001t0008g0003 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.229-303T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383470 | ||||||
| chr4:53383560
|
G | T | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229-213G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383560 | ||||||
| chr4:53383697
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.229-76A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 4/17 | chr4 | 53383697 | ||||||
| chr4:53383887
|
T | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332+11T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53383887 | ||||||
| chr4:53383896
|
G | A | 1 | a0001c0001t0003g0025 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.332+20G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53383896 | ||||||
| chr4:53384022
|
T | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.332+146T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384022 | ||||||
| chr4:53384036
|
A | G | 1 | a0001c0001t0002g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332+160A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384036 | ||||||
| chr4:53384040
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+164T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384040 | ||||||
| chr4:53384058
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.332+182C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384058 | ||||||
| chr4:53384121
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+245G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384121 | ||||||
| chr4:53384188
|
C | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+312C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384188 | ||||||
| chr4:53384257
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+381T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384257 | ||||||
| chr4:53384368
|
C | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.332+492C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384368 | ||||||
| chr4:53384406
|
C | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+530C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384406 | ||||||
| chr4:53384630
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+754G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384630 | ||||||
| chr4:53384687
|
T | G | 3 | a0001c0001t0004g0101a0001c0001t0004g0110a0001c0001t0004g0111 | 3 | NA18944.hp2 NA18970.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.332+811T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384687 | ||||||
| chr4:53384761
|
C | T | 46 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(43): Show | 47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.332+885C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384761 | ||||||
| chr4:53384785
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+909G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384785 | ||||||
| chr4:53384996
|
C | A | 1 | a0001c0001t0017g0026 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.332+1120C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53384996 | ||||||
| chr4:53385028
|
A | G | 1 | a0001c0001t0005g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.332+1152A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385028 | ||||||
| chr4:53385130
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.332+1254A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385130 | ||||||
| chr4:53385142
|
C | T | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.332+1266C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385142 | ||||||
| chr4:53385238
|
C | T | 1 | a0001c0001t0002g0308 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.332+1362C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385238 | ||||||
| chr4:53385427
|
T | C | 1 | a0001c0001t0005g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.332+1551T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385427 | ||||||
| chr4:53385491
|
G | A | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.332+1615G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385491 | ||||||
| chr4:53385551
|
A | G | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(73): Show | 78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.332+1675A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53385551 | ||||||
| chr4:53386037
|
A | AT | 81 | a0001c0001t0001g0162a0001c0001t0001g0290a0001c0001t0002g0010others(78): Show | 83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.332+2177dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53386037 | |||||
| chr4:53386037
|
A | ATT | 8 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0070others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.332+2176_332+2177d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53386037 | |||||
| chr4:53386053
|
T | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.332+2177T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386053 | ||||||
| chr4:53386055
|
C | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.332+2179C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386055 | ||||||
| chr4:53386260
|
A | G | 6 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(3): Show | 6 | HG00597.hp1 HG02165.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.332+2384A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386260 | ||||||
| chr4:53386268
|
G | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2392G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386268 | ||||||
| chr4:53386291
|
G | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.332+2415G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386291 | ||||||
| chr4:53386347
|
A | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.332+2471A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386347 | ||||||
| chr4:53386470
|
G | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2594G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386470 | ||||||
| chr4:53386490
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.332+2614A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386490 | ||||||
| chr4:53386529
|
A | G | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.332+2653A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386529 | ||||||
| chr4:53386675
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.332+2799C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386675 | ||||||
| chr4:53386676
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2800G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386676 | ||||||
| chr4:53386715
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2839T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386715 | ||||||
| chr4:53386796
|
A | G | 1 | a0001c0001t0004g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.332+2920A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386796 | ||||||
| chr4:53386817
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.332+2941T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386817 | ||||||
| chr4:53386945
|
A | G | 1 | a0001c0001t0005g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-2864A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386945 | ||||||
| chr4:53386955
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333-2854C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53386955 | ||||||
| chr4:53387436
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-2373C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387436 | ||||||
| chr4:53387697
|
C | T | 1 | a0001c0001t0005g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-2112C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387697 | ||||||
| chr4:53387759
|
G | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.333-2050G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387759 | ||||||
| chr4:53387806
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.333-2003A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387806 | ||||||
| chr4:53387824
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-1985G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387824 | ||||||
| chr4:53387864
|
A | G | 1 | a0001c0001t0005g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333-1945A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387864 | ||||||
| chr4:53387979
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.333-1830G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53387979 | ||||||
| chr4:53388005
|
A | T | 1 | a0001c0001t0005g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.333-1804A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388005 | ||||||
| chr4:53388207
|
T | C | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.333-1602T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388207 | ||||||
| chr4:53388344
|
CT | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(285): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.333-1452delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53388344 | |||||
| chr4:53388442
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.333-1367C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388442 | ||||||
| chr4:53388582
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333-1227G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388582 | ||||||
| chr4:53388631
|
G | A | 1 | a0001c0001t0002g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.333-1178G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388631 | ||||||
| chr4:53388635
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.333-1174G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388635 | ||||||
| chr4:53388689
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0151others(41): Show | 46 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.333-1120G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388689 | ||||||
| chr4:53388689
|
G | T | 1 | a0001c0001t0002g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.333-1120G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388689 | ||||||
| chr4:53388703
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-1106T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53388703 | ||||||
| chr4:53388976
|
GTATTA | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.333-827_333-823del others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53388976 | |||||
| chr4:53389190
|
G | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0284 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.333-619G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389190 | ||||||
| chr4:53389203
|
A | G | 1 | a0001c0001t0017g0026 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.333-606A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389203 | ||||||
| chr4:53389455
|
C | CT | 6 | a0001c0001t0001g0274a0001c0001t0001g0284a0001c0001t0002g0350others(3): Show | 6 | HG02055.hp2 HG02970.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.333-343dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53389455 | |||||
| chr4:53389455
|
CT | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(280): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.333-343delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 53389455 | |||||
| chr4:53389599
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-210C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389599 | ||||||
| chr4:53389626
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.333-183T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389626 | ||||||
| chr4:53389700
|
A | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-109A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389700 | ||||||
| chr4:53389720
|
T | C | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.333-89T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389720 | ||||||
| chr4:53389789
|
T | G | 9 | a0001c0001t0002g0305a0001c0001t0002g0313a0001c0001t0002g0324others(6): Show | 9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.333-20T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 5/17 | chr4 | 53389789 | ||||||
| chr4:53389892
|
G | A | 1 | a0001c0001t0019g0366 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.397+19G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53389892 | ||||||
| chr4:53390000
|
G | A | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.397+127G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390000 | ||||||
| chr4:53390024
|
C | T | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+151C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390024 | ||||||
| chr4:53390080
|
G | A | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+207G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390080 | ||||||
| chr4:53390088
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.397+215A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390088 | ||||||
| chr4:53390125
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0283 | 2 | NA18964.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.397+252A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390125 | ||||||
| chr4:53390232
|
G | A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.398-289G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390232 | ||||||
| chr4:53390283
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.398-238A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390283 | ||||||
| chr4:53390310
|
G | A | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.398-211G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390310 | ||||||
| chr4:53390311
|
C | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.398-210C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390311 | ||||||
| chr4:53390473
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.398-48T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 6/17 | chr4 | 53390473 | ||||||
| chr4:53390677
|
C | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+49C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390677 | ||||||
| chr4:53390859
|
C | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-150C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390859 | ||||||
| chr4:53390867
|
A | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.506-142A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390867 | ||||||
| chr4:53390870
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0002g0314 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.506-139T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390870 | ||||||
| chr4:53390908
|
A | G | 1 | a0001c0001t0002g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.506-101A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390908 | ||||||
| chr4:53390964
|
A | T | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.506-45A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 7/17 | chr4 | 53390964 | ||||||
| chr4:53391216
|
A | G | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.636+77A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391216 | ||||||
| chr4:53391304
|
G | A | 10 | a0001c0001t0002g0305a0001c0001t0002g0313a0001c0001t0002g0324others(7): Show | 10 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.637-126G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391304 | ||||||
| chr4:53391363
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.637-67G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 8/17 | chr4 | 53391363 | ||||||
| chr4:53391698
|
A | G | 50 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.705+200A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391698 | ||||||
| chr4:53391844
|
A | C | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.705+346A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391844 | ||||||
| chr4:53391928
|
G | A | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.705+430G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391928 | ||||||
| chr4:53391946
|
A | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.705+448A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53391946 | ||||||
| chr4:53392382
|
TG | T | 7 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG01261.hp1 HG02683.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.705+885delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392382 | ||||||
| chr4:53392413
|
C | G | 1 | a0001c0001t0002g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.705+915C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392413 | ||||||
| chr4:53392702
|
T | C | 1 | a0001c0001t0010g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.705+1204T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392702 | ||||||
| chr4:53392715
|
AAG | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+1221_705+1222d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53392715 | |||||
| chr4:53392944
|
T | C | 1 | a0001c0001t0002g0330 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.705+1446T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53392944 | ||||||
| chr4:53393239
|
A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+1741A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393239 | ||||||
| chr4:53393241
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.705+1743G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393241 | ||||||
| chr4:53393450
|
G | A | 81 | a0001c0001t0001g0165a0001c0001t0002g0010a0001c0001t0002g0011others(78): Show | 83 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.705+1952G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393450 | ||||||
| chr4:53393489
|
A | T | 1 | a0001c0001t0003g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.705+1991A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393489 | ||||||
| chr4:53393567
|
G | GAAA | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+2070_705+2072d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393567 | |||||
| chr4:53393616
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.705+2118A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393616 | ||||||
| chr4:53393621
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.705+2123G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393621 | ||||||
| chr4:53393695
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.705+2197C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393695 | ||||||
| chr4:53393762
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705+2264C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393762 | ||||||
| chr4:53393764
|
G | GCCC | 14 | a0001c0001t0003g0018a0001c0001t0003g0037a0001c0001t0003g0038others(11): Show | 15 | HG01175.hp2 HG01256.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.705+2281_705+2283d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
G | GCCCC | 20 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0032others(17): Show | 21 | HG00323.hp2 HG00741.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.705+2280_705+2283d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
G | GCCCCCCC others(3): Show |
1 | a0001c0001t0003g0027 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.705+2274_705+2283d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
G | GCCCCCCC others(4): Show |
1 | a0001c0001t0003g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.705+2273_705+2283d others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
GCCCC | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0152others(49): Show | 54 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.705+2280_705+2283d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
GCCCCC | G | 62 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0189others(59): Show | 63 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.705+2279_705+2283d others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
GCCCCCC | G | 23 | a0001c0001t0001g0150a0001c0001t0001g0207a0001c0001t0001g0210others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.705+2278_705+2283d others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
GCCCCCCC others(3): Show |
G | 54 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(51): Show | 59 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.705+2274_705+2283d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393764
|
GCCCCCCC others(5): Show |
G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+2272_705+2283d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53393764 | |||||
| chr4:53393776
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.705+2278C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393776 | ||||||
| chr4:53393781
|
C | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG01167.hp2 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.705+2283C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53393781 | ||||||
| chr4:53394383
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0271 | 2 | NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.705+2885A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394383 | ||||||
| chr4:53394508
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+3010A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394508 | ||||||
| chr4:53394516
|
C | T | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.705+3018C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394516 | ||||||
| chr4:53394745
|
CTG | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+3249_705+3250d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53394745 | |||||
| chr4:53394755
|
T | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.705+3257T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394755 | ||||||
| chr4:53394770
|
C | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(103): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.705+3272C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53394770 | ||||||
| chr4:53395268
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705+3770T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395268 | ||||||
| chr4:53395479
|
G | C | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.705+3981G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395479 | ||||||
| chr4:53395575
|
C | T | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.705+4077C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395575 | ||||||
| chr4:53395746
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-3984G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395746 | ||||||
| chr4:53395756
|
G | C | 1 | a0001c0001t0003g0046 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.706-3974G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53395756 | ||||||
| chr4:53395919
|
A | AT | 215 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(212): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.706-3798dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53395919 | |||||
| chr4:53395919
|
A | ATT | 78 | a0001c0001t0001g0293a0001c0001t0002g0010a0001c0001t0002g0011others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-3799_706-3798d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53395919 | |||||
| chr4:53396009
|
C | T | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-3721C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396009 | ||||||
| chr4:53396040
|
G | A | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3690G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396040 | ||||||
| chr4:53396138
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.706-3592C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396138 | ||||||
| chr4:53396153
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.706-3577A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396153 | ||||||
| chr4:53396296
|
G | C | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3434G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396296 | ||||||
| chr4:53396377
|
T | C | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.706-3353T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396377 | ||||||
| chr4:53396407
|
CT | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.706-3314delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396407 | |||||
| chr4:53396459
|
T | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.706-3271T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396459 | ||||||
| chr4:53396469
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.706-3261G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396469 | ||||||
| chr4:53396479
|
C | A | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.706-3251C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396479 | ||||||
| chr4:53396550
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-3180C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396550 | ||||||
| chr4:53396657
|
G | A | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.706-3073G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396657 | ||||||
| chr4:53396788
|
A | C | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.706-2942A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53396788 | ||||||
| chr4:53396829
|
GTC | G | 46 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(43): Show | 47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.706-2895_706-2894d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396829 | |||||
| chr4:53396917
|
A | AT | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.706-2807dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53396917 | |||||
| chr4:53397015
|
A | G | 1 | a0001c0001t0005g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.706-2715A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397015 | ||||||
| chr4:53397186
|
G | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-2544G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397186 | ||||||
| chr4:53397457
|
G | A | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-2273G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397457 | ||||||
| chr4:53397465
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.706-2265C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397465 | ||||||
| chr4:53397591
|
C | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.706-2139C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397591 | ||||||
| chr4:53397631
|
A | G | 1 | a0001c0001t0002g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.706-2099A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397631 | ||||||
| chr4:53397707
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.706-2023G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397707 | ||||||
| chr4:53397752
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.706-1978A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397752 | ||||||
| chr4:53397757
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-1973T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397757 | ||||||
| chr4:53397825
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.706-1905G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397825 | ||||||
| chr4:53397938
|
T | C | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.706-1792T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397938 | ||||||
| chr4:53397950
|
G | A | 1 | a0001c0001t0004g0006 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.706-1780G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397950 | ||||||
| chr4:53397988
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0258others(1): Show | 4 | HG01109.hp2 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-1742G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53397988 | ||||||
| chr4:53398007
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.706-1723C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398007 | ||||||
| chr4:53398022
|
G | A | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.706-1708G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398022 | ||||||
| chr4:53398144
|
A | G | 1 | a0001c0001t0003g0079 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.706-1586A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398144 | ||||||
| chr4:53398261
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.706-1469T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398261 | ||||||
| chr4:53398284
|
A | C | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-1446A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398284 | ||||||
| chr4:53398376
|
T | C | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.706-1354T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398376 | ||||||
| chr4:53398582
|
T | C | 1 | a0001c0001t0013g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.706-1148T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398582 | ||||||
| chr4:53398637
|
A | AT | 61 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0164others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.706-1090dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 53398637 | |||||
| chr4:53398765
|
G | C | 1 | a0001c0001t0002g0309 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.706-965G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398765 | ||||||
| chr4:53398830
|
A | C | 1 | a0001c0001t0003g0065 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.706-900A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398830 | ||||||
| chr4:53398875
|
G | A | 4 | a0001c0001t0004g0107a0001c0001t0004g0115a0001c0001t0004g0138others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-855G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53398875 | ||||||
| chr4:53399166
|
A | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.706-564A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399166 | ||||||
| chr4:53399271
|
T | C | 1 | a0001c0001t0004g0103 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.706-459T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399271 | ||||||
| chr4:53399320
|
A | G | 2 | a0001c0001t0003g0036a0001c0001t0003g0064 | 2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.706-410A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399320 | ||||||
| chr4:53399333
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.706-397A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399333 | ||||||
| chr4:53399500
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.706-230G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 9/17 | chr4 | 53399500 | ||||||
| chr4:53399865
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.815+26T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53399865 | ||||||
| chr4:53399994
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.815+155C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53399994 | ||||||
| chr4:53400012
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+173A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400012 | ||||||
| chr4:53400072
|
G | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.815+233G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400072 | ||||||
| chr4:53400500
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+661A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400500 | ||||||
| chr4:53400548
|
G | A | 20 | a0001c0001t0003g0014a0001c0001t0003g0028a0001c0001t0003g0029others(17): Show | 20 | HG00323.hp2 HG02004.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.815+709G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400548 | ||||||
| chr4:53400706
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+867C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400706 | ||||||
| chr4:53400842
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.815+1003C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400842 | ||||||
| chr4:53400917
|
A | G | 1 | a0001c0001t0002g0349 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.815+1078A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400917 | ||||||
| chr4:53400993
|
A | G | 1 | a0001c0001t0002g0348 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.815+1154A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53400993 | ||||||
| chr4:53401020
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.815+1181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401020 | ||||||
| chr4:53401041
|
G | A | 83 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(80): Show | 86 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.815+1202G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401041 | ||||||
| chr4:53401156
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.815+1317T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401156 | ||||||
| chr4:53401166
|
G | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+1327G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401166 | ||||||
| chr4:53401267
|
T | G | 2 | a0001c0001t0006g0030a0001c0001t0016g0031 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.815+1428T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401267 | ||||||
| chr4:53401268
|
G | A | 1 | a0001c0001t0003g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.815+1429G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401268 | ||||||
| chr4:53401363
|
C | T | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+1524C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401363 | ||||||
| chr4:53401799
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+1960G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53401799 | ||||||
| chr4:53402184
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.815+2345T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402184 | ||||||
| chr4:53402332
|
TG | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+2498delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53402332 | |||||
| chr4:53402377
|
CAGG | C | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.815+2541_815+2543d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53402377 | |||||
| chr4:53402536
|
A | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+2697A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402536 | ||||||
| chr4:53402546
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.815+2707A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402546 | ||||||
| chr4:53402657
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+2818A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402657 | ||||||
| chr4:53402873
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.815+3034A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402873 | ||||||
| chr4:53402929
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+3090G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53402929 | ||||||
| chr4:53403006
|
T | C | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815+3167T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403006 | ||||||
| chr4:53403099
|
T | C | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.815+3260T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403099 | ||||||
| chr4:53403107
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.815+3268A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403107 | ||||||
| chr4:53403402
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.815+3563G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403402 | ||||||
| chr4:53403478
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.815+3639C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403478 | ||||||
| chr4:53403529
|
T | A | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(73): Show | 78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.815+3690T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403529 | ||||||
| chr4:53403531
|
C | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+3692C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403531 | ||||||
| chr4:53403547
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+3708C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403547 | ||||||
| chr4:53403740
|
G | C | 1 | a0001c0001t0003g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.815+3901G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403740 | ||||||
| chr4:53403998
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.815+4159G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53403998 | ||||||
| chr4:53404010
|
C | CT | 110 | a0001c0001t0001g0155a0001c0001t0001g0260a0001c0001t0003g0378others(107): Show | 117 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.815+4183dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | |||||
| chr4:53404010
|
C | CTT | 107 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(104): Show | 109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.815+4182_815+4183d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | |||||
| chr4:53404010
|
CT | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+4183delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53404010 | |||||
| chr4:53404133
|
T | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0205 | 2 | HG01255.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.815+4294T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404133 | ||||||
| chr4:53404177
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.815+4338C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404177 | ||||||
| chr4:53404252
|
T | C | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.815+4413T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404252 | ||||||
| chr4:53404256
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+4417C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404256 | ||||||
| chr4:53404308
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+4469G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404308 | ||||||
| chr4:53404464
|
A | G | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.815+4625A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404464 | ||||||
| chr4:53404489
|
T | C | 1 | a0001c0001t0002g0315 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.815+4650T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404489 | ||||||
| chr4:53404516
|
C | G | 1 | a0001c0001t0002g0309 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.815+4677C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404516 | ||||||
| chr4:53404564
|
A | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+4725A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404564 | ||||||
| chr4:53404564
|
A | G | 15 | a0001c0001t0006g0004a0001c0001t0006g0030a0001c0001t0006g0062others(12): Show | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.815+4725A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404564 | ||||||
| chr4:53404612
|
C | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.815+4773C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404612 | ||||||
| chr4:53404671
|
G | C | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.815+4832G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404671 | ||||||
| chr4:53404870
|
G | A | 1 | a0001c0001t0006g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.815+5031G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404870 | ||||||
| chr4:53404877
|
T | C | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+5038T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404877 | ||||||
| chr4:53404889
|
T | C | 1 | a0001c0001t0002g0367 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.815+5050T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404889 | ||||||
| chr4:53404910
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.815+5071C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404910 | ||||||
| chr4:53404933
|
G | A | 1 | a0001c0001t0004g0118 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.815+5094G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404933 | ||||||
| chr4:53404952
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.815+5113G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53404952 | ||||||
| chr4:53405030
|
G | A | 1 | a0001c0001t0004g0119 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.815+5191G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405030 | ||||||
| chr4:53405054
|
T | G | 1 | a0001c0001t0004g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.815+5215T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405054 | ||||||
| chr4:53405090
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.815+5251G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405090 | ||||||
| chr4:53405103
|
T | C | 1 | a0001c0001t0002g0324 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.815+5264T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405103 | ||||||
| chr4:53405217
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.815+5378C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405217 | ||||||
| chr4:53405223
|
A | G | 1 | a0001c0001t0001g0290 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.815+5384A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405223 | ||||||
| chr4:53405326
|
C | T | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5487C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405326 | ||||||
| chr4:53405330
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+5491A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405330 | ||||||
| chr4:53405440
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.815+5601C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405440 | ||||||
| chr4:53405441
|
T | G | 1 | a0001c0001t0002g0347 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.815+5602T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405441 | ||||||
| chr4:53405444
|
A | C | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5605A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405444 | ||||||
| chr4:53405450
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+5611C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405450 | ||||||
| chr4:53405477
|
C | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+5638C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405477 | ||||||
| chr4:53405488
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+5649C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405488 | ||||||
| chr4:53405534
|
A | G | 1 | a0001c0001t0009g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.815+5695A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405534 | ||||||
| chr4:53405539
|
G | C | 1 | a0001c0001t0002g0331 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.815+5700G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405539 | ||||||
| chr4:53405600
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.815+5761G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405600 | ||||||
| chr4:53405608
|
A | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0321others(2): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.815+5769A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405608 | ||||||
| chr4:53405642
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.815+5803A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405642 | ||||||
| chr4:53405647
|
A | C | 1 | a0001c0001t0011g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.815+5808A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405647 | ||||||
| chr4:53405661
|
G | C | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+5822G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405661 | ||||||
| chr4:53405667
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+5828G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405667 | ||||||
| chr4:53405682
|
C | A | 1 | a0001c0001t0013g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+5843C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405682 | ||||||
| chr4:53405683
|
T | C | 1 | a0001c0001t0013g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+5844T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405683 | ||||||
| chr4:53405735
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.815+5896G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405735 | ||||||
| chr4:53405839
|
G | A | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.815+6000G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405839 | ||||||
| chr4:53405873
|
T | C | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.815+6034T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405873 | ||||||
| chr4:53405891
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6052A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405891 | ||||||
| chr4:53405894
|
T | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6055T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405894 | ||||||
| chr4:53405911
|
G | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6072G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405911 | ||||||
| chr4:53405915
|
C | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6076C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405915 | ||||||
| chr4:53405916
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6077A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405916 | ||||||
| chr4:53405924
|
G | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+6085G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405924 | ||||||
| chr4:53405994
|
C | G | 1 | a0001c0001t0002g0349 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.815+6155C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53405994 | ||||||
| chr4:53406043
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(154): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.815+6204A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406043 | ||||||
| chr4:53406076
|
T | C | 1 | a0001c0001t0011g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.815+6237T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406076 | ||||||
| chr4:53406087
|
A | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6248A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406087 | ||||||
| chr4:53406166
|
A | G | 1 | a0001c0001t0002g0346 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.815+6327A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406166 | ||||||
| chr4:53406182
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.815+6343T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406182 | ||||||
| chr4:53406220
|
AG | A | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.815+6384delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53406220 | |||||
| chr4:53406222
|
G | T | 1 | a0001c0001t0004g0103 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.815+6383G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406222 | ||||||
| chr4:53406236
|
G | C | 46 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(43): Show | 47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.815+6397G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406236 | ||||||
| chr4:53406255
|
T | G | 3 | a0001c0001t0005g0149a0001c0001t0005g0231a0001c0001t0005g0232 | 3 | HG00408.hp1 HG02165.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.815+6416T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406255 | ||||||
| chr4:53406303
|
A | G | 2 | a0001c0001t0007g0132a0001c0001t0007g0133 | 2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.815+6464A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406303 | ||||||
| chr4:53406323
|
G | A | 83 | a0001c0001t0001g0204a0001c0001t0001g0286a0001c0001t0002g0010others(80): Show | 85 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.815+6484G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406323 | ||||||
| chr4:53406403
|
T | G | 50 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.815+6564T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406403 | ||||||
| chr4:53406441
|
G | C | 1 | a0001c0001t0006g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.815+6602G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406441 | ||||||
| chr4:53406449
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+6610G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406449 | ||||||
| chr4:53406492
|
C | T | 50 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.815+6653C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406492 | ||||||
| chr4:53406494
|
G | A | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+6655G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406494 | ||||||
| chr4:53406533
|
T | G | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.815+6694T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406533 | ||||||
| chr4:53406554
|
C | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+6715C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406554 | ||||||
| chr4:53406556
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6717A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406556 | ||||||
| chr4:53406581
|
A | T | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.815+6742A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406581 | ||||||
| chr4:53406604
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.815+6765C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406604 | ||||||
| chr4:53406617
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+6778C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406617 | ||||||
| chr4:53406715
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+6876A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406715 | ||||||
| chr4:53406743
|
T | C | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.815+6904T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406743 | ||||||
| chr4:53406753
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.815+6914G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406753 | ||||||
| chr4:53406766
|
A | C | 9 | a0001c0001t0003g0081a0001c0001t0003g0083a0001c0001t0003g0084others(6): Show | 9 | HG02040.hp2 HG02074.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.815+6927A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406766 | ||||||
| chr4:53406802
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.815+6963T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406802 | ||||||
| chr4:53406881
|
G | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.815+7042G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406881 | ||||||
| chr4:53406912
|
T | C | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.815+7073T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406912 | ||||||
| chr4:53406925
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.815+7086A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406925 | ||||||
| chr4:53406963
|
G | C | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.815+7124G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406963 | ||||||
| chr4:53406999
|
C | G | 9 | a0001c0001t0002g0305a0001c0001t0002g0313a0001c0001t0002g0324others(6): Show | 9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.815+7160C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53406999 | ||||||
| chr4:53407007
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0293 | 2 | HG00733.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.815+7168T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407007 | ||||||
| chr4:53407070
|
C | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.815+7231C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407070 | ||||||
| chr4:53407107
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.815+7268G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407107 | ||||||
| chr4:53407292
|
T | G | 61 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0164others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.816-7323T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407292 | ||||||
| chr4:53407320
|
C | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.816-7295C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407320 | ||||||
| chr4:53407338
|
C | G | 1 | a0001c0001t0011g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.816-7277C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407338 | ||||||
| chr4:53407338
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.816-7277C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407338 | ||||||
| chr4:53407432
|
A | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-7183A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407432 | ||||||
| chr4:53407458
|
G | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0190 | 3 | HG00673.hp1 HG02083.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.816-7157G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407458 | ||||||
| chr4:53407527
|
T | C | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-7088T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407527 | ||||||
| chr4:53407549
|
A | G | 7 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0246others(4): Show | 7 | NA18940.hp2 NA18945.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.816-7066A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407549 | ||||||
| chr4:53407581
|
CGTT | C | 46 | a0001c0001t0001g0188a0001c0001t0005g0009a0001c0001t0005g0012others(43): Show | 47 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.816-7032_816-7030d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53407581 | |||||
| chr4:53407586
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.816-7029G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407586 | ||||||
| chr4:53407613
|
T | TA | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-7000dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53407613 | |||||
| chr4:53407724
|
A | G | 4 | a0001c0001t0006g0004a0001c0001t0006g0063a0001c0001t0006g0067others(1): Show | 5 | HG01358.hp1 HG01361.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.816-6891A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407724 | ||||||
| chr4:53407836
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-6779G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407836 | ||||||
| chr4:53407847
|
G | T | 1 | a0001c0001t0002g0345 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.816-6768G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407847 | ||||||
| chr4:53407863
|
C | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.816-6752C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407863 | ||||||
| chr4:53407987
|
C | G | 5 | a0001c0001t0002g0367a0001c0001t0002g0369a0001c0001t0002g0370others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-6628C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53407987 | ||||||
| chr4:53408015
|
G | A | 1 | a0001c0001t0005g0252 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.816-6600G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408015 | ||||||
| chr4:53408017
|
A | G | 371 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(368): Show | 383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.816-6598A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408017 | ||||||
| chr4:53408017
|
A | T | 1 | a0001c0001t0007g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816-6598A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408017 | ||||||
| chr4:53408085
|
A | G | 1 | a0001c0001t0004g0107 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.816-6530A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408085 | ||||||
| chr4:53408087
|
C | G | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816-6528C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408087 | ||||||
| chr4:53408090
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-6525C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408090 | ||||||
| chr4:53408170
|
G | A | 1 | a0001c0001t0002g0308 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.816-6445G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408170 | ||||||
| chr4:53408193
|
G | T | 55 | a0001c0001t0001g0150a0001c0001t0001g0197a0001c0001t0001g0198others(52): Show | 55 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.816-6422G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408193 | ||||||
| chr4:53408354
|
G | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-6261G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408354 | ||||||
| chr4:53408356
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-6259A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408356 | ||||||
| chr4:53408399
|
C | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.816-6216C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408399 | ||||||
| chr4:53408416
|
C | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-6199C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408416 | ||||||
| chr4:53408435
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-6180C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408435 | ||||||
| chr4:53408457
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.816-6158C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408457 | ||||||
| chr4:53408462
|
G | A | 2 | a0001c0001t0002g0351a0001c0001t0003g0036 | 2 | HG02698.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.816-6153G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408462 | ||||||
| chr4:53408557
|
G | A | 1 | a0001c0001t0002g0359 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.816-6058G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408557 | ||||||
| chr4:53408637
|
A | T | 1 | a0001c0001t0002g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.816-5978A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408637 | ||||||
| chr4:53408681
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816-5934G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408681 | ||||||
| chr4:53408773
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.816-5842T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408773 | ||||||
| chr4:53408814
|
C | T | 3 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0235 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.816-5801C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408814 | ||||||
| chr4:53408832
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5783G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408832 | ||||||
| chr4:53408843
|
T | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0321others(2): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.816-5772T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408843 | ||||||
| chr4:53408844
|
G | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0321others(2): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.816-5771G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408844 | ||||||
| chr4:53408888
|
A | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.816-5727A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408888 | ||||||
| chr4:53408943
|
TC | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-5670delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53408943 | |||||
| chr4:53408951
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816-5664T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408951 | ||||||
| chr4:53408955
|
T | G | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-5660T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408955 | ||||||
| chr4:53408971
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5644G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408971 | ||||||
| chr4:53408982
|
T | A | 46 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(43): Show | 47 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.816-5633T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53408982 | ||||||
| chr4:53409042
|
C | G | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-5573C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409042 | ||||||
| chr4:53409152
|
G | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-5463G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409152 | ||||||
| chr4:53409262
|
C | G | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.816-5353C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409262 | ||||||
| chr4:53409320
|
A | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-5295A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409320 | ||||||
| chr4:53409326
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816-5289G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409326 | ||||||
| chr4:53409362
|
C | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.816-5253C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409362 | ||||||
| chr4:53409427
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0014g0289 | 2 | NA18939.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.816-5188G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409427 | ||||||
| chr4:53409434
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.816-5181C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409434 | ||||||
| chr4:53409477
|
C | T | 3 | a0001c0001t0002g0361a0001c0001t0002g0362a0001c0001t0002g0363 | 3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.816-5138C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409477 | ||||||
| chr4:53409497
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-5118C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409497 | ||||||
| chr4:53409510
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.816-5105C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409510 | ||||||
| chr4:53409613
|
C | G | 2 | a0001c0001t0005g0196a0001c0001t0005g0279 | 2 | HG00323.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.816-5002C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409613 | ||||||
| chr4:53409640
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0152others(10): Show | 15 | HG01346.hp1 HG01952.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.816-4975C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409640 | ||||||
| chr4:53409696
|
G | A | 1 | a0001c0001t0006g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816-4919G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409696 | ||||||
| chr4:53409725
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.816-4890C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409725 | ||||||
| chr4:53409780
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-4835A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409780 | ||||||
| chr4:53409811
|
C | T | 1 | a0001c0001t0002g0343 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.816-4804C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409811 | ||||||
| chr4:53409820
|
C | T | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.816-4795C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409820 | ||||||
| chr4:53409915
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-4700A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409915 | ||||||
| chr4:53409931
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.816-4684C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409931 | ||||||
| chr4:53409975
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-4640C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409975 | ||||||
| chr4:53409986
|
C | T | 1 | a0001c0001t0004g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.816-4629C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53409986 | ||||||
| chr4:53410040
|
C | T | 3 | a0001c0001t0006g0063a0001c0001t0010g0374a0001c0001t0011g0373 | 3 | HG02055.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-4575C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410040 | ||||||
| chr4:53410081
|
G | A | 2 | a0001c0001t0004g0135a0001c0001t0009g0147 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.816-4534G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410081 | ||||||
| chr4:53410136
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816-4479C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410136 | ||||||
| chr4:53410151
|
A | G | 3 | a0001c0001t0002g0361a0001c0001t0002g0362a0001c0001t0002g0363 | 3 | HG00558.hp1 NA18957.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.816-4464A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410151 | ||||||
| chr4:53410219
|
A | C | 1 | a0001c0001t0004g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.816-4396A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410219 | ||||||
| chr4:53410236
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.816-4379T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410236 | ||||||
| chr4:53410273
|
A | G | 4 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0003g0065others(1): Show | 4 | NA18968.hp1 NA19003.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-4342A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410273 | ||||||
| chr4:53410330
|
G | A | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.816-4285G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410330 | ||||||
| chr4:53410341
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.816-4274C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410341 | ||||||
| chr4:53410399
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-4216A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410399 | ||||||
| chr4:53410476
|
C | T | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.816-4139C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410476 | ||||||
| chr4:53410495
|
A | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-4120A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410495 | ||||||
| chr4:53410515
|
G | C | 3 | a0001c0001t0002g0332a0001c0001t0002g0349a0001c0001t0002g0360 | 3 | NA18971.hp1 NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.816-4100G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410515 | ||||||
| chr4:53410556
|
A | G | 1 | a0001c0001t0005g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.816-4059A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410556 | ||||||
| chr4:53410741
|
C | T | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.816-3874C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410741 | ||||||
| chr4:53410805
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-3810A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410805 | ||||||
| chr4:53410844
|
C | T | 4 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0003g0378others(1): Show | 4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-3771C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410844 | ||||||
| chr4:53410908
|
C | T | 1 | a0001c0001t0005g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.816-3707C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410908 | ||||||
| chr4:53410967
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.816-3648A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410967 | ||||||
| chr4:53410971
|
TG | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.816-3636delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53410971 | |||||
| chr4:53410976
|
G | A | 2 | a0001c0001t0002g0333a0001c0001t0002g0348 | 2 | HG00597.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.816-3639G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53410976 | ||||||
| chr4:53411022
|
G | A | 15 | a0001c0001t0006g0004a0001c0001t0006g0030a0001c0001t0006g0062others(12): Show | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.816-3593G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411022 | ||||||
| chr4:53411133
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0241 | 2 | HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.816-3482A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411133 | ||||||
| chr4:53411152
|
G | A | 46 | a0001c0001t0001g0188a0001c0001t0005g0009a0001c0001t0005g0012others(43): Show | 47 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.816-3463G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411152 | ||||||
| chr4:53411320
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.816-3295A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411320 | ||||||
| chr4:53411330
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-3285C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411330 | ||||||
| chr4:53411349
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.816-3266C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411349 | ||||||
| chr4:53411375
|
G | A | 1 | a0001c0001t0006g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.816-3240G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411375 | ||||||
| chr4:53411480
|
T | C | 3 | a0001c0001t0006g0030a0001c0001t0006g0062a0001c0001t0016g0031 | 3 | HG01884.hp2 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.816-3135T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411480 | ||||||
| chr4:53411481
|
A | AT | 77 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(74): Show | 79 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.816-3126dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53411481 | |||||
| chr4:53411550
|
C | T | 1 | a0001c0001t0002g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.816-3065C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411550 | ||||||
| chr4:53411625
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.816-2990G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411625 | ||||||
| chr4:53411633
|
A | C | 6 | a0001c0001t0004g0101a0001c0001t0004g0110a0001c0001t0004g0111others(3): Show | 6 | NA18939.hp1 NA18940.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.816-2982A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411633 | ||||||
| chr4:53411701
|
T | C | 2 | a0001c0001t0006g0070a0001c0001t0006g0071 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-2914T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411701 | ||||||
| chr4:53411937
|
C | G | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.816-2678C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411937 | ||||||
| chr4:53411977
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-2638C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53411977 | ||||||
| chr4:53411987
|
A | AC | 9 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(6): Show | 9 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.816-2623dupC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53411987 | |||||
| chr4:53412006
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816-2609A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412006 | ||||||
| chr4:53412052
|
T | G | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.816-2563T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412052 | ||||||
| chr4:53412266
|
A | G | 1 | a0001c0001t0005g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.816-2349A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412266 | ||||||
| chr4:53412563
|
T | C | 1 | a0001c0001t0010g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.816-2052T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412563 | ||||||
| chr4:53412623
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.816-1992A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412623 | ||||||
| chr4:53412739
|
G | T | 2 | a0001c0001t0006g0070a0001c0001t0006g0071 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-1876G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412739 | ||||||
| chr4:53412740
|
C | T | 2 | a0001c0001t0006g0070a0001c0001t0006g0071 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.816-1875C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412740 | ||||||
| chr4:53412954
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816-1661C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53412954 | ||||||
| chr4:53413011
|
G | A | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816-1604G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413011 | ||||||
| chr4:53413032
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-1583G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413032 | ||||||
| chr4:53413036
|
C | T | 1 | a0001c0001t0004g0005 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.816-1579C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413036 | ||||||
| chr4:53413125
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(154): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.816-1490A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413125 | ||||||
| chr4:53413216
|
T | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.816-1399T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413216 | ||||||
| chr4:53413602
|
T | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-1013T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413602 | ||||||
| chr4:53413639
|
G | T | 1 | a0001c0001t0005g0256 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.816-976G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413639 | ||||||
| chr4:53413656
|
T | G | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816-959T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413656 | ||||||
| chr4:53413782
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-833T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413782 | ||||||
| chr4:53413826
|
T | A | 1 | a0001c0001t0004g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.816-789T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413826 | ||||||
| chr4:53413862
|
A | G | 1 | a0001c0001t0004g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.816-753A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413862 | ||||||
| chr4:53413921
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-694C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413921 | ||||||
| chr4:53413932
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.816-683T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53413932 | ||||||
| chr4:53414493
|
G | T | 1 | a0001c0001t0004g0109 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.816-122G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | chr4 | 53414493 | ||||||
| chr4:53414538
|
GA | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(232): Show | 241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.816-64delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 53414538 | |||||
| chr4:53414801
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.923+79A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414801 | ||||||
| chr4:53414904
|
C | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+182C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414904 | ||||||
| chr4:53414908
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+186C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414908 | ||||||
| chr4:53414985
|
G | A | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296 | 3 | HG01358.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.923+263G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53414985 | ||||||
| chr4:53415023
|
C | T | 3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0303 | 3 | NA18960.hp1 NA19079.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.923+301C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415023 | ||||||
| chr4:53415055
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+333C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415055 | ||||||
| chr4:53415061
|
A | C | 1 | a0001c0001t0004g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.923+339A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415061 | ||||||
| chr4:53415175
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.923+453A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415175 | ||||||
| chr4:53415185
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.923+463G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415185 | ||||||
| chr4:53415528
|
T | G | 1 | a0001c0001t0003g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.923+806T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415528 | ||||||
| chr4:53415529
|
G | GT | 17 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(14): Show | 17 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.923+818dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53415529 | |||||
| chr4:53415529
|
G | GTT | 153 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(150): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.923+817_923+818dup others(2): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53415529 | |||||
| chr4:53415530
|
T | G | 1 | a0001c0001t0002g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.923+808T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415530 | ||||||
| chr4:53415547
|
G | T | 1 | a0001c0001t0006g0004 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.923+825G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415547 | ||||||
| chr4:53415553
|
G | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.923+831G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415553 | ||||||
| chr4:53415564
|
T | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.923+842T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415564 | ||||||
| chr4:53415571
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+849C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415571 | ||||||
| chr4:53415824
|
A | G | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.923+1102A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415824 | ||||||
| chr4:53415976
|
A | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+1254A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53415976 | ||||||
| chr4:53416023
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.923+1301C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416023 | ||||||
| chr4:53416085
|
A | C | 1 | a0001c0001t0009g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.923+1363A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416085 | ||||||
| chr4:53416119
|
A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1397A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416119 | ||||||
| chr4:53416170
|
A | G | 4 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0007g0001others(1): Show | 5 | NA18956.hp2 NA18963.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+1448A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416170 | ||||||
| chr4:53416236
|
A | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+1514A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416236 | ||||||
| chr4:53416427
|
C | G | 6 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0370others(3): Show | 6 | HG00642.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+1705C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416427 | ||||||
| chr4:53416431
|
A | G | 1 | a0001c0001t0003g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.923+1709A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416431 | ||||||
| chr4:53416529
|
G | A | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1807G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416529 | ||||||
| chr4:53416987
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0187 | 2 | HG00280.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.923+2265A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416987 | ||||||
| chr4:53416999
|
A | G | 1 | a0001c0001t0004g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.923+2277A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53416999 | ||||||
| chr4:53417146
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+2424C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417146 | ||||||
| chr4:53417182
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2460C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417182 | ||||||
| chr4:53417236
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.923+2514T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417236 | ||||||
| chr4:53417328
|
C | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.923+2606C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417328 | ||||||
| chr4:53417407
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+2685C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417407 | ||||||
| chr4:53417629
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.923+2907C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417629 | ||||||
| chr4:53417642
|
C | CA | 113 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(110): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.923+2944dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | |||||
| chr4:53417642
|
C | CAA | 84 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0001t0001g0171others(81): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.923+2943_923+2944d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | |||||
| chr4:53417642
|
C | CAAA | 14 | a0001c0001t0001g0170a0001c0001t0004g0005a0001c0001t0004g0094others(11): Show | 15 | HG02135.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+2942_923+2944d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | |||||
| chr4:53417642
|
CA | C | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(73): Show | 78 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(75): Show |
intron_variant | MODIFIER | c.923+2944delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417642 | |||||
| chr4:53417662
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+2940A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417662 | ||||||
| chr4:53417702
|
AGCTACTT others(9): Show |
A | 4 | a0001c0001t0001g0013a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+2997_923+3012d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417702 | |||||
| chr4:53417738
|
A | AACACACA others(3): Show |
1 | a0001c0001t0011g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+3033_923+3042d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | |||||
| chr4:53417738
|
A | AACACACA others(5): Show |
2 | a0001c0001t0002g0311a0001c0001t0002g0354 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.923+3031_923+3042d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | |||||
| chr4:53417738
|
A | AACACACA others(7): Show |
1 | a0001c0001t0002g0365 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.923+3029_923+3042d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417738 | |||||
| chr4:53417755
|
ACACACAC others(31): Show |
A | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+3035_923+3072d others(40): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417755 | |||||
| chr4:53417755
|
ACACACAC others(33): Show |
A | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.923+3035_923+3074d others(42): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417755 | |||||
| chr4:53417759
|
ACACACTC others(7): Show |
A | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | NA18959.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.923+3039_923+3052d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(9): Show |
A | 6 | a0001c0001t0003g0075a0001c0001t0003g0078a0001c0001t0003g0081others(3): Show | 6 | NA18944.hp1 NA18955.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+3039_923+3054d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(11): Show |
A | 9 | a0001c0001t0003g0032a0001c0001t0003g0034a0001c0001t0003g0045others(6): Show | 9 | HG00621.hp1 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3039_923+3056d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(13): Show |
A | 38 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0028others(35): Show | 38 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.923+3039_923+3058d others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(15): Show |
A | 9 | a0001c0001t0003g0027a0001c0001t0003g0038a0001c0001t0006g0069others(6): Show | 9 | HG00673.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3039_923+3060d others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(17): Show |
A | 3 | a0001c0001t0006g0063a0001c0001t0006g0067a0001c0001t0006g0090 | 3 | HG02572.hp2 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.923+3039_923+3062d others(26): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(19): Show |
A | 2 | a0001c0001t0003g0033a0001c0001t0006g0004 | 3 | HG01358.hp1 HG01361.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.923+3039_923+3064d others(28): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417759
|
ACACACTC others(21): Show |
A | 1 | a0001c0001t0003g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.923+3039_923+3066d others(30): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417759 | |||||
| chr4:53417761
|
ACACTCTC others(9): Show |
A | 2 | a0001c0001t0003g0039a0001c0001t0003g0080 | 2 | HG02027.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.923+3041_923+3056d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | |||||
| chr4:53417761
|
ACACTCTC others(11): Show |
A | 4 | a0001c0001t0003g0042a0001c0001t0003g0046a0001c0001t0003g0061others(1): Show | 4 | HG02056.hp1 HG04199.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+3041_923+3058d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | |||||
| chr4:53417761
|
ACACTCTC others(23): Show |
A | 2 | a0001c0001t0004g0137a0001c0001t0004g0146 | 2 | HG01099.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.923+3041_923+3070d others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417761 | |||||
| chr4:53417763
|
ACTCT | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0265a0001c0001t0002g0302others(4): Show | 7 | HG02135.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+3095_923+3098d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCT | A | 10 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0179others(7): Show | 10 | HG01081.hp1 HG01515.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.923+3093_923+3098d others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(1): Show |
A | 19 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0171others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+3091_923+3098d others(10): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(3): Show |
A | 23 | a0001c0001t0001g0185a0001c0001t0001g0197a0001c0001t0001g0216others(20): Show | 23 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+3089_923+3098d others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(5): Show |
A | 37 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0166others(34): Show | 37 | HG00280.hp1 HG00558.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+3087_923+3098d others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(7): Show |
A | 33 | a0001c0001t0001g0150a0001c0001t0001g0173a0001c0001t0001g0180others(30): Show | 33 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.923+3085_923+3098d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(9): Show |
A | 6 | a0001c0001t0001g0152a0001c0001t0005g0012a0001c0001t0005g0233others(3): Show | 6 | HG02135.hp2 HG02451.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.923+3083_923+3098d others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(11): Show |
A | 28 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0153others(25): Show | 30 | HG00408.hp1 HG01346.hp1 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.923+3081_923+3098d others(20): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(13): Show |
A | 21 | a0001c0001t0001g0293a0001c0001t0002g0319a0001c0001t0002g0335others(18): Show | 22 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.923+3079_923+3098d others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(15): Show |
A | 11 | a0001c0001t0001g0261a0001c0001t0002g0315a0001c0001t0002g0326others(8): Show | 12 | HG02486.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.923+3077_923+3098d others(24): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(17): Show |
A | 12 | a0001c0001t0002g0305a0001c0001t0002g0308a0001c0001t0002g0317others(9): Show | 12 | HG00597.hp2 HG02129.hp2 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+3075_923+3098d others(26): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(19): Show |
A | 25 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(22): Show | 26 | HG00558.hp1 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.923+3073_923+3098d others(28): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(21): Show |
A | 7 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0342others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+3071_923+3098d others(30): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(23): Show |
A | 47 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(44): Show | 51 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.923+3069_923+3098d others(32): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(25): Show |
A | 2 | a0001c0001t0002g0306a0001c0001t0002g0314 | 2 | HG02523.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.923+3067_923+3098d others(34): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417763
|
ACTCTCTC others(27): Show |
A | 1 | a0001c0001t0004g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.923+3065_923+3098d others(36): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53417763 | |||||
| chr4:53417765
|
T | A | 9 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3043T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417765 | ||||||
| chr4:53417767
|
T | A | 9 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+3045T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417767 | ||||||
| chr4:53417769
|
T | A | 12 | a0001c0001t0001g0198a0001c0001t0001g0265a0001c0001t0002g0302others(9): Show | 12 | HG02055.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+3047T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417769 | ||||||
| chr4:53417771
|
T | A | 19 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0179others(16): Show | 19 | HG01081.hp1 HG01515.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+3049T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417771 | ||||||
| chr4:53417773
|
T | A | 31 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0169others(28): Show | 31 | HG00621.hp2 HG00673.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.923+3051T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417773 | ||||||
| chr4:53417775
|
T | A | 46 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0171others(43): Show | 46 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.923+3053T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417775 | ||||||
| chr4:53417777
|
T | A | 54 | a0001c0001t0001g0013a0001c0001t0001g0165a0001c0001t0001g0166others(51): Show | 54 | HG00280.hp1 HG00558.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.923+3055T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417777 | ||||||
| chr4:53417779
|
T | A | 66 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0165others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.923+3057T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417779 | ||||||
| chr4:53417781
|
T | A | 51 | a0001c0001t0001g0152a0001c0001t0001g0173a0001c0001t0001g0181others(48): Show | 51 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.923+3059T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417781 | ||||||
| chr4:53417783
|
T | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0152others(60): Show | 65 | HG00408.hp1 HG00642.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.923+3061T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417783 | ||||||
| chr4:53417785
|
T | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0152others(54): Show | 60 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.923+3063T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417785 | ||||||
| chr4:53417787
|
T | A | 45 | a0001c0001t0001g0261a0001c0001t0001g0293a0001c0001t0002g0302others(42): Show | 46 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.923+3065T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417787 | ||||||
| chr4:53417789
|
T | A | 39 | a0001c0001t0001g0293a0001c0001t0002g0302a0001c0001t0002g0305others(36): Show | 39 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.923+3067T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417789 | ||||||
| chr4:53417791
|
T | A | 59 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(56): Show | 60 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.923+3069T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417791 | ||||||
| chr4:53417793
|
T | A | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3071T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417793 | ||||||
| chr4:53417795
|
T | A | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3073T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417795 | ||||||
| chr4:53417797
|
T | A | 68 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(65): Show | 70 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.923+3075T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417797 | ||||||
| chr4:53417799
|
T | A | 68 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(65): Show | 70 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.923+3077T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417799 | ||||||
| chr4:53417801
|
T | A | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.923+3079T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417801 | ||||||
| chr4:53417803
|
T | A | 65 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(62): Show | 67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.923+3081T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417803 | ||||||
| chr4:53417805
|
T | A | 61 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(58): Show | 63 | HG00558.hp1 HG00642.hp2 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.923+3083T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417805 | ||||||
| chr4:53417807
|
T | A | 26 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0305others(23): Show | 27 | HG00642.hp2 HG01261.hp1 HG02129.hp2 others(24): Show |
intron_variant | MODIFIER | c.923+3085T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417807 | ||||||
| chr4:53417809
|
T | A | 3 | a0001c0001t0002g0314a0001c0001t0002g0316a0001c0001t0002g0325 | 3 | HG02683.hp1 HG03239.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.923+3087T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417809 | ||||||
| chr4:53417811
|
T | A | 3 | a0001c0001t0002g0314a0001c0001t0002g0316a0001c0001t0002g0325 | 3 | HG02683.hp1 HG03239.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.923+3089T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417811 | ||||||
| chr4:53417813
|
T | A | 2 | a0001c0001t0002g0314a0001c0001t0002g0316 | 2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.923+3091T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417813 | ||||||
| chr4:53417820
|
C | A | 1 | a0001c0001t0003g0033 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.923+3098C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417820 | ||||||
| chr4:53417849
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.923+3127A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417849 | ||||||
| chr4:53417891
|
T | G | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.923+3169T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53417891 | ||||||
| chr4:53418051
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01071.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.923+3329A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418051 | ||||||
| chr4:53418237
|
G | A | 54 | a0001c0001t0002g0332a0001c0001t0002g0349a0001c0001t0002g0360others(51): Show | 58 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.923+3515G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418237 | ||||||
| chr4:53418281
|
C | CTAAA | 44 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0151others(41): Show | 46 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.923+3574_923+3577d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53418281 | |||||
| chr4:53418537
|
A | G | 2 | a0001c0001t0003g0036a0001c0001t0003g0064 | 2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.923+3815A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418537 | ||||||
| chr4:53418700
|
A | G | 8 | a0001c0001t0005g0199a0001c0001t0005g0200a0001c0001t0005g0201others(5): Show | 8 | HG01255.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+3978A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418700 | ||||||
| chr4:53418738
|
T | C | 1 | a0001c0001t0005g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.923+4016T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418738 | ||||||
| chr4:53418746
|
G | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+4024G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418746 | ||||||
| chr4:53418858
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.923+4136A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53418858 | ||||||
| chr4:53419553
|
A | G | 78 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(75): Show | 80 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.923+4831A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419553 | ||||||
| chr4:53419600
|
C | T | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+4878C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419600 | ||||||
| chr4:53419710
|
C | G | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.923+4988C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419710 | ||||||
| chr4:53419725
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+5003G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419725 | ||||||
| chr4:53419739
|
C | A | 1 | a0001c0001t0004g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.923+5017C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419739 | ||||||
| chr4:53419785
|
A | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.923+5063A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419785 | ||||||
| chr4:53419846
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+5124C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419846 | ||||||
| chr4:53419886
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923+5164G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419886 | ||||||
| chr4:53419928
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.923+5206G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419928 | ||||||
| chr4:53419941
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.923+5219G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53419941 | ||||||
| chr4:53420054
|
C | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.923+5332C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420054 | ||||||
| chr4:53420059
|
G | A | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.923+5337G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420059 | ||||||
| chr4:53420069
|
G | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.923+5347G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420069 | ||||||
| chr4:53420130
|
G | A | 1 | a0001c0001t0006g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.923+5408G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420130 | ||||||
| chr4:53420156
|
C | T | 2 | a0001c0001t0004g0005a0001c0001t0004g0094 | 3 | HG02486.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.923+5434C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420156 | ||||||
| chr4:53420176
|
C | T | 1 | a0001c0001t0004g0139 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.923+5454C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420176 | ||||||
| chr4:53420197
|
C | CA | 76 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0151others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.923+5503dupA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420197
|
C | CAA | 71 | a0001c0001t0001g0002a0001c0001t0001g0152a0001c0001t0001g0153others(68): Show | 74 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.923+5502_923+5503d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420197
|
C | CAAA | 34 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0290others(31): Show | 37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.923+5501_923+5503d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420197
|
C | CAAAA | 15 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0004g0113others(12): Show | 15 | HG00140.hp1 HG00423.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+5500_923+5503d others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420197
|
CA | C | 65 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0025others(62): Show | 66 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.923+5503delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420197
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0004g0001a0001c0001t0004g0102a0001c0001t0004g0103others(3): Show | 7 | NA18941.hp2 NA18956.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5495_923+5503d others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420197 | |||||
| chr4:53420199
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.923+5487_923+5488i others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420199 | |||||
| chr4:53420200
|
A | AAAAAAAA others(3): Show |
12 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+5487_923+5488i others(12): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420200 | |||||
| chr4:53420201
|
A | AAAAAAAA others(2): Show |
59 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(56): Show | 61 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.923+5487_923+5488i others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420201 | |||||
| chr4:53420210
|
A | C | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5488A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420210 | ||||||
| chr4:53420212
|
A | C | 12 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.923+5490A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420212 | ||||||
| chr4:53420213
|
A | C | 61 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(58): Show | 63 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(60): Show |
intron_variant | MODIFIER | c.923+5491A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420213 | ||||||
| chr4:53420217
|
A | AAAAACAA others(2): Show |
7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+5499_923+5500i others(11): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420217 | |||||
| chr4:53420226
|
C | A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.923+5504C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420226 | ||||||
| chr4:53420284
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.923+5562T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420284 | ||||||
| chr4:53420317
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.924-5555A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420317 | ||||||
| chr4:53420392
|
G | T | 1 | a0001c0001t0005g0256 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.924-5480G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420392 | ||||||
| chr4:53420393
|
C | T | 1 | a0001c0001t0005g0256 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.924-5479C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420393 | ||||||
| chr4:53420423
|
C | G | 1 | a0001c0001t0003g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.924-5449C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420423 | ||||||
| chr4:53420429
|
CA | C | 16 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(13): Show | 16 | HG01257.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.924-5424delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420429 | |||||
| chr4:53420448
|
AGAT | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(145): Show | 151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5423_924-5421d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420448 | ||||||
| chr4:53420451
|
TAAATC | T | 6 | a0001c0001t0001g0217a0001c0001t0001g0240a0001c0001t0001g0272others(3): Show | 6 | HG02735.hp2 HG03239.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.924-5419_924-5415d others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420451 | |||||
| chr4:53420453
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(145): Show | 151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5419A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420453 | ||||||
| chr4:53420455
|
TC | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(145): Show | 151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.924-5416delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420455 | ||||||
| chr4:53420527
|
T | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-5345T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420527 | ||||||
| chr4:53420563
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-5309A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420563 | ||||||
| chr4:53420589
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.924-5283G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420589 | ||||||
| chr4:53420614
|
A | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-5258A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420614 | ||||||
| chr4:53420631
|
C | G | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.924-5241C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420631 | ||||||
| chr4:53420718
|
AG | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-5152delG | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 53420718 | |||||
| chr4:53420736
|
A | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.924-5136A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420736 | ||||||
| chr4:53420796
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.924-5076A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420796 | ||||||
| chr4:53420807
|
T | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-5065T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53420807 | ||||||
| chr4:53421070
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.924-4802G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421070 | ||||||
| chr4:53421382
|
A | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-4490A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421382 | ||||||
| chr4:53421530
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.924-4342T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421530 | ||||||
| chr4:53421589
|
T | A | 76 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(73): Show | 78 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.924-4283T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421589 | ||||||
| chr4:53421874
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.924-3998G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53421874 | ||||||
| chr4:53422024
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.924-3848T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422024 | ||||||
| chr4:53422410
|
A | G | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.924-3462A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422410 | ||||||
| chr4:53422457
|
C | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924-3415C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422457 | ||||||
| chr4:53422639
|
T | C | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.924-3233T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422639 | ||||||
| chr4:53422722
|
A | T | 47 | a0001c0001t0004g0111a0001c0001t0005g0009a0001c0001t0005g0012others(44): Show | 48 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.924-3150A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422722 | ||||||
| chr4:53422724
|
T | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(111): Show | 116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.924-3148T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422724 | ||||||
| chr4:53422860
|
A | C | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.924-3012A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422860 | ||||||
| chr4:53422868
|
C | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-3004C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422868 | ||||||
| chr4:53422880
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.924-2992G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422880 | ||||||
| chr4:53422913
|
G | A | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924-2959G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53422913 | ||||||
| chr4:53423014
|
G | A | 1 | a0001c0001t0010g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.924-2858G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423014 | ||||||
| chr4:53423195
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(153): Show | 159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.924-2677G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423195 | ||||||
| chr4:53423213
|
G | A | 7 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0246others(4): Show | 7 | NA18940.hp2 NA18945.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.924-2659G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423213 | ||||||
| chr4:53423463
|
A | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.924-2409A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423463 | ||||||
| chr4:53423525
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.924-2347A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423525 | ||||||
| chr4:53423549
|
C | T | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.924-2323C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423549 | ||||||
| chr4:53423564
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.924-2308T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423564 | ||||||
| chr4:53423574
|
G | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-2298G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423574 | ||||||
| chr4:53423615
|
T | G | 1 | a0001c0001t0003g0088 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.924-2257T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423615 | ||||||
| chr4:53423659
|
G | A | 1 | a0001c0001t0011g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.924-2213G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423659 | ||||||
| chr4:53423663
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.924-2209A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423663 | ||||||
| chr4:53423671
|
A | C | 1 | a0001c0001t0005g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.924-2201A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423671 | ||||||
| chr4:53423772
|
T | C | 1 | a0001c0001t0002g0333 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.924-2100T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423772 | ||||||
| chr4:53423811
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.924-2061T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53423811 | ||||||
| chr4:53424035
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.924-1837T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424035 | ||||||
| chr4:53424062
|
A | G | 4 | a0001c0001t0005g0193a0001c0001t0005g0194a0001c0001t0005g0195others(1): Show | 4 | NA18961.hp1 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1810A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424062 | ||||||
| chr4:53424242
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.924-1630A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424242 | ||||||
| chr4:53424310
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.924-1562A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424310 | ||||||
| chr4:53424510
|
A | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.924-1362A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53424510 | ||||||
| chr4:53425053
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.924-819G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425053 | ||||||
| chr4:53425070
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.924-802C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425070 | ||||||
| chr4:53425197
|
T | C | 1 | a0001c0001t0002g0357 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-675T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425197 | ||||||
| chr4:53425210
|
A | T | 4 | a0001c0001t0005g0276a0001c0001t0005g0277a0001c0001t0005g0279others(1): Show | 4 | NA18971.hp2 NA18990.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-662A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425210 | ||||||
| chr4:53425230
|
G | C | 1 | a0001c0001t0002g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.924-642G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425230 | ||||||
| chr4:53425294
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.924-578T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425294 | ||||||
| chr4:53425426
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0271 | 2 | NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.924-446T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425426 | ||||||
| chr4:53425595
|
C | G | 4 | a0001c0001t0004g0107a0001c0001t0004g0115a0001c0001t0004g0138others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-277C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425595 | ||||||
| chr4:53425833
|
A | G | 8 | a0001c0001t0003g0025a0001c0001t0003g0027a0001c0001t0003g0057others(5): Show | 8 | HG00544.hp1 HG00673.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.924-39A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425833 | ||||||
| chr4:53425837
|
G | A | 6 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0179others(3): Show | 6 | HG00140.hp2 HG01169.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-35G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 11/17 | chr4 | 53425837 | ||||||
| chr4:53426017
|
A | G | 1 | a0001c0001t0002g0346 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1017+52A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426017 | ||||||
| chr4:53426109
|
T | C | 1 | a0001c0001t0006g0004 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1017+144T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426109 | ||||||
| chr4:53426211
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1017+246T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426211 | ||||||
| chr4:53426278
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0003g0375 | 2 | HG00423.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1017+313G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426278 | ||||||
| chr4:53426624
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1017+659T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426624 | ||||||
| chr4:53426929
|
CT | C | 8 | a0001c0001t0004g0007a0001c0001t0004g0113a0001c0001t0004g0120others(5): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1017+971delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 53426929 | |||||
| chr4:53426981
|
G | A | 1 | a0001c0001t0005g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1017+1016G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53426981 | ||||||
| chr4:53427012
|
A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1018-1015A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427012 | ||||||
| chr4:53427170
|
G | T | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1018-857G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427170 | ||||||
| chr4:53427223
|
T | G | 1 | a0001c0001t0002g0355 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1018-804T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427223 | ||||||
| chr4:53427345
|
A | T | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1018-682A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427345 | ||||||
| chr4:53427376
|
G | T | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1018-651G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427376 | ||||||
| chr4:53427381
|
T | G | 2 | a0001c0001t0004g0005a0001c0001t0004g0094 | 3 | HG02486.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1018-646T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427381 | ||||||
| chr4:53427527
|
C | G | 1 | a0001c0001t0002g0358 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1018-500C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427527 | ||||||
| chr4:53427777
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1018-250G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427777 | ||||||
| chr4:53427865
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1018-162C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427865 | ||||||
| chr4:53427875
|
A | T | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1018-152A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 12/17 | chr4 | 53427875 | ||||||
| chr4:53428371
|
A | G | 11 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(8): Show | 11 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174+188A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428371 | ||||||
| chr4:53428393
|
A | G | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+210A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428393 | ||||||
| chr4:53428423
|
A | G | 1 | a0001c0001t0005g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1174+240A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428423 | ||||||
| chr4:53428439
|
A | C | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1174+256A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428439 | ||||||
| chr4:53428464
|
A | G | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+281A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428464 | ||||||
| chr4:53428510
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1174+327G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428510 | ||||||
| chr4:53428595
|
GTCT | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0151others(37): Show | 42 | HG00140.hp2 HG00280.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1174+419_1174+421d others(5): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53428595 | |||||
| chr4:53428767
|
T | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0001g0272others(1): Show | 4 | NA18954.hp1 NA18956.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+584T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428767 | ||||||
| chr4:53428774
|
G | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+591G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428774 | ||||||
| chr4:53428841
|
G | A | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1174+658G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53428841 | ||||||
| chr4:53429002
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1174+819G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429002 | ||||||
| chr4:53429060
|
G | C | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1174+877G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429060 | ||||||
| chr4:53429065
|
G | A | 50 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1174+882G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429065 | ||||||
| chr4:53429465
|
T | G | 9 | a0001c0001t0005g0149a0001c0001t0005g0191a0001c0001t0005g0229others(6): Show | 9 | HG00408.hp1 HG02165.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+1282T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429465 | ||||||
| chr4:53429630
|
G | A | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+1447G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429630 | ||||||
| chr4:53429786
|
T | C | 1 | a0001c0001t0013g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1174+1603T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429786 | ||||||
| chr4:53429953
|
G | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(213): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1174+1770G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429953 | ||||||
| chr4:53429957
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0258others(1): Show | 4 | HG01109.hp2 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+1774C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53429957 | ||||||
| chr4:53430214
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+2031A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430214 | ||||||
| chr4:53430240
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1174+2057A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430240 | ||||||
| chr4:53430248
|
C | G | 15 | a0001c0001t0006g0004a0001c0001t0006g0030a0001c0001t0006g0062others(12): Show | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174+2065C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430248 | ||||||
| chr4:53430250
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+2067A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430250 | ||||||
| chr4:53430256
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1174+2073C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430256 | ||||||
| chr4:53430341
|
C | CT | 62 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0155others(59): Show | 63 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1174+2182dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53430341 | |||||
| chr4:53430341
|
CT | C | 123 | a0001c0001t0001g0190a0001c0001t0001g0240a0001c0001t0002g0010others(120): Show | 130 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1174+2182delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53430341 | |||||
| chr4:53430412
|
G | A | 1 | a0001c0001t0005g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1174+2229G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430412 | ||||||
| chr4:53430585
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+2402C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430585 | ||||||
| chr4:53430825
|
G | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+2642G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430825 | ||||||
| chr4:53430837
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+2654A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430837 | ||||||
| chr4:53430984
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1174+2801C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53430984 | ||||||
| chr4:53431047
|
A | G | 6 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174+2864A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431047 | ||||||
| chr4:53431073
|
G | A | 4 | a0001c0001t0003g0376a0001c0001t0003g0377a0001c0001t0003g0378others(1): Show | 4 | NA18973.hp1 NA18981.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174+2890G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431073 | ||||||
| chr4:53431149
|
T | A | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1174+2966T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431149 | ||||||
| chr4:53431277
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1174+3094A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431277 | ||||||
| chr4:53431353
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1174+3170A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431353 | ||||||
| chr4:53431366
|
C | T | 1 | a0001c0001t0005g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1174+3183C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431366 | ||||||
| chr4:53431541
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1174+3358A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431541 | ||||||
| chr4:53431582
|
T | G | 1 | a0001c0001t0005g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174+3399T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431582 | ||||||
| chr4:53431584
|
C | A | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+3401C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431584 | ||||||
| chr4:53431608
|
TTTTTG | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1174+3445_1174+344 others(9): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53431608 | |||||
| chr4:53431633
|
C | T | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1174+3450C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431633 | ||||||
| chr4:53431652
|
T | A | 1 | a0001c0001t0003g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1174+3469T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431652 | ||||||
| chr4:53431737
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1174+3554G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431737 | ||||||
| chr4:53431771
|
A | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+3588A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431771 | ||||||
| chr4:53431910
|
T | G | 2 | a0001c0001t0002g0307a0001c0001t0002g0337 | 2 | HG02056.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1174+3727T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53431910 | ||||||
| chr4:53432086
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0183 | 2 | HG00673.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1174+3903A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432086 | ||||||
| chr4:53432157
|
A | AGGCTGAG others(11): Show |
1 | a0001c0001t0004g0123 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1174+3975_1174+399 others(22): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432157 | |||||
| chr4:53432171
|
A | G | 224 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0163others(221): Show | 228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1174+3988A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432171 | ||||||
| chr4:53432199
|
C | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1174+4016C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432199 | ||||||
| chr4:53432270
|
C | T | 141 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0001g0163others(138): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1174+4087C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432270 | ||||||
| chr4:53432272
|
C | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+4089C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432272 | ||||||
| chr4:53432398
|
CA | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0151a0001c0001t0001g0152others(114): Show | 120 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1174+4241delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432398
|
CAA | C | 57 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0246others(54): Show | 60 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174+4240_1174+424 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432398
|
CAAA | C | 70 | a0001c0001t0001g0150a0001c0001t0001g0163a0001c0001t0001g0164others(67): Show | 71 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1174+4239_1174+424 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432398
|
CAAAA | C | 123 | a0001c0001t0001g0013a0001c0001t0001g0166a0001c0001t0001g0169others(120): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1174+4238_1174+424 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432398
|
CAAAAA | C | 8 | a0001c0001t0001g0168a0001c0001t0001g0181a0001c0001t0001g0187others(5): Show | 8 | HG01070.hp2 HG01243.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+4237_1174+424 others(9): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432398
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0008g0003 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+4221_1174+424 others(25): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53432398 | |||||
| chr4:53432438
|
T | C | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1174+4255T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432438 | ||||||
| chr4:53432494
|
G | A | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174+4311G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432494 | ||||||
| chr4:53432679
|
A | T | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+4496A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432679 | ||||||
| chr4:53432839
|
G | A | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1174+4656G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53432839 | ||||||
| chr4:53433156
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1174+4973C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433156 | ||||||
| chr4:53433189
|
G | T | 1 | a0001c0001t0003g0079 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1174+5006G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433189 | ||||||
| chr4:53433213
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(225): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1174+5030T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433213 | ||||||
| chr4:53433304
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1174+5121C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433304 | ||||||
| chr4:53433402
|
T | G | 1 | a0001c0001t0002g0331 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1174+5219T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433402 | ||||||
| chr4:53433438
|
T | C | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174+5255T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433438 | ||||||
| chr4:53433498
|
GTCA | G | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1174+5320_1174+532 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53433498 | |||||
| chr4:53433517
|
AT | A | 370 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(367): Show | 382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.1174+5345delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53433517 | |||||
| chr4:53433716
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1174+5533G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433716 | ||||||
| chr4:53433838
|
C | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1174+5655C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433838 | ||||||
| chr4:53433922
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1174+5739C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433922 | ||||||
| chr4:53433936
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1174+5753T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433936 | ||||||
| chr4:53433960
|
G | C | 37 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(34): Show | 38 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1174+5777G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53433960 | ||||||
| chr4:53434079
|
C | T | 1 | a0001c0001t0004g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1174+5896C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434079 | ||||||
| chr4:53434091
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1174+5908G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434091 | ||||||
| chr4:53434147
|
T | TAC | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174+5964_1174+596 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434147 | ||||||
| chr4:53434252
|
A | T | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174+6069A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434252 | ||||||
| chr4:53434354
|
G | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+6171G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434354 | ||||||
| chr4:53434355
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1174+6172C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434355 | ||||||
| chr4:53434424
|
A | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1174+6241A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434424 | ||||||
| chr4:53434429
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1174+6246G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434429 | ||||||
| chr4:53434471
|
A | AT | 7 | a0001c0001t0005g0205a0001c0001t0005g0228a0001c0001t0005g0230others(4): Show | 8 | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+6305dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53434471 | |||||
| chr4:53434471
|
AT | A | 68 | a0001c0001t0001g0150a0001c0001t0001g0197a0001c0001t0001g0198others(65): Show | 68 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1174+6305delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53434471 | |||||
| chr4:53434618
|
T | G | 7 | a0001c0001t0002g0367a0001c0001t0002g0368a0001c0001t0002g0369others(4): Show | 7 | HG00642.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1174+6435T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434618 | ||||||
| chr4:53434674
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0286a0001c0001t0012g0226others(1): Show | 4 | HG01884.hp1 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174+6491G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434674 | ||||||
| chr4:53434760
|
G | A | 3 | a0001c0001t0005g0277a0001c0001t0005g0279a0001c0001t0005g0285 | 3 | NA18971.hp2 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1174+6577G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434760 | ||||||
| chr4:53434889
|
T | A | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1174+6706T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434889 | ||||||
| chr4:53434994
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1174+6811A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53434994 | ||||||
| chr4:53435826
|
CGT | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(233): Show | 242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1175-6819_1175-681 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53435826 | |||||
| chr4:53435856
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175-6797G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435856 | ||||||
| chr4:53435885
|
G | A | 5 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0321others(2): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-6768G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435885 | ||||||
| chr4:53435993
|
A | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-6660A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53435993 | ||||||
| chr4:53436003
|
A | G | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1175-6650A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436003 | ||||||
| chr4:53436077
|
G | GT | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1175-6575dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53436077 | |||||
| chr4:53436133
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1175-6520A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436133 | ||||||
| chr4:53436530
|
T | C | 3 | a0001c0001t0002g0315a0001c0001t0002g0319a0001c0001t0002g0320 | 3 | HG02698.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1175-6123T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53436530 | ||||||
| chr4:53436856
|
AC | A | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1175-5792delC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53436856 | |||||
| chr4:53437098
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | NA18964.hp1 NA18987.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1175-5555G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437098 | ||||||
| chr4:53437147
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0002g0331 | 2 | HG00733.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1175-5506C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437147 | ||||||
| chr4:53437148
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1175-5505G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437148 | ||||||
| chr4:53437300
|
A | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1175-5353A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437300 | ||||||
| chr4:53437326
|
C | CAA | 46 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0028others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1175-5301_1175-530 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
C | CAAA | 12 | a0001c0001t0003g0032a0001c0001t0003g0034a0001c0001t0003g0035others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1175-5302_1175-530 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
C | CAAAA | 7 | a0001c0001t0003g0027a0001c0001t0006g0004a0001c0001t0006g0063others(4): Show | 8 | HG00673.hp2 HG01358.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-5303_1175-530 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0006g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175-5313_1175-530 others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CA | C | 14 | a0001c0001t0002g0318a0001c0001t0002g0324a0001c0001t0002g0328others(11): Show | 15 | HG00423.hp2 HG01261.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.1175-5300delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CAA | C | 109 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0172others(106): Show | 115 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1175-5301_1175-530 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CAAA | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(145): Show | 152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1175-5302_1175-530 others(7): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CAAAA | C | 11 | a0001c0001t0001g0236a0001c0001t0001g0263a0001c0001t0001g0293others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1175-5303_1175-530 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0002g0302a0001c0001t0002g0310a0001c0001t0002g0311others(6): Show | 9 | HG02630.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-5309_1175-530 others(14): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437326
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-5313_1175-530 others(18): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437326 | |||||
| chr4:53437354
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1175-5299G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437354 | ||||||
| chr4:53437375
|
T | C | 5 | a0001c0001t0002g0302a0001c0001t0002g0355a0001c0001t0002g0356others(2): Show | 5 | HG02630.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1175-5278T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437375 | ||||||
| chr4:53437659
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-4994A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437659 | ||||||
| chr4:53437699
|
T | TTTTA | 60 | a0001c0001t0001g0204a0001c0001t0002g0302a0001c0001t0002g0309others(57): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1175-4931_1175-492 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53437699 | |||||
| chr4:53437744
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1175-4909G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437744 | ||||||
| chr4:53437881
|
A | G | 12 | a0001c0001t0003g0014a0001c0001t0003g0046a0001c0001t0003g0049others(9): Show | 12 | HG02074.hp1 NA18953.hp2 NA18968.hp1 others(9): Show |
intron_variant | MODIFIER | c.1175-4772A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53437881 | ||||||
| chr4:53438017
|
G | A | 1 | a0001c0001t0002g0332 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1175-4636G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438017 | ||||||
| chr4:53438053
|
G | T | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1175-4600G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438053 | ||||||
| chr4:53438341
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1175-4312A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438341 | ||||||
| chr4:53438668
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1175-3985T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438668 | ||||||
| chr4:53438752
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1175-3901A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438752 | ||||||
| chr4:53438758
|
C | G | 15 | a0001c0001t0006g0004a0001c0001t0006g0030a0001c0001t0006g0062others(12): Show | 16 | HG01358.hp1 HG01361.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1175-3895C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438758 | ||||||
| chr4:53438806
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0015 | 3 | HG03130.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1175-3847G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438806 | ||||||
| chr4:53438889
|
C | G | 1 | a0001c0001t0004g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1175-3764C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53438889 | ||||||
| chr4:53439049
|
T | C | 1 | a0001c0001t0003g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1175-3604T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439049 | ||||||
| chr4:53439095
|
T | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1175-3558T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439095 | ||||||
| chr4:53439237
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(107): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1175-3416A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439237 | ||||||
| chr4:53439312
|
T | C | 1 | a0001c0001t0002g0368 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1175-3341T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439312 | ||||||
| chr4:53439450
|
A | G | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-3203A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439450 | ||||||
| chr4:53439589
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-3064T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439589 | ||||||
| chr4:53439729
|
C | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1175-2924C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439729 | ||||||
| chr4:53439798
|
T | TAG | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-2854_1175-285 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53439798 | |||||
| chr4:53439935
|
G | A | 1 | a0001c0001t0004g0145 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1175-2718G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53439935 | ||||||
| chr4:53440049
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1175-2604C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440049 | ||||||
| chr4:53440074
|
T | G | 1 | a0001c0001t0005g0230 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1175-2579T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440074 | ||||||
| chr4:53440097
|
C | A | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1175-2556C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440097 | ||||||
| chr4:53440273
|
A | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1175-2380A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440273 | ||||||
| chr4:53440422
|
T | C | 1 | a0001c0001t0003g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1175-2231T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440422 | ||||||
| chr4:53440436
|
G | C | 1 | a0001c0001t0004g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1175-2217G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440436 | ||||||
| chr4:53440794
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1175-1859C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440794 | ||||||
| chr4:53440804
|
C | T | 1 | a0001c0001t0005g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1175-1849C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440804 | ||||||
| chr4:53440969
|
T | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1175-1684T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53440969 | ||||||
| chr4:53441102
|
T | G | 1 | a0001c0001t0003g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1175-1551T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441102 | ||||||
| chr4:53441147
|
T | TTTTA | 4 | a0001c0001t0004g0096a0001c0001t0004g0098a0001c0001t0004g0099others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1482_1175-147 others(8): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 53441147 | |||||
| chr4:53441168
|
T | C | 1 | a0001c0001t0003g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1175-1485T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441168 | ||||||
| chr4:53441172
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175-1481T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441172 | ||||||
| chr4:53441708
|
C | T | 3 | a0001c0001t0005g0277a0001c0001t0005g0279a0001c0001t0005g0285 | 3 | NA18971.hp2 NA19082.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1175-945C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441708 | ||||||
| chr4:53441809
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1175-844A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441809 | ||||||
| chr4:53441951
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1175-702A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53441951 | ||||||
| chr4:53442240
|
A | G | 1 | a0001c0001t0002g0369 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1175-413A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442240 | ||||||
| chr4:53442255
|
G | A | 2 | a0001c0001t0006g0070a0001c0001t0006g0071 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1175-398G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442255 | ||||||
| chr4:53442437
|
G | A | 50 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(47): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1175-216G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 13/17 | chr4 | 53442437 | ||||||
| chr4:53442975
|
T | C | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1229+268T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53442975 | ||||||
| chr4:53443010
|
A | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1229+303A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443010 | ||||||
| chr4:53443063
|
G | A | 1 | a0001c0001t0009g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1229+356G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443063 | ||||||
| chr4:53443134
|
A | G | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1229+427A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443134 | ||||||
| chr4:53443298
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1229+591G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443298 | ||||||
| chr4:53443372
|
AAT | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1229+669_1229+670d others(4): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 53443372 | |||||
| chr4:53443374
|
T | C | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229+667T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443374 | ||||||
| chr4:53443395
|
T | C | 1 | a0001c0001t0010g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1230-653T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443395 | ||||||
| chr4:53443477
|
A | G | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230-571A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443477 | ||||||
| chr4:53443542
|
C | T | 1 | a0001c0001t0002g0364 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1230-506C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443542 | ||||||
| chr4:53443549
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230-499A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443549 | ||||||
| chr4:53443635
|
A | G | 45 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0149others(42): Show | 46 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230-413A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443635 | ||||||
| chr4:53443669
|
C | T | 2 | a0001c0001t0010g0374a0001c0001t0011g0373 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1230-379C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443669 | ||||||
| chr4:53443891
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(150): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1230-157C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53443891 | ||||||
| chr4:53444019
|
A | G | 1 | a0001c0001t0003g0037 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1230-29A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53444019 | ||||||
| chr4:53444021
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1230-27A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 14/17 | chr4 | 53444021 | ||||||
| chr4:53444114
|
T | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(154): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1285+11T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444114 | ||||||
| chr4:53444173
|
TA | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+75delA | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53444173 | |||||
| chr4:53444341
|
C | T | 56 | a0001c0001t0001g0150a0001c0001t0001g0189a0001c0001t0001g0197others(53): Show | 56 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1285+238C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444341 | ||||||
| chr4:53444379
|
C | T | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+276C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444379 | ||||||
| chr4:53444383
|
A | G | 52 | a0001c0001t0003g0014a0001c0001t0004g0001a0001c0001t0004g0006others(49): Show | 56 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1285+280A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444383 | ||||||
| chr4:53444422
|
G | A | 11 | a0001c0001t0004g0008a0001c0001t0004g0112a0001c0001t0004g0118others(8): Show | 12 | HG00423.hp2 HG02080.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.1285+319G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444422 | ||||||
| chr4:53444466
|
T | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(293): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1285+363T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444466 | ||||||
| chr4:53444585
|
A | T | 65 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(62): Show | 67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285+482A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444585 | ||||||
| chr4:53444602
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1285+499A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444602 | ||||||
| chr4:53444811
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+708A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53444811 | ||||||
| chr4:53445108
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+1005C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445108 | ||||||
| chr4:53445176
|
G | C | 4 | a0001c0001t0004g0096a0001c0001t0004g0098a0001c0001t0004g0099others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+1073G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445176 | ||||||
| chr4:53445381
|
C | A | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+1278C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445381 | ||||||
| chr4:53445531
|
A | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1285+1428A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445531 | ||||||
| chr4:53445706
|
T | G | 1 | a0001c0001t0002g0304 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1285+1603T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445706 | ||||||
| chr4:53445813
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1285+1710C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445813 | ||||||
| chr4:53445836
|
A | T | 1 | a0001c0001t0001g0282 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1285+1733A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445836 | ||||||
| chr4:53445902
|
T | C | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285+1799T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445902 | ||||||
| chr4:53445905
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+1802T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445905 | ||||||
| chr4:53445950
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+1847T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53445950 | ||||||
| chr4:53446084
|
C | T | 1 | a0001c0001t0015g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1285+1981C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446084 | ||||||
| chr4:53446147
|
G | A | 1 | a0001c0001t0006g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1285+2044G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446147 | ||||||
| chr4:53446161
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+2058T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446161 | ||||||
| chr4:53446170
|
T | G | 1 | a0001c0001t0002g0317 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1285+2067T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446170 | ||||||
| chr4:53446199
|
C | CT | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285+2106dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446199 | |||||
| chr4:53446199
|
CT | C | 76 | a0001c0001t0003g0014a0001c0001t0003g0025a0001c0001t0003g0027others(73): Show | 77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1285+2106delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446199 | |||||
| chr4:53446203
|
T | A | 1 | a0001c0001t0018g0215 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1285+2100T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446203 | ||||||
| chr4:53446539
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1285+2436A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446539 | ||||||
| chr4:53446585
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+2482A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446585 | ||||||
| chr4:53446830
|
T | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1285+2727T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446830 | ||||||
| chr4:53446939
|
TTTTTTGT others(5): Show |
T | 1 | a0001c0001t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1285+2854_1285+286 others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53446939 | |||||
| chr4:53446945
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+2842G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53446945 | ||||||
| chr4:53447549
|
C | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+3446C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447549 | ||||||
| chr4:53447610
|
A | G | 3 | a0001c0001t0002g0336a0001c0001t0002g0347a0001c0001t0002g0353 | 3 | HG02602.hp2 HG03942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+3507A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447610 | ||||||
| chr4:53447648
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1285+3545A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447648 | ||||||
| chr4:53447706
|
C | T | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+3603C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447706 | ||||||
| chr4:53447799
|
G | A | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1285+3696G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447799 | ||||||
| chr4:53447859
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1285+3756C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447859 | ||||||
| chr4:53447919
|
A | G | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+3816A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53447919 | ||||||
| chr4:53448020
|
G | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285+3917G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448020 | ||||||
| chr4:53448095
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1285+3992A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448095 | ||||||
| chr4:53448251
|
T | C | 65 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(62): Show | 67 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285+4148T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448251 | ||||||
| chr4:53448383
|
A | G | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1285+4280A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448383 | ||||||
| chr4:53448661
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1286-4259A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53448661 | ||||||
| chr4:53449100
|
T | C | 1 | a0001c0001t0007g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1286-3820T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449100 | ||||||
| chr4:53449432
|
T | C | 1 | a0001c0001t0002g0339 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1286-3488T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449432 | ||||||
| chr4:53449602
|
C | G | 1 | a0001c0001t0003g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1286-3318C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449602 | ||||||
| chr4:53449623
|
T | C | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286-3297T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449623 | ||||||
| chr4:53449703
|
T | C | 1 | a0001c0001t0005g0231 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1286-3217T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449703 | ||||||
| chr4:53449751
|
T | C | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-3169T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449751 | ||||||
| chr4:53449965
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1286-2955G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53449965 | ||||||
| chr4:53450047
|
T | C | 12 | a0001c0001t0003g0032a0001c0001t0003g0034a0001c0001t0003g0036others(9): Show | 12 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286-2873T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450047 | ||||||
| chr4:53450328
|
T | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1286-2592T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450328 | ||||||
| chr4:53450329
|
A | G | 1 | a0001c0001t0017g0026 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1286-2591A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450329 | ||||||
| chr4:53450450
|
C | G | 1 | a0001c0001t0004g0006 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1286-2470C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450450 | ||||||
| chr4:53450498
|
C | T | 2 | a0001c0001t0005g0231a0001c0001t0005g0232 | 2 | HG02165.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1286-2422C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450498 | ||||||
| chr4:53450529
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0066 | 2 | HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1286-2391C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450529 | ||||||
| chr4:53450756
|
T | C | 59 | a0001c0001t0004g0001a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 64 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1286-2164T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450756 | ||||||
| chr4:53450764
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1286-2156T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450764 | ||||||
| chr4:53450765
|
C | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1286-2155C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450765 | ||||||
| chr4:53450815
|
A | G | 8 | a0001c0001t0004g0007a0001c0001t0004g0113a0001c0001t0004g0120others(5): Show | 9 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286-2105A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450815 | ||||||
| chr4:53450963
|
C | CT | 12 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0305others(9): Show | 12 | HG02129.hp2 HG03130.hp1 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.1286-1941dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53450963 | |||||
| chr4:53450963
|
CTT | C | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286-1942_1286-194 others(6): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53450963 | |||||
| chr4:53450984
|
T | C | 1 | a0001c0001t0002g0346 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1286-1936T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53450984 | ||||||
| chr4:53451325
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1286-1595T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451325 | ||||||
| chr4:53451439
|
T | G | 7 | a0001c0001t0002g0305a0001c0001t0002g0325a0001c0001t0002g0326others(4): Show | 7 | HG02129.hp2 HG04184.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1286-1481T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451439 | ||||||
| chr4:53451568
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1286-1352A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451568 | ||||||
| chr4:53451575
|
C | CT | 236 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(233): Show | 242 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1286-1331dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53451575 | |||||
| chr4:53451610
|
A | G | 8 | a0001c0001t0004g0005a0001c0001t0004g0094a0001c0001t0004g0095others(5): Show | 9 | HG02486.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1310A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451610 | ||||||
| chr4:53451885
|
CT | C | 140 | a0001c0001t0001g0186a0001c0001t0002g0010a0001c0001t0002g0011others(137): Show | 148 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1286-1019delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 53451885 | |||||
| chr4:53451894
|
T | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0278 | 2 | HG02135.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1286-1026T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451894 | ||||||
| chr4:53451898
|
T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(150): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1286-1022T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53451898 | ||||||
| chr4:53452019
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1286-901G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452019 | ||||||
| chr4:53452039
|
G | A | 2 | a0001c0001t0002g0364a0001c0001t0002g0365 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1286-881G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452039 | ||||||
| chr4:53452143
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1286-777A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452143 | ||||||
| chr4:53452247
|
C | T | 6 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0179others(3): Show | 6 | HG00140.hp2 HG01169.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286-673C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452247 | ||||||
| chr4:53452452
|
G | A | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1286-468G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452452 | ||||||
| chr4:53452584
|
G | T | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1286-336G>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452584 | ||||||
| chr4:53452608
|
C | T | 2 | a0001c0001t0002g0338a0001c0001t0002g0340 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1286-312C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452608 | ||||||
| chr4:53452731
|
T | G | 1 | a0001c0001t0001g0297 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1286-189T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452731 | ||||||
| chr4:53452805
|
T | G | 1 | a0001c0001t0010g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1286-115T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452805 | ||||||
| chr4:53452844
|
C | A | 372 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(369): Show | 384 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1286-76C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 15/17 | chr4 | 53452844 | ||||||
| chr4:53453195
|
G | A | 1 | a0001c0001t0003g0046 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1499+62G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453195 | ||||||
| chr4:53453443
|
T | C | 1 | a0001c0001t0005g0254 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1499+310T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453443 | ||||||
| chr4:53453565
|
A | G | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1499+432A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453565 | ||||||
| chr4:53453669
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1499+536T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453669 | ||||||
| chr4:53453744
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1499+611C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453744 | ||||||
| chr4:53453872
|
T | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0299a0001c0001t0002g0321others(2): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+739T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453872 | ||||||
| chr4:53453921
|
A | T | 5 | a0001c0001t0002g0309a0001c0001t0002g0310a0001c0001t0002g0311others(2): Show | 5 | HG02109.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499+788A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453921 | ||||||
| chr4:53453968
|
C | T | 9 | a0001c0001t0002g0305a0001c0001t0002g0313a0001c0001t0002g0324others(6): Show | 9 | HG02129.hp2 HG03927.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1499+835C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53453968 | ||||||
| chr4:53454339
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1499+1206A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454339 | ||||||
| chr4:53454443
|
C | T | 1 | a0001c0001t0012g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1499+1310C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454443 | ||||||
| chr4:53454450
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(234): Show | 243 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1499+1317C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454450 | ||||||
| chr4:53454481
|
C | A | 2 | a0001c0001t0003g0014a0001c0001t0003g0046 | 2 | NA19068.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1499+1348C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454481 | ||||||
| chr4:53454505
|
T | C | 7 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0070others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1499+1372T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454505 | ||||||
| chr4:53454535
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1499+1402G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454535 | ||||||
| chr4:53454652
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1499+1519T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454652 | ||||||
| chr4:53454655
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1499+1522A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454655 | ||||||
| chr4:53454993
|
T | A | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499+1860T>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53454993 | ||||||
| chr4:53455030
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1499+1897C>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455030 | ||||||
| chr4:53455149
|
T | C | 58 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(55): Show | 60 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.1499+2016T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455149 | ||||||
| chr4:53455270
|
A | G | 31 | a0001c0001t0002g0011a0001c0001t0002g0300a0001c0001t0002g0301others(28): Show | 32 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1499+2137A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455270 | ||||||
| chr4:53455446
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(106): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1499+2313G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455446 | ||||||
| chr4:53455531
|
G | C | 1 | a0001c0001t0002g0318 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1499+2398G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455531 | ||||||
| chr4:53455835
|
G | A | 1 | a0001c0001t0002g0370 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1499+2702G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455835 | ||||||
| chr4:53455847
|
C | CT | 51 | a0001c0001t0004g0001a0001c0001t0004g0006a0001c0001t0004g0007others(48): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1499+2720dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53455847 | |||||
| chr4:53455940
|
A | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(292): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1500-2713A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53455940 | ||||||
| chr4:53456237
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0015g0016 | 4 | HG03130.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1500-2416T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456237 | ||||||
| chr4:53456529
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1500-2124G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456529 | ||||||
| chr4:53456545
|
ATTTTAGC others(2): Show |
A | 154 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1500-2106_1500-209 others(13): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53456545 | |||||
| chr4:53456919
|
G | A | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1500-1734G>A | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53456919 | ||||||
| chr4:53457101
|
T | C | 1 | a0001c0001t0005g0277 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1500-1552T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457101 | ||||||
| chr4:53457116
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1500-1537C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457116 | ||||||
| chr4:53457147
|
C | G | 66 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(63): Show | 68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1500-1506C>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457147 | ||||||
| chr4:53457178
|
A | G | 1 | a0001c0001t0002g0329 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1500-1475A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457178 | ||||||
| chr4:53457658
|
T | G | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1500-995T>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457658 | ||||||
| chr4:53457740
|
G | C | 1 | a0001c0001t0002g0352 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1500-913G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53457740 | ||||||
| chr4:53458006
|
G | GC | 10 | a0001c0001t0002g0302a0001c0001t0002g0309a0001c0001t0002g0310others(7): Show | 10 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1500-641dupC | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 53458006 | |||||
| chr4:53458058
|
A | G | 4 | a0001c0001t0001g0293a0001c0001t0008g0003a0001c0001t0008g0015others(1): Show | 5 | HG00733.hp2 HG03130.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500-595A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458058 | ||||||
| chr4:53458212
|
A | G | 80 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(77): Show | 82 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1500-441A>G | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458212 | ||||||
| chr4:53458218
|
A | C | 1 | a0001c0001t0005g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1500-435A>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458218 | ||||||
| chr4:53458227
|
T | C | 2 | a0001c0001t0009g0147a0001c0001t0009g0148 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1500-426T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458227 | ||||||
| chr4:53458284
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1500-369T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 16/17 | chr4 | 53458284 | ||||||
| chr4:53458824
|
A | T | 58 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0299others(55): Show | 60 | HG00558.hp1 HG00597.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.1637+34A>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458824 | ||||||
| chr4:53458899
|
G | C | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1637+109G>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458899 | ||||||
| chr4:53458918
|
C | T | 1 | a0001c0001t0004g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1637+128C>T | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53458918 | ||||||
| chr4:53459149
|
AACTGATT others(7): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1638-150_1638-137d others(16): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459149 | |||||
| chr4:53459255
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1638-47T>C | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | chr4 | 53459255 | ||||||
| chr4:53459277
|
C | CT | 100 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0150others(97): Show | 102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
splice_region_variant&intron_variant | LOW | c.1638-5dupT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | |||||
| chr4:53459277
|
C | CTT | 123 | a0001c0001t0001g0153a0001c0001t0001g0184a0001c0001t0001g0185others(120): Show | 126 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.1638-6_1638-5dupTT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | |||||
| chr4:53459277
|
C | CTTT | 6 | a0001c0001t0001g0245a0001c0001t0005g0230a0001c0001t0008g0003others(3): Show | 7 | HG02055.hp2 HG03130.hp1 HG03486.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1638-7_1638-5dupTT others(1): Show |
FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 | |||||
| chr4:53459277
|
CT | C | 50 | a0001c0001t0003g0019a0001c0001t0004g0001a0001c0001t0004g0005others(47): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1638-5delT | FIP1L1 | ENSG00000145216.17 | transcript | ENST00000337488.11 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 53459277 |