Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2313 |
|---|---|
| ensemblid | ENSG00000151702.18 |
| hgncid | 3749 |
| symbol | FLI1 |
| name | Fli-1 proto-oncogene, ETS transcription factor |
| refseq_nuc | NM_002017.5 |
| refseq_prot | NP_002008.2 |
| ensembl_nuc | ENST00000527786.7 |
| ensembl_prot | ENSP00000433488.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 128694072 |
| end | 128813267 |
| strand | + |
| ver | v1.2 |
| region | chr11:128694072-128813267 |
| region5000 | chr11:128689072-128818267 |
| regionname0 | FLI1_chr11_128694072_128813267 |
| regionname5000 | FLI1_chr11_128689072_128818267 |
| 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 | 452 | 322 | 83 | 57 | 140 | 6 | 34 | 102 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0002 | 0/0 | 452 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0003 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| 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 | 1359 | 214 | 36 | 47 | 99 | 5 | 25 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0002 | 0/0 | 1359 | 48 | 21 | 5 | 20 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0003 | 0/0 | 1359 | 33 | 10 | 2 | 15 | 1 | 5 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0004 | 0/0 | 1359 | 19 | 13 | 2 | 2 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0005 | 0/0 | 1359 | 5 | 0 | 1 | 4 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0006 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0007 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0008 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0011 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0012 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| 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 | 1/0 | 2467 | 220 | 53 | 38 | 100 | 3 | 25 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0002 | 0/1 | 2021 | 56 | 3 | 16 | 27 | 2 | 7 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0003 | 0/0 | 2467 | 15 | 14 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0004 | 0/0 | 2020 | 13 | 0 | 1 | 12 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0005 | 0/0 | 2020 | 9 | 8 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0006 | 0/0 | 2467 | 3 | 0 | 0 | 3 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0007 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0008 | 0/0 | 2466 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0009 | 0/0 | 2467 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0010 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0011 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0012 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0013 | 0/0 | 2466 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0014 | 0/0 | 2467 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0015 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0016 | 0/0 | 2467 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0017 | 0/0 | 2467 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| t0018 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| 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 | 1359 | 214 | 36 | 47 | 99 | 5 | 25 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0002 | 0/0 | 1359 | 48 | 21 | 5 | 20 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0003 | 0/0 | 1359 | 33 | 10 | 2 | 15 | 1 | 5 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0004 | 0/0 | 1359 | 19 | 13 | 2 | 2 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0006 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0007 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0008 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0011 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0012 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0002c0005 | 0/0 | 1359 | 5 | 0 | 1 | 4 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0003c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3825 | 134 | 23 | 31 | 61 | 2 | 16 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0002 | 0/1 | 3379 | 51 | 3 | 14 | 24 | 2 | 7 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0004 | 0/0 | 3378 | 13 | 0 | 1 | 12 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0005 | 0/0 | 3378 | 8 | 8 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0008 | 0/0 | 3824 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0009 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0010 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0012 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0013 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0014 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0016 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0001t0017 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0002t0001 | 0/0 | 3825 | 42 | 20 | 2 | 18 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0002t0002 | 0/0 | 3379 | 4 | 0 | 2 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0002t0005 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0002t0018 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0003t0001 | 0/0 | 3825 | 23 | 4 | 1 | 12 | 1 | 5 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0003t0003 | 0/0 | 3825 | 6 | 5 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0003t0006 | 0/0 | 3825 | 3 | 0 | 0 | 3 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0003t0007 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0004t0001 | 0/0 | 3825 | 11 | 5 | 2 | 2 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0004t0003 | 0/0 | 3825 | 7 | 7 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0004t0011 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0006t0001 | 0/0 | 3825 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0007t0003 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0008t0001 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0009t0001 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0010t0002 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0011t0003 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0001c0012t0015 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0002c0005t0001 | 0/0 | 3825 | 5 | 0 | 1 | 4 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| a0003c0013t0001 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | copy fasta | chr11 | 128689072 | 128818267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0013g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0016g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0017g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0018g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0007t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0008t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0010t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0011t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0012t0015g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0003c0013t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0317 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0264 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0076 | EUR | FIN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00609 | hp1 | a0001 | c0001 | t0013 | g0111 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0169 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0318 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0201 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0308 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01258 | hp2 | a0001 | c0001 | t0017 | g0303 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0218 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0167 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02055 | hp1 | a0001 | c0002 | t0018 | g0015 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0277 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0313 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02148 | hp1 | a0002 | c0005 | t0001 | g0191 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02165 | hp2 | a0001 | c0010 | t0002 | g0312 | EAS | CDX | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0166 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0311 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02451 | hp2 | a0001 | c0012 | t0015 | g0084 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02622 | hp2 | a0001 | c0004 | t0003 | g0283 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0309 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02717 | hp1 | a0003 | c0013 | t0001 | g0080 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0088 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0190 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0255 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0214 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0225 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03453 | hp1 | a0001 | c0011 | t0003 | g0093 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0077 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0112 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03710 | hp2 | a0001 | c0001 | t0014 | g0092 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0171 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0298 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0270 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0023 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0275 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0162 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0304 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0041 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18971 | hp1 | a0002 | c0005 | t0001 | g0300 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18983 | hp1 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18991 | hp1 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18992 | hp2 | a0001 | c0003 | t0006 | g0223 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19005 | hp1 | a0001 | c0009 | t0001 | g0143 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19007 | hp1 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19012 | hp1 | a0001 | c0006 | t0001 | g0064 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19043 | hp1 | a0001 | c0003 | t0007 | g0147 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19058 | hp1 | a0002 | c0005 | t0001 | g0051 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0239 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0249 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19077 | hp2 | a0002 | c0005 | t0001 | g0117 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0267 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ASW | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | GIH | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0070 | SAS | GIH | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0096 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0287 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18955 | hp2 | a0002 | c0005 | t0001 | g0279 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20300 | hp1 | a0001 | c0004 | t0011 | g0108 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA21309 | hp1 | a0001 | c0007 | t0003 | g0021 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0105 | REF | REF | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128758170
|
C | T | 1 | a0003 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.74C>T | p.Ala25Val | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/9 | 261/3825 | 74/1359 | 25/452 | chr11 | 128758170 | ||
| chr11:128810806
|
G | A | 1 | a0002 | 5 | HG02148.hp1 NA18955.hp2 NA18971.hp1 others(2): Show |
missense_variant | MODERATE | c.1177G>A | p.Ala393Thr | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1364/3825 | 1177/1359 | 393/452 | chr11 | 128810806 | ||
| chr11:128812821
|
AGGACTTT others(686): Show |
A | 1 | a0001 | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
splice_region_variant | LOW | c.*1834_*2526del | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | chr11 | 128812821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128758291
|
C | T | 2 | a0001c0011a0001c0012 | 2 | HG02451.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.195C>T | p.Asn65Asn | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/9 | 382/3825 | 195/1359 | 65/452 | chr11 | 128758291 | ||
| chr11:128768166
|
C | T | 2 | a0001c0009a0001c0010 | 2 | HG02165.hp2 NA19005.hp1 |
synonymous_variant | LOW | c.279C>T | p.Gly93Gly | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/9 | 466/3825 | 279/1359 | 93/452 | chr11 | 128768166 | ||
| chr11:128781998
|
A | G | 6 | a0001c0002a0001c0004a0001c0009others(3): Show | 71 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(68): Show |
synonymous_variant | LOW | c.630A>G | p.Gln210Gln | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/9 | 817/3825 | 630/1359 | 210/452 | chr11 | 128781998 | ||
| chr11:128805397
|
T | A | 7 | a0001c0003a0001c0004a0001c0006others(4): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
synonymous_variant | LOW | c.687T>A | p.Ala229Ala | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/9 | 874/3825 | 687/1359 | 229/452 | chr11 | 128805397 | ||
| chr11:128807205
|
G | C | 1 | a0001c0006 | 2 | NA19007.hp1 NA19012.hp1 |
synonymous_variant | LOW | c.747G>C | p.Thr249Thr | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/9 | 934/3825 | 747/1359 | 249/452 | chr11 | 128807205 | ||
| chr11:128810565
|
G | A | 1 | a0001c0007 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.936G>A | p.Thr312Thr | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1123/3825 | 936/1359 | 312/452 | chr11 | 128810565 | ||
| chr11:128810571
|
C | G | 1 | a0001c0008 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.942C>G | p.Pro314Pro | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1129/3825 | 942/1359 | 314/452 | chr11 | 128810571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128811091
|
T | G | 1 | a0001c0003t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 103 | chr11 | 128811091 | |||||
| chr11:128811309
|
T | C | 2 | a0001c0001t0005a0001c0002t0005 | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 321 | chr11 | 128811309 | |||||
| chr11:128811338
|
T | C | 2 | a0001c0001t0008a0001c0001t0009 | 2 | HG00323.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*350T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 350 | chr11 | 128811338 | |||||
| chr11:128811352
|
G | A | 1 | a0001c0001t0010 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*364G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 364 | chr11 | 128811352 | |||||
| chr11:128811388
|
G | A | 1 | a0001c0004t0011 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 400 | chr11 | 128811388 | |||||
| chr11:128811574
|
C | T | 1 | a0001c0003t0006 | 3 | NA18983.hp1 NA18991.hp1 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*586C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 586 | chr11 | 128811574 | |||||
| chr11:128811593
|
A | G | 1 | a0001c0002t0018 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 605 | chr11 | 128811593 | |||||
| chr11:128811616
|
A | C | 5 | a0001c0003t0003a0001c0003t0007a0001c0004t0003others(2): Show | 16 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*628A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 628 | chr11 | 128811616 | |||||
| chr11:128811674
|
G | A | 1 | a0001c0001t0012 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 686 | chr11 | 128811674 | |||||
| chr11:128811691
|
AT | A | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(2): Show | 24 | HG00323.hp1 HG00609.hp1 HG01123.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*718delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 718 | INFO_REALIGN_3_PRIME | chr11 | 128811691 | ||||
| chr11:128811706
|
T | A | 1 | a0001c0003t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 718 | chr11 | 128811706 | |||||
| chr11:128812013
|
T | C | 1 | a0001c0001t0014 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1025T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1025 | chr11 | 128812013 | |||||
| chr11:128812187
|
G | A | 1 | a0001c0012t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1199 | chr11 | 128812187 | |||||
| chr11:128812347
|
T | C | 1 | a0001c0001t0016 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1359T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1359 | chr11 | 128812347 | |||||
| chr11:128812565
|
C | A | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(3): Show | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1577C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1577 | chr11 | 128812565 | |||||
| chr11:128812711
|
G | T | 6 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(3): Show | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1723G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1723 | chr11 | 128812711 | |||||
| chr11:128812817
|
G | A | 1 | a0001c0001t0017 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1829G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | 1829 | chr11 | 128812817 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128694294
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+18G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694294 | ||||||
| chr11:128694346
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.18+70G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694346 | ||||||
| chr11:128694351
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+75G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694351 | ||||||
| chr11:128694396
|
C | T | 3 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0002t0001g0323 | 3 | NA18939.hp1 NA18990.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.18+120C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694396 | ||||||
| chr11:128694462
|
GC | G | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+189delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128694462 | |||||
| chr11:128694478
|
AC | A | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+205delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128694478 | |||||
| chr11:128694497
|
GC | G | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+226delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128694497 | |||||
| chr11:128694514
|
CCG | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+239_18+240delCG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694514 | ||||||
| chr11:128694518
|
C | G | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+242C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694518 | ||||||
| chr11:128694542
|
CG | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+270delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128694542 | |||||
| chr11:128694581
|
CA | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+306delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694581 | ||||||
| chr11:128694587
|
A | G | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+311A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694587 | ||||||
| chr11:128694592
|
A | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+316A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694592 | ||||||
| chr11:128694648
|
C | G | 1 | a0001c0001t0002g0320 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.18+372C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694648 | ||||||
| chr11:128694650
|
CG | C | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.18+375delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694650 | ||||||
| chr11:128694707
|
G | A | 2 | a0001c0003t0003g0008a0001c0004t0001g0009 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.18+431G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694707 | ||||||
| chr11:128694711
|
G | T | 1 | a0001c0001t0002g0319 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.18+435G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694711 | ||||||
| chr11:128694782
|
G | C | 1 | a0001c0001t0002g0010 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.18+506G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694782 | ||||||
| chr11:128694832
|
C | A | 104 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(101): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.18+556C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694832 | ||||||
| chr11:128694856
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+580G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694856 | ||||||
| chr11:128694899
|
A | C | 221 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.18+623A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694899 | ||||||
| chr11:128694977
|
C | A | 1 | a0001c0003t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+701C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694977 | ||||||
| chr11:128695101
|
T | C | 220 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.18+825T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695101 | ||||||
| chr11:128695139
|
C | T | 33 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0295others(30): Show | 33 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.18+863C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695139 | ||||||
| chr11:128695248
|
G | A | 1 | a0001c0003t0003g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+972G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695248 | ||||||
| chr11:128695249
|
T | C | 6 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+973T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695249 | ||||||
| chr11:128695264
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+988G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695264 | ||||||
| chr11:128695471
|
G | T | 1 | a0001c0004t0011g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.18+1195G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695471 | ||||||
| chr11:128695855
|
A | G | 7 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+1579A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695855 | ||||||
| chr11:128695899
|
C | G | 3 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0002t0001g0207 | 3 | HG01074.hp1 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.18+1623C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695899 | ||||||
| chr11:128696001
|
C | T | 1 | a0001c0003t0003g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+1725C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696001 | ||||||
| chr11:128696020
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+1744G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696020 | ||||||
| chr11:128696167
|
A | C | 1 | a0001c0001t0002g0317 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.18+1891A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696167 | ||||||
| chr11:128696237
|
A | G | 1 | a0001c0002t0001g0286 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.18+1961A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696237 | ||||||
| chr11:128696263
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(172): Show | 178 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.18+1987G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696263 | ||||||
| chr11:128696438
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.18+2162A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696438 | ||||||
| chr11:128696492
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.18+2216C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696492 | ||||||
| chr11:128696497
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.18+2221A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696497 | ||||||
| chr11:128696672
|
A | T | 1 | a0001c0002t0001g0315 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.18+2396A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696672 | ||||||
| chr11:128696682
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.18+2406G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696682 | ||||||
| chr11:128696709
|
G | T | 1 | a0001c0001t0002g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.18+2433G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696709 | ||||||
| chr11:128696775
|
T | C | 1 | a0001c0001t0013g0111 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.18+2499T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696775 | ||||||
| chr11:128696953
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.18+2677G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128696953 | ||||||
| chr11:128697063
|
C | T | 2 | a0001c0002t0001g0101a0001c0002t0001g0102 | 2 | NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.18+2787C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697063 | ||||||
| chr11:128697113
|
G | A | 2 | a0001c0002t0001g0216a0001c0003t0001g0217 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.18+2837G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697113 | ||||||
| chr11:128697121
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.18+2845C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697121 | ||||||
| chr11:128697149
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+2873T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697149 | ||||||
| chr11:128697163
|
T | C | 1 | a0001c0003t0001g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+2887T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697163 | ||||||
| chr11:128697371
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+3095C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697371 | ||||||
| chr11:128697600
|
G | A | 3 | a0001c0001t0002g0219a0001c0003t0003g0218a0001c0004t0001g0220 | 3 | HG01884.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.18+3324G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697600 | ||||||
| chr11:128697981
|
G | A | 38 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0295others(35): Show | 38 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.18+3705G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128697981 | ||||||
| chr11:128698006
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+3730C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698006 | ||||||
| chr11:128698034
|
TC | T | 220 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.18+3760delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698034 | |||||
| chr11:128698089
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18+3813C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698089 | ||||||
| chr11:128698189
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0002g0221a0001c0003t0006g0004others(1): Show | 5 | NA18983.hp1 NA18991.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3913G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698189 | ||||||
| chr11:128698274
|
A | C | 2 | a0001c0001t0001g0202a0001c0002t0001g0203 | 2 | HG02074.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.18+3998A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698274 | ||||||
| chr11:128698318
|
C | G | 1 | a0001c0002t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+4042C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698318 | ||||||
| chr11:128698382
|
G | A | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4106G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698382 | ||||||
| chr11:128698594
|
T | C | 166 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(163): Show | 169 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.18+4318T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698594 | ||||||
| chr11:128698685
|
G | A | 1 | a0001c0003t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+4409G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698685 | ||||||
| chr11:128698711
|
C | CGT | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG01255.hp1 HG01255.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+4457_18+4458dup others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | CGTGTGT | 3 | a0001c0001t0001g0224a0001c0003t0003g0218a0001c0004t0003g0225 | 3 | HG01884.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.18+4453_18+4458dup others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | CGTGTGTG others(1): Show |
44 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(41): Show | 45 | HG00639.hp2 HG01261.hp1 HG01993.hp1 others(42): Show |
intron_variant | MODIFIER | c.18+4451_18+4458dup others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | CGTGTGTG others(3): Show |
12 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0269others(9): Show | 12 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+4449_18+4458dup others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | CGTGTGTG others(5): Show |
2 | a0001c0004t0003g0277a0001c0011t0003g0093 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+4447_18+4458dup others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | CGTGTGTG others(7): Show |
1 | a0001c0004t0001g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.18+4445_18+4458dup others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698711
|
C | T | 1 | a0001c0004t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+4435C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698711 | ||||||
| chr11:128698711
|
CGT | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0288a0001c0001t0001g0293others(38): Show | 41 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+4457_18+4458del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698711 | |||||
| chr11:128698712
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0103 | 2 | NA18948.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.18+4436G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698712 | ||||||
| chr11:128698733
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.18+4457T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698733 | ||||||
| chr11:128698733
|
T | TGTGTGTG others(3): Show |
18 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(15): Show | 19 | HG00099.hp2 HG00642.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(5): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0002g0025others(3): Show | 6 | HG01081.hp2 HG01109.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(5): Show |
2 | a0001c0002t0001g0029a0001c0002t0001g0030 | 2 | HG01109.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(7): Show |
78 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0032others(75): Show | 79 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0014g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+4458_18+4459ins others(16): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0001g0095a0001c0002t0001g0094a0001c0002t0005g0096 | 3 | HG00673.hp1 HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698733
|
T | TGTGTGTG others(9): Show |
3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0099 | 3 | HG01070.hp2 HG03654.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.18+4458_18+4459ins others(16): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698733 | |||||
| chr11:128698735
|
A | T | 9 | a0001c0001t0001g0224a0001c0001t0002g0219a0001c0002t0001g0215others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+4459A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698735 | ||||||
| chr11:128698737
|
A | T | 5 | a0001c0001t0001g0224a0001c0002t0001g0215a0001c0002t0001g0216others(2): Show | 5 | HG02922.hp1 HG03225.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+4461A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698737 | ||||||
| chr11:128698787
|
GCA | G | 4 | a0001c0001t0002g0194a0001c0003t0001g0195a0001c0003t0001g0196others(1): Show | 4 | NA18951.hp2 NA18970.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4513_18+4514del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128698787 | |||||
| chr11:128698796
|
A | G | 2 | a0001c0001t0005g0284a0001c0002t0001g0285 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+4520A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698796 | ||||||
| chr11:128698804
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0010g0090a0001c0002t0001g0002others(2): Show | 6 | HG02486.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+4528C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698804 | ||||||
| chr11:128698842
|
C | T | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4566C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698842 | ||||||
| chr11:128698933
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(175): Show | 181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.18+4657G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698933 | ||||||
| chr11:128699048
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(115): Show | 120 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.18+4772C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699048 | ||||||
| chr11:128699415
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.18+5139T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699415 | ||||||
| chr11:128699427
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.18+5151G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699427 | ||||||
| chr11:128699520
|
C | T | 52 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(49): Show | 53 | HG00639.hp2 HG01261.hp1 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.18+5244C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699520 | ||||||
| chr11:128699559
|
T | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(105): Show | 110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.18+5283T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699559 | ||||||
| chr11:128699674
|
C | T | 107 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(104): Show | 109 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.18+5398C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699674 | ||||||
| chr11:128699698
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0005g0280a0001c0001t0005g0281others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+5422A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699698 | ||||||
| chr11:128699736
|
G | A | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+5460G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699736 | ||||||
| chr11:128699932
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0005g0280a0001c0001t0005g0281others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+5656G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699932 | ||||||
| chr11:128699980
|
C | T | 6 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+5704C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699980 | ||||||
| chr11:128700004
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.18+5728G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700004 | ||||||
| chr11:128700108
|
C | A | 1 | a0001c0001t0001g0269 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.18+5832C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700108 | ||||||
| chr11:128700453
|
A | C | 5 | a0001c0001t0001g0006a0001c0001t0005g0280a0001c0001t0005g0281others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+6177A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700453 | ||||||
| chr11:128700466
|
G | C | 1 | a0001c0001t0002g0289 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+6190G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700466 | ||||||
| chr11:128700565
|
C | A | 1 | a0001c0001t0002g0116 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.18+6289C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700565 | ||||||
| chr11:128700589
|
T | A | 6 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+6313T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700589 | ||||||
| chr11:128700690
|
A | G | 2 | a0001c0003t0001g0313a0001c0010t0002g0312 | 2 | HG02083.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.18+6414A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700690 | ||||||
| chr11:128700731
|
G | C | 3 | a0001c0001t0001g0119a0001c0001t0002g0118a0002c0005t0001g0117 | 3 | NA18942.hp2 NA19000.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.18+6455G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700731 | ||||||
| chr11:128700770
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+6494G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700770 | ||||||
| chr11:128700881
|
A | G | 2 | a0001c0002t0005g0096a0001c0011t0003g0093 | 2 | HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+6605A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700881 | ||||||
| chr11:128700903
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.18+6627G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128700903 | ||||||
| chr11:128701019
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.18+6743G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701019 | ||||||
| chr11:128701040
|
C | T | 1 | a0001c0003t0001g0197 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.18+6764C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701040 | ||||||
| chr11:128701146
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+6870T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701146 | ||||||
| chr11:128701148
|
A | G | 177 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(174): Show | 180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.18+6872A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701148 | ||||||
| chr11:128701185
|
T | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(175): Show | 181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.18+6909T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701185 | ||||||
| chr11:128701329
|
GA | G | 178 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(175): Show | 181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.18+7063delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128701329 | |||||
| chr11:128701362
|
A | G | 181 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(178): Show | 184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.18+7086A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701362 | ||||||
| chr11:128701533
|
C | A | 1 | a0001c0001t0004g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.18+7257C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701533 | ||||||
| chr11:128701749
|
C | A | 27 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0121others(24): Show | 27 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+7473C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701749 | ||||||
| chr11:128701761
|
G | C | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+7485G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701761 | ||||||
| chr11:128701815
|
T | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.18+7539T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701815 | ||||||
| chr11:128701881
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.18+7605T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701881 | ||||||
| chr11:128701899
|
C | T | 1 | a0001c0004t0001g0267 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+7623C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701899 | ||||||
| chr11:128702269
|
A | T | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+7993A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128702269 | ||||||
| chr11:128702359
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.18+8083C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128702359 | ||||||
| chr11:128702499
|
G | A | 2 | a0001c0001t0005g0284a0001c0002t0001g0285 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+8223G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128702499 | ||||||
| chr11:128702790
|
A | T | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+8514A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128702790 | ||||||
| chr11:128702865
|
G | GAA | 124 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(121): Show | 126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.18+8602_18+8603dup others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128702865 | |||||
| chr11:128702865
|
G | GAAA | 13 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0258others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.18+8601_18+8603dup others(3): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128702865 | |||||
| chr11:128702865
|
G | GAAAA | 42 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(39): Show | 43 | HG00639.hp2 HG01261.hp1 HG01993.hp1 others(40): Show |
intron_variant | MODIFIER | c.18+8600_18+8603dup others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128702865 | |||||
| chr11:128703248
|
T | C | 1 | a0001c0011t0003g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.18+8972T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703248 | ||||||
| chr11:128703490
|
C | T | 46 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(43): Show | 47 | HG00639.hp2 HG01261.hp1 HG01993.hp1 others(44): Show |
intron_variant | MODIFIER | c.18+9214C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703490 | ||||||
| chr11:128703567
|
G | A | 3 | a0001c0001t0005g0280a0001c0001t0005g0281a0001c0001t0005g0282 | 3 | HG02818.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.18+9291G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703567 | ||||||
| chr11:128703610
|
C | T | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.18+9334C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703610 | ||||||
| chr11:128703678
|
A | G | 7 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+9402A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703678 | ||||||
| chr11:128703725
|
C | G | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+9449C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703725 | ||||||
| chr11:128703757
|
C | T | 1 | a0001c0004t0003g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+9481C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703757 | ||||||
| chr11:128703791
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0002g0221a0001c0003t0006g0004others(1): Show | 5 | NA18983.hp1 NA18991.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+9515C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703791 | ||||||
| chr11:128703811
|
C | G | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+9535C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703811 | ||||||
| chr11:128703830
|
G | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0005g0210others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+9554G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703830 | ||||||
| chr11:128703837
|
C | T | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.18+9561C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703837 | ||||||
| chr11:128703842
|
C | CA | 82 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(79): Show | 82 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+9587dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128703842 | |||||
| chr11:128703842
|
C | CAA | 45 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0037others(42): Show | 47 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.18+9586_18+9587dup others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128703842 | |||||
| chr11:128703842
|
C | CAAA | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(5): Show | 8 | HG01243.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+9585_18+9587dup others(3): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128703842 | |||||
| chr11:128703857
|
A | C | 3 | a0001c0001t0001g0137a0001c0001t0002g0139a0001c0001t0004g0138 | 3 | NA18939.hp2 NA18947.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.18+9581A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703857 | ||||||
| chr11:128703862
|
AAC | A | 10 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0272others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+9588_18+9589del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128703862 | |||||
| chr11:128703863
|
A | C | 5 | a0001c0001t0001g0006a0001c0001t0005g0280a0001c0001t0005g0281others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+9587A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703863 | ||||||
| chr11:128703863
|
AC | A | 71 | a0001c0001t0001g0106a0001c0001t0001g0222a0001c0001t0001g0230others(68): Show | 72 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.18+9588delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703863 | ||||||
| chr11:128703864
|
C | A | 222 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(219): Show | 224 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.18+9588C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703864 | ||||||
| chr11:128704220
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+9944G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704220 | ||||||
| chr11:128704255
|
C | T | 71 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0222others(68): Show | 72 | HG00099.hp2 HG00639.hp2 HG01167.hp2 others(69): Show |
intron_variant | MODIFIER | c.18+9979C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704255 | ||||||
| chr11:128704278
|
G | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(174): Show | 180 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.18+10002G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704278 | ||||||
| chr11:128704291
|
AC | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0224others(9): Show | 12 | HG02109.hp1 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+10018delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128704291 | |||||
| chr11:128704349
|
G | C | 1 | a0001c0001t0004g0229 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.18+10073G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704349 | ||||||
| chr11:128704457
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+10181G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704457 | ||||||
| chr11:128704782
|
C | A | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+10506C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704782 | ||||||
| chr11:128704960
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.18+10684A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704960 | ||||||
| chr11:128704962
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.18+10686G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128704962 | ||||||
| chr11:128705086
|
G | C | 1 | a0001c0001t0002g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.18+10810G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705086 | ||||||
| chr11:128705105
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.18+10829A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705105 | ||||||
| chr11:128705129
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.18+10853G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705129 | ||||||
| chr11:128705155
|
T | A | 4 | a0001c0001t0001g0224a0001c0002t0001g0216a0001c0003t0001g0217others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+10879T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705155 | ||||||
| chr11:128705237
|
G | A | 35 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0295others(32): Show | 35 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.18+10961G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705237 | ||||||
| chr11:128705237
|
G | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+10961G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705237 | ||||||
| chr11:128705348
|
A | G | 1 | a0001c0002t0002g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.18+11072A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705348 | ||||||
| chr11:128705437
|
C | G | 51 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(48): Show | 52 | HG00639.hp2 HG01261.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.18+11161C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705437 | ||||||
| chr11:128705448
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(102): Show | 107 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.18+11172G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705448 | ||||||
| chr11:128705535
|
T | A | 53 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(50): Show | 54 | HG00639.hp2 HG01261.hp1 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.18+11259T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705535 | ||||||
| chr11:128705602
|
G | A | 1 | a0001c0003t0003g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+11326G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705602 | ||||||
| chr11:128705714
|
C | G | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+11438C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705714 | ||||||
| chr11:128705878
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+11602C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705878 | ||||||
| chr11:128705879
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.18+11603G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128705879 | ||||||
| chr11:128706109
|
T | G | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+11833T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706109 | ||||||
| chr11:128706112
|
A | T | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+11836A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706112 | ||||||
| chr11:128706244
|
C | G | 2 | a0001c0001t0005g0284a0001c0002t0001g0285 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+11968C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706244 | ||||||
| chr11:128706278
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+12002C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706278 | ||||||
| chr11:128706297
|
C | T | 1 | a0002c0005t0001g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.18+12021C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706297 | ||||||
| chr11:128706499
|
C | A | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+12223C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706499 | ||||||
| chr11:128706637
|
A | T | 2 | a0001c0001t0005g0284a0001c0002t0001g0285 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+12361A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706637 | ||||||
| chr11:128706727
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+12451C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706727 | ||||||
| chr11:128706767
|
T | C | 8 | a0001c0001t0001g0226a0001c0001t0001g0230a0001c0001t0001g0232others(5): Show | 8 | HG02129.hp1 NA18940.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+12491T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706767 | ||||||
| chr11:128706779
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.18+12503A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128706779 | ||||||
| chr11:128707068
|
G | A | 2 | a0001c0001t0002g0087a0001c0002t0001g0094 | 2 | HG01243.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.18+12792G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707068 | ||||||
| chr11:128707144
|
T | C | 52 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0227others(49): Show | 53 | HG00639.hp2 HG01261.hp1 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.18+12868T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707144 | ||||||
| chr11:128707185
|
A | G | 1 | a0001c0002t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.18+12909A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707185 | ||||||
| chr11:128707262
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+12986C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707262 | ||||||
| chr11:128707479
|
C | T | 1 | a0001c0003t0001g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.18+13203C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707479 | ||||||
| chr11:128707531
|
G | A | 1 | a0001c0001t0010g0090 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.18+13255G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707531 | ||||||
| chr11:128707576
|
C | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(106): Show | 111 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.18+13300C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707576 | ||||||
| chr11:128707577
|
T | G | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+13301T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707577 | ||||||
| chr11:128707587
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18+13311T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707587 | ||||||
| chr11:128707630
|
A | T | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+13354A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707630 | ||||||
| chr11:128707705
|
T | A | 2 | a0001c0001t0005g0284a0001c0002t0001g0285 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+13429T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707705 | ||||||
| chr11:128707729
|
G | C | 34 | a0001c0001t0001g0288a0001c0001t0001g0293a0001c0001t0001g0295others(31): Show | 34 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.18+13453G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707729 | ||||||
| chr11:128707814
|
C | A | 1 | a0001c0002t0002g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.18+13538C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707814 | ||||||
| chr11:128707844
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.18+13568T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707844 | ||||||
| chr11:128707946
|
A | T | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+13670A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128707946 | ||||||
| chr11:128708152
|
T | G | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.18+13876T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708152 | ||||||
| chr11:128708154
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18+13878C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708154 | ||||||
| chr11:128708185
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+13909C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708185 | ||||||
| chr11:128708262
|
T | C | 111 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(108): Show | 113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.18+13986T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708262 | ||||||
| chr11:128708282
|
A | G | 1 | a0001c0001t0004g0174 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.18+14006A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708282 | ||||||
| chr11:128708377
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+14101C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708377 | ||||||
| chr11:128708604
|
C | T | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+14328C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708604 | ||||||
| chr11:128708606
|
T | G | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+14330T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708606 | ||||||
| chr11:128708611
|
A | C | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+14335A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708611 | ||||||
| chr11:128708789
|
G | A | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+14513G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708789 | ||||||
| chr11:128708847
|
A | C | 1 | a0001c0001t0002g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.18+14571A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128708847 | ||||||
| chr11:128709526
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.18+15250C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128709526 | ||||||
| chr11:128709830
|
C | T | 8 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(5): Show | 8 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+15554C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128709830 | ||||||
| chr11:128710351
|
C | T | 2 | a0001c0002t0005g0096a0001c0011t0003g0093 | 2 | HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+16075C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710351 | ||||||
| chr11:128710360
|
C | G | 4 | a0001c0001t0005g0280a0001c0001t0005g0281a0001c0001t0005g0282others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+16084C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710360 | ||||||
| chr11:128710396
|
G | T | 1 | a0001c0001t0002g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.18+16120G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710396 | ||||||
| chr11:128710455
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.18+16179T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710455 | ||||||
| chr11:128710461
|
C | A | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+16185C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710461 | ||||||
| chr11:128710683
|
T | C | 2 | a0001c0001t0001g0019a0001c0002t0001g0030 | 2 | HG01109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.18+16407T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710683 | ||||||
| chr11:128710982
|
G | A | 1 | a0002c0005t0001g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.18+16706G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128710982 | ||||||
| chr11:128711156
|
A | C | 1 | a0001c0003t0003g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+16880A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128711156 | ||||||
| chr11:128711450
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0103 | 2 | NA18948.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.18+17174G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128711450 | ||||||
| chr11:128711667
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.18+17391C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128711667 | ||||||
| chr11:128711713
|
A | G | 4 | a0001c0001t0010g0090a0001c0002t0001g0002a0001c0002t0001g0091others(1): Show | 5 | HG02486.hp2 HG03195.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+17437A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128711713 | ||||||
| chr11:128711924
|
T | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0054 | 3 | HG00738.hp1 HG01261.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.18+17648T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128711924 | ||||||
| chr11:128712362
|
G | A | 2 | a0001c0002t0001g0296a0001c0003t0003g0311 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.18+18086G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712362 | ||||||
| chr11:128712379
|
T | C | 5 | a0001c0001t0001g0259a0001c0001t0002g0219a0001c0003t0003g0218others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+18103T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712379 | ||||||
| chr11:128712499
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.18+18223C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712499 | ||||||
| chr11:128712595
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+18319G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712595 | ||||||
| chr11:128712619
|
T | C | 26 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0259others(23): Show | 26 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+18343T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712619 | ||||||
| chr11:128712662
|
T | C | 11 | a0001c0001t0001g0106a0001c0001t0001g0224a0001c0001t0001g0260others(8): Show | 11 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.18+18386T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712662 | ||||||
| chr11:128712742
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0100others(11): Show | 14 | HG00642.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+18466C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712742 | ||||||
| chr11:128712968
|
T | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0113others(4): Show | 7 | HG01891.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+18692T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128712968 | ||||||
| chr11:128713049
|
C | T | 170 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.18+18773C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713049 | ||||||
| chr11:128713120
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+18844C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713120 | ||||||
| chr11:128713165
|
C | G | 39 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0089others(36): Show | 42 | HG01074.hp2 HG01081.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.18+18889C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713165 | ||||||
| chr11:128713359
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+19083C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713359 | ||||||
| chr11:128713458
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+19182G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713458 | ||||||
| chr11:128713615
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.18+19339G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713615 | ||||||
| chr11:128713616
|
C | CA | 14 | a0001c0001t0001g0019a0001c0001t0001g0230a0001c0001t0001g0273others(11): Show | 14 | HG01109.hp1 HG02015.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+19352dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128713616 | |||||
| chr11:128713680
|
T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+19404T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713680 | ||||||
| chr11:128713684
|
G | T | 1 | a0001c0001t0001g0297 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18+19408G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713684 | ||||||
| chr11:128713950
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.18+19674G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128713950 | ||||||
| chr11:128714080
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.18+19804C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714080 | ||||||
| chr11:128714205
|
G | GA | 34 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0142others(31): Show | 34 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.18+19950dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128714205 | |||||
| chr11:128714205
|
GA | G | 114 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0028others(111): Show | 117 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.18+19950delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128714205 | |||||
| chr11:128714216
|
A | C | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.18+19940A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714216 | ||||||
| chr11:128714221
|
A | C | 1 | a0001c0003t0001g0306 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.18+19945A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714221 | ||||||
| chr11:128714263
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18+19987G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714263 | ||||||
| chr11:128714315
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.18+20039C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714315 | ||||||
| chr11:128714425
|
C | T | 312 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(309): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.18+20149C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714425 | ||||||
| chr11:128714655
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.18+20379A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714655 | ||||||
| chr11:128714710
|
C | CT | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.18+20453dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128714710 | |||||
| chr11:128714710
|
C | CTT | 16 | a0001c0001t0001g0037a0001c0001t0001g0049a0001c0001t0001g0097others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.18+20452_18+20453d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128714710 | |||||
| chr11:128714770
|
G | A | 1 | a0002c0005t0001g0300 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.18+20494G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714770 | ||||||
| chr11:128714846
|
C | CCGTG | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+20570_18+20571i others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714846 | ||||||
| chr11:128714848
|
A | AGG | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+20572_18+20573i others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714848 | ||||||
| chr11:128714849
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+20573C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714849 | ||||||
| chr11:128714870
|
A | C | 79 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0033others(76): Show | 80 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.18+20594A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714870 | ||||||
| chr11:128714918
|
G | A | 301 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.18+20642G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714918 | ||||||
| chr11:128714929
|
A | G | 301 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.18+20653A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714929 | ||||||
| chr11:128715072
|
C | T | 2 | a0001c0001t0009g0255a0001c0002t0001g0256 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+20796C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715072 | ||||||
| chr11:128715100
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.18+20824C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715100 | ||||||
| chr11:128715132
|
G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+20856G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715132 | ||||||
| chr11:128715147
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.18+20871C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715147 | ||||||
| chr11:128715325
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0172 | 2 | HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.18+21049C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715325 | ||||||
| chr11:128715520
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+21244G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715520 | ||||||
| chr11:128715527
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+21251T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715527 | ||||||
| chr11:128715722
|
G | C | 2 | a0001c0001t0001g0184a0001c0001t0002g0204 | 2 | HG00140.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.18+21446G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715722 | ||||||
| chr11:128715754
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.18+21478A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128715754 | ||||||
| chr11:128716029
|
G | A | 53 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0037others(50): Show | 55 | HG00642.hp2 HG01074.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.18+21753G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716029 | ||||||
| chr11:128716128
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+21852G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716128 | ||||||
| chr11:128716131
|
G | T | 1 | a0001c0001t0002g0139 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.18+21855G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716131 | ||||||
| chr11:128716248
|
A | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0002g0243 | 3 | NA18975.hp2 NA18983.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.18+21972A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716248 | ||||||
| chr11:128716260
|
C | A | 155 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.18+21984C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716260 | ||||||
| chr11:128716367
|
G | C | 159 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.18+22091G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716367 | ||||||
| chr11:128716828
|
A | G | 1 | a0001c0004t0001g0298 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.18+22552A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716828 | ||||||
| chr11:128716873
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.18+22597C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716873 | ||||||
| chr11:128716925
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18+22649C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716925 | ||||||
| chr11:128717178
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0213a0001c0002t0001g0030others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+22902T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717178 | ||||||
| chr11:128717353
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+23077G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717353 | ||||||
| chr11:128717401
|
C | T | 3 | a0001c0001t0005g0284a0001c0003t0003g0035a0001c0004t0001g0009 | 3 | HG01891.hp2 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.18+23125C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717401 | ||||||
| chr11:128717508
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+23232C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717508 | ||||||
| chr11:128717516
|
C | T | 153 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.18+23240C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717516 | ||||||
| chr11:128717965
|
T | G | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+23689T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128717965 | ||||||
| chr11:128718058
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+23782T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128718058 | ||||||
| chr11:128718446
|
TC | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(72): Show | 76 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+24175delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128718446 | |||||
| chr11:128718720
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.18+24444G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128718720 | ||||||
| chr11:128718895
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+24619T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128718895 | ||||||
| chr11:128719062
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+24786T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719062 | ||||||
| chr11:128719278
|
T | TA | 118 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.18+25016dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719278 | |||||
| chr11:128719312
|
G | C | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+25036G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719312 | ||||||
| chr11:128719356
|
C | CGT | 5 | a0001c0001t0001g0097a0001c0001t0001g0297a0001c0001t0001g0310others(2): Show | 5 | HG02602.hp2 HG02630.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+25119_18+25120d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
C | CGTGT | 12 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0058others(9): Show | 13 | HG01081.hp2 HG01884.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+25117_18+25120d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
C | CGTGTGT | 31 | a0001c0001t0001g0033a0001c0001t0001g0149a0001c0001t0001g0150others(28): Show | 32 | HG00558.hp1 HG00639.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.18+25115_18+25120d others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
C | CGTGTGTG others(1): Show |
16 | a0001c0001t0001g0059a0001c0001t0001g0182a0001c0001t0001g0244others(13): Show | 16 | HG00438.hp1 HG00673.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+25113_18+25120d others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
C | CGTGTGTG others(3): Show |
5 | a0001c0001t0001g0060a0001c0001t0001g0154a0001c0001t0001g0208others(2): Show | 5 | HG00408.hp1 HG01074.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+25111_18+25120d others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGT | C | 11 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+25119_18+25120d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGT | C | 8 | a0001c0001t0001g0089a0001c0001t0001g0156a0001c0001t0001g0259others(5): Show | 8 | HG02572.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+25117_18+25120d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGT | C | 10 | a0001c0001t0005g0281a0001c0001t0005g0282a0001c0001t0005g0284others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+25115_18+25120d others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0049others(23): Show | 26 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+25113_18+25120d others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGTG others(3): Show |
C | 12 | a0001c0001t0001g0039a0001c0001t0001g0137a0001c0001t0001g0205others(9): Show | 12 | HG00408.hp2 HG02622.hp1 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+25111_18+25120d others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGTG others(5): Show |
C | 166 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.18+25109_18+25120d others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0001g0022a0001c0002t0001g0094 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.18+25105_18+25120d others(18): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719356
|
CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0001g0263a0001c0001t0002g0265 | 2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.18+25103_18+25120d others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128719356 | |||||
| chr11:128719487
|
T | C | 2 | a0001c0001t0001g0022a0001c0002t0001g0094 | 2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.18+25211T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719487 | ||||||
| chr11:128719577
|
C | T | 117 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.18+25301C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719577 | ||||||
| chr11:128719604
|
G | T | 1 | a0001c0003t0001g0306 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.18+25328G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719604 | ||||||
| chr11:128719607
|
G | A | 54 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(51): Show | 56 | HG00597.hp1 HG00597.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.18+25331G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719607 | ||||||
| chr11:128719866
|
G | C | 94 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(91): Show | 96 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.18+25590G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128719866 | ||||||
| chr11:128720052
|
G | C | 298 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(295): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.18+25776G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720052 | ||||||
| chr11:128720428
|
C | T | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+26152C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720428 | ||||||
| chr11:128720449
|
T | C | 2 | a0001c0001t0001g0254a0001c0001t0004g0122 | 2 | NA18954.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.18+26173T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720449 | ||||||
| chr11:128720580
|
G | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+26304G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720580 | ||||||
| chr11:128720621
|
A | T | 1 | a0001c0003t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.18+26345A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720621 | ||||||
| chr11:128720688
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18+26412T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720688 | ||||||
| chr11:128720771
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+26495C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720771 | ||||||
| chr11:128720990
|
C | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG01261.hp2 HG02300.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.18+26714C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128720990 | ||||||
| chr11:128721381
|
A | G | 9 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0233others(6): Show | 9 | HG00408.hp1 HG00438.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+27105A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128721381 | ||||||
| chr11:128721702
|
T | G | 297 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.18+27426T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128721702 | ||||||
| chr11:128721715
|
G | A | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.18+27439G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128721715 | ||||||
| chr11:128721974
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0274a0001c0001t0005g0027others(2): Show | 5 | HG00642.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+27698A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128721974 | ||||||
| chr11:128722137
|
G | A | 92 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(89): Show | 94 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.18+27861G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722137 | ||||||
| chr11:128722339
|
G | A | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+28063G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722339 | ||||||
| chr11:128722354
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.18+28078C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722354 | ||||||
| chr11:128722420
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.18+28144C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722420 | ||||||
| chr11:128722497
|
C | T | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0262others(1): Show | 4 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+28221C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722497 | ||||||
| chr11:128722617
|
C | T | 1 | a0001c0004t0001g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.18+28341C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722617 | ||||||
| chr11:128722636
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0068a0001c0001t0001g0126others(1): Show | 4 | HG00558.hp2 HG00609.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+28360T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722636 | ||||||
| chr11:128722649
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0005g0280 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+28373T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722649 | ||||||
| chr11:128722742
|
A | G | 297 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.18+28466A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722742 | ||||||
| chr11:128722822
|
G | A | 2 | a0001c0001t0001g0324a0001c0004t0003g0041 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.18+28546G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722822 | ||||||
| chr11:128722932
|
C | T | 92 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(89): Show | 94 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.18+28656C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722932 | ||||||
| chr11:128722995
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+28719T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128722995 | ||||||
| chr11:128723119
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18+28843G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723119 | ||||||
| chr11:128723167
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0002g0065a0001c0001t0002g0131others(1): Show | 4 | NA18953.hp2 NA18969.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+28891C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723167 | ||||||
| chr11:128723291
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+29015C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723291 | ||||||
| chr11:128723293
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0310a0001c0001t0002g0081others(1): Show | 4 | HG00735.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+29017G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723293 | ||||||
| chr11:128723329
|
A | G | 1 | a0001c0003t0003g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+29053A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723329 | ||||||
| chr11:128723386
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(62): Show | 67 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+29110A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723386 | ||||||
| chr11:128723388
|
G | A | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0262others(1): Show | 4 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+29112G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723388 | ||||||
| chr11:128723598
|
G | A | 297 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.18+29322G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723598 | ||||||
| chr11:128723651
|
G | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(78): Show | 83 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.18+29375G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723651 | ||||||
| chr11:128723912
|
G | T | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.18+29636G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723912 | ||||||
| chr11:128723933
|
A | AT | 61 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0057others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+29683dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128723933 | |||||
| chr11:128723933
|
A | ATT | 54 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0050others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.18+29682_18+29683d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128723933 | |||||
| chr11:128723933
|
A | ATTT | 13 | a0001c0001t0001g0048a0001c0001t0001g0260a0001c0001t0001g0261others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+29681_18+29683d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128723933 | |||||
| chr11:128723933
|
AT | A | 87 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(84): Show | 89 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.18+29683delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128723933 | |||||
| chr11:128723982
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+29706G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128723982 | ||||||
| chr11:128724266
|
C | T | 118 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.18+29990C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724266 | ||||||
| chr11:128724282
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0002g0317 | 2 | HG00099.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.18+30006C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724282 | ||||||
| chr11:128724310
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+30034C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724310 | ||||||
| chr11:128724334
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.18+30058G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724334 | ||||||
| chr11:128724714
|
C | T | 1 | a0001c0003t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.18+30438C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724714 | ||||||
| chr11:128724735
|
G | T | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.18+30459G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724735 | ||||||
| chr11:128724765
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0002g0320a0002c0005t0001g0191 | 3 | HG02056.hp1 HG02148.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.18+30489G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724765 | ||||||
| chr11:128724956
|
C | T | 297 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.18+30680C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724956 | ||||||
| chr11:128724980
|
G | A | 175 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 179 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.18+30704G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724980 | ||||||
| chr11:128724989
|
C | T | 2 | a0001c0002t0001g0030a0001c0003t0003g0013 | 2 | HG01109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.18+30713C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724989 | ||||||
| chr11:128725067
|
G | A | 1 | a0001c0003t0001g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.18+30791G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725067 | ||||||
| chr11:128725094
|
G | C | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+30818G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725094 | ||||||
| chr11:128725274
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+30998A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725274 | ||||||
| chr11:128725278
|
A | G | 175 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 179 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.18+31002A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725278 | ||||||
| chr11:128725399
|
C | T | 1 | a0001c0003t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.18+31123C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725399 | ||||||
| chr11:128725638
|
TTCTCTCT others(5): Show |
T | 4 | a0001c0001t0001g0012a0001c0001t0001g0068a0001c0001t0001g0126others(1): Show | 4 | HG00558.hp2 HG00609.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+31371_18+31382d others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128725638 | |||||
| chr11:128725643
|
TCTCC | T | 188 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0026others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.18+31371_18+31374d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128725643 | |||||
| chr11:128725645
|
TCC | T | 91 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(88): Show | 93 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.18+31371_18+31372d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128725645 | |||||
| chr11:128725647
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0079a0001c0001t0001g0100others(11): Show | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+31371C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725647 | ||||||
| chr11:128725662
|
C | G | 66 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0062others(63): Show | 68 | HG00597.hp1 HG00597.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.18+31386C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725662 | ||||||
| chr11:128725662
|
CTGTG | C | 3 | a0001c0001t0001g0211a0001c0001t0005g0210a0001c0001t0005g0212 | 3 | HG02615.hp1 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.18+31396_18+31399d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128725662 | |||||
| chr11:128725664
|
G | C | 194 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.18+31388G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725664 | ||||||
| chr11:128725666
|
G | C | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.18+31390G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725666 | ||||||
| chr11:128725778
|
C | T | 3 | a0001c0001t0017g0303a0001c0002t0001g0296a0001c0003t0003g0311 | 3 | HG01258.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.18+31502C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725778 | ||||||
| chr11:128725984
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18+31708C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128725984 | ||||||
| chr11:128726122
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.18+31846G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726122 | ||||||
| chr11:128726320
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.19-31795T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726320 | ||||||
| chr11:128726376
|
G | A | 83 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(80): Show | 85 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.19-31739G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726376 | ||||||
| chr11:128726474
|
T | A | 52 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0062others(49): Show | 54 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-31641T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726474 | ||||||
| chr11:128726526
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.19-31589C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726526 | ||||||
| chr11:128726629
|
G | A | 1 | a0001c0003t0001g0128 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.19-31486G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726629 | ||||||
| chr11:128726937
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(84): Show | 88 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.19-31178G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128726937 | ||||||
| chr11:128727003
|
A | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(17): Show | 20 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.19-31112A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727003 | ||||||
| chr11:128727101
|
T | C | 2 | a0001c0003t0003g0008a0001c0004t0003g0283 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.19-31014T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727101 | ||||||
| chr11:128727120
|
A | T | 293 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.19-30995A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727120 | ||||||
| chr11:128727151
|
A | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.19-30964A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727151 | ||||||
| chr11:128727262
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-30853G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727262 | ||||||
| chr11:128727418
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.19-30697G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727418 | ||||||
| chr11:128727467
|
G | A | 15 | a0001c0001t0001g0028a0001c0001t0001g0059a0001c0001t0001g0149others(12): Show | 15 | HG00639.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-30648G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727467 | ||||||
| chr11:128727505
|
G | A | 95 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(92): Show | 97 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.19-30610G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727505 | ||||||
| chr11:128727549
|
G | C | 65 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0058others(62): Show | 66 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.19-30566G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727549 | ||||||
| chr11:128727647
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0208 | 2 | HG01074.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-30468C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727647 | ||||||
| chr11:128727822
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0012t0015g0084 | 3 | HG01891.hp1 HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.19-30293C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727822 | ||||||
| chr11:128727860
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.19-30255T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727860 | ||||||
| chr11:128727912
|
G | T | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-30203G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727912 | ||||||
| chr11:128727965
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-30150A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727965 | ||||||
| chr11:128728102
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0004g0308 | 2 | HG01175.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.19-30013G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728102 | ||||||
| chr11:128728163
|
C | T | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-29952C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728163 | ||||||
| chr11:128728174
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.19-29941G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728174 | ||||||
| chr11:128728381
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.19-29734C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728381 | ||||||
| chr11:128728382
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-29733G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728382 | ||||||
| chr11:128728386
|
T | C | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-29729T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728386 | ||||||
| chr11:128728553
|
G | A | 1 | a0001c0003t0003g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-29562G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728553 | ||||||
| chr11:128728731
|
A | G | 1 | a0001c0002t0001g0315 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.19-29384A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728731 | ||||||
| chr11:128728915
|
C | A | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-29200C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728915 | ||||||
| chr11:128728920
|
A | G | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-29195A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128728920 | ||||||
| chr11:128729127
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-28988G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128729127 | ||||||
| chr11:128729165
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.19-28950G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128729165 | ||||||
| chr11:128729313
|
G | C | 2 | a0001c0002t0001g0001a0001c0002t0001g0216 | 3 | HG02922.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-28802G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128729313 | ||||||
| chr11:128729710
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.19-28405A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128729710 | ||||||
| chr11:128730061
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-28054G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730061 | ||||||
| chr11:128730155
|
C | A | 4 | a0001c0001t0001g0022a0001c0002t0001g0141a0001c0004t0001g0009others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-27960C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730155 | ||||||
| chr11:128730311
|
C | T | 289 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(286): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.19-27804C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730311 | ||||||
| chr11:128730372
|
T | C | 3 | a0001c0001t0001g0098a0001c0002t0001g0052a0001c0003t0001g0072 | 3 | NA18981.hp1 NA18999.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.19-27743T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730372 | ||||||
| chr11:128730407
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0068a0001c0002t0002g0043 | 3 | HG00609.hp2 HG02083.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.19-27708G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730407 | ||||||
| chr11:128730486
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-27629G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730486 | ||||||
| chr11:128730702
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0100a0001c0001t0001g0213others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-27413G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730702 | ||||||
| chr11:128730832
|
G | A | 6 | a0001c0001t0001g0019a0001c0002t0001g0094a0001c0003t0003g0008others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-27283G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730832 | ||||||
| chr11:128730855
|
C | T | 293 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.19-27260C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730855 | ||||||
| chr11:128730979
|
G | A | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-27136G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128730979 | ||||||
| chr11:128731052
|
G | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.19-27063G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731052 | ||||||
| chr11:128731204
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.19-26911T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731204 | ||||||
| chr11:128731300
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.19-26815A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731300 | ||||||
| chr11:128731303
|
TG | T | 59 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0058others(56): Show | 60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.19-26805delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128731303 | |||||
| chr11:128731310
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.19-26805G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731310 | ||||||
| chr11:128731479
|
C | CT | 289 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.19-26626dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128731479 | |||||
| chr11:128731622
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19-26493A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731622 | ||||||
| chr11:128731688
|
G | A | 2 | a0001c0002t0001g0001a0001c0002t0001g0216 | 3 | HG02922.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-26427G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731688 | ||||||
| chr11:128731725
|
G | T | 293 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.19-26390G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731725 | ||||||
| chr11:128731831
|
T | C | 62 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(59): Show | 64 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-26284T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731831 | ||||||
| chr11:128731860
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19-26255T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731860 | ||||||
| chr11:128731896
|
C | T | 62 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(59): Show | 64 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-26219C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731896 | ||||||
| chr11:128731897
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-26218G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731897 | ||||||
| chr11:128731975
|
G | C | 293 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.19-26140G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731975 | ||||||
| chr11:128731995
|
T | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0216 | 3 | HG01074.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-26120T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731995 | ||||||
| chr11:128732002
|
C | CA | 275 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.19-26102dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128732002 | |||||
| chr11:128732002
|
C | CAA | 7 | a0001c0001t0001g0022a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-26103_19-26102d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128732002 | |||||
| chr11:128732009
|
A | AG | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-26106_19-26105i others(3): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732009 | ||||||
| chr11:128732251
|
C | T | 62 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(59): Show | 64 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-25864C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732251 | ||||||
| chr11:128732267
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0157a0001c0001t0001g0257others(3): Show | 7 | HG00673.hp2 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-25848G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732267 | ||||||
| chr11:128732338
|
G | A | 1 | a0001c0001t0008g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.19-25777G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732338 | ||||||
| chr11:128732579
|
T | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.19-25536T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732579 | ||||||
| chr11:128732612
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0244 | 2 | NA18975.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.19-25503C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732612 | ||||||
| chr11:128732889
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0240 | 2 | HG00597.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.19-25226G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732889 | ||||||
| chr11:128732932
|
A | G | 60 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(57): Show | 61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.19-25183A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128732932 | ||||||
| chr11:128733076
|
A | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-25039A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733076 | ||||||
| chr11:128733098
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-25017T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733098 | ||||||
| chr11:128733129
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0094 | 3 | HG01074.hp1 HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19-24986G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733129 | ||||||
| chr11:128733176
|
GT | G | 287 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.19-24928delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128733176 | |||||
| chr11:128733250
|
T | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.19-24865T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733250 | ||||||
| chr11:128733253
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19-24862A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733253 | ||||||
| chr11:128733314
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0216 | 3 | HG01074.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-24801C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733314 | ||||||
| chr11:128733417
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.19-24698C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733417 | ||||||
| chr11:128733508
|
C | T | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-24607C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733508 | ||||||
| chr11:128733633
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-24482C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733633 | ||||||
| chr11:128733877
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.19-24238C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733877 | ||||||
| chr11:128733946
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.19-24169G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128733946 | ||||||
| chr11:128734115
|
C | T | 228 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.19-24000C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734115 | ||||||
| chr11:128734127
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.19-23988G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734127 | ||||||
| chr11:128734159
|
G | T | 2 | a0001c0001t0002g0231a0001c0003t0001g0162 | 2 | HG02129.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.19-23956G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734159 | ||||||
| chr11:128734160
|
G | T | 8 | a0001c0001t0001g0089a0001c0001t0001g0156a0001c0001t0001g0259others(5): Show | 8 | HG02572.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-23955G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734160 | ||||||
| chr11:128734196
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-23919G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734196 | ||||||
| chr11:128734270
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.19-23845C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734270 | ||||||
| chr11:128734271
|
G | A | 1 | a0001c0004t0003g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-23844G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734271 | ||||||
| chr11:128734279
|
C | T | 139 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0020others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.19-23836C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734279 | ||||||
| chr11:128734304
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.19-23811C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734304 | ||||||
| chr11:128734337
|
G | T | 117 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.19-23778G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734337 | ||||||
| chr11:128734370
|
G | A | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0022others(111): Show | 116 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.19-23745G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734370 | ||||||
| chr11:128734490
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 13 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-23625G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734490 | ||||||
| chr11:128734561
|
G | A | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-23554G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734561 | ||||||
| chr11:128734808
|
C | T | 2 | a0001c0003t0003g0008a0001c0004t0003g0283 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.19-23307C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734808 | ||||||
| chr11:128734860
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-23255C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734860 | ||||||
| chr11:128734988
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-23127G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734988 | ||||||
| chr11:128735048
|
G | A | 1 | a0001c0002t0005g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-23067G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735048 | ||||||
| chr11:128735165
|
T | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0288a0001c0001t0005g0038others(8): Show | 11 | HG01123.hp2 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-22950T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735165 | ||||||
| chr11:128735185
|
T | C | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-22930T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735185 | ||||||
| chr11:128735274
|
T | A | 175 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(172): Show | 179 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.19-22841T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735274 | ||||||
| chr11:128735304
|
T | C | 292 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(289): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.19-22811T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735304 | ||||||
| chr11:128735405
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-22710G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735405 | ||||||
| chr11:128735583
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-22532G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735583 | ||||||
| chr11:128735659
|
G | A | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-22456G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735659 | ||||||
| chr11:128735706
|
C | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0089others(15): Show | 18 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-22409C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735706 | ||||||
| chr11:128735830
|
A | T | 1 | a0001c0003t0001g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19-22285A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735830 | ||||||
| chr11:128735939
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19-22176G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735939 | ||||||
| chr11:128735961
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0010g0090others(5): Show | 9 | HG01099.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-22154T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128735961 | ||||||
| chr11:128736179
|
G | A | 1 | a0001c0002t0001g0164 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.19-21936G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128736179 | ||||||
| chr11:128736437
|
T | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0173 | 3 | HG01074.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19-21678T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128736437 | ||||||
| chr11:128736452
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.19-21663G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128736452 | ||||||
| chr11:128736613
|
C | T | 118 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.19-21502C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128736613 | ||||||
| chr11:128736809
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0173 | 3 | HG01074.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19-21306T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128736809 | ||||||
| chr11:128737143
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(10): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-20972T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737143 | ||||||
| chr11:128737166
|
G | T | 51 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0058others(48): Show | 52 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.19-20949G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737166 | ||||||
| chr11:128737188
|
G | C | 62 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(59): Show | 64 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-20927G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737188 | ||||||
| chr11:128737237
|
C | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0208a0001c0002t0001g0173 | 3 | HG01074.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19-20878C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737237 | ||||||
| chr11:128737345
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-20770C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737345 | ||||||
| chr11:128737395
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-20720C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737395 | ||||||
| chr11:128737406
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.19-20709G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737406 | ||||||
| chr11:128737424
|
A | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-20691A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737424 | ||||||
| chr11:128737457
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0208 | 2 | HG01074.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-20658T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737457 | ||||||
| chr11:128737572
|
G | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0089others(15): Show | 18 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-20543G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737572 | ||||||
| chr11:128737701
|
A | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0113others(12): Show | 15 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-20414A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737701 | ||||||
| chr11:128737714
|
T | C | 296 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(293): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.19-20401T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737714 | ||||||
| chr11:128737716
|
T | C | 2 | a0001c0001t0001g0324a0001c0004t0003g0041 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.19-20399T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737716 | ||||||
| chr11:128737723
|
G | T | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-20392G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737723 | ||||||
| chr11:128737799
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19-20316G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737799 | ||||||
| chr11:128737799
|
G | C | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-20316G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737799 | ||||||
| chr11:128737799
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.19-20316G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737799 | ||||||
| chr11:128737824
|
A | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0089others(15): Show | 18 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-20291A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737824 | ||||||
| chr11:128737831
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-20284C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737831 | ||||||
| chr11:128737840
|
T | C | 9 | a0001c0001t0001g0211a0001c0001t0002g0031a0001c0001t0002g0104others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20275T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737840 | ||||||
| chr11:128737863
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0100a0001c0001t0001g0213others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-20252C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128737863 | ||||||
| chr11:128738014
|
G | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0089others(15): Show | 18 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-20101G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738014 | ||||||
| chr11:128738099
|
A | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.19-20016A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738099 | ||||||
| chr11:128738168
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-19947C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738168 | ||||||
| chr11:128738346
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-19769C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738346 | ||||||
| chr11:128738359
|
G | C | 1 | a0001c0001t0005g0284 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.19-19756G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738359 | ||||||
| chr11:128738370
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-19745C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738370 | ||||||
| chr11:128738382
|
C | T | 1 | a0001c0002t0005g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-19733C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738382 | ||||||
| chr11:128738536
|
G | T | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-19579G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738536 | ||||||
| chr11:128738598
|
C | A | 1 | a0001c0001t0002g0118 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-19517C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738598 | ||||||
| chr11:128738756
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0004g0122 | 2 | NA18954.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.19-19359G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738756 | ||||||
| chr11:128738759
|
G | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-19356G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738759 | ||||||
| chr11:128738834
|
C | G | 18 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0089others(15): Show | 18 | HG01074.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-19281C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738834 | ||||||
| chr11:128738857
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.19-19258G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128738857 | ||||||
| chr11:128739124
|
A | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(10): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-18991A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739124 | ||||||
| chr11:128739197
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.19-18918G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739197 | ||||||
| chr11:128739397
|
C | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0113others(12): Show | 15 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-18718C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739397 | ||||||
| chr11:128739427
|
C | A | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-18688C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739427 | ||||||
| chr11:128739432
|
CT | C | 3 | a0001c0002t0001g0203a0001c0003t0001g0128a0001c0003t0001g0313 | 3 | HG01975.hp1 HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.19-18682delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739432 | ||||||
| chr11:128739500
|
A | C | 16 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0113others(13): Show | 16 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-18615A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739500 | ||||||
| chr11:128739610
|
G | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0048others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.19-18505G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739610 | ||||||
| chr11:128739614
|
T | G | 16 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0113others(13): Show | 16 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-18501T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739614 | ||||||
| chr11:128739679
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-18436C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739679 | ||||||
| chr11:128739730
|
G | GA | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-18376dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128739730 | |||||
| chr11:128739958
|
G | T | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-18157G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739958 | ||||||
| chr11:128739995
|
C | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0288a0001c0001t0005g0038others(8): Show | 11 | HG01123.hp2 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-18120C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739995 | ||||||
| chr11:128739996
|
G | A | 2 | a0001c0001t0004g0174a0001c0002t0001g0101 | 2 | NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.19-18119G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128739996 | ||||||
| chr11:128740096
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-18019C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740096 | ||||||
| chr11:128740110
|
T | C | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-18005T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740110 | ||||||
| chr11:128740266
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.19-17849A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740266 | ||||||
| chr11:128740285
|
T | C | 1 | a0001c0009t0001g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.19-17830T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740285 | ||||||
| chr11:128740368
|
C | T | 273 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(270): Show | 277 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.19-17747C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740368 | ||||||
| chr11:128740416
|
T | C | 57 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0033others(54): Show | 59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-17699T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740416 | ||||||
| chr11:128740442
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(10): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-17673G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740442 | ||||||
| chr11:128740461
|
C | T | 113 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.19-17654C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740461 | ||||||
| chr11:128740716
|
A | G | 1 | a0001c0001t0002g0292 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.19-17399A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740716 | ||||||
| chr11:128740780
|
C | T | 1 | a0001c0003t0001g0270 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-17335C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740780 | ||||||
| chr11:128740992
|
C | A | 93 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(90): Show | 94 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.19-17123C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128740992 | ||||||
| chr11:128741008
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(10): Show | 13 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-17107C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741008 | ||||||
| chr11:128741009
|
G | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0224others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-17106G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741009 | ||||||
| chr11:128741094
|
T | C | 4 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0218others(1): Show | 5 | HG01884.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-17021T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741094 | ||||||
| chr11:128741130
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.19-16985A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741130 | ||||||
| chr11:128741168
|
C | G | 2 | a0001c0002t0001g0203a0001c0003t0001g0313 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.19-16947C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741168 | ||||||
| chr11:128741265
|
C | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(16): Show | 19 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-16850C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741265 | ||||||
| chr11:128741266
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-16849G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741266 | ||||||
| chr11:128741286
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-16829G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741286 | ||||||
| chr11:128741308
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0224others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-16807G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741308 | ||||||
| chr11:128741329
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0086a0001c0001t0001g0185others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-16786G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741329 | ||||||
| chr11:128741388
|
G | A | 292 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(289): Show | 296 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.19-16727G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741388 | ||||||
| chr11:128741440
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-16675C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741440 | ||||||
| chr11:128741461
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-16654C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741461 | ||||||
| chr11:128741475
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-16640G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741475 | ||||||
| chr11:128741568
|
C | T | 4 | a0001c0001t0001g0293a0001c0001t0002g0054a0001c0001t0002g0290others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-16547C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741568 | ||||||
| chr11:128741583
|
T | A | 1 | a0001c0001t0001g0310 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.19-16532T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741583 | ||||||
| chr11:128741583
|
T | C | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-16532T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741583 | ||||||
| chr11:128741623
|
G | A | 114 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.19-16492G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741623 | ||||||
| chr11:128741732
|
C | A | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-16383C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741732 | ||||||
| chr11:128741733
|
G | C | 191 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(188): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.19-16382G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741733 | ||||||
| chr11:128741891
|
C | T | 1 | a0001c0002t0002g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.19-16224C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741891 | ||||||
| chr11:128741896
|
G | T | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-16219G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741896 | ||||||
| chr11:128741993
|
G | C | 19 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0113others(16): Show | 19 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-16122G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741993 | ||||||
| chr11:128741998
|
T | C | 1 | a0001c0001t0017g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.19-16117T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128741998 | ||||||
| chr11:128742001
|
A | T | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-16114A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742001 | ||||||
| chr11:128742023
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(9): Show | 12 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-16092C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742023 | ||||||
| chr11:128742049
|
CTT | C | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0224others(2): Show | 5 | HG01891.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-16063_19-16062d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128742049 | |||||
| chr11:128742168
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-15947G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742168 | ||||||
| chr11:128742300
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0156others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-15815G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742300 | ||||||
| chr11:128742355
|
T | G | 292 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(289): Show | 296 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.19-15760T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742355 | ||||||
| chr11:128742569
|
A | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0226a0001c0001t0001g0230others(4): Show | 7 | HG00423.hp1 HG00609.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-15546A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742569 | ||||||
| chr11:128742642
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19-15473C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742642 | ||||||
| chr11:128742689
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-15426G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742689 | ||||||
| chr11:128742728
|
C | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-15387C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742728 | ||||||
| chr11:128742818
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0208 | 2 | HG01074.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-15297C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742818 | ||||||
| chr11:128742833
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0316a0001c0001t0002g0082others(4): Show | 7 | HG02129.hp2 HG02523.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-15282C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742833 | ||||||
| chr11:128742834
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-15281G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742834 | ||||||
| chr11:128742842
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0208 | 2 | HG01074.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.19-15273G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742842 | ||||||
| chr11:128743128
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0213a0001c0002t0001g0030others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-14987C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743128 | ||||||
| chr11:128743329
|
C | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-14786C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743329 | ||||||
| chr11:128743405
|
T | TA | 6 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0208others(3): Show | 6 | HG01074.hp1 HG02300.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-14689dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128743405 | |||||
| chr11:128743405
|
TA | T | 21 | a0001c0001t0001g0058a0001c0001t0001g0113a0001c0001t0001g0114others(18): Show | 22 | HG01169.hp2 HG01243.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.19-14689delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128743405 | |||||
| chr11:128743405
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-14700_19-14689d others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128743405 | |||||
| chr11:128743482
|
C | T | 2 | a0001c0003t0003g0008a0001c0004t0003g0283 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.19-14633C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743482 | ||||||
| chr11:128743501
|
A | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0226a0001c0001t0001g0230others(4): Show | 7 | HG00423.hp1 HG00609.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-14614A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743501 | ||||||
| chr11:128743559
|
A | G | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-14556A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743559 | ||||||
| chr11:128743583
|
GGA | G | 57 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0033others(54): Show | 59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-14529_19-14528d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128743583 | |||||
| chr11:128743727
|
G | GC | 57 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0033others(54): Show | 59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-14383dupC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128743727 | |||||
| chr11:128743733
|
A | G | 57 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0033others(54): Show | 59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-14382A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743733 | ||||||
| chr11:128743746
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(17): Show | 20 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.19-14369G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743746 | ||||||
| chr11:128743824
|
T | C | 75 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0062others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.19-14291T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743824 | ||||||
| chr11:128743837
|
G | A | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-14278G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743837 | ||||||
| chr11:128743846
|
C | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-14269C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743846 | ||||||
| chr11:128743889
|
C | A | 6 | a0001c0001t0001g0019a0001c0002t0001g0001a0001c0003t0003g0008others(3): Show | 7 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-14226C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743889 | ||||||
| chr11:128743993
|
T | C | 289 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(286): Show | 293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.19-14122T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128743993 | ||||||
| chr11:128744070
|
A | C | 1 | a0001c0004t0001g0239 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.19-14045A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744070 | ||||||
| chr11:128744108
|
G | A | 75 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0062others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.19-14007G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744108 | ||||||
| chr11:128744168
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0002g0046 | 2 | HG00621.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.19-13947C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744168 | ||||||
| chr11:128744171
|
G | A | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19-13944G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744171 | ||||||
| chr11:128744218
|
G | T | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-13897G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744218 | ||||||
| chr11:128744256
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.19-13859G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744256 | ||||||
| chr11:128744341
|
G | C | 210 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(207): Show | 212 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.19-13774G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744341 | ||||||
| chr11:128744485
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-13630T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744485 | ||||||
| chr11:128744516
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.19-13599A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744516 | ||||||
| chr11:128744551
|
C | T | 1 | a0001c0001t0017g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.19-13564C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744551 | ||||||
| chr11:128744571
|
T | C | 1 | a0001c0002t0005g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-13544T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744571 | ||||||
| chr11:128744662
|
C | G | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-13453C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744662 | ||||||
| chr11:128744781
|
A | C | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-13334A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744781 | ||||||
| chr11:128744786
|
A | T | 1 | a0001c0002t0001g0153 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19-13329A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128744786 | ||||||
| chr11:128745154
|
T | C | 78 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(75): Show | 80 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.19-12961T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745154 | ||||||
| chr11:128745253
|
CAG | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(33): Show | 36 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.19-12859_19-12858d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128745253 | |||||
| chr11:128745329
|
G | A | 2 | a0001c0002t0001g0209a0001c0004t0001g0009 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.19-12786G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745329 | ||||||
| chr11:128745484
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-12631G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745484 | ||||||
| chr11:128745591
|
A | G | 119 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.19-12524A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745591 | ||||||
| chr11:128745630
|
C | G | 2 | a0001c0009t0001g0143a0001c0010t0002g0312 | 2 | HG02165.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.19-12485C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745630 | ||||||
| chr11:128745740
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.19-12375C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128745740 | ||||||
| chr11:128746001
|
A | G | 2 | a0001c0002t0001g0094a0001c0002t0001g0173 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-12114A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746001 | ||||||
| chr11:128746385
|
C | T | 4 | a0001c0001t0005g0284a0001c0002t0001g0209a0001c0003t0003g0035others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-11730C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746385 | ||||||
| chr11:128746416
|
G | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.19-11699G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746416 | ||||||
| chr11:128746510
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19-11605A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746510 | ||||||
| chr11:128746564
|
C | T | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-11551C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746564 | ||||||
| chr11:128746637
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.19-11478C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746637 | ||||||
| chr11:128746638
|
G | A | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-11477G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746638 | ||||||
| chr11:128746699
|
C | T | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-11416C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746699 | ||||||
| chr11:128746708
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-11407A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746708 | ||||||
| chr11:128746774
|
A | C | 1 | a0001c0003t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-11341A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746774 | ||||||
| chr11:128746879
|
A | G | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-11236A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128746879 | ||||||
| chr11:128747141
|
C | A | 1 | a0002c0005t0001g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.19-10974C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747141 | ||||||
| chr11:128747144
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0273a0001c0001t0002g0010 | 3 | HG02056.hp2 NA18989.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.19-10971G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747144 | ||||||
| chr11:128747263
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.19-10852G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747263 | ||||||
| chr11:128747336
|
G | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.19-10779G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747336 | ||||||
| chr11:128747394
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-10721G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747394 | ||||||
| chr11:128747423
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0230a0001c0001t0001g0232 | 3 | NA18940.hp1 NA18967.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.19-10692T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747423 | ||||||
| chr11:128747468
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.19-10647T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747468 | ||||||
| chr11:128747623
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0005g0280a0001c0004t0001g0167 | 3 | HG01981.hp2 HG02818.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.19-10492G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747623 | ||||||
| chr11:128747744
|
G | T | 1 | a0001c0002t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-10371G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128747744 | ||||||
| chr11:128748131
|
T | C | 278 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(275): Show | 281 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.19-9984T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748131 | ||||||
| chr11:128748132
|
G | A | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-9983G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748132 | ||||||
| chr11:128748170
|
C | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0049others(24): Show | 27 | HG00642.hp2 HG00735.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.19-9945C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748170 | ||||||
| chr11:128748506
|
G | A | 1 | a0001c0001t0002g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.19-9609G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748506 | ||||||
| chr11:128748698
|
G | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-9417G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748698 | ||||||
| chr11:128748711
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0003t0003g0008 | 3 | HG02258.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19-9404G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748711 | ||||||
| chr11:128748763
|
C | A | 1 | a0001c0001t0002g0320 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.19-9352C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748763 | ||||||
| chr11:128748794
|
A | G | 73 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(70): Show | 75 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.19-9321A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748794 | ||||||
| chr11:128748975
|
T | C | 6 | a0001c0001t0005g0284a0001c0002t0001g0001a0001c0002t0001g0209others(3): Show | 7 | HG01891.hp2 HG02723.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-9140T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748975 | ||||||
| chr11:128748984
|
T | C | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-9131T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128748984 | ||||||
| chr11:128749019
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.19-9096G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749019 | ||||||
| chr11:128749048
|
C | T | 15 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0068others(12): Show | 15 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-9067C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749048 | ||||||
| chr11:128749355
|
G | C | 2 | a0001c0001t0001g0019a0001c0003t0003g0218 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.19-8760G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749355 | ||||||
| chr11:128749359
|
G | A | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-8756G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749359 | ||||||
| chr11:128749419
|
C | T | 71 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(68): Show | 73 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.19-8696C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749419 | ||||||
| chr11:128749426
|
C | T | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-8689C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749426 | ||||||
| chr11:128749488
|
C | T | 1 | a0001c0004t0001g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.19-8627C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749488 | ||||||
| chr11:128749546
|
C | T | 206 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(203): Show | 208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.19-8569C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749546 | ||||||
| chr11:128749673
|
T | C | 2 | a0001c0002t0001g0001a0001c0002t0001g0173 | 3 | HG03130.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19-8442T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749673 | ||||||
| chr11:128749798
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0002g0219a0001c0001t0012g0309others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-8317T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749798 | ||||||
| chr11:128749880
|
G | A | 151 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.19-8235G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749880 | ||||||
| chr11:128749896
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-8219G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749896 | ||||||
| chr11:128749937
|
C | T | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-8178C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749937 | ||||||
| chr11:128749940
|
A | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0173 | 3 | HG03130.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19-8175A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749940 | ||||||
| chr11:128749968
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0156a0001c0001t0001g0213others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8147G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128749968 | ||||||
| chr11:128750027
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-8088C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750027 | ||||||
| chr11:128750109
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0089others(9): Show | 13 | HG01243.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-8006G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750109 | ||||||
| chr11:128750169
|
C | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.19-7946C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750169 | ||||||
| chr11:128750237
|
C | T | 89 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(86): Show | 90 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.19-7878C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750237 | ||||||
| chr11:128750346
|
T | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0001others(4): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-7769T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750346 | ||||||
| chr11:128750401
|
G | A | 3 | a0001c0002t0001g0209a0001c0004t0001g0009a0001c0004t0003g0023 | 3 | HG02976.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.19-7714G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750401 | ||||||
| chr11:128750554
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0127a0001c0001t0004g0122others(1): Show | 4 | HG00673.hp1 HG02056.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-7561G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750554 | ||||||
| chr11:128750572
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-7543C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750572 | ||||||
| chr11:128750633
|
T | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0001others(4): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-7482T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750633 | ||||||
| chr11:128750634
|
A | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0001others(4): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-7481A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750634 | ||||||
| chr11:128750675
|
G | A | 5 | a0001c0001t0001g0234a0001c0001t0002g0219a0001c0001t0004g0189others(2): Show | 5 | HG02109.hp2 HG02145.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-7440G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750675 | ||||||
| chr11:128750730
|
C | T | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-7385C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750730 | ||||||
| chr11:128750866
|
A | T | 90 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(87): Show | 91 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-7249A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750866 | ||||||
| chr11:128750867
|
A | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0001others(4): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-7248A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128750867 | ||||||
| chr11:128751148
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0005g0280 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-6967T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751148 | ||||||
| chr11:128751342
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.19-6773T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751342 | ||||||
| chr11:128751348
|
T | C | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-6767T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751348 | ||||||
| chr11:128751354
|
T | C | 1 | a0001c0004t0011g0108 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19-6761T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751354 | ||||||
| chr11:128751358
|
C | CT | 7 | a0001c0001t0001g0022a0001c0001t0001g0079a0001c0001t0001g0100others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6742dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128751358 | |||||
| chr11:128751358
|
CT | C | 65 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0050others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.19-6742delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128751358 | |||||
| chr11:128751424
|
A | G | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-6691A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751424 | ||||||
| chr11:128751488
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0310a0001c0001t0002g0081others(2): Show | 5 | HG00735.hp1 HG02602.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-6627C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751488 | ||||||
| chr11:128751549
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0170 | 2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.19-6566C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751549 | ||||||
| chr11:128751566
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0127a0001c0001t0004g0122others(1): Show | 4 | HG00673.hp1 HG02056.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-6549G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751566 | ||||||
| chr11:128751619
|
C | T | 1 | a0001c0003t0001g0016 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.19-6496C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751619 | ||||||
| chr11:128751809
|
TG | T | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-6303delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128751809 | |||||
| chr11:128751812
|
G | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.19-6303G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751812 | ||||||
| chr11:128751819
|
T | A | 90 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(87): Show | 91 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-6296T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751819 | ||||||
| chr11:128751824
|
G | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-6291G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751824 | ||||||
| chr11:128751825
|
G | GT | 14 | a0001c0001t0001g0193a0001c0001t0001g0202a0001c0001t0001g0222others(11): Show | 14 | HG00673.hp2 HG01981.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-6290_19-6289ins others(1): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751825 | ||||||
| chr11:128751825
|
G | GTTTT | 3 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218 | 3 | HG01884.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.19-6290_19-6289ins others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751825 | ||||||
| chr11:128751826
|
G | T | 319 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.19-6289G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751826 | ||||||
| chr11:128751830
|
G | GT | 9 | a0001c0001t0001g0110a0001c0001t0001g0184a0001c0001t0002g0087others(6): Show | 9 | HG00140.hp2 HG01891.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-6272dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128751830 | |||||
| chr11:128751830
|
G | GTT | 6 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0001others(3): Show | 7 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6273_19-6272dup others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128751830 | |||||
| chr11:128751830
|
G | T | 77 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0062others(74): Show | 79 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.19-6285G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751830 | ||||||
| chr11:128751831
|
T | G | 1 | a0001c0002t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19-6284T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751831 | ||||||
| chr11:128751845
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0002t0001g0094others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-6270T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751845 | ||||||
| chr11:128751922
|
A | C | 84 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0037others(81): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.19-6193A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751922 | ||||||
| chr11:128751980
|
C | A | 1 | a0001c0001t0002g0003 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.19-6135C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128751980 | ||||||
| chr11:128752037
|
G | A | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-6078G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752037 | ||||||
| chr11:128752040
|
A | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0288a0001c0001t0005g0038others(8): Show | 11 | HG01123.hp2 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-6075A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752040 | ||||||
| chr11:128752062
|
G | A | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.19-6053G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752062 | ||||||
| chr11:128752188
|
C | T | 1 | a0001c0002t0001g0276 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.19-5927C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752188 | ||||||
| chr11:128752205
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19-5910G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752205 | ||||||
| chr11:128752442
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0172a0001c0001t0001g0295 | 3 | HG00735.hp2 HG01496.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.19-5673T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752442 | ||||||
| chr11:128752736
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.19-5379A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752736 | ||||||
| chr11:128752896
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19-5219C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128752896 | ||||||
| chr11:128753021
|
G | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0173 | 3 | HG03130.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19-5094G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753021 | ||||||
| chr11:128753440
|
C | G | 73 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(70): Show | 75 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-4675C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753440 | ||||||
| chr11:128753467
|
G | A | 2 | a0001c0002t0001g0209a0001c0004t0001g0009 | 2 | HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.19-4648G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753467 | ||||||
| chr11:128753498
|
T | C | 2 | a0001c0002t0001g0266a0001c0004t0001g0220 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.19-4617T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753498 | ||||||
| chr11:128753547
|
G | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0213a0001c0002t0001g0030others(2): Show | 5 | HG01109.hp1 HG02109.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-4568G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753547 | ||||||
| chr11:128753670
|
A | T | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-4445A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753670 | ||||||
| chr11:128753804
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.19-4311C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753804 | ||||||
| chr11:128753900
|
TG | T | 21 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(18): Show | 21 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-4211delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128753900 | |||||
| chr11:128753912
|
A | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(16): Show | 19 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-4203A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753912 | ||||||
| chr11:128753975
|
C | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0185a0001c0001t0002g0047 | 3 | HG00140.hp1 HG01123.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-4140C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128753975 | ||||||
| chr11:128754081
|
AT | A | 85 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(82): Show | 86 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-4032delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754081 | |||||
| chr11:128754091
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.19-4024C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754091 | ||||||
| chr11:128754133
|
A | G | 285 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(282): Show | 289 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.19-3982A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754133 | ||||||
| chr11:128754235
|
A | ATG | 29 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0049others(26): Show | 30 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-3839_19-3838dup others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
A | ATGTG | 19 | a0001c0001t0001g0020a0001c0001t0001g0142a0001c0001t0001g0144others(16): Show | 19 | HG01169.hp2 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-3841_19-3838dup others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
A | ATGTGTG | 5 | a0001c0001t0001g0089a0001c0001t0002g0025a0001c0001t0002g0078others(2): Show | 5 | HG01109.hp2 HG02965.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-3843_19-3838dup others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATG | A | 44 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0058others(41): Show | 44 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.19-3839_19-3838del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTG | A | 91 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0059others(88): Show | 93 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.19-3841_19-3838del others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTGTG | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0032others(43): Show | 47 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.19-3843_19-3838del others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTGTGT others(1): Show |
A | 46 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0050others(43): Show | 46 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-3845_19-3838del others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTGTGT others(3): Show |
A | 4 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0231others(1): Show | 4 | HG00609.hp2 HG02129.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-3847_19-3838del others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0016g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.19-3849_19-3838del others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754235
|
ATGTGTGT others(7): Show |
A | 6 | a0001c0001t0001g0039a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG01074.hp1 HG01891.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-3851_19-3838del others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128754235 | |||||
| chr11:128754274
|
T | C | 2 | a0001c0001t0001g0297a0001c0003t0001g0024 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19-3841T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754274 | ||||||
| chr11:128754276
|
T | C | 73 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(70): Show | 75 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.19-3839T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754276 | ||||||
| chr11:128754309
|
G | A | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-3806G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754309 | ||||||
| chr11:128754391
|
T | G | 1 | a0002c0005t0001g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.19-3724T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754391 | ||||||
| chr11:128754641
|
T | C | 116 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(113): Show | 116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-3474T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754641 | ||||||
| chr11:128754775
|
C | T | 1 | a0001c0001t0002g0320 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.19-3340C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754775 | ||||||
| chr11:128754916
|
A | G | 70 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(67): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.19-3199A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128754916 | ||||||
| chr11:128755117
|
T | C | 73 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(70): Show | 75 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-2998T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755117 | ||||||
| chr11:128755121
|
C | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(278): Show | 285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.19-2994C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755121 | ||||||
| chr11:128755339
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.19-2776C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755339 | ||||||
| chr11:128755416
|
A | C | 1 | a0001c0002t0001g0266 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-2699A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755416 | ||||||
| chr11:128755486
|
C | T | 1 | a0001c0003t0001g0294 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.19-2629C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755486 | ||||||
| chr11:128755487
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-2628G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755487 | ||||||
| chr11:128755710
|
G | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-2405G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755710 | ||||||
| chr11:128755839
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0004g0122 | 2 | HG00673.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.19-2276C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755839 | ||||||
| chr11:128755912
|
C | T | 85 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(82): Show | 86 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-2203C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755912 | ||||||
| chr11:128755926
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0003t0003g0008 | 3 | HG02258.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19-2189C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128755926 | ||||||
| chr11:128756348
|
C | T | 9 | a0001c0001t0001g0183a0001c0001t0001g0202a0001c0001t0001g0235others(6): Show | 9 | HG00597.hp1 HG02074.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-1767C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756348 | ||||||
| chr11:128756614
|
A | G | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19-1501A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756614 | ||||||
| chr11:128756891
|
G | A | 70 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(67): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.19-1224G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756891 | ||||||
| chr11:128756914
|
G | A | 4 | a0001c0001t0001g0098a0001c0002t0001g0052a0001c0002t0002g0085others(1): Show | 4 | NA18981.hp1 NA18985.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-1201G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756914 | ||||||
| chr11:128756946
|
G | A | 5 | a0001c0001t0001g0066a0001c0001t0001g0160a0001c0001t0002g0065others(2): Show | 5 | NA18953.hp2 NA18969.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-1169G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756946 | ||||||
| chr11:128756983
|
A | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0170a0001c0004t0001g0077 | 3 | HG03688.hp1 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.19-1132A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128756983 | ||||||
| chr11:128757016
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0017g0303 | 2 | HG01099.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.19-1099G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757016 | ||||||
| chr11:128757042
|
TTTTTTCT others(7): Show |
T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-1069_19-1056del others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757042 | |||||
| chr11:128757044
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0001g0211 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-1069_19-1068ins others(19): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTC | 55 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 55 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.19-1005_19-1002dup others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTCTCT others(13): Show |
1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19-1066_19-1065ins others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTCTTT others(1): Show |
34 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0149others(31): Show | 34 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.19-1009_19-1002dup others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTCTTT others(5): Show |
18 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0182others(15): Show | 18 | HG00738.hp1 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-1013_19-1002dup others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTCTTT others(9): Show |
8 | a0001c0001t0001g0075a0001c0001t0001g0095a0001c0001t0001g0172others(5): Show | 8 | HG00621.hp1 HG00673.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-1017_19-1002dup others(16): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
T | TTTTCTTT others(21): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0145 | 2 | HG00735.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.19-1029_19-1002dup others(28): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTC | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0039others(39): Show | 43 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.19-1005_19-1002del others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTCTTT others(1): Show |
T | 30 | a0001c0001t0001g0037a0001c0001t0001g0106a0001c0001t0001g0119others(27): Show | 31 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.19-1009_19-1002del others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTCTTT others(5): Show |
T | 57 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0089others(54): Show | 58 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.19-1013_19-1002del others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTCTTT others(9): Show |
T | 4 | a0001c0001t0001g0110a0001c0001t0001g0263a0001c0001t0004g0229others(1): Show | 4 | HG00099.hp2 HG02683.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1017_19-1002del others(16): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTCTTT others(21): Show |
T | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19-1029_19-1002del others(28): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757044
|
TTTTCTTT others(29): Show |
T | 3 | a0001c0001t0002g0219a0001c0004t0001g0267a0001c0004t0001g0287 | 3 | HG02109.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19-1037_19-1002del others(36): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757044 | |||||
| chr11:128757049
|
T | C | 1 | a0001c0001t0005g0284 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.19-1066T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757049 | ||||||
| chr11:128757050
|
T | C | 2 | a0001c0003t0003g0008a0001c0004t0003g0283 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.19-1065T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757050 | ||||||
| chr11:128757053
|
T | C | 1 | a0001c0003t0003g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-1062T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757053 | ||||||
| chr11:128757054
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-1061T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757054 | ||||||
| chr11:128757060
|
C | CTTTCTTT others(8): Show |
2 | a0001c0002t0001g0030a0001c0003t0001g0217 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19-1054_19-1040dup others(15): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757060 | |||||
| chr11:128757064
|
C | CTTTCTTT others(4): Show |
1 | a0001c0003t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-1050_19-1040dup others(11): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757064 | |||||
| chr11:128757080
|
C | CTTTCTTT others(5): Show |
1 | a0001c0001t0013g0111 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.19-1024_19-1023ins others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757080 | |||||
| chr11:128757094
|
T | TTCTTTCT others(5): Show |
1 | a0001c0003t0001g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-1010_19-1009ins others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757094 | |||||
| chr11:128757102
|
T | C | 73 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(70): Show | 75 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-1013T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757102 | ||||||
| chr11:128757114
|
C | T | 2 | a0001c0001t0002g0103a0001c0011t0003g0093 | 2 | HG03453.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.19-1001C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757114 | ||||||
| chr11:128757117
|
T | TTTCTTTC others(15): Show |
1 | a0001c0001t0002g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.19-994_19-993insTT others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 128757117 | |||||
| chr11:128757643
|
G | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-472G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757643 | ||||||
| chr11:128757663
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.19-452G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757663 | ||||||
| chr11:128757664
|
C | T | 2 | a0001c0001t0001g0019a0001c0003t0003g0218 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.19-451C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757664 | ||||||
| chr11:128757782
|
T | C | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19-333T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757782 | ||||||
| chr11:128757831
|
T | A | 67 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(64): Show | 68 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.19-284T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757831 | ||||||
| chr11:128757845
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-270C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757845 | ||||||
| chr11:128757871
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-244C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757871 | ||||||
| chr11:128757876
|
T | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-239T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757876 | ||||||
| chr11:128757888
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-227T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757888 | ||||||
| chr11:128757889
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-226C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757889 | ||||||
| chr11:128757890
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-225C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757890 | ||||||
| chr11:128757894
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-221C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757894 | ||||||
| chr11:128757895
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-220C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757895 | ||||||
| chr11:128757896
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-219C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757896 | ||||||
| chr11:128757898
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-217C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757898 | ||||||
| chr11:128757903
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-212C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757903 | ||||||
| chr11:128757922
|
A | T | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-193A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757922 | ||||||
| chr11:128757933
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19-182C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757933 | ||||||
| chr11:128757992
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0005g0280 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19-123C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128757992 | ||||||
| chr11:128758020
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.19-95G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128758020 | ||||||
| chr11:128758094
|
G | C | 2 | a0001c0001t0005g0284a0001c0003t0003g0035 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-21G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128758094 | ||||||
| chr11:128758447
|
C | G | 3 | a0001c0001t0001g0074a0001c0001t0002g0044a0001c0003t0001g0070 | 3 | HG03491.hp1 HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.230+121C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758447 | ||||||
| chr11:128758528
|
C | A | 91 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(88): Show | 93 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.230+202C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758528 | ||||||
| chr11:128758528
|
C | G | 194 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(191): Show | 196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.230+202C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758528 | ||||||
| chr11:128758575
|
C | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0142others(24): Show | 28 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.230+249C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758575 | ||||||
| chr11:128758711
|
G | T | 67 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(64): Show | 68 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.230+385G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758711 | ||||||
| chr11:128758733
|
C | T | 66 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(63): Show | 67 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.230+407C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758733 | ||||||
| chr11:128758861
|
T | C | 188 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(185): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.230+535T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758861 | ||||||
| chr11:128758943
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.230+617C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758943 | ||||||
| chr11:128758958
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230+632G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758958 | ||||||
| chr11:128758980
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(182): Show | 187 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.230+654A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758980 | ||||||
| chr11:128759008
|
C | G | 1 | a0001c0001t0012g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.230+682C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759008 | ||||||
| chr11:128759040
|
C | T | 190 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0020others(187): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.230+714C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759040 | ||||||
| chr11:128759066
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0001t0005g0280others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+740G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759066 | ||||||
| chr11:128759107
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.230+781G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759107 | ||||||
| chr11:128759201
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.230+875A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759201 | ||||||
| chr11:128759257
|
T | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0086a0001c0001t0001g0185others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.230+931T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759257 | ||||||
| chr11:128759424
|
G | A | 22 | a0001c0001t0001g0062a0001c0001t0001g0126a0001c0001t0001g0140others(19): Show | 23 | HG00423.hp2 HG00558.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.230+1098G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759424 | ||||||
| chr11:128759487
|
T | G | 126 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(123): Show | 127 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.230+1161T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759487 | ||||||
| chr11:128759495
|
G | T | 218 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(215): Show | 221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.230+1169G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759495 | ||||||
| chr11:128759510
|
T | C | 1 | a0001c0003t0003g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.230+1184T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759510 | ||||||
| chr11:128759613
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.230+1287A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759613 | ||||||
| chr11:128759766
|
C | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.230+1440C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759766 | ||||||
| chr11:128759766
|
C | T | 214 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.230+1440C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759766 | ||||||
| chr11:128759858
|
A | C | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+1532A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759858 | ||||||
| chr11:128759976
|
G | C | 214 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.230+1650G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759976 | ||||||
| chr11:128760139
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.230+1813C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760139 | ||||||
| chr11:128760276
|
G | T | 93 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0028others(90): Show | 95 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.230+1950G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760276 | ||||||
| chr11:128760414
|
C | T | 294 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(291): Show | 298 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.230+2088C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760414 | ||||||
| chr11:128760431
|
G | C | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230+2105G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760431 | ||||||
| chr11:128760434
|
C | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230+2108C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760434 | ||||||
| chr11:128760442
|
C | T | 2 | a0001c0001t0001g0068a0001c0003t0001g0306 | 2 | HG02083.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.230+2116C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760442 | ||||||
| chr11:128760454
|
A | C | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230+2128A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760454 | ||||||
| chr11:128760473
|
G | A | 1 | a0001c0001t0005g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.230+2147G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760473 | ||||||
| chr11:128760520
|
CT | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0179a0001c0001t0001g0199others(6): Show | 9 | HG00639.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.230+2219delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128760520 | |||||
| chr11:128760520
|
CTTTT | C | 106 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0026others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.230+2216_230+2219d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128760520 | |||||
| chr11:128760523
|
T | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0028others(62): Show | 66 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.230+2197T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760523 | ||||||
| chr11:128760524
|
T | A | 2 | a0001c0001t0004g0189a0001c0002t0001g0286 | 2 | NA18942.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.230+2198T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760524 | ||||||
| chr11:128760540
|
T | C | 70 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(67): Show | 71 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.230+2214T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760540 | ||||||
| chr11:128760791
|
G | T | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0049others(29): Show | 32 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.230+2465G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760791 | ||||||
| chr11:128760806
|
G | A | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.230+2480G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760806 | ||||||
| chr11:128760907
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+2581G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760907 | ||||||
| chr11:128760927
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.230+2601C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760927 | ||||||
| chr11:128760932
|
G | A | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+2606G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760932 | ||||||
| chr11:128760953
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.230+2627C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760953 | ||||||
| chr11:128760980
|
G | A | 4 | a0001c0001t0001g0293a0001c0001t0002g0054a0001c0001t0002g0290others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.230+2654G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760980 | ||||||
| chr11:128760983
|
C | G | 1 | a0001c0004t0001g0298 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.230+2657C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128760983 | ||||||
| chr11:128761149
|
G | A | 4 | a0001c0001t0001g0019a0001c0002t0001g0266a0001c0003t0003g0218others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+2823G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761149 | ||||||
| chr11:128761335
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+3009C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761335 | ||||||
| chr11:128761339
|
T | C | 1 | a0001c0003t0001g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.230+3013T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761339 | ||||||
| chr11:128761371
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.230+3045C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761371 | ||||||
| chr11:128761543
|
A | G | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.230+3217A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761543 | ||||||
| chr11:128761886
|
C | G | 1 | a0001c0004t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.230+3560C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761886 | ||||||
| chr11:128761996
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.230+3670C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128761996 | ||||||
| chr11:128762109
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.230+3783T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762109 | ||||||
| chr11:128762249
|
T | C | 1 | a0001c0009t0001g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.230+3923T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762249 | ||||||
| chr11:128762363
|
T | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(169): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.230+4037T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762363 | ||||||
| chr11:128762660
|
T | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(165): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.230+4334T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762660 | ||||||
| chr11:128762710
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.230+4384C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762710 | ||||||
| chr11:128762792
|
G | A | 168 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(165): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.230+4466G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762792 | ||||||
| chr11:128762956
|
C | CAA | 6 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0001t0005g0284others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.230+4643_230+4644d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128762956 | |||||
| chr11:128762956
|
CA | C | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.230+4644delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128762956 | |||||
| chr11:128762975
|
G | A | 1 | a0001c0002t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.230+4649G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762975 | ||||||
| chr11:128762997
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.230+4671A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128762997 | ||||||
| chr11:128763038
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0020others(165): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.230+4712A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763038 | ||||||
| chr11:128763161
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.230+4835G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763161 | ||||||
| chr11:128763223
|
A | G | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(275): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.231-4895A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763223 | ||||||
| chr11:128763386
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.231-4732G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763386 | ||||||
| chr11:128763402
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0297others(8): Show | 11 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.231-4716A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763402 | ||||||
| chr11:128763414
|
A | G | 66 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0033others(63): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.231-4704A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763414 | ||||||
| chr11:128763519
|
A | T | 1 | a0001c0003t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.231-4599A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763519 | ||||||
| chr11:128763633
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0100a0001c0003t0003g0008others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-4485A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763633 | ||||||
| chr11:128763699
|
A | C | 2 | a0001c0004t0001g0220a0001c0012t0015g0084 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.231-4419A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763699 | ||||||
| chr11:128763703
|
C | T | 7 | a0001c0001t0001g0245a0001c0001t0001g0272a0001c0001t0004g0174others(4): Show | 7 | HG01981.hp2 HG02165.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.231-4415C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763703 | ||||||
| chr11:128763724
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.231-4394T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763724 | ||||||
| chr11:128763756
|
A | AG | 29 | a0001c0001t0001g0062a0001c0001t0001g0079a0001c0001t0001g0126others(26): Show | 30 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.231-4360dupG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128763756 | |||||
| chr11:128763759
|
A | G | 69 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(66): Show | 71 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.231-4359A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763759 | ||||||
| chr11:128763770
|
C | T | 31 | a0001c0001t0001g0062a0001c0001t0001g0079a0001c0001t0001g0126others(28): Show | 32 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.231-4348C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763770 | ||||||
| chr11:128763829
|
C | T | 4 | a0001c0001t0004g0151a0001c0001t0004g0238a0001c0001t0004g0291others(1): Show | 4 | HG02129.hp2 NA18982.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-4289C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763829 | ||||||
| chr11:128763999
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.231-4119C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763999 | ||||||
| chr11:128764000
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-4118G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764000 | ||||||
| chr11:128764056
|
C | T | 40 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0032others(37): Show | 42 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.231-4062C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764056 | ||||||
| chr11:128764057
|
G | A | 13 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0205others(10): Show | 13 | HG00621.hp2 HG02622.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.231-4061G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764057 | ||||||
| chr11:128764102
|
C | T | 4 | a0001c0001t0001g0168a0001c0002t0002g0146a0001c0004t0001g0166others(1): Show | 4 | HG00423.hp2 HG01981.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-4016C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764102 | ||||||
| chr11:128764261
|
C | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 48 | HG01074.hp1 HG01099.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.231-3857C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764261 | ||||||
| chr11:128764322
|
C | T | 1 | a0001c0007t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.231-3796C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764322 | ||||||
| chr11:128764330
|
C | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0213a0001c0001t0001g0259others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.231-3788C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764330 | ||||||
| chr11:128764344
|
A | T | 1 | a0001c0001t0001g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231-3774A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764344 | ||||||
| chr11:128764550
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.231-3568G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764550 | ||||||
| chr11:128764603
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0003t0001g0264 | 3 | HG00099.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.231-3515C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764603 | ||||||
| chr11:128764752
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0022others(1): Show | 4 | HG00642.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-3366G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764752 | ||||||
| chr11:128764769
|
C | A | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.231-3349C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764769 | ||||||
| chr11:128764865
|
C | T | 28 | a0001c0001t0001g0066a0001c0001t0001g0086a0001c0001t0001g0129others(25): Show | 28 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.231-3253C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764865 | ||||||
| chr11:128764878
|
T | C | 7 | a0001c0001t0001g0211a0001c0001t0002g0219a0001c0002t0001g0275others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.231-3240T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764878 | ||||||
| chr11:128764886
|
A | G | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.231-3232A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764886 | ||||||
| chr11:128764955
|
G | A | 2 | a0001c0001t0001g0073a0001c0002t0002g0085 | 2 | NA18985.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.231-3163G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128764955 | ||||||
| chr11:128765048
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.231-3070G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765048 | ||||||
| chr11:128765050
|
C | T | 1 | a0001c0003t0003g0311 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.231-3068C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765050 | ||||||
| chr11:128765227
|
A | C | 1 | a0001c0002t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.231-2891A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765227 | ||||||
| chr11:128765236
|
G | A | 1 | a0001c0001t0014g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.231-2882G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765236 | ||||||
| chr11:128765489
|
G | A | 51 | a0001c0001t0001g0020a0001c0001t0001g0049a0001c0001t0001g0057others(48): Show | 51 | HG00423.hp2 HG00609.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.231-2629G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765489 | ||||||
| chr11:128765540
|
A | G | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.231-2578A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765540 | ||||||
| chr11:128765783
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0324 | 2 | HG02300.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.231-2335C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765783 | ||||||
| chr11:128765784
|
A | G | 268 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(265): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.231-2334A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765784 | ||||||
| chr11:128765807
|
G | A | 2 | a0001c0002t0001g0001a0001c0003t0001g0217 | 3 | HG03130.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-2311G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765807 | ||||||
| chr11:128765813
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.231-2305G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765813 | ||||||
| chr11:128765818
|
CTG | C | 9 | a0001c0001t0001g0100a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01884.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.231-2296_231-2295d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128765818 | |||||
| chr11:128765820
|
G | C | 2 | a0001c0006t0001g0064a0001c0006t0001g0236 | 2 | NA19007.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.231-2298G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765820 | ||||||
| chr11:128765870
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0002g0204 | 2 | HG00140.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.231-2248G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765870 | ||||||
| chr11:128765922
|
A | C | 1 | a0001c0001t0005g0284 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.231-2196A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765922 | ||||||
| chr11:128765958
|
A | G | 272 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(269): Show | 275 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.231-2160A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128765958 | ||||||
| chr11:128766010
|
G | A | 3 | a0001c0003t0001g0107a0001c0004t0003g0225a0001c0011t0003g0093 | 3 | HG03225.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.231-2108G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766010 | ||||||
| chr11:128766052
|
A | C | 2 | a0001c0002t0001g0216a0001c0002t0005g0096 | 2 | HG01123.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.231-2066A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766052 | ||||||
| chr11:128766150
|
G | C | 2 | a0001c0001t0001g0208a0001c0011t0003g0093 | 2 | HG01074.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.231-1968G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766150 | ||||||
| chr11:128766184
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0032others(44): Show | 49 | HG01074.hp1 HG01099.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.231-1934T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766184 | ||||||
| chr11:128766194
|
A | G | 1 | a0001c0003t0001g0313 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.231-1924A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766194 | ||||||
| chr11:128766254
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231-1864C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766254 | ||||||
| chr11:128766294
|
C | T | 1 | a0001c0001t0008g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.231-1824C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766294 | ||||||
| chr11:128766338
|
G | A | 109 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(106): Show | 111 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.231-1780G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766338 | ||||||
| chr11:128766346
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.231-1772C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766346 | ||||||
| chr11:128766485
|
C | T | 1 | a0001c0003t0007g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.231-1633C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766485 | ||||||
| chr11:128766559
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.231-1559G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766559 | ||||||
| chr11:128766589
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.231-1529T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766589 | ||||||
| chr11:128766613
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-1505G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766613 | ||||||
| chr11:128766733
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-1385G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766733 | ||||||
| chr11:128766791
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.231-1327C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766791 | ||||||
| chr11:128766803
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231-1315T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766803 | ||||||
| chr11:128766810
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.231-1308G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766810 | ||||||
| chr11:128766828
|
G | A | 2 | a0001c0002t0001g0001a0001c0003t0001g0217 | 3 | HG03130.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-1290G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766828 | ||||||
| chr11:128766950
|
T | TTCTCCTT others(13): Show |
37 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.231-1160_231-1141d others(22): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128766950 | |||||
| chr11:128766959
|
G | GCCTT | 4 | a0001c0001t0001g0278a0001c0001t0002g0042a0001c0001t0002g0221others(1): Show | 4 | NA18940.hp2 NA18955.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-1156_231-1153d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128766959 | |||||
| chr11:128766964
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.231-1154C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128766964 | ||||||
| chr11:128767005
|
G | GCAGCGGG others(12): Show |
2 | a0001c0001t0001g0274a0001c0001t0005g0027 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.231-1109_231-1091d others(21): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 128767005 | |||||
| chr11:128767102
|
A | T | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.231-1016A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767102 | ||||||
| chr11:128767114
|
C | A | 1 | a0001c0002t0001g0061 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.231-1004C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767114 | ||||||
| chr11:128767161
|
A | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(117): Show | 122 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.231-957A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767161 | ||||||
| chr11:128767225
|
G | C | 1 | a0001c0003t0003g0311 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.231-893G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767225 | ||||||
| chr11:128767242
|
T | A | 1 | a0001c0001t0004g0308 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.231-876T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767242 | ||||||
| chr11:128767334
|
A | G | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.231-784A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767334 | ||||||
| chr11:128767364
|
T | C | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(17): Show | 21 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.231-754T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767364 | ||||||
| chr11:128767402
|
C | T | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(17): Show | 21 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.231-716C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767402 | ||||||
| chr11:128767483
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.231-635A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767483 | ||||||
| chr11:128767518
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.231-600T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767518 | ||||||
| chr11:128767529
|
G | A | 104 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(101): Show | 106 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.231-589G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767529 | ||||||
| chr11:128767574
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.231-544A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767574 | ||||||
| chr11:128767681
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.231-437G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767681 | ||||||
| chr11:128767732
|
C | T | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.231-386C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767732 | ||||||
| chr11:128767747
|
G | A | 4 | a0001c0002t0001g0173a0001c0003t0007g0147a0001c0004t0001g0009others(1): Show | 4 | HG02622.hp2 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.231-371G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767747 | ||||||
| chr11:128767758
|
G | A | 8 | a0001c0001t0001g0039a0001c0002t0001g0029a0001c0002t0001g0034others(5): Show | 8 | HG01884.hp1 HG02723.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.231-360G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767758 | ||||||
| chr11:128767812
|
GT | G | 22 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(19): Show | 24 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.231-305delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767812 | ||||||
| chr11:128767830
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.231-288G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767830 | ||||||
| chr11:128767841
|
G | A | 84 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0059others(81): Show | 86 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.231-277G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767841 | ||||||
| chr11:128767887
|
G | A | 1 | a0001c0003t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.231-231G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767887 | ||||||
| chr11:128767904
|
C | T | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(17): Show | 21 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.231-214C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767904 | ||||||
| chr11:128767977
|
A | G | 16 | a0001c0001t0001g0039a0001c0002t0001g0029a0001c0002t0001g0034others(13): Show | 16 | HG01123.hp2 HG01884.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.231-141A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767977 | ||||||
| chr11:128768006
|
C | A | 22 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0089others(19): Show | 24 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.231-112C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128768006 | ||||||
| chr11:128768321
|
TG | T | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(255): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.385+56delG | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768321 | |||||
| chr11:128768323
|
G | C | 1 | a0001c0001t0002g0010 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.385+51G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768323 | ||||||
| chr11:128768332
|
G | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0213a0001c0003t0003g0318others(1): Show | 4 | HG01099.hp2 HG02109.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+60G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768332 | ||||||
| chr11:128768337
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.385+65A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768337 | ||||||
| chr11:128768471
|
G | C | 2 | a0001c0002t0001g0094a0001c0003t0003g0008 | 2 | HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.385+199G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768471 | ||||||
| chr11:128768516
|
TA | T | 264 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(261): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.385+259delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768516 | |||||
| chr11:128768516
|
TAA | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0100a0001c0002t0001g0029others(6): Show | 9 | HG02723.hp1 HG02965.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.385+258_385+259del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768516 | |||||
| chr11:128768533
|
A | T | 66 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0086others(63): Show | 66 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.385+261A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768533 | ||||||
| chr11:128768560
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.385+288A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768560 | ||||||
| chr11:128768688
|
C | CA | 11 | a0001c0001t0001g0156a0001c0001t0001g0245a0001c0001t0002g0025others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+439dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768688 | |||||
| chr11:128768688
|
CA | C | 164 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(161): Show | 168 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.385+439delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768688 | |||||
| chr11:128768688
|
CAA | C | 75 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0074others(72): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.385+438_385+439del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768688 | |||||
| chr11:128768688
|
CAAA | C | 7 | a0001c0001t0005g0038a0001c0001t0005g0210a0001c0001t0005g0212others(4): Show | 7 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+437_385+439del others(3): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768688 | |||||
| chr11:128768738
|
C | CTGCCCTT | 10 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0002g0262others(7): Show | 10 | HG00323.hp1 HG01123.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+468_385+474dup others(7): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128768738 | |||||
| chr11:128768756
|
T | C | 72 | a0001c0001t0001g0033a0001c0001t0001g0059a0001c0001t0001g0074others(69): Show | 72 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.385+484T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768756 | ||||||
| chr11:128768848
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.385+576C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768848 | ||||||
| chr11:128768876
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0160 | 3 | HG02080.hp1 NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.385+604C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768876 | ||||||
| chr11:128768882
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.385+610C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128768882 | ||||||
| chr11:128769234
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0002g0069 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.385+962A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769234 | ||||||
| chr11:128769438
|
T | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0033others(114): Show | 117 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.385+1166T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769438 | ||||||
| chr11:128769444
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.385+1172G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769444 | ||||||
| chr11:128769479
|
T | G | 182 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(179): Show | 186 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.385+1207T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769479 | ||||||
| chr11:128769881
|
G | A | 96 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(93): Show | 100 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.385+1609G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769881 | ||||||
| chr11:128769935
|
C | T | 126 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(123): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.385+1663C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769935 | ||||||
| chr11:128769949
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.385+1677G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769949 | ||||||
| chr11:128770020
|
T | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(236): Show | 243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.385+1748T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770020 | ||||||
| chr11:128770050
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.385+1778T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770050 | ||||||
| chr11:128770192
|
G | A | 2 | a0001c0001t0002g0262a0001c0003t0003g0218 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.385+1920G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770192 | ||||||
| chr11:128770370
|
A | G | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.385+2098A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770370 | ||||||
| chr11:128770377
|
G | A | 22 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0177others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.385+2105G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770377 | ||||||
| chr11:128770512
|
G | A | 2 | a0001c0002t0001g0030a0001c0002t0001g0141 | 2 | HG01109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.385+2240G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770512 | ||||||
| chr11:128770582
|
T | G | 2 | a0001c0001t0002g0262a0001c0003t0003g0218 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.386-2200T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770582 | ||||||
| chr11:128770686
|
T | C | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-2096T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770686 | ||||||
| chr11:128770877
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.386-1905A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770877 | ||||||
| chr11:128770953
|
G | A | 63 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0079others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.386-1829G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128770953 | ||||||
| chr11:128771122
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-1660A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771122 | ||||||
| chr11:128771143
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.386-1639C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771143 | ||||||
| chr11:128771193
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.386-1589C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771193 | ||||||
| chr11:128771238
|
A | G | 1 | a0001c0004t0001g0298 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.386-1544A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771238 | ||||||
| chr11:128771261
|
T | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0097a0001c0001t0001g0106others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.386-1521T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771261 | ||||||
| chr11:128771400
|
C | T | 2 | a0001c0001t0001g0022a0001c0004t0001g0287 | 2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.386-1382C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771400 | ||||||
| chr11:128771402
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.386-1380C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771402 | ||||||
| chr11:128771573
|
C | T | 191 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(188): Show | 195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.386-1209C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771573 | ||||||
| chr11:128771962
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.386-820A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128771962 | ||||||
| chr11:128772028
|
CCA | C | 12 | a0001c0001t0001g0048a0001c0001t0001g0127a0001c0001t0001g0129others(9): Show | 12 | HG00609.hp1 HG01099.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-705_386-704del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACA | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0152a0001c0001t0001g0157others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.386-707_386-704del others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACA | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0211a0001c0001t0001g0224others(5): Show | 8 | HG00323.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-709_386-704del others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(1): Show |
C | 15 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0187others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-711_386-704del others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(3): Show |
C | 68 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0055others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.386-713_386-704del others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(5): Show |
C | 137 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0026others(134): Show | 141 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.386-715_386-704del others(12): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(7): Show |
C | 30 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0097others(27): Show | 30 | HG00323.hp2 HG00673.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.386-717_386-704del others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(9): Show |
C | 10 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0100others(7): Show | 10 | HG00642.hp2 HG00735.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-719_386-704del others(16): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(11): Show |
C | 3 | a0001c0002t0001g0173a0001c0007t0003g0021a0001c0012t0015g0084 | 3 | HG02451.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.386-721_386-704del others(18): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(13): Show |
C | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.386-723_386-704del others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(15): Show |
C | 3 | a0001c0001t0001g0208a0001c0003t0001g0107a0001c0011t0003g0093 | 3 | HG01074.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.386-725_386-704del others(22): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772028
|
CCACACAC others(19): Show |
C | 2 | a0001c0001t0002g0262a0001c0003t0003g0218 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.386-729_386-704del others(26): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772028 | |||||
| chr11:128772057
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.386-725C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772057 | ||||||
| chr11:128772069
|
CACACACA others(3): Show |
C | 1 | a0001c0004t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.386-704_386-695del others(10): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 128772069 | |||||
| chr11:128772073
|
C | T | 2 | a0001c0007t0003g0021a0001c0012t0015g0084 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.386-709C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772073 | ||||||
| chr11:128772100
|
G | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0074others(64): Show | 67 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.386-682G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772100 | ||||||
| chr11:128772265
|
C | T | 194 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(191): Show | 198 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.386-517C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772265 | ||||||
| chr11:128772383
|
G | A | 1 | a0001c0001t0012g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.386-399G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772383 | ||||||
| chr11:128772416
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0259a0001c0002t0018g0015others(1): Show | 4 | HG02055.hp1 HG02809.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-366T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772416 | ||||||
| chr11:128772493
|
C | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0074others(64): Show | 67 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.386-289C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772493 | ||||||
| chr11:128772643
|
G | C | 15 | a0001c0001t0001g0095a0001c0001t0001g0152a0001c0001t0004g0125others(12): Show | 15 | HG00423.hp1 HG00673.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.386-139G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772643 | ||||||
| chr11:128772705
|
G | C | 2 | a0001c0004t0001g0214a0001c0004t0003g0283 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.386-77G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772705 | ||||||
| chr11:128772717
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.386-65G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772717 | ||||||
| chr11:128772740
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386-42A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772740 | ||||||
| chr11:128773069
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.589+84G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128773069 | ||||||
| chr11:128773084
|
C | T | 31 | a0001c0001t0001g0033a0001c0001t0001g0097a0001c0001t0001g0106others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.589+99C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128773084 | ||||||
| chr11:128773658
|
A | C | 162 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.589+673A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128773658 | ||||||
| chr11:128773705
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.589+720A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128773705 | ||||||
| chr11:128773754
|
G | T | 63 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0079others(60): Show | 63 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.589+769G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128773754 | ||||||
| chr11:128774093
|
A | T | 1 | a0001c0002t0002g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.589+1108A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774093 | ||||||
| chr11:128774115
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.589+1130C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774115 | ||||||
| chr11:128774177
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0259a0001c0002t0018g0015others(1): Show | 4 | HG02055.hp1 HG02809.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.589+1192G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774177 | ||||||
| chr11:128774286
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.589+1301G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774286 | ||||||
| chr11:128774342
|
T | A | 2 | a0001c0001t0002g0262a0001c0003t0003g0218 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.589+1357T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774342 | ||||||
| chr11:128774440
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.589+1455T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774440 | ||||||
| chr11:128774512
|
C | T | 97 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.589+1527C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774512 | ||||||
| chr11:128774687
|
C | T | 2 | a0001c0002t0001g0216a0001c0002t0005g0096 | 2 | HG01123.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.589+1702C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774687 | ||||||
| chr11:128774774
|
G | A | 2 | a0001c0004t0001g0214a0001c0004t0003g0283 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.589+1789G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774774 | ||||||
| chr11:128774804
|
G | A | 9 | a0001c0001t0001g0039a0001c0001t0005g0027a0001c0002t0001g0029others(6): Show | 9 | HG02572.hp1 HG02723.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.589+1819G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774804 | ||||||
| chr11:128774821
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.589+1836T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774821 | ||||||
| chr11:128774846
|
T | A | 129 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(126): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.589+1861T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774846 | ||||||
| chr11:128774887
|
G | A | 97 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.589+1902G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774887 | ||||||
| chr11:128774922
|
T | TA | 127 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.589+1939dupA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 128774922 | |||||
| chr11:128774925
|
C | A | 127 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.589+1940C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774925 | ||||||
| chr11:128774991
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.589+2006T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774991 | ||||||
| chr11:128775152
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.589+2167T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775152 | ||||||
| chr11:128775162
|
G | T | 229 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(226): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.589+2177G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775162 | ||||||
| chr11:128775175
|
G | T | 102 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.589+2190G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775175 | ||||||
| chr11:128775187
|
A | C | 8 | a0001c0001t0001g0018a0001c0002t0001g0094a0001c0002t0001g0216others(5): Show | 8 | HG00642.hp2 HG01123.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.589+2202A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775187 | ||||||
| chr11:128775374
|
A | C | 225 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.589+2389A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775374 | ||||||
| chr11:128775441
|
C | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(221): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.589+2456C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775441 | ||||||
| chr11:128775554
|
A | G | 77 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0079others(74): Show | 78 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.589+2569A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775554 | ||||||
| chr11:128775590
|
G | T | 1 | a0001c0002t0001g0275 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.589+2605G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775590 | ||||||
| chr11:128775635
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0259a0001c0002t0018g0015 | 3 | HG02055.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.589+2650T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775635 | ||||||
| chr11:128775688
|
C | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.589+2703C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775688 | ||||||
| chr11:128775699
|
A | T | 102 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0058others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.589+2714A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775699 | ||||||
| chr11:128775716
|
T | C | 235 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(232): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.589+2731T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775716 | ||||||
| chr11:128775731
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.589+2746G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775731 | ||||||
| chr11:128775749
|
G | A | 1 | a0001c0003t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.589+2764G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775749 | ||||||
| chr11:128775808
|
G | C | 1 | a0001c0001t0002g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.589+2823G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775808 | ||||||
| chr11:128776077
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0288a0001c0001t0010g0090 | 3 | HG02647.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.589+3092A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776077 | ||||||
| chr11:128776291
|
C | A | 104 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(101): Show | 107 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.589+3306C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776291 | ||||||
| chr11:128776341
|
G | C | 5 | a0001c0002t0001g0094a0001c0003t0003g0008a0001c0004t0001g0009others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.589+3356G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776341 | ||||||
| chr11:128776416
|
C | T | 1 | a0001c0004t0001g0169 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.589+3431C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776416 | ||||||
| chr11:128776434
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.589+3449T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776434 | ||||||
| chr11:128776491
|
A | T | 203 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(200): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.589+3506A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776491 | ||||||
| chr11:128776505
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.589+3520G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776505 | ||||||
| chr11:128776638
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.589+3653G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128776638 | ||||||
| chr11:128777140
|
C | T | 1 | a0001c0003t0001g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.589+4155C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777140 | ||||||
| chr11:128777251
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.589+4266C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777251 | ||||||
| chr11:128777262
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.589+4277T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777262 | ||||||
| chr11:128777295
|
G | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0033others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.589+4310G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777295 | ||||||
| chr11:128777341
|
GA | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(130): Show | 135 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.589+4365delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 128777341 | |||||
| chr11:128777482
|
T | C | 4 | a0001c0002t0001g0203a0001c0002t0001g0285a0001c0003t0001g0264others(1): Show | 4 | HG00099.hp2 HG00621.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-4476T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777482 | ||||||
| chr11:128777530
|
A | G | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(244): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.590-4428A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777530 | ||||||
| chr11:128777532
|
T | C | 1 | a0001c0004t0003g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.590-4426T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777532 | ||||||
| chr11:128777649
|
G | A | 1 | a0001c0007t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.590-4309G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777649 | ||||||
| chr11:128777688
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.590-4270G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777688 | ||||||
| chr11:128777691
|
C | T | 105 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0066others(102): Show | 105 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.590-4267C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777691 | ||||||
| chr11:128777840
|
G | GC | 112 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0032others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.590-4113dupC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 128777840 | |||||
| chr11:128777925
|
C | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.590-4033C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777925 | ||||||
| chr11:128777936
|
C | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.590-4022C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128777936 | ||||||
| chr11:128778036
|
T | A | 1 | a0001c0001t0002g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.590-3922T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778036 | ||||||
| chr11:128778066
|
T | C | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.590-3892T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778066 | ||||||
| chr11:128778107
|
T | C | 133 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0032others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.590-3851T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778107 | ||||||
| chr11:128778269
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.590-3689G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778269 | ||||||
| chr11:128778460
|
T | G | 1 | a0001c0002t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.590-3498T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778460 | ||||||
| chr11:128778503
|
G | A | 1 | a0001c0004t0003g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.590-3455G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778503 | ||||||
| chr11:128778653
|
G | A | 16 | a0001c0001t0001g0039a0001c0001t0001g0089a0001c0002t0001g0001others(13): Show | 18 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.590-3305G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778653 | ||||||
| chr11:128778663
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.590-3295C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778663 | ||||||
| chr11:128778725
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.590-3233A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778725 | ||||||
| chr11:128778734
|
C | T | 26 | a0001c0001t0001g0089a0001c0002t0001g0001a0001c0002t0001g0002others(23): Show | 28 | HG01109.hp1 HG01123.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.590-3224C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778734 | ||||||
| chr11:128778926
|
G | A | 1 | a0001c0004t0001g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.590-3032G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128778926 | ||||||
| chr11:128778961
|
GC | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0100others(61): Show | 64 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.590-2992delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 128778961 | |||||
| chr11:128779034
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0001t0001g0297others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-2924T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779034 | ||||||
| chr11:128779071
|
A | G | 225 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.590-2887A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779071 | ||||||
| chr11:128779207
|
C | T | 1 | a0001c0001t0005g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.590-2751C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779207 | ||||||
| chr11:128779365
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0005g0038others(7): Show | 10 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.590-2593G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779365 | ||||||
| chr11:128779539
|
A | G | 1 | a0001c0003t0001g0270 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.590-2419A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779539 | ||||||
| chr11:128779647
|
G | C | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.590-2311G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779647 | ||||||
| chr11:128779708
|
G | A | 24 | a0001c0001t0001g0089a0001c0002t0001g0001a0001c0002t0001g0002others(21): Show | 26 | HG01109.hp1 HG01123.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.590-2250G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779708 | ||||||
| chr11:128779735
|
A | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0226a0001c0001t0001g0230others(4): Show | 7 | NA18940.hp1 NA18947.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.590-2223A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779735 | ||||||
| chr11:128779852
|
C | A | 1 | a0001c0002t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-2106C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779852 | ||||||
| chr11:128779852
|
C | G | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(49): Show | 54 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.590-2106C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779852 | ||||||
| chr11:128779857
|
A | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.590-2101A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779857 | ||||||
| chr11:128779956
|
G | A | 76 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0039others(73): Show | 76 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.590-2002G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779956 | ||||||
| chr11:128779988
|
T | A | 53 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(50): Show | 55 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.590-1970T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779988 | ||||||
| chr11:128780134
|
C | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0032others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.590-1824C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780134 | ||||||
| chr11:128780171
|
A | T | 46 | a0001c0001t0001g0100a0001c0001t0001g0211a0001c0001t0004g0253others(43): Show | 46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.590-1787A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780171 | ||||||
| chr11:128780271
|
G | T | 45 | a0001c0001t0001g0100a0001c0001t0001g0211a0001c0002t0001g0036others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.590-1687G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780271 | ||||||
| chr11:128780307
|
A | G | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(49): Show | 54 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.590-1651A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780307 | ||||||
| chr11:128780376
|
G | A | 164 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.590-1582G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780376 | ||||||
| chr11:128780421
|
C | T | 8 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0001t0001g0297others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-1537C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780421 | ||||||
| chr11:128780424
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.590-1534C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780424 | ||||||
| chr11:128780464
|
A | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.590-1494A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780464 | ||||||
| chr11:128780474
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.590-1484A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780474 | ||||||
| chr11:128780527
|
G | A | 107 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0032others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.590-1431G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780527 | ||||||
| chr11:128780531
|
G | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.590-1427G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780531 | ||||||
| chr11:128780548
|
T | C | 1 | a0001c0001t0012g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.590-1410T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780548 | ||||||
| chr11:128780595
|
CA | C | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(49): Show | 54 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.590-1355delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 128780595 | |||||
| chr11:128780697
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.590-1261G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780697 | ||||||
| chr11:128780794
|
C | T | 1 | a0001c0002t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.590-1164C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780794 | ||||||
| chr11:128780867
|
G | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0005g0038others(7): Show | 10 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.590-1091G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780867 | ||||||
| chr11:128780876
|
A | G | 98 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(95): Show | 100 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.590-1082A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780876 | ||||||
| chr11:128780897
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.590-1061C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780897 | ||||||
| chr11:128780898
|
G | A | 28 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.590-1060G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128780898 | ||||||
| chr11:128781029
|
AAT | A | 3 | a0001c0002t0005g0096a0001c0004t0003g0190a0001c0011t0003g0093 | 3 | HG01123.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.590-928_590-927del others(2): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781029 | ||||||
| chr11:128781030
|
A | G | 95 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(92): Show | 97 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.590-928A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781030 | ||||||
| chr11:128781057
|
C | T | 108 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(105): Show | 110 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.590-901C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781057 | ||||||
| chr11:128781188
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.590-770G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781188 | ||||||
| chr11:128781189
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.590-769G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781189 | ||||||
| chr11:128781324
|
A | G | 70 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(67): Show | 72 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.590-634A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781324 | ||||||
| chr11:128781377
|
G | C | 62 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(59): Show | 64 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.590-581G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781377 | ||||||
| chr11:128781423
|
G | A | 5 | a0001c0002t0001g0002a0001c0002t0001g0091a0001c0002t0001g0120others(2): Show | 6 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-535G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781423 | ||||||
| chr11:128781442
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.590-516G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781442 | ||||||
| chr11:128781633
|
A | G | 45 | a0001c0001t0001g0100a0001c0002t0001g0036a0001c0002t0001g0052others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.590-325A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781633 | ||||||
| chr11:128781830
|
C | T | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.590-128C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781830 | ||||||
| chr11:128782117
|
G | T | 323 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.655+94G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782117 | ||||||
| chr11:128782158
|
A | AG | 217 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.655+135_655+136ins others(1): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782158 | ||||||
| chr11:128782194
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+171A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782194 | ||||||
| chr11:128782243
|
T | G | 70 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(67): Show | 72 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.655+220T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782243 | ||||||
| chr11:128782284
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655+261A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782284 | ||||||
| chr11:128782321
|
T | C | 5 | a0001c0002t0001g0002a0001c0002t0001g0091a0001c0002t0001g0120others(2): Show | 6 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+298T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782321 | ||||||
| chr11:128782480
|
G | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0124others(2): Show | 5 | HG00558.hp2 HG02015.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+457G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782480 | ||||||
| chr11:128782558
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(108): Show | 113 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.655+535T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782558 | ||||||
| chr11:128782565
|
G | A | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.655+542G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782565 | ||||||
| chr11:128782676
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.655+653C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782676 | ||||||
| chr11:128782720
|
A | G | 8 | a0001c0002t0001g0209a0001c0002t0005g0096a0001c0004t0001g0009others(5): Show | 8 | HG01123.hp2 HG02109.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.655+697A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782720 | ||||||
| chr11:128782732
|
A | C | 70 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(67): Show | 72 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.655+709A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128782732 | ||||||
| chr11:128783001
|
G | T | 1 | a0001c0002t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+978G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783001 | ||||||
| chr11:128783003
|
G | A | 68 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(65): Show | 70 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.655+980G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783003 | ||||||
| chr11:128783025
|
G | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0032others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.655+1002G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783025 | ||||||
| chr11:128783137
|
A | G | 1 | a0001c0001t0005g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.655+1114A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783137 | ||||||
| chr11:128783140
|
T | C | 1 | a0001c0003t0003g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.655+1117T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783140 | ||||||
| chr11:128783214
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+1191C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783214 | ||||||
| chr11:128783394
|
A | G | 69 | a0001c0001t0001g0100a0001c0002t0001g0001a0001c0002t0001g0002others(66): Show | 71 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.655+1371A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783394 | ||||||
| chr11:128783453
|
C | A | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655+1430C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783453 | ||||||
| chr11:128783621
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.655+1598C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783621 | ||||||
| chr11:128783639
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.655+1616A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783639 | ||||||
| chr11:128783718
|
G | C | 32 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(29): Show | 32 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+1695G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783718 | ||||||
| chr11:128783746
|
C | T | 1 | a0001c0003t0001g0304 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.655+1723C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128783746 | ||||||
| chr11:128784024
|
A | C | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+2001A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784024 | ||||||
| chr11:128784063
|
G | A | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+2040G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784063 | ||||||
| chr11:128784178
|
T | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0001t0001g0297others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.655+2155T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784178 | ||||||
| chr11:128784208
|
T | G | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2185T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784208 | ||||||
| chr11:128784209
|
G | T | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2186G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784209 | ||||||
| chr11:128784210
|
T | C | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2187T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784210 | ||||||
| chr11:128784220
|
T | TCTC | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0055others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.655+2245_655+2247d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
T | TCTCCTCC others(2): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0226others(2): Show | 5 | HG01167.hp1 HG02922.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+2239_655+2247d others(11): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
T | TCTCCTCC others(5): Show |
1 | a0001c0001t0001g0097 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.655+2236_655+2247d others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
T | TCTCCTCC others(8): Show |
1 | a0001c0003t0007g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655+2233_655+2247d others(17): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
T | TCTCCTCC others(11): Show |
2 | a0001c0001t0001g0259a0001c0002t0001g0209 | 2 | NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655+2230_655+2247d others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTC | T | 15 | a0001c0001t0001g0033a0001c0001t0002g0045a0001c0001t0002g0065others(12): Show | 16 | HG01256.hp1 HG01433.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+2245_655+2247d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTCCTC | T | 21 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0126others(18): Show | 21 | HG00558.hp2 HG00733.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.655+2242_655+2247d others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTCCTCC others(8): Show |
T | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+2233_655+2247d others(17): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTCCTCC others(11): Show |
T | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.655+2230_655+2247d others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTCCTCC others(14): Show |
T | 9 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0001t0001g0297others(6): Show | 9 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+2227_655+2247d others(23): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784220
|
TCTCCTCC others(17): Show |
T | 101 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0039others(98): Show | 101 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.655+2224_655+2247d others(26): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784220 | |||||
| chr11:128784240
|
T | A | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2217T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784240 | ||||||
| chr11:128784251
|
C | T | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2228C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784251 | ||||||
| chr11:128784252
|
T | C | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2229T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784252 | ||||||
| chr11:128784268
|
C | CCTCCTCC others(17): Show |
1 | a0001c0003t0001g0304 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.655+2247_655+2248i others(26): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTCC others(14): Show |
6 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0079others(3): Show | 6 | HG02080.hp1 NA18942.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+2247_655+2248i others(23): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTCC others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.655+2247_655+2248i others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTCC others(11): Show |
2 | a0001c0001t0001g0020a0001c0003t0001g0011 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.655+2247_655+2248i others(20): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTCC others(8): Show |
2 | a0001c0001t0002g0231a0001c0003t0001g0217 | 2 | HG02129.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.655+2247_655+2248i others(17): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTG | 3 | a0001c0001t0001g0213a0001c0004t0001g0220a0001c0004t0003g0190 | 3 | HG02109.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.655+2247_655+2248i others(8): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTCCTGC others(5): Show |
11 | a0001c0001t0001g0127a0001c0001t0001g0248a0001c0001t0001g0271others(8): Show | 11 | HG00438.hp2 HG02056.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.655+2247_655+2248i others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTG | 11 | a0001c0001t0001g0274a0001c0002t0001g0001a0001c0002t0001g0029others(8): Show | 12 | HG01123.hp2 HG02109.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2249_655+2251d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTGCTGC others(2): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG02074.hp1 HG02080.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+2251_655+2252i others(11): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | CCTGCTGC others(5): Show |
3 | a0001c0001t0002g0204a0001c0001t0008g0076a0001c0003t0001g0112 | 3 | HG00140.hp2 HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.655+2251_655+2252i others(14): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784268 | |||||
| chr11:128784268
|
C | G | 14 | a0001c0001t0005g0027a0001c0002t0001g0002a0001c0002t0001g0030others(11): Show | 15 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.655+2245C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784268 | ||||||
| chr11:128784327
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.655+2304C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784327 | ||||||
| chr11:128784349
|
A | G | 214 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.655+2326A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784349 | ||||||
| chr11:128784395
|
C | T | 58 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(55): Show | 60 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.655+2372C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784395 | ||||||
| chr11:128784460
|
T | G | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2437T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784460 | ||||||
| chr11:128784536
|
T | C | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(56): Show | 61 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.655+2513T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784536 | ||||||
| chr11:128784630
|
T | C | 1 | a0001c0001t0014g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.655+2607T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784630 | ||||||
| chr11:128784636
|
C | T | 1 | a0001c0002t0005g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.655+2613C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784636 | ||||||
| chr11:128784705
|
C | CT | 7 | a0001c0001t0001g0156a0001c0001t0001g0224a0001c0001t0001g0297others(4): Show | 7 | HG01099.hp2 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+2683dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784705 | |||||
| chr11:128784719
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.655+2696C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784719 | ||||||
| chr11:128784757
|
T | A | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+2734T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784757 | ||||||
| chr11:128784846
|
G | C | 1 | a0001c0004t0003g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655+2823G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784846 | ||||||
| chr11:128784857
|
C | CTG | 27 | a0001c0001t0001g0142a0001c0001t0005g0027a0001c0002t0001g0001others(24): Show | 29 | HG00609.hp2 HG00621.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.655+2854_655+2855d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128784857 | |||||
| chr11:128784861
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.655+2838G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784861 | ||||||
| chr11:128784879
|
C | G | 15 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0029others(12): Show | 17 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+2856C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128784879 | ||||||
| chr11:128785282
|
G | A | 26 | a0001c0001t0005g0027a0001c0002t0001g0001a0001c0002t0001g0002others(23): Show | 28 | HG01109.hp1 HG01123.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.655+3259G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128785282 | ||||||
| chr11:128785587
|
T | C | 1 | a0002c0005t0001g0191 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.655+3564T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128785587 | ||||||
| chr11:128785882
|
A | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.655+3859A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128785882 | ||||||
| chr11:128785925
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0213others(2): Show | 5 | HG02109.hp1 HG03098.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+3902C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128785925 | ||||||
| chr11:128785947
|
A | C | 58 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0048others(55): Show | 58 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.655+3924A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128785947 | ||||||
| chr11:128786062
|
G | C | 1 | a0001c0001t0002g0221 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.655+4039G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786062 | ||||||
| chr11:128786069
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+4046A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786069 | ||||||
| chr11:128786091
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.655+4068C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786091 | ||||||
| chr11:128786234
|
T | G | 2 | a0001c0003t0003g0218a0001c0004t0003g0283 | 2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.655+4211T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786234 | ||||||
| chr11:128786262
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0055others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+4239G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786262 | ||||||
| chr11:128786349
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.655+4326C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786349 | ||||||
| chr11:128786378
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.655+4355T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786378 | ||||||
| chr11:128786417
|
A | T | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.655+4394A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786417 | ||||||
| chr11:128786471
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+4448A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786471 | ||||||
| chr11:128786610
|
C | A | 60 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0059others(57): Show | 60 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.655+4587C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786610 | ||||||
| chr11:128786611
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655+4588G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786611 | ||||||
| chr11:128786632
|
C | T | 1 | a0001c0002t0001g0286 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.655+4609C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786632 | ||||||
| chr11:128786831
|
A | G | 3 | a0001c0003t0003g0035a0001c0003t0003g0318a0001c0004t0003g0088 | 3 | HG01099.hp2 HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.655+4808A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128786831 | ||||||
| chr11:128787010
|
T | C | 1 | a0001c0003t0001g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+4987T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787010 | ||||||
| chr11:128787101
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.655+5078G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787101 | ||||||
| chr11:128787244
|
G | A | 2 | a0001c0003t0001g0070a0001c0004t0001g0214 | 2 | HG03130.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.655+5221G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787244 | ||||||
| chr11:128787320
|
A | T | 1 | a0001c0002t0001g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+5297A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787320 | ||||||
| chr11:128787695
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(44): Show | 48 | HG00642.hp2 HG01099.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+5672C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787695 | ||||||
| chr11:128787807
|
A | AT | 257 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(254): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.655+5801dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128787807 | |||||
| chr11:128787807
|
A | ATT | 13 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0246others(10): Show | 13 | HG01123.hp2 HG01891.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+5800_655+5801d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128787807 | |||||
| chr11:128787837
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.655+5814C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787837 | ||||||
| chr11:128787899
|
C | T | 1 | a0001c0003t0003g0311 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.655+5876C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787899 | ||||||
| chr11:128787933
|
A | C | 1 | a0001c0002t0001g0130 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.655+5910A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128787933 | ||||||
| chr11:128788013
|
C | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.655+5990C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788013 | ||||||
| chr11:128788061
|
C | T | 63 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0014others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.655+6038C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788061 | ||||||
| chr11:128788093
|
A | G | 5 | a0001c0003t0001g0011a0001c0004t0001g0009a0001c0004t0001g0287others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+6070A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788093 | ||||||
| chr11:128788268
|
A | G | 136 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.655+6245A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788268 | ||||||
| chr11:128788328
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.655+6305G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788328 | ||||||
| chr11:128788383
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.655+6360T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788383 | ||||||
| chr11:128788397
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.655+6374A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788397 | ||||||
| chr11:128788507
|
A | G | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.655+6484A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788507 | ||||||
| chr11:128788577
|
T | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.655+6554T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788577 | ||||||
| chr11:128788609
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+6586C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788609 | ||||||
| chr11:128788747
|
A | G | 67 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+6724A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788747 | ||||||
| chr11:128788874
|
C | G | 1 | a0001c0002t0001g0153 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.655+6851C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788874 | ||||||
| chr11:128788963
|
T | G | 1 | a0001c0001t0001g0271 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.655+6940T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788963 | ||||||
| chr11:128789178
|
T | C | 67 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+7155T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789178 | ||||||
| chr11:128789253
|
G | C | 1 | a0001c0001t0002g0319 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.655+7230G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789253 | ||||||
| chr11:128789289
|
A | G | 11 | a0001c0003t0001g0107a0001c0003t0003g0008a0001c0003t0003g0013others(8): Show | 11 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.655+7266A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789289 | ||||||
| chr11:128789339
|
G | A | 1 | a0001c0007t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+7316G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789339 | ||||||
| chr11:128789371
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.655+7348G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789371 | ||||||
| chr11:128789479
|
G | A | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+7456G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789479 | ||||||
| chr11:128789532
|
C | T | 2 | a0001c0004t0003g0041a0001c0011t0003g0093 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.655+7509C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789532 | ||||||
| chr11:128789592
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.655+7569C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789592 | ||||||
| chr11:128789645
|
C | T | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+7622C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789645 | ||||||
| chr11:128789758
|
G | A | 47 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(44): Show | 48 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.655+7735G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789758 | ||||||
| chr11:128789886
|
G | A | 67 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+7863G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128789886 | ||||||
| chr11:128790009
|
A | C | 11 | a0001c0003t0001g0107a0001c0003t0003g0008a0001c0003t0003g0013others(8): Show | 11 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.655+7986A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790009 | ||||||
| chr11:128790044
|
ATG | A | 16 | a0001c0001t0001g0032a0001c0001t0001g0288a0001c0001t0002g0289others(13): Show | 16 | HG00735.hp1 HG01099.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+8036_655+8037d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790044 | |||||
| chr11:128790048
|
G | A | 5 | a0001c0003t0001g0011a0001c0004t0001g0009a0001c0004t0001g0287others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+8025G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790048 | ||||||
| chr11:128790058
|
G | GCA | 111 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.655+8035_655+8036i others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790058 | ||||||
| chr11:128790063
|
T | TTC | 63 | a0001c0001t0002g0003a0001c0001t0002g0014a0001c0001t0002g0025others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.655+8040_655+8041i others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790063 | ||||||
| chr11:128790064
|
G | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(44): Show | 48 | HG00642.hp2 HG01123.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+8041G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790064 | ||||||
| chr11:128790065
|
C | T | 64 | a0001c0001t0002g0003a0001c0001t0002g0014a0001c0001t0002g0025others(61): Show | 65 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.655+8042C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790065 | ||||||
| chr11:128790066
|
A | G | 111 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.655+8043A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790066 | ||||||
| chr11:128790067
|
T | TTC | 6 | a0001c0001t0004g0123a0001c0003t0003g0013a0001c0003t0003g0318others(3): Show | 6 | HG01099.hp2 HG02055.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+8044_655+8045i others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790067 | ||||||
| chr11:128790068
|
G | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0288a0001c0001t0002g0289others(7): Show | 10 | HG00735.hp1 HG02109.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+8045G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790068 | ||||||
| chr11:128790069
|
C | CGT | 51 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0199others(48): Show | 52 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+8072_655+8073d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790069 | |||||
| chr11:128790069
|
C | T | 117 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.655+8046C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790069 | ||||||
| chr11:128790069
|
CGT | C | 11 | a0001c0001t0001g0060a0001c0001t0001g0089a0001c0001t0001g0324others(8): Show | 12 | HG00408.hp1 HG01109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+8072_655+8073d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790069 | |||||
| chr11:128790069
|
CGTGT | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0258a0001c0002t0001g0203others(1): Show | 4 | HG02074.hp2 HG02451.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+8070_655+8073d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790069 | |||||
| chr11:128790093
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 27 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+8070T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790093 | ||||||
| chr11:128790093
|
T | TGC | 6 | a0001c0001t0001g0032a0001c0001t0001g0156a0001c0001t0001g0274others(3): Show | 6 | HG02615.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+8071_655+8072i others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790093 | |||||
| chr11:128790103
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.655+8080T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790103 | ||||||
| chr11:128790125
|
C | A | 67 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+8102C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790125 | ||||||
| chr11:128790230
|
T | C | 3 | a0001c0001t0004g0151a0001c0001t0004g0238a0001c0001t0004g0291 | 3 | HG02129.hp2 NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.655+8207T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790230 | ||||||
| chr11:128790253
|
A | AT | 54 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 56 | HG00642.hp2 HG01109.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.655+8243dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790253 | |||||
| chr11:128790253
|
A | ATT | 67 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+8242_655+8243d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790253 | |||||
| chr11:128790253
|
A | ATTTT | 10 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(7): Show | 10 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+8240_655+8243d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128790253 | |||||
| chr11:128790267
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.655+8244C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790267 | ||||||
| chr11:128790271
|
G | A | 33 | a0001c0001t0002g0014a0001c0001t0002g0025a0001c0001t0002g0031others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+8248G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790271 | ||||||
| chr11:128790313
|
A | G | 73 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.655+8290A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790313 | ||||||
| chr11:128790408
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.655+8385A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790408 | ||||||
| chr11:128790492
|
T | C | 1 | a0001c0004t0001g0009 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+8469T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790492 | ||||||
| chr11:128790851
|
A | G | 127 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.655+8828A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790851 | ||||||
| chr11:128790854
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.655+8831G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790854 | ||||||
| chr11:128790856
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.655+8833T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790856 | ||||||
| chr11:128790979
|
C | G | 66 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(63): Show | 67 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.655+8956C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790979 | ||||||
| chr11:128791337
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.655+9314C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791337 | ||||||
| chr11:128791462
|
A | G | 13 | a0001c0001t0001g0089a0001c0001t0001g0324a0001c0002t0001g0001others(10): Show | 14 | HG01109.hp1 HG02572.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.655+9439A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791462 | ||||||
| chr11:128791526
|
C | T | 3 | a0001c0001t0002g0099a0001c0001t0002g0104a0001c0003t0001g0217 | 3 | HG00733.hp2 HG01070.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.655+9503C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791526 | ||||||
| chr11:128791574
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.655+9551A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791574 | ||||||
| chr11:128791755
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.655+9732G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791755 | ||||||
| chr11:128791775
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.655+9752A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791775 | ||||||
| chr11:128791778
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(127): Show | 132 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.655+9755A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791778 | ||||||
| chr11:128791924
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655+9901C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791924 | ||||||
| chr11:128791932
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.655+9909C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791932 | ||||||
| chr11:128791933
|
G | A | 1 | a0001c0002t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.655+9910G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791933 | ||||||
| chr11:128791958
|
G | A | 129 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.655+9935G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791958 | ||||||
| chr11:128792074
|
C | T | 3 | a0001c0003t0001g0161a0001c0003t0001g0304a0001c0003t0001g0313 | 3 | HG02015.hp1 HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.655+10051C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792074 | ||||||
| chr11:128792207
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.655+10184T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792207 | ||||||
| chr11:128792211
|
C | G | 1 | a0001c0001t0001g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.655+10188C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792211 | ||||||
| chr11:128792215
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0307 | 2 | NA19068.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.655+10192C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792215 | ||||||
| chr11:128792274
|
A | G | 2 | a0001c0004t0003g0041a0001c0011t0003g0093 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.655+10251A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792274 | ||||||
| chr11:128792455
|
G | A | 129 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.655+10432G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792455 | ||||||
| chr11:128792675
|
TC | T | 129 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(126): Show | 131 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.655+10653delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792675 | ||||||
| chr11:128792684
|
T | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.655+10661T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792684 | ||||||
| chr11:128792719
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.655+10696T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792719 | ||||||
| chr11:128792723
|
G | C | 7 | a0001c0001t0001g0089a0001c0001t0001g0324a0001c0002t0001g0001others(4): Show | 8 | HG01109.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.655+10700G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792723 | ||||||
| chr11:128792795
|
T | C | 3 | a0001c0003t0001g0128a0001c0004t0001g0166a0001c0004t0001g0167 | 3 | HG01975.hp1 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.655+10772T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792795 | ||||||
| chr11:128793055
|
C | T | 2 | a0001c0003t0001g0024a0001c0003t0001g0112 | 2 | HG02572.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.655+11032C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793055 | ||||||
| chr11:128793066
|
C | T | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.655+11043C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793066 | ||||||
| chr11:128793068
|
G | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.655+11045G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793068 | ||||||
| chr11:128793073
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.655+11050G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793073 | ||||||
| chr11:128793215
|
G | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0206a0001c0001t0001g0274others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+11192G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793215 | ||||||
| chr11:128793231
|
T | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0033others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.655+11208T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793231 | ||||||
| chr11:128793356
|
G | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.655+11333G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793356 | ||||||
| chr11:128793360
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655+11337C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793360 | ||||||
| chr11:128793562
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+11539C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793562 | ||||||
| chr11:128793686
|
G | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.655+11663G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793686 | ||||||
| chr11:128793742
|
T | A | 59 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.656-11624T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793742 | ||||||
| chr11:128793797
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.656-11569C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793797 | ||||||
| chr11:128793930
|
G | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-11436G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793930 | ||||||
| chr11:128793936
|
G | A | 12 | a0001c0001t0002g0025a0001c0001t0002g0047a0001c0001t0002g0053others(9): Show | 12 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-11430G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793936 | ||||||
| chr11:128794013
|
G | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.656-11353G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794013 | ||||||
| chr11:128794019
|
C | T | 1 | a0001c0007t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-11347C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794019 | ||||||
| chr11:128794020
|
G | T | 1 | a0001c0001t0002g0103 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.656-11346G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794020 | ||||||
| chr11:128794112
|
A | G | 59 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.656-11254A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794112 | ||||||
| chr11:128794117
|
C | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(29): Show | 33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.656-11249C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794117 | ||||||
| chr11:128794133
|
C | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-11233C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794133 | ||||||
| chr11:128794200
|
A | G | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-11166A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794200 | ||||||
| chr11:128794282
|
T | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-11084T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794282 | ||||||
| chr11:128794343
|
G | A | 137 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.656-11023G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794343 | ||||||
| chr11:128794370
|
T | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-10996T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794370 | ||||||
| chr11:128794387
|
G | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-10979G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794387 | ||||||
| chr11:128794620
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0075others(3): Show | 6 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-10746C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794620 | ||||||
| chr11:128794670
|
T | C | 15 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(12): Show | 15 | HG01123.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.656-10696T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794670 | ||||||
| chr11:128794695
|
C | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-10671C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794695 | ||||||
| chr11:128794740
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0235a0001c0001t0001g0247 | 3 | HG04228.hp1 NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.656-10626G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794740 | ||||||
| chr11:128794846
|
T | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-10520T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794846 | ||||||
| chr11:128794894
|
G | A | 32 | a0001c0001t0002g0014a0001c0001t0002g0025a0001c0001t0002g0031others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.656-10472G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794894 | ||||||
| chr11:128794946
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.656-10420C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128794946 | ||||||
| chr11:128795382
|
G | A | 3 | a0001c0004t0001g0214a0001c0004t0001g0220a0001c0004t0001g0267 | 3 | HG03130.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.656-9984G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795382 | ||||||
| chr11:128795559
|
A | AT | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.656-9789dupT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128795559 | |||||
| chr11:128795559
|
A | ATT | 44 | a0001c0001t0001g0208a0001c0001t0001g0324a0001c0001t0002g0010others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.656-9790_656-9789d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128795559 | |||||
| chr11:128795559
|
A | ATTT | 49 | a0001c0001t0001g0089a0001c0001t0002g0003a0001c0001t0002g0042others(46): Show | 50 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.656-9791_656-9789d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128795559 | |||||
| chr11:128795559
|
A | ATTTT | 12 | a0001c0001t0002g0082a0001c0001t0005g0027a0001c0001t0005g0038others(9): Show | 12 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.656-9792_656-9789d others(6): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128795559 | |||||
| chr11:128795579
|
A | T | 2 | a0001c0001t0005g0281a0001c0001t0005g0282 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.656-9787A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795579 | ||||||
| chr11:128795637
|
G | A | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-9729G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795637 | ||||||
| chr11:128795644
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.656-9722G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795644 | ||||||
| chr11:128795676
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.656-9690G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795676 | ||||||
| chr11:128795802
|
T | G | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-9564T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795802 | ||||||
| chr11:128795815
|
G | T | 1 | a0001c0001t0012g0309 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-9551G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795815 | ||||||
| chr11:128795872
|
T | C | 10 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(7): Show | 10 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-9494T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795872 | ||||||
| chr11:128795956
|
A | G | 1 | a0001c0003t0003g0218 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-9410A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128795956 | ||||||
| chr11:128796006
|
A | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-9360A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796006 | ||||||
| chr11:128796092
|
A | AC | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-9268dupC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128796092 | |||||
| chr11:128796210
|
C | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-9156C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796210 | ||||||
| chr11:128796212
|
A | G | 12 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0124others(9): Show | 12 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-9154A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796212 | ||||||
| chr11:128796335
|
T | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-9031T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796335 | ||||||
| chr11:128796379
|
G | A | 51 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(48): Show | 52 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.656-8987G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796379 | ||||||
| chr11:128796564
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.656-8802T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796564 | ||||||
| chr11:128796701
|
G | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-8665G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796701 | ||||||
| chr11:128796852
|
A | G | 59 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.656-8514A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796852 | ||||||
| chr11:128796931
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.656-8435C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796931 | ||||||
| chr11:128796932
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-8434G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128796932 | ||||||
| chr11:128797133
|
G | A | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-8233G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797133 | ||||||
| chr11:128797165
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.656-8201C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797165 | ||||||
| chr11:128797185
|
C | G | 1 | a0003c0013t0001g0080 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656-8181C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797185 | ||||||
| chr11:128797501
|
A | C | 53 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(50): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-7865A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797501 | ||||||
| chr11:128797533
|
T | C | 65 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(62): Show | 66 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.656-7833T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797533 | ||||||
| chr11:128797574
|
T | C | 1 | a0001c0003t0001g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.656-7792T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797574 | ||||||
| chr11:128797723
|
C | T | 2 | a0001c0003t0001g0107a0001c0004t0003g0023 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.656-7643C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797723 | ||||||
| chr11:128797752
|
G | C | 59 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.656-7614G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797752 | ||||||
| chr11:128797761
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.656-7605G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797761 | ||||||
| chr11:128797907
|
C | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.656-7459C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797907 | ||||||
| chr11:128797909
|
C | T | 11 | a0001c0003t0001g0107a0001c0003t0003g0008a0001c0003t0003g0013others(8): Show | 11 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.656-7457C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797909 | ||||||
| chr11:128797969
|
G | A | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-7397G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128797969 | ||||||
| chr11:128798038
|
A | G | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-7328A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798038 | ||||||
| chr11:128798053
|
G | C | 56 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(53): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-7313G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798053 | ||||||
| chr11:128798069
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-7297G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798069 | ||||||
| chr11:128798105
|
A | G | 56 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(53): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-7261A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798105 | ||||||
| chr11:128798196
|
G | A | 2 | a0001c0001t0002g0082a0001c0003t0001g0070 | 2 | NA19085.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.656-7170G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798196 | ||||||
| chr11:128798197
|
T | C | 45 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(42): Show | 46 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-7169T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798197 | ||||||
| chr11:128798225
|
T | C | 6 | a0001c0001t0002g0065a0001c0001t0002g0131a0001c0001t0002g0243others(3): Show | 6 | NA18953.hp2 NA18969.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-7141T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798225 | ||||||
| chr11:128798298
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.656-7068G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798298 | ||||||
| chr11:128798330
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.656-7036C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798330 | ||||||
| chr11:128798398
|
GA | G | 45 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(42): Show | 46 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-6967delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798398 | ||||||
| chr11:128798407
|
G | A | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-6959G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798407 | ||||||
| chr11:128798446
|
C | T | 2 | a0001c0002t0001g0036a0001c0002t0001g0256 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.656-6920C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798446 | ||||||
| chr11:128798702
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.656-6664C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798702 | ||||||
| chr11:128798768
|
G | A | 5 | a0001c0003t0001g0132a0001c0003t0001g0195a0001c0003t0001g0196others(2): Show | 5 | HG00408.hp2 NA18951.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-6598G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798768 | ||||||
| chr11:128798817
|
A | G | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-6549A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798817 | ||||||
| chr11:128798945
|
G | A | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.656-6421G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798945 | ||||||
| chr11:128798979
|
T | G | 1 | a0001c0001t0017g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.656-6387T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128798979 | ||||||
| chr11:128799020
|
A | ATAT | 7 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0095others(4): Show | 7 | HG00673.hp1 HG02056.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-6314_656-6312d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799020 | |||||
| chr11:128799020
|
ATAT | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(2): Show | 5 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-6314_656-6312d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799020 | |||||
| chr11:128799037
|
A | ATTTTTTT others(19): Show |
1 | a0001c0003t0003g0311 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.656-6327_656-6326i others(28): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799037 | |||||
| chr11:128799037
|
A | T | 14 | a0001c0001t0002g0025a0001c0001t0002g0042a0001c0001t0002g0047others(11): Show | 14 | HG01109.hp2 HG01123.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-6329A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799037 | ||||||
| chr11:128799039
|
TA | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0231a0001c0001t0004g0291 | 3 | HG02129.hp1 NA18939.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.656-6326delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799039 | ||||||
| chr11:128799040
|
A | ATTTTTTT others(18): Show |
1 | a0001c0003t0007g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656-6324_656-6323i others(27): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799040 | |||||
| chr11:128799040
|
A | T | 67 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0025others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.656-6326A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799040 | ||||||
| chr11:128799042
|
T | A | 1 | a0001c0001t0002g0289 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.656-6324T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799042 | ||||||
| chr11:128799042
|
TA | T | 7 | a0001c0001t0002g0082a0001c0003t0001g0024a0001c0003t0001g0070others(4): Show | 7 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-6323delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799042 | ||||||
| chr11:128799043
|
A | T | 100 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0039others(97): Show | 101 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.656-6323A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799043 | ||||||
| chr11:128799046
|
A | T | 163 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.656-6320A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799046 | ||||||
| chr11:128799049
|
A | T | 175 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.656-6317A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799049 | ||||||
| chr11:128799052
|
A | ATTT | 51 | a0001c0001t0001g0026a0001c0001t0001g0059a0001c0001t0001g0062others(48): Show | 51 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.656-6312_656-6310d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799052 | |||||
| chr11:128799052
|
A | ATTTTTTT others(4): Show |
1 | a0001c0003t0003g0013 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.656-6310_656-6309i others(13): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128799052 | |||||
| chr11:128799052
|
A | T | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(224): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.656-6314A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799052 | ||||||
| chr11:128799279
|
C | T | 45 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(42): Show | 46 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-6087C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799279 | ||||||
| chr11:128799292
|
C | T | 36 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0042others(33): Show | 37 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.656-6074C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799292 | ||||||
| chr11:128799701
|
G | A | 77 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.656-5665G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799701 | ||||||
| chr11:128799768
|
G | T | 2 | a0001c0001t0001g0208a0001c0001t0010g0090 | 2 | HG01074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-5598G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799768 | ||||||
| chr11:128799829
|
C | G | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-5537C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799829 | ||||||
| chr11:128799873
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.656-5493C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799873 | ||||||
| chr11:128799880
|
T | A | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-5486T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799880 | ||||||
| chr11:128799925
|
C | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.656-5441C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799925 | ||||||
| chr11:128799963
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-5403G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799963 | ||||||
| chr11:128799976
|
A | G | 1 | a0001c0004t0003g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.656-5390A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799976 | ||||||
| chr11:128800016
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-5350G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800016 | ||||||
| chr11:128800072
|
G | C | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-5294G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800072 | ||||||
| chr11:128800199
|
A | G | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-5167A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800199 | ||||||
| chr11:128800206
|
G | A | 1 | a0001c0004t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-5160G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800206 | ||||||
| chr11:128800213
|
A | G | 1 | a0001c0004t0003g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.656-5153A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800213 | ||||||
| chr11:128800220
|
C | T | 45 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(42): Show | 46 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-5146C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800220 | ||||||
| chr11:128800232
|
A | G | 1 | a0001c0002t0001g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.656-5134A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800232 | ||||||
| chr11:128800295
|
A | T | 56 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(53): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-5071A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800295 | ||||||
| chr11:128800413
|
T | C | 185 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.656-4953T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800413 | ||||||
| chr11:128800444
|
C | T | 7 | a0001c0001t0001g0089a0001c0001t0001g0324a0001c0002t0001g0001others(4): Show | 8 | HG01109.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-4922C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800444 | ||||||
| chr11:128800471
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-4895G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800471 | ||||||
| chr11:128800569
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.656-4797G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800569 | ||||||
| chr11:128800583
|
A | G | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-4783A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800583 | ||||||
| chr11:128800623
|
CTT | C | 56 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(53): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-4741_656-4740d others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128800623 | |||||
| chr11:128800626
|
T | C | 1 | a0001c0002t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.656-4740T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128800626 | ||||||
| chr11:128801043
|
A | G | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-4323A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801043 | ||||||
| chr11:128801206
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.656-4160C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801206 | ||||||
| chr11:128801318
|
C | T | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.656-4048C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801318 | ||||||
| chr11:128801611
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0010g0090 | 2 | HG01074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-3755C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801611 | ||||||
| chr11:128801628
|
A | G | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-3738A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801628 | ||||||
| chr11:128801837
|
A | C | 59 | a0001c0001t0001g0140a0001c0001t0001g0157a0001c0001t0001g0299others(56): Show | 60 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.656-3529A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801837 | ||||||
| chr11:128801885
|
G | A | 7 | a0001c0001t0005g0038a0001c0001t0005g0210a0001c0001t0005g0212others(4): Show | 7 | HG01891.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-3481G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128801885 | ||||||
| chr11:128802055
|
C | A | 44 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.656-3311C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802055 | ||||||
| chr11:128802121
|
G | A | 3 | a0001c0004t0003g0041a0001c0004t0003g0225a0001c0011t0003g0093 | 3 | HG03225.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.656-3245G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802121 | ||||||
| chr11:128802289
|
G | A | 44 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.656-3077G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802289 | ||||||
| chr11:128802300
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.656-3066C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802300 | ||||||
| chr11:128802429
|
G | A | 1 | a0001c0003t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.656-2937G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802429 | ||||||
| chr11:128802613
|
T | G | 55 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(52): Show | 56 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.656-2753T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802613 | ||||||
| chr11:128802686
|
A | C | 134 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.656-2680A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802686 | ||||||
| chr11:128802729
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.656-2637A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802729 | ||||||
| chr11:128802746
|
A | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0224 | 2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656-2620A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802746 | ||||||
| chr11:128802755
|
C | A | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-2611C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802755 | ||||||
| chr11:128802881
|
T | C | 1 | a0001c0001t0004g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.656-2485T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802881 | ||||||
| chr11:128802923
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-2443G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802923 | ||||||
| chr11:128802931
|
C | T | 29 | a0001c0003t0001g0016a0001c0003t0001g0072a0001c0003t0001g0083others(26): Show | 30 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.656-2435C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128802931 | ||||||
| chr11:128803032
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.656-2334G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803032 | ||||||
| chr11:128803095
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.656-2271G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803095 | ||||||
| chr11:128803123
|
C | G | 3 | a0001c0002t0001g0001a0001c0002t0001g0029a0001c0002t0001g0296 | 4 | HG02723.hp1 HG03130.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2243C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803123 | ||||||
| chr11:128803127
|
TC | T | 155 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.656-2236delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128803127 | |||||
| chr11:128803158
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.656-2208G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803158 | ||||||
| chr11:128803218
|
C | T | 4 | a0001c0001t0002g0014a0001c0001t0002g0103a0001c0001t0002g0139others(1): Show | 4 | NA18939.hp2 NA18948.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2148C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803218 | ||||||
| chr11:128803236
|
T | TACC | 44 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.656-2127_656-2125d others(5): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 128803236 | |||||
| chr11:128803284
|
A | C | 46 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(43): Show | 47 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-2082A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803284 | ||||||
| chr11:128803340
|
G | A | 46 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(43): Show | 47 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-2026G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803340 | ||||||
| chr11:128803402
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.656-1964A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803402 | ||||||
| chr11:128803456
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-1910C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803456 | ||||||
| chr11:128803573
|
T | C | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-1793T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803573 | ||||||
| chr11:128803574
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-1792G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803574 | ||||||
| chr11:128803639
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.656-1727C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803639 | ||||||
| chr11:128803750
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-1616G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803750 | ||||||
| chr11:128803967
|
C | G | 1 | a0001c0002t0001g0215 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-1399C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128803967 | ||||||
| chr11:128804681
|
C | T | 55 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(52): Show | 56 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.656-685C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804681 | ||||||
| chr11:128804737
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.656-629G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804737 | ||||||
| chr11:128804790
|
C | T | 2 | a0001c0002t0001g0052a0001c0002t0001g0276 | 2 | NA18985.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.656-576C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804790 | ||||||
| chr11:128804885
|
G | A | 1 | a0001c0001t0002g0243 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.656-481G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804885 | ||||||
| chr11:128804908
|
A | G | 1 | a0001c0002t0005g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.656-458A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804908 | ||||||
| chr11:128804919
|
G | A | 7 | a0001c0001t0001g0089a0001c0001t0001g0324a0001c0002t0001g0001others(4): Show | 8 | HG01109.hp1 HG02723.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-447G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804919 | ||||||
| chr11:128804952
|
G | A | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.656-414G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804952 | ||||||
| chr11:128804986
|
C | T | 57 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.656-380C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128804986 | ||||||
| chr11:128805069
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01167.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.656-297G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128805069 | ||||||
| chr11:128805074
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.656-292A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128805074 | ||||||
| chr11:128805220
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.656-146G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128805220 | ||||||
| chr11:128805341
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.656-25A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128805341 | ||||||
| chr11:128805465
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0226a0001c0001t0001g0230others(3): Show | 6 | NA18940.hp1 NA18947.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.721+34G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805465 | ||||||
| chr11:128805506
|
C | T | 57 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.721+75C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805506 | ||||||
| chr11:128805653
|
G | A | 1 | a0001c0003t0001g0016 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.721+222G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805653 | ||||||
| chr11:128805689
|
A | T | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.721+258A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805689 | ||||||
| chr11:128805762
|
T | G | 77 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.721+331T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805762 | ||||||
| chr11:128805769
|
T | C | 57 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.721+338T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805769 | ||||||
| chr11:128805777
|
C | T | 2 | a0001c0003t0001g0161a0001c0003t0001g0313 | 2 | HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.721+346C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805777 | ||||||
| chr11:128805797
|
T | C | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.721+366T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805797 | ||||||
| chr11:128805803
|
C | A | 5 | a0001c0003t0001g0011a0001c0004t0001g0009a0001c0004t0001g0287others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.721+372C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128805803 | ||||||
| chr11:128806188
|
TATTA | T | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.721+762_721+765del others(4): Show |
FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 128806188 | |||||
| chr11:128806265
|
C | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.721+834C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806265 | ||||||
| chr11:128806309
|
T | A | 57 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.722-871T>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806309 | ||||||
| chr11:128806342
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.722-838T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806342 | ||||||
| chr11:128806606
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.722-574G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806606 | ||||||
| chr11:128806805
|
G | A | 5 | a0001c0003t0001g0011a0001c0004t0001g0009a0001c0004t0001g0287others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.722-375G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806805 | ||||||
| chr11:128806841
|
G | A | 1 | a0001c0002t0001g0286 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.722-339G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806841 | ||||||
| chr11:128806973
|
G | T | 43 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(40): Show | 44 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.722-207G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806973 | ||||||
| chr11:128806981
|
T | C | 1 | a0001c0004t0001g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.722-199T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128806981 | ||||||
| chr11:128807018
|
A | G | 43 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(40): Show | 44 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.722-162A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128807018 | ||||||
| chr11:128807085
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0078a0001c0001t0002g0148others(2): Show | 6 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.722-95C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 6/8 | chr11 | 128807085 | ||||||
| chr11:128807453
|
G | A | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+214G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128807453 | ||||||
| chr11:128807510
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0118 | 2 | HG02056.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.781+271G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128807510 | ||||||
| chr11:128807564
|
C | T | 44 | a0001c0003t0001g0011a0001c0003t0001g0016a0001c0003t0001g0024others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.781+325C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128807564 | ||||||
| chr11:128807800
|
G | C | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+561G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128807800 | ||||||
| chr11:128808229
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.782-928G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808229 | ||||||
| chr11:128808265
|
C | T | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.782-892C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808265 | ||||||
| chr11:128808330
|
A | C | 32 | a0001c0001t0002g0014a0001c0001t0002g0025a0001c0001t0002g0031others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.782-827A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808330 | ||||||
| chr11:128808410
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.782-747A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808410 | ||||||
| chr11:128808442
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.782-715G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808442 | ||||||
| chr11:128808467
|
G | A | 1 | a0001c0003t0001g0306 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.782-690G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808467 | ||||||
| chr11:128808542
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.782-615G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808542 | ||||||
| chr11:128808725
|
AT | A | 96 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.782-429delT | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 128808725 | |||||
| chr11:128808728
|
T | C | 10 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(7): Show | 10 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-429T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808728 | ||||||
| chr11:128808728
|
TA | T | 11 | a0001c0001t0001g0208a0001c0001t0010g0090a0001c0003t0001g0024others(8): Show | 11 | HG01074.hp1 HG02572.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.782-418delA | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 128808728 | |||||
| chr11:128808729
|
A | C | 96 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(93): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.782-428A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128808729 | ||||||
| chr11:128809087
|
T | C | 1 | a0001c0012t0015g0084 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.782-70T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128809087 | ||||||
| chr11:128809110
|
A | G | 12 | a0001c0003t0001g0107a0001c0003t0003g0008a0001c0003t0003g0013others(9): Show | 12 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-47A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128809110 | ||||||
| chr11:128809123
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG02074.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.782-34A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 7/8 | chr11 | 128809123 | ||||||
| chr11:128809305
|
G | C | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.829+101G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809305 | ||||||
| chr11:128809316
|
G | C | 134 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+112G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809316 | ||||||
| chr11:128809427
|
A | G | 6 | a0001c0001t0001g0140a0001c0002t0001g0061a0001c0002t0001g0063others(3): Show | 6 | HG00423.hp1 NA18956.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.829+223A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809427 | ||||||
| chr11:128809459
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.829+255T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809459 | ||||||
| chr11:128809487
|
C | T | 2 | a0001c0003t0003g0311a0001c0003t0007g0147 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.829+283C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809487 | ||||||
| chr11:128809506
|
G | A | 29 | a0001c0003t0001g0016a0001c0003t0001g0072a0001c0003t0001g0083others(26): Show | 30 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.829+302G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809506 | ||||||
| chr11:128809513
|
A | G | 3 | a0001c0004t0003g0041a0001c0004t0003g0225a0001c0011t0003g0093 | 3 | HG03225.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.829+309A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809513 | ||||||
| chr11:128809518
|
A | G | 73 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.829+314A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809518 | ||||||
| chr11:128809548
|
G | A | 1 | a0001c0004t0003g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.829+344G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809548 | ||||||
| chr11:128809548
|
G | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG00639.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.829+344G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809548 | ||||||
| chr11:128809555
|
G | A | 68 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.829+351G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809555 | ||||||
| chr11:128809566
|
A | G | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.829+362A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809566 | ||||||
| chr11:128809652
|
T | C | 14 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(11): Show | 14 | HG01123.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.829+448T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809652 | ||||||
| chr11:128809671
|
G | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0033others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.829+467G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809671 | ||||||
| chr11:128809685
|
G | C | 1 | a0001c0002t0001g0001 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.829+481G>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809685 | ||||||
| chr11:128809746
|
C | T | 29 | a0001c0003t0001g0016a0001c0003t0001g0072a0001c0003t0001g0083others(26): Show | 30 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.829+542C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809746 | ||||||
| chr11:128809920
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.830-539T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128809920 | ||||||
| chr11:128810022
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.830-437C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128810022 | ||||||
| chr11:128810025
|
GC | G | 9 | a0001c0001t0005g0027a0001c0001t0005g0038a0001c0001t0005g0210others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-430delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 128810025 | |||||
| chr11:128810258
|
C | T | 29 | a0001c0003t0001g0016a0001c0003t0001g0072a0001c0003t0001g0083others(26): Show | 30 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.830-201C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128810258 | ||||||
| chr11:128810296
|
A | G | 6 | a0001c0003t0001g0024a0001c0003t0001g0070a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-163A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128810296 | ||||||
| chr11:128810381
|
C | G | 2 | a0001c0003t0001g0024a0001c0003t0001g0112 | 2 | HG02572.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.830-78C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128810381 |