Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDGTI others(447): Show |
chr11 | 128689072 | 128818267 |
| a0002 | 0/0 | 452 | 5 | 0 | 1 | 4 | 0 | 0 | 4 | FLI1_chr11_128689072_128818267 | FLI1 | MDGTI others(447): Show |
chr11 | 128689072 | 128818267 |
| a0003 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | MDGTI others(447): Show |
chr11 | 128689072 | 128818267 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 214 | 36 | 47 | 99 | 5 | 25 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0002 | 0/0 | 1356 | 48 | 21 | 5 | 20 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0003 | 0/0 | 1356 | 33 | 10 | 2 | 15 | 1 | 5 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0004 | 0/0 | 1356 | 19 | 13 | 2 | 2 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0006 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0007 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0008 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0009 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0011 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0001c0012 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0002c0005 | 0/0 | 1356 | 5 | 0 | 1 | 4 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
chr11 | 128689072 | 128818267 | ||
| a0003c0013 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | ATGGA others(1351): Show |
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 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0002 | 0/1 | 3379 | 51 | 3 | 14 | 24 | 2 | 7 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3374): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0004 | 0/0 | 3378 | 13 | 0 | 1 | 12 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3373): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0005 | 0/0 | 3378 | 8 | 8 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3373): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0008 | 0/0 | 3824 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3819): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0009 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0010 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0012 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0013 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3819): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0014 | 0/0 | 3825 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0016 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0001t0017 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0002t0001 | 0/0 | 3825 | 42 | 20 | 2 | 18 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0002t0002 | 0/0 | 3379 | 4 | 0 | 2 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3374): Show |
chr11 | 128689072 | 128818267 |
| a0001c0002t0005 | 0/0 | 3378 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3373): Show |
chr11 | 128689072 | 128818267 |
| a0001c0002t0018 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0003t0001 | 0/0 | 3825 | 23 | 4 | 1 | 12 | 1 | 5 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0003t0003 | 0/0 | 3825 | 6 | 5 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0003t0006 | 0/0 | 3825 | 3 | 0 | 0 | 3 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0003t0007 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0004t0001 | 0/0 | 3825 | 11 | 5 | 2 | 2 | 0 | 2 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0004t0003 | 0/0 | 3825 | 7 | 7 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0004t0011 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0006t0001 | 0/0 | 3825 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0007t0003 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0008t0001 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0009t0001 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0010t0002 | 0/0 | 3379 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3374): Show |
chr11 | 128689072 | 128818267 |
| a0001c0011t0003 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0001c0012t0015 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0002c0005t0001 | 0/0 | 3825 | 5 | 0 | 1 | 4 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| a0003c0013t0001 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | CTCTT others(3820): Show |
chr11 | 128689072 | 128818267 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0013 | 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 |
| 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 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0101 | 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 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0117 | 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 |
| a0001c0001t0001g0122 | 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 |
| a0001c0001t0001g0125 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0148 | 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 |
| a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0186 | 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 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0256 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0001g0322 | 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 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0050 | 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 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0121 | 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 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0156 | 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 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0004g0296 | 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 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0005g0279 | 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 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0009g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0010g0098 | 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 |
| a0001c0001t0014g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0016g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0001t0017g0302 | 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 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0210 | 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 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0002t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0089 | 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 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0001g0305 | 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 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0003g0317 | 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 |
| a0001c0003t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0003t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0001g0293 | 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 |
| a0001c0004t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0004t0003g0282 | 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 |
| a0001c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0007t0003g0057 | 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 |
| a0001c0009t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0010t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0011t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0001c0012t0015g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0002c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| a0003c0013t0001g0086 | 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 | g0316 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0232 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | GBR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0080 | 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 | g0063 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | 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 | g0034 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0179 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | CHS | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0209 | 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 | g0059 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0317 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0202 | 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 | g0185 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01258 | hp2 | a0001 | c0001 | t0017 | g0302 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0219 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0126 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0177 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0168 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02055 | hp1 | a0001 | c0002 | t0018 | g0024 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02055 | hp2 | a0001 | c0004 | t0003 | g0276 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02148 | hp1 | a0002 | c0005 | t0001 | g0192 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02165 | hp2 | a0001 | c0010 | t0002 | g0311 | EAS | CDX | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0176 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0289 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02451 | hp2 | a0001 | c0012 | t0015 | g0090 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0016 | 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 | g0212 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02622 | hp2 | a0001 | c0004 | t0003 | g0282 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0292 | 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 | g0287 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0233 | 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 | g0086 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0022 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02965 | hp2 | a0001 | c0004 | t0003 | g0096 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0191 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0266 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0097 | 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 | g0215 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0098 | AFR | ESN | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0226 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03453 | hp1 | a0001 | c0011 | t0003 | g0100 | 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 | g0078 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0218 | 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 | g0322 | AFR | GWD | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | 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 | g0029 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0081 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | 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 | g0180 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03710 | hp2 | a0001 | c0001 | t0014 | g0062 | SAS | PJL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0038 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0181 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0036 | 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 | g0293 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0273 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0092 | 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 | g0237 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0303 | EAS | CHB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0032 | 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 | g0321 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0129 | 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 | g0120 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18971 | hp1 | a0002 | c0005 | t0001 | g0298 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0058 | 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 | g0251 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0006 | 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 | g0173 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18992 | hp2 | a0001 | c0003 | t0006 | g0224 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19005 | hp1 | a0001 | c0009 | t0001 | g0141 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19007 | hp1 | a0001 | c0006 | t0001 | g0245 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19012 | hp1 | a0001 | c0006 | t0001 | g0067 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19043 | hp1 | a0001 | c0003 | t0007 | g0145 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19058 | hp1 | a0002 | c0005 | t0001 | g0048 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0260 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19077 | hp2 | a0002 | c0005 | t0001 | g0115 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0235 | 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 | g0175 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0270 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ASW | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0267 | SAS | GIH | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | GIH | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0095 | AMR | CLM | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0286 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | MSL | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA18955 | hp2 | a0002 | c0005 | t0001 | g0278 | 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 | g0210 | AFR | USA | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA21309 | hp1 | a0001 | c0007 | t0003 | g0057 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0320 | REF | REF | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0151 | REF | REF | FLI1_chr11_128689072_128818267 | FLI1 | chr11 | 128689072 | 128818267 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 77 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(74): Show |
splice_region_variant | LOW | c.*1834_*2526del | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 9/9 | chr11 | 128812821 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128758291 | C | T | 2 | a0001c0011 a0001c0012 |
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 | a0001c0009 a0001c0010 |
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 | a0001c0002 a0001c0004 a0001c0009 others(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 | a0001c0003 a0001c0004 a0001c0006 others(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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0005 a0001c0002t0005 |
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 | a0001c0001t0008 a0001c0001t0009 |
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 | a0001c0003t0003 a0001c0003t0007 a0001c0004t0003 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(3): Show |
77 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(74): 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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(3): Show |
77 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(74): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:128694294 | G | T | 1 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0008 | 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 | 2 | a0001c0001t0002g0006 a0001c0002t0001g0321 |
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 | |||||||
| chr11:128694648 | C | G | 1 | a0001c0001t0002g0319 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.18+372C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128694648 | |||||||
| chr11:128694707 | G | A | 2 | a0001c0003t0003g0009 a0001c0004t0001g0010 |
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 | a0001c0001t0002g0318 | 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 | a0001c0001t0002g0011 | 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 | 103 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(100): Show |
105 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(102): 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 | 218 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): 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 | a0001c0003t0001g0012 | 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 | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.18+825T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128695101 | |||||||
| chr11:128695139 | C | T | 32 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0292 others(29): 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 | a0001c0003t0003g0317 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0002t0001g0208 |
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 | a0001c0003t0003g0317 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0002g0316 | 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 | a0001c0002t0001g0285 | 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 | 174 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(171): 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0002g0205 | 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 | a0001c0002t0001g0314 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0013 | 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 | a0001c0002t0001g0102 a0001c0002t0001g0103 |
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 | a0001c0002t0001g0217 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0287 | 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 | a0001c0002t0001g0313 | 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 | a0001c0001t0002g0220 a0001c0003t0003g0219 a0001c0004t0001g0221 |
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 | 37 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0292 others(34): 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 | a0001c0002t0001g0216 | 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 | 217 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0222 a0001c0003t0006g0004 others(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 | a0001c0001t0001g0203 a0001c0002t0001g0204 |
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 | a0001c0002t0001g0284 | 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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | 164 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(161): Show |
168 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(165): 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 | a0001c0003t0003g0014 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(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 | a0001c0001t0001g0225 a0001c0003t0003g0219 a0001c0004t0003g0226 |
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 |
43 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0240 others(40): 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0272 others(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 | a0001c0004t0003g0276 a0001c0011t0003g0100 |
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 | a0001c0004t0001g0215 | 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 | a0001c0004t0001g0286 | 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 | 40 | a0001c0001t0001g0008 a0001c0001t0001g0287 a0001c0001t0001g0290 others(37): 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 | a0001c0001t0002g0015 a0001c0001t0002g0104 |
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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0059 a0001c0001t0002g0035 others(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 | a0001c0002t0001g0025 a0001c0002t0001g0051 |
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 |
77 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(75): 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 | a0001c0001t0014g0062 | 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 | a0001c0001t0001g0046 a0001c0002t0001g0018 a0001c0002t0005g0095 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0076 a0001c0001t0002g0083 |
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 | a0001c0001t0001g0225 a0001c0001t0002g0220 a0001c0002t0001g0216 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0216 a0001c0002t0001g0217 others(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 | a0001c0001t0002g0195 a0001c0003t0001g0196 a0001c0003t0001g0197 others(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 | a0001c0001t0005g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0097 a0001c0001t0010g0098 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | 176 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(173): Show |
180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.18+4657G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128698933 | |||||||
| chr11:128699048 | C | T | 117 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(114): Show |
119 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(116): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0002g0271 | 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 | 51 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0235 others(48): 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 | 107 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(104): Show |
109 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.18+5283T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128699559 | |||||||
| chr11:128699674 | C | T | 106 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(103): Show |
108 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(105): 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 | a0001c0001t0001g0008 a0001c0001t0005g0279 a0001c0001t0005g0280 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | a0001c0001t0001g0008 a0001c0001t0005g0279 a0001c0001t0005g0280 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0001t0002g0016 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0008 a0001c0001t0005g0279 a0001c0001t0005g0280 others(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 | a0001c0001t0002g0288 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0003t0001g0312 a0001c0010t0002g0311 |
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 | a0001c0001t0001g0117 a0001c0001t0002g0116 a0002c0005t0001g0115 |
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 | a0001c0002t0001g0118 | 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 | a0001c0002t0005g0095 a0001c0011t0003g0100 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0206 | 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 | a0001c0003t0001g0198 | 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 | a0001c0004t0001g0286 | 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 | 175 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(172): Show |
179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.18+6872A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701148 | |||||||
| chr11:128701185 | T | C | 176 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(173): Show |
180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.18+6909T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128701185 | |||||||
| chr11:128701329 | GA | G | 176 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(173): Show |
180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): 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 | 179 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
183 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(180): 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | 219 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): 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 | a0001c0001t0001g0138 | 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 | a0001c0004t0001g0270 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0002g0318 | 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 | a0001c0001t0005g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0101 a0001c0001t0001g0235 others(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 | 41 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0240 others(38): 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 | a0001c0011t0003g0100 | 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 | 45 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0240 others(42): 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 | a0001c0001t0005g0279 a0001c0001t0005g0280 a0001c0001t0005g0281 |
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 | a0001c0004t0001g0010 | 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | a0001c0004t0003g0191 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0222 a0001c0003t0006g0004 others(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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0005g0211 others(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 | a0001c0001t0004g0190 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0137 a0001c0001t0004g0136 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0274 others(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 | a0001c0001t0001g0008 a0001c0001t0005g0279 a0001c0001t0005g0280 others(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 | 70 | a0001c0001t0001g0005 a0001c0001t0001g0106 a0001c0001t0001g0223 others(67): Show |
71 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.18+9588delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128703863 | |||||||
| chr11:128703864 | C | A | 222 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(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 | a0001c0002t0001g0139 | 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 | 70 | a0001c0001t0001g0005 a0001c0001t0001g0212 a0001c0001t0001g0214 others(67): 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 | 176 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(173): 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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0225 others(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 | a0001c0001t0004g0239 | 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 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0225 a0001c0002t0001g0217 a0001c0003t0001g0218 others(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 | 34 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0292 others(31): 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | a0001c0002t0002g0091 | 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 | 50 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0240 others(47): 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 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(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 | 52 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0235 others(49): 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 | a0001c0003t0003g0317 | 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 | a0001c0012t0015g0090 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0005g0283 a0001c0002t0001g0284 |
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 | a0001c0002t0001g0216 | 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 | a0002c0005t0001g0048 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0005g0283 a0001c0002t0001g0284 |
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 | a0001c0001t0001g0322 | 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 | 7 | a0001c0001t0001g0005 a0001c0001t0001g0240 a0001c0001t0001g0242 others(4): 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0002g0093 a0001c0002t0001g0018 |
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 | 51 | a0001c0001t0001g0005 a0001c0001t0001g0223 a0001c0001t0001g0235 others(48): 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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0202 | 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 | a0001c0003t0001g0089 | 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 | a0001c0001t0010g0098 | 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 | 108 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(105): Show |
110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0005g0283 a0001c0002t0001g0284 |
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 | 33 | a0001c0001t0001g0287 a0001c0001t0001g0290 a0001c0001t0001g0292 others(30): 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 | a0001c0002t0002g0144 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0002g0015 | 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 | 220 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(217): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | 110 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(107): Show |
112 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(109): 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 | a0001c0001t0004g0188 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0015 | 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 | a0001c0001t0002g0015 | 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 | a0001c0003t0003g0219 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | a0001c0002t0005g0095 a0001c0011t0003g0100 |
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 | a0001c0001t0005g0279 a0001c0001t0005g0280 a0001c0001t0005g0281 others(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 | a0001c0001t0002g0087 | 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 | a0001c0001t0002g0050 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0051 |
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 | a0002c0005t0001g0048 | 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 | a0001c0003t0003g0317 | 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 | a0001c0001t0002g0015 a0001c0001t0002g0104 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
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 | a0001c0001t0010g0098 a0001c0002t0001g0002 a0001c0002t0001g0099 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0053 |
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 | a0001c0002t0001g0291 a0001c0003t0003g0289 |
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 | a0001c0001t0001g0227 a0001c0001t0002g0220 a0001c0003t0003g0219 others(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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0227 others(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 | 10 | a0001c0001t0001g0106 a0001c0001t0001g0225 a0001c0001t0001g0228 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(7): 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 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0183 others(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 | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0097 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0322 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0235 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | a0001c0001t0001g0292 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0140 others(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 | 113 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0046 others(110): 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0292 | 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 | a0001c0001t0001g0199 | 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 | 309 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0001c0001t0002g0233 | 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 | 276 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(273): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0043 others(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 | a0002c0005t0001g0298 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | 78 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0059 others(75): 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 | 298 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.18+20642G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128714918 | |||||||
| chr11:128714929 | A | G | 298 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(295): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0009g0266 a0001c0002t0001g0267 |
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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0169 a0001c0001t0002g0205 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0045 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0002g0137 | 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 | a0001c0001t0001g0251 a0001c0001t0001g0254 a0001c0001t0002g0253 |
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 | 153 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.18+21984C>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128716260 | |||||||
| chr11:128716367 | G | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): 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 | a0001c0004t0001g0293 | 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 | a0001c0002t0001g0049 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0214 a0001c0002t0001g0051 others(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 | a0001c0001t0005g0283 a0001c0003t0003g0022 a0001c0004t0001g0010 |
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 | a0001c0001t0001g0094 | 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 | 151 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0214 | 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 | a0001c0002t0001g0208 | 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 | a0001c0001t0001g0202 | 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 | 116 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0029 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0292 a0001c0001t0001g0310 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0154 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0158 a0001c0001t0001g0254 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0160 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0148 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0097 a0001c0001t0001g0163 a0001c0001t0001g0227 others(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 | a0001c0001t0005g0280 a0001c0001t0005g0281 a0001c0001t0005g0283 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0206 others(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 | 163 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0027 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): 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 | a0001c0001t0001g0094 a0001c0002t0001g0018 |
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 | a0001c0001t0001g0231 a0001c0001t0002g0233 |
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 | a0001c0001t0001g0094 a0001c0002t0001g0018 |
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 | 115 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0029 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): 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 | 53 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(50): 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 | 93 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(90): 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 | 295 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): 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 | a0001c0001t0001g0265 a0001c0001t0004g0120 |
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 | a0001c0012t0015g0090 | 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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0164 | 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0242 others(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 | 294 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0236 a0001c0001t0005g0044 others(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 | 91 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(88): 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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0230 others(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 | a0001c0004t0001g0215 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0008 a0001c0001t0005g0279 |
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 | 294 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): 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 | a0001c0001t0001g0322 a0001c0004t0003g0032 |
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 | 91 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(88): 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 | a0001c0002t0001g0018 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0069 a0001c0001t0002g0068 a0001c0001t0002g0129 others(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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0310 a0001c0001t0002g0087 others(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 | a0001c0003t0003g0009 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0230 others(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 | 294 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0059 others(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 | a0001c0004t0001g0010 | 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 | 60 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0056 others(57): 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 | 53 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0046 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(50): 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 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | 86 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0045 others(83): 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 | a0001c0001t0001g0094 | 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 | 116 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0029 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): 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 | a0001c0001t0001g0092 a0001c0001t0002g0316 |
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 | a0001c0002t0001g0018 | 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 | a0001c0001t0002g0016 | 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 | a0001c0003t0001g0130 | 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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0001t0001g0125 a0001c0001t0002g0319 a0002c0005t0001g0192 |
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 | 294 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.18+30680C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128724956 | |||||||
| chr11:128724980 | G | A | 174 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): 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 | a0001c0002t0001g0051 a0001c0003t0003g0014 |
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 | a0001c0002t0001g0018 | 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 | a0001c0002t0001g0187 | 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 | 174 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): 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 | a0001c0003t0001g0181 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0124 others(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 | 186 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): 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 | 90 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(87): 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 | a0001c0001t0001g0052 a0001c0001t0001g0085 a0001c0001t0001g0101 others(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 | 65 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0065 others(62): 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 | a0001c0001t0001g0212 a0001c0001t0005g0211 a0001c0001t0005g0213 |
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 | 192 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): 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 | a0001c0004t0001g0010 | 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 | a0001c0001t0017g0302 a0001c0002t0001g0291 a0001c0003t0003g0289 |
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 | a0001c0001t0001g0101 | 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 | a0001c0002t0001g0066 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0085 | 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 | a0001c0003t0001g0126 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0140 others(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 | a0001c0003t0003g0009 a0001c0004t0003g0282 |
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 | 290 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.19-30995A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128727120 | |||||||
| chr11:128727151 | A | G | 195 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): 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 | a0001c0001t0001g0094 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0154 others(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 | 94 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0029 others(91): 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 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0012t0015g0090 |
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 | a0001c0001t0001g0272 | 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0042 a0001c0001t0004g0308 |
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 | a0001c0004t0001g0010 | 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 | a0001c0001t0001g0154 | 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 | a0001c0002t0001g0018 | 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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0003t0003g0009 | 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 | a0001c0002t0001g0314 | 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 | a0001c0002t0001g0139 | 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 | a0001c0004t0001g0010 | 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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0175 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0217 |
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 | a0001c0001t0001g0183 | 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0094 a0001c0002t0001g0139 a0001c0004t0001g0010 others(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 | 286 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): 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 | a0001c0001t0001g0076 a0001c0002t0001g0049 a0001c0003t0001g0075 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0002t0002g0034 |
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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0101 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0018 a0001c0003t0003g0009 others(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 | 290 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): 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 | a0001c0004t0001g0010 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0124 | 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 | a0001c0001t0002g0016 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | 98 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(95): 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 | 286 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): 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 | a0001c0002t0001g0128 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0217 |
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 | 290 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.19-26390G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128731725 | |||||||
| chr11:128731831 | T | C | 61 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(58): 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 | a0001c0002t0001g0189 | 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 | 61 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(58): 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 | a0001c0002t0001g0187 | 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 | 290 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0217 |
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 | 272 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(269): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): 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 | a0001c0001t0001g0094 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | 61 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(58): 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 | a0001c0001t0001g0027 a0001c0001t0001g0164 a0001c0001t0001g0268 others(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 | a0001c0001t0008g0080 | 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 | 98 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(95): 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 | a0001c0001t0001g0251 a0001c0001t0001g0254 |
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 | a0001c0001t0001g0113 a0001c0001t0001g0250 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0018 |
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 | 284 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0217 |
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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | a0001c0002t0001g0018 | 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 | a0001c0001t0002g0295 | 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 | a0001c0001t0001g0013 | 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 | 225 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.19-24000C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734115 | |||||||
| chr11:128734127 | G | A | 98 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0043 others(95): 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 | a0001c0001t0002g0241 a0001c0003t0001g0170 |
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 | a0001c0001t0001g0097 a0001c0001t0001g0163 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0119 | 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 | a0001c0004t0003g0191 | 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 | 137 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): 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 | a0001c0001t0001g0127 | 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 | 115 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.19-23778G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128734337 | |||||||
| chr11:128734370 | G | A | 113 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0029 others(110): 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 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0003t0003g0009 a0001c0004t0003g0282 |
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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0008 | 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 | a0001c0002t0005g0095 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0287 a0001c0001t0005g0028 others(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 | a0001c0002t0001g0187 | 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 | 174 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(171): 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 | 289 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(286): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0003t0001g0089 | 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 | a0001c0001t0002g0233 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0010g0098 others(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 | a0001c0002t0001g0173 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0187 |
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 | a0001c0001t0001g0255 | 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 | 116 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0187 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | 61 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(58): 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 a0001c0002t0001g0187 |
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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | 293 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(290): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): 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 | a0001c0001t0001g0322 a0001c0004t0003g0032 |
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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0002t0001g0021 | 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0002t0001g0018 | 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 | a0001c0001t0001g0212 a0001c0001t0002g0016 a0001c0001t0002g0105 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0101 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0005g0283 | 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 | a0001c0002t0001g0187 | 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 | a0001c0002t0005g0095 | 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0265 a0001c0001t0004g0120 |
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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0001t0002g0297 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0002g0072 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | a0001c0002t0001g0204 a0001c0003t0001g0126 a0001c0003t0001g0312 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | 55 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0042 others(52): Show |
55 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(52): 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0287 a0001c0001t0005g0028 others(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 | a0001c0001t0004g0188 a0001c0002t0001g0102 |
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 | a0001c0002t0001g0217 | 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 | a0001c0002t0001g0139 | 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 | a0001c0009t0001g0141 | 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 | 270 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(267): Show |
276 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(273): 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 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | 111 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0037 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): 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 | a0001c0001t0002g0297 | 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 | a0001c0003t0001g0273 | 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 | 92 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0045 others(89): 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0219 others(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 | a0001c0002t0001g0304 | 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 | a0001c0002t0001g0204 a0001c0003t0001g0312 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0140 others(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 | a0001c0002t0001g0187 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0172 others(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 | 289 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(286): Show |
295 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(292): 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 | a0001c0002t0001g0217 | 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 | a0001c0002t0001g0018 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0301 a0001c0001t0002g0053 a0001c0001t0002g0295 others(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 | a0001c0004t0001g0010 | 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 | 112 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): 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 | a0001c0002t0001g0018 | 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 | 189 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): 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 | a0001c0002t0002g0091 | 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0017g0302 | 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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0225 others(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 | a0001c0002t0001g0018 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0163 others(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 | 289 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(286): Show |
295 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.19-15760T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 1/8 | chr11 | 128742355 | |||||||
| chr11:128742569 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0153 a0001c0001t0001g0240 others(3): 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 | a0001c0001t0001g0140 | 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 | a0001c0002t0001g0217 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0127 a0001c0001t0001g0315 a0001c0001t0002g0088 others(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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0214 a0001c0002t0001g0051 others(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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0003t0003g0009 a0001c0004t0003g0282 |
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 | 6 | a0001c0001t0001g0005 a0001c0001t0001g0153 a0001c0001t0001g0240 others(3): 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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0140 others(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 | 74 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(71): 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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0001 a0001c0003t0003g0009 others(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 | 286 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(283): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): 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 | a0001c0004t0001g0249 | 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 | 74 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(71): 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 | a0001c0001t0001g0079 a0001c0001t0002g0040 |
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 | a0001c0004t0001g0010 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0071 | 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 | 208 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(205): Show |
211 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(208): 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 | a0001c0002t0001g0234 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0017g0302 | 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 | a0001c0002t0005g0095 | 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 | a0001c0004t0001g0221 | 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 | a0001c0002t0001g0187 | 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 | a0001c0002t0001g0159 | 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 | 77 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(74): 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 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0045 others(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 | a0001c0002t0001g0210 a0001c0004t0001g0010 |
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 | a0001c0002t0001g0187 | 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 | 117 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): 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 | a0001c0009t0001g0141 a0001c0010t0002g0311 |
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 | a0001c0001t0001g0045 | 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 | a0001c0002t0001g0018 a0001c0002t0001g0187 |
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 | a0001c0001t0005g0283 a0001c0002t0001g0210 a0001c0003t0003g0022 others(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 | 114 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0029 others(111): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): 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 | a0001c0001t0001g0200 | 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 | a0001c0002t0001g0217 | 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 | a0001c0002t0001g0187 | 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 | a0001c0003t0001g0012 | 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 | a0001c0012t0015g0090 | 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 | a0002c0005t0001g0048 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0259 a0001c0001t0002g0011 |
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 | a0001c0002t0001g0139 | 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 | 114 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0029 others(111): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): 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 | a0001c0002t0001g0187 | 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 | 2 | a0001c0001t0001g0005 a0001c0001t0001g0240 |
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 | a0001c0001t0001g0235 | 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 | a0001c0001t0002g0036 a0001c0001t0005g0279 a0001c0004t0001g0177 |
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 | a0001c0002t0001g0313 | 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 | 275 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(272): Show |
280 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(277): 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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0271 | 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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0003t0003g0009 |
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 | a0001c0001t0002g0319 | 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 | 71 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(68): 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 | a0001c0001t0005g0283 a0001c0002t0001g0001 a0001c0002t0001g0210 others(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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0052 a0001c0003t0003g0219 |
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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | 69 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(66): 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 | a0001c0004t0001g0179 | 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 | 205 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(202): Show |
207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): 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 | a0001c0002t0001g0001 a0001c0002t0001g0187 |
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 | a0001c0001t0001g0052 a0001c0001t0002g0220 a0001c0001t0012g0309 others(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 | 150 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0029 others(147): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): 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 | a0001c0001t0001g0101 | 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 | a0001c0004t0001g0221 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0187 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0163 a0001c0001t0001g0214 others(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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | 110 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0037 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0001 others(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 | a0001c0002t0001g0210 a0001c0004t0001g0010 a0001c0004t0003g0023 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0125 a0001c0001t0004g0120 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0243 a0001c0001t0002g0220 a0001c0001t0004g0190 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0008 a0001c0001t0005g0279 |
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 | a0001c0001t0002g0300 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0101 others(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 | 64 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0046 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0310 a0001c0001t0002g0087 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0125 a0001c0001t0004g0120 others(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 | a0001c0003t0001g0038 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | 316 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(313): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0043 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0203 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 |
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 | 316 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(313): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0001g0110 a0001c0001t0001g0169 a0001c0001t0002g0093 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0001 others(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 | 75 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0052 others(72): 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 | a0001c0002t0001g0021 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0002t0001g0018 others(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 | 82 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0052 others(79): 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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0287 a0001c0001t0005g0028 others(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 | a0001c0001t0004g0190 | 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 | a0001c0002t0001g0238 | 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 | a0001c0004t0001g0081 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0182 a0001c0001t0001g0290 |
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 | a0001c0001t0002g0053 | 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 | a0001c0001t0002g0083 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0187 |
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 | 71 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(68): 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 | a0001c0002t0001g0210 a0001c0004t0001g0010 |
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 | a0001c0002t0001g0234 a0001c0004t0001g0221 |
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 | a0001c0001t0001g0163 a0001c0001t0001g0214 a0001c0002t0001g0051 others(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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0002g0041 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0045 others(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 | a0001c0002t0001g0049 | 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 | 282 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(279): Show |
288 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(285): 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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0140 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0097 a0001c0001t0002g0035 a0001c0001t0002g0084 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(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 | 89 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0061 others(86): 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 | 45 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(43): 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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0258 a0001c0001t0002g0220 a0001c0001t0002g0241 others(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 | a0001c0001t0016g0260 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0183 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0292 a0001c0003t0001g0031 |
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 | 71 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(68): 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0002c0005t0001g0048 | 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 | 115 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): 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 | a0001c0001t0002g0319 | 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 | 68 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(65): 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 | 71 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(68): 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 | 278 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(275): Show |
284 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(281): 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 | a0001c0001t0001g0135 | 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 | a0001c0002t0001g0234 | 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 | a0001c0003t0001g0305 | 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 | a0001c0004t0003g0282 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0046 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0003t0003g0009 |
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 | 8 | a0001c0001t0001g0161 a0001c0001t0001g0203 a0001c0001t0001g0244 others(5): 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 | a0001c0003t0003g0219 | 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 | 68 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(65): 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 | a0001c0001t0001g0076 a0001c0002t0001g0049 a0001c0002t0002g0091 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0167 a0001c0001t0002g0068 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0180 a0001c0004t0001g0081 |
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 | a0001c0001t0001g0158 a0001c0001t0017g0302 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0079 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0143 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0106 a0001c0001t0001g0117 others(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 | 54 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0069 others(51): Show |
57 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(54): 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 | a0001c0001t0001g0110 a0001c0001t0001g0231 a0001c0001t0004g0239 others(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 | a0001c0003t0003g0219 | 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 | a0001c0001t0002g0220 a0001c0004t0001g0270 a0001c0004t0001g0286 |
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 | a0001c0001t0005g0283 | 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 | a0001c0003t0003g0009 a0001c0004t0003g0282 |
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 | a0001c0003t0003g0022 | 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 | a0001c0001t0001g0101 | 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 | a0001c0002t0001g0051 a0001c0003t0001g0218 |
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 | a0001c0003t0003g0014 | 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 | a0001c0003t0001g0012 | 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 | 71 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0065 others(68): 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 | a0001c0001t0002g0104 a0001c0011t0003g0100 |
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 | a0001c0001t0002g0104 | 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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0052 a0001c0003t0003g0219 |
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 | a0001c0012t0015g0090 | 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 | 66 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(63): 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0002t0001g0102 | 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 | a0001c0001t0001g0008 a0001c0001t0005g0279 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0005g0283 a0001c0003t0003g0022 |
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 | a0001c0001t0001g0078 a0001c0001t0002g0036 a0001c0003t0001g0073 |
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 | 90 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0043 others(87): 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 | 192 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(189): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.230+202C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128758528 | |||||||
| chr11:128758575 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0082 others(23): 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 | 66 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(63): 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 | 65 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(62): 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 | 186 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(183): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): 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 | a0001c0001t0001g0020 | 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 | a0001c0002t0001g0187 | 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 | 183 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(183): 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 | 188 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0027 others(185): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0005g0279 others(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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0124 a0001c0001t0001g0138 others(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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.230+1161T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128759487 | |||||||
| chr11:128759495 | G | T | 216 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(213): Show |
220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): 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 | a0001c0003t0003g0009 | 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 | a0001c0001t0001g0272 | 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 | 212 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(209): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | 212 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(209): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): 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 | a0001c0002t0001g0049 | 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 | 92 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0043 others(89): 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 | 291 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(288): Show |
297 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(294): 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 | a0001c0012t0015g0090 | 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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0071 a0001c0003t0001g0306 |
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 | a0001c0012t0015g0090 | 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 | a0001c0001t0005g0044 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0149 a0001c0001t0001g0200 others(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 | 105 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0037 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0045 others(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 | a0001c0001t0004g0190 a0001c0002t0001g0285 |
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 | 69 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0069 others(66): 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 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0001c0002t0001g0313 | 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 | a0001c0001t0001g0301 a0001c0001t0002g0053 a0001c0001t0002g0295 others(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 | a0001c0004t0001g0293 | 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 | a0001c0001t0001g0052 a0001c0002t0001g0234 a0001c0003t0003g0219 others(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 | a0001c0001t0001g0101 | 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 | a0001c0003t0001g0089 | 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 | a0001c0001t0001g0242 | 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 | a0001c0004t0001g0221 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0027 | 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 | a0001c0009t0001g0141 | 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 | 171 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(168): 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 | 167 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(164): 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 | a0001c0001t0001g0135 | 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 | 167 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(164): 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0005g0283 others(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 | 168 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(165): 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 | a0001c0002t0001g0210 | 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 | a0001c0002t0001g0139 | 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 | 167 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(164): 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 | 275 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(272): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0058 others(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 | a0001c0003t0001g0130 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0003t0003g0009 others(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 | a0001c0004t0001g0221 a0001c0012t0015g0090 |
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 | a0001c0001t0001g0255 a0001c0001t0001g0274 a0001c0001t0004g0188 others(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 | a0001c0001t0001g0199 | 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 | 28 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0124 others(25): 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 | 67 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0043 others(64): Show |
70 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.231-4359A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128763759 | |||||||
| chr11:128763770 | C | T | 30 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0124 others(27): 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 | a0001c0001t0004g0156 a0001c0001t0004g0248 a0001c0001t0004g0296 others(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 | a0001c0001t0001g0152 | 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 | 39 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0045 others(36): Show |
41 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(38): 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 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0178 a0001c0002t0002g0144 a0001c0004t0001g0176 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0052 others(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 | a0001c0007t0003g0057 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0214 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0003t0001g0232 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0094 others(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 | a0001c0002t0001g0217 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0212 a0001c0001t0002g0220 a0001c0002t0001g0237 others(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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0077 a0001c0002t0002g0091 |
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 | a0001c0001t0002g0105 | 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 | a0001c0003t0003g0289 | 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 | a0001c0002t0001g0051 | 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 | a0001c0001t0014g0062 | 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 | 50 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0058 others(47): 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 | a0001c0003t0003g0219 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0322 |
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 | 265 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(262): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): 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 | a0001c0002t0001g0001 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0101 a0001c0001t0005g0028 a0001c0001t0005g0211 others(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 | a0001c0006t0001g0067 a0001c0006t0001g0245 |
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 | a0001c0001t0001g0169 a0001c0001t0002g0205 |
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 | a0001c0001t0005g0283 | 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 | 269 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(266): Show |
274 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(271): 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 | a0001c0003t0001g0107 a0001c0004t0003g0226 a0001c0011t0003g0100 |
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 | a0001c0002t0001g0217 a0001c0002t0005g0095 |
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 | a0001c0001t0001g0209 a0001c0011t0003g0100 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0003t0001g0312 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0008g0080 | 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 | 108 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0027 others(105): 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 | a0001c0001t0002g0271 | 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 | a0001c0003t0007g0145 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0094 | 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 | a0001c0002t0001g0074 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0037 | 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 | a0001c0002t0001g0001 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0277 a0001c0001t0002g0033 a0001c0001t0002g0222 others(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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0236 a0001c0001t0005g0044 |
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 | a0001c0004t0003g0282 | 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 | a0001c0002t0001g0064 | 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 | 118 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0017 others(115): 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 | a0001c0003t0003g0289 | 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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | a0001c0001t0002g0016 | 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 | 99 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0054 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.231-600T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 2/8 | chr11 | 128767518 | |||||||
| chr11:128767529 | G | A | 103 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0027 others(100): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0059 | 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 | a0001c0002t0001g0187 a0001c0003t0007g0145 a0001c0004t0001g0010 others(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 | a0001c0001t0001g0029 a0001c0002t0001g0021 a0001c0002t0001g0025 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0182 | 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 | 83 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0061 others(80): Show |
85 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(82): 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 | a0001c0003t0001g0218 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0029 a0001c0002t0001g0021 a0001c0002t0001g0025 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0097 others(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 | 256 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(253): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0214 a0001c0003t0003g0317 others(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 | a0001c0001t0001g0261 | 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 | a0001c0002t0001g0018 a0001c0003t0003g0009 |
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 | 261 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(258): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): 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 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0002t0001g0021 others(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 | 65 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0092 others(62): Show |
65 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(62): 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0255 a0001c0001t0002g0035 others(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 | 162 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): 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 | 74 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0078 others(71): Show |
74 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(71): 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 | a0001c0001t0005g0028 a0001c0001t0005g0211 a0001c0001t0005g0213 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0236 a0001c0001t0002g0230 others(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 | 71 | a0001c0001t0001g0020 a0001c0001t0001g0061 a0001c0001t0001g0078 others(68): Show |
71 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(68): 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0167 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0142 a0001c0001t0002g0072 |
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 | 116 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0020 others(113): Show |
116 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(113): 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 | a0001c0001t0001g0017 | 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 | 179 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(176): Show |
185 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.385+1207T>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128769479 | |||||||
| chr11:128769881 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0027 others(91): 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 | 124 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0017 others(121): 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 | a0001c0004t0003g0282 | 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 | 236 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): 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 | a0001c0001t0002g0230 | 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 | a0001c0001t0002g0230 a0001c0003t0003g0219 |
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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0106 a0001c0001t0001g0147 others(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 | a0001c0002t0001g0051 a0001c0002t0001g0139 |
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 | a0001c0001t0002g0230 a0001c0003t0003g0219 |
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 | a0001c0002t0001g0187 | 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 | a0001c0001t0002g0083 | 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 | 62 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0085 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(59): 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 | a0001c0002t0001g0074 | 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 | a0001c0001t0002g0220 | 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 | a0001c0001t0001g0101 | 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 | a0001c0004t0001g0293 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0094 a0001c0004t0001g0286 |
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 | 188 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(185): Show |
194 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(191): 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0153 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0212 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0056 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0054 others(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 | 134 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0027 others(131): Show |
140 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(137): 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 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0101 others(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 | a0001c0002t0001g0187 a0001c0007t0003g0057 a0001c0012t0015g0090 |
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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0209 a0001c0003t0001g0107 a0001c0011t0003g0100 |
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 | a0001c0001t0002g0230 a0001c0003t0003g0219 |
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 | a0001c0001t0001g0257 | 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 | a0001c0004t0001g0286 | 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 | a0001c0007t0003g0057 a0001c0012t0015g0090 |
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 | 66 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0078 others(63): Show |
66 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.386-682G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 3/8 | chr11 | 128772100 | |||||||
| chr11:128772265 | C | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(188): Show |
197 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(194): 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 | a0001c0001t0001g0052 a0001c0001t0001g0227 a0001c0002t0018g0024 others(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 | 66 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0078 others(63): Show |
66 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(63): 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 | a0001c0001t0001g0046 a0001c0001t0001g0157 a0001c0001t0004g0123 others(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 | a0001c0004t0001g0215 a0001c0004t0003g0282 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0225 | 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 | a0001c0002t0001g0187 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0106 others(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 | 160 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(157): 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 | a0001c0001t0005g0279 | 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 | 62 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0085 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(59): 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 | a0001c0002t0002g0091 | 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 | a0001c0001t0002g0300 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0227 a0001c0002t0018g0024 others(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 | a0001c0001t0002g0150 | 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 | a0001c0001t0002g0230 a0001c0003t0003g0219 |
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 | a0001c0001t0001g0250 | 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 | 96 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0060 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): 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 | a0001c0002t0001g0217 a0001c0002t0005g0095 |
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 | a0001c0004t0001g0215 a0001c0004t0003g0282 |
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 | a0001c0001t0001g0029 a0001c0001t0005g0044 a0001c0002t0001g0021 others(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 | a0001c0001t0001g0082 | 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 | 127 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0017 others(124): 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 | 96 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0060 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.589+1902G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128774887 | |||||||
| chr11:128774922 | T | TA | 125 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0017 others(122): 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 | 125 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0017 others(122): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0002g0039 | 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 | 226 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.589+2177G>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775162 | |||||||
| chr11:128775175 | G | T | 101 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0060 others(98): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): 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 | a0001c0001t0001g0045 a0001c0002t0001g0018 a0001c0002t0001g0217 others(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 | 222 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.589+2389A>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775374 | |||||||
| chr11:128775441 | C | G | 221 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(218): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.589+2456C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775441 | |||||||
| chr11:128775554 | A | G | 75 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0078 others(72): Show |
77 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(74): 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 | a0001c0002t0001g0237 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0227 a0001c0002t0018g0024 |
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 | 100 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0060 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.589+2703C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775688 | |||||||
| chr11:128775699 | A | T | 101 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0060 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.589+2714A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128775699 | |||||||
| chr11:128775716 | T | C | 232 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0013 others(229): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): 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 | a0001c0001t0001g0045 | 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 | a0001c0003t0001g0073 | 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0287 a0001c0001t0010g0098 |
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 | 102 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0027 others(99): 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 | a0001c0002t0001g0018 a0001c0003t0003g0009 a0001c0004t0001g0010 others(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 | a0001c0004t0001g0179 | 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 | a0001c0001t0001g0154 | 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 | 200 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(197): Show |
205 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(202): 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 | a0001c0001t0001g0059 | 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 | a0001c0003t0001g0170 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0002t0001g0204 a0001c0002t0001g0284 a0001c0003t0001g0232 others(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 | 246 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(243): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): 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 | a0001c0004t0003g0191 | 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 | a0001c0007t0003g0057 | 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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0046 others(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 | 111 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0042 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): 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 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0002g0241 | 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 | a0001c0004t0003g0282 | 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 | 132 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0029 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): 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 | a0001c0001t0001g0269 | 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 | a0001c0002t0001g0284 | 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 | a0001c0004t0003g0226 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0002t0001g0001 others(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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0097 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0004t0001g0081 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0225 a0001c0001t0001g0292 others(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 | 224 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): 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 | a0001c0001t0005g0211 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0005g0028 others(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 | a0001c0003t0001g0273 | 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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0097 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | 6 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0240 others(3): 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 | a0001c0002t0001g0118 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | 223 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.590-2101A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128779857 | |||||||
| chr11:128779956 | G | A | 75 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0029 others(72): Show |
75 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(72): 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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | 108 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): 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 | a0001c0001t0001g0101 a0001c0001t0001g0212 a0001c0001t0004g0264 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0212 a0001c0002t0001g0018 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | 163 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): 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 | a0001c0001t0001g0163 a0001c0001t0001g0225 a0001c0001t0001g0292 others(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 | a0001c0002t0001g0204 | 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 | 223 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): 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 | a0001c0001t0001g0155 | 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 | 106 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): 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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0002t0001g0139 | 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 | a0001c0002t0001g0284 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0005g0028 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0002t0005g0095 a0001c0004t0003g0191 a0001c0011t0003g0100 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
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 | a0001c0001t0002g0040 | 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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0002t0001g0002 a0001c0002t0001g0099 a0001c0002t0001g0118 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0018 a0001c0002t0001g0026 others(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 | a0001c0001t0002g0040 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.590-128C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 4/8 | chr11 | 128781830 | |||||||
| chr11:128782158 | A | AG | 217 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0214 | 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 | a0001c0002t0001g0002 a0001c0002t0001g0099 a0001c0002t0001g0118 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0027 others(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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0077 | 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 | a0001c0002t0001g0210 a0001c0002t0005g0095 a0001c0004t0001g0010 others(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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0002t0001g0313 | 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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | a0001c0001t0005g0044 | 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 | a0001c0003t0003g0009 | 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 | a0001c0002t0001g0313 | 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 | a0001c0001t0001g0101 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0003t0001g0303 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0225 a0001c0001t0001g0292 others(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 | a0001c0001t0004g0121 | 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0054 others(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 |
4 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0134 others(1): 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 | a0001c0001t0001g0017 | 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 | a0001c0003t0007g0145 | 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 | a0001c0001t0001g0227 a0001c0002t0001g0210 |
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 | a0001c0001t0001g0020 a0001c0001t0002g0039 a0001c0001t0002g0068 others(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 | 20 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0124 others(17): Show |
20 | HG00558.hp2 HG00733.hp2 HG00738.hp1 others(17): 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 | a0001c0002t0001g0139 | 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 | a0001c0003t0003g0219 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0225 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0042 others(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 | a0001c0001t0004g0121 | 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0004g0121 | 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 | a0001c0003t0001g0303 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0056 a0001c0003t0001g0012 |
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 | a0001c0001t0002g0241 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0214 a0001c0004t0001g0221 a0001c0004t0003g0191 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0259 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0236 a0001c0002t0001g0001 a0001c0002t0001g0021 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0153 a0001c0001t0001g0161 others(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 | a0001c0001t0002g0205 a0001c0001t0008g0080 a0001c0003t0001g0112 |
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 | a0001c0001t0005g0044 a0001c0002t0001g0002 a0001c0002t0001g0051 others(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 | a0001c0002t0001g0074 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0004g0121 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0056 others(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 | a0001c0001t0014g0062 | 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 | a0001c0002t0005g0095 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0225 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0004g0121 | 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 | a0001c0004t0003g0282 | 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 | a0001c0001t0001g0140 a0001c0001t0005g0044 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0021 others(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 | a0001c0001t0005g0044 a0001c0002t0001g0001 a0001c0002t0001g0002 others(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 | a0002c0005t0001g0192 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0002g0222 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(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 | a0001c0003t0003g0219 a0001c0004t0003g0282 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0125 | 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 | a0001c0002t0001g0285 | 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 | a0001c0003t0003g0022 a0001c0003t0003g0317 a0001c0004t0003g0096 |
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 | a0001c0001t0001g0047 | 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 | a0001c0003t0001g0073 a0001c0004t0001g0215 |
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 | a0001c0002t0001g0210 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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 | 254 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): 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 | a0001c0001t0001g0140 a0001c0001t0001g0184 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0299 | 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 | a0001c0003t0003g0289 | 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 | a0001c0002t0001g0128 | 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 | 118 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(115): Show |
121 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.655+5990C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128788013 | |||||||
| chr11:128788061 | C | T | 61 | a0001c0001t0001g0206 a0001c0001t0002g0003 a0001c0001t0002g0006 others(58): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): 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 | a0001c0003t0001g0012 a0001c0004t0001g0010 a0001c0004t0001g0286 others(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 | 134 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(131): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0002g0295 | 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0004g0121 | 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): 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 | a0001c0003t0001g0218 | 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 | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): 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 | a0001c0002t0001g0159 | 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 | a0001c0001t0001g0275 | 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 | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): 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 | a0001c0001t0002g0318 | 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 | a0001c0003t0001g0107 a0001c0003t0003g0009 a0001c0003t0003g0014 others(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 | a0001c0007t0003g0057 | 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 | a0001c0001t0001g0290 | 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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0004t0003g0032 a0001c0011t0003g0100 |
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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): 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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): 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 | a0001c0003t0001g0107 a0001c0003t0003g0009 a0001c0003t0003g0014 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0287 a0001c0001t0002g0288 others(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 | a0001c0003t0001g0012 a0001c0004t0001g0010 a0001c0004t0001g0286 others(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 | 109 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): 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 | 62 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(59): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): 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 | 46 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(43): 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 | 63 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.655+8042C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790065 | |||||||
| chr11:128790066 | A | G | 109 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): 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 | a0001c0001t0004g0121 a0001c0003t0003g0014 a0001c0003t0003g0317 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0287 a0001c0001t0002g0288 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0200 others(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 | 115 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(112): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): 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 | a0001c0001t0001g0063 a0001c0001t0001g0097 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0269 a0001c0002t0001g0204 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0163 a0001c0001t0001g0236 others(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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.655+8080T>C | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790103 | |||||||
| chr11:128790125 | C | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): 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 | a0001c0001t0004g0156 a0001c0001t0004g0248 a0001c0001t0004g0296 |
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 | 53 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(50): 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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0015 others(63): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): 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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.655+8244C>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790267 | |||||||
| chr11:128790271 | G | A | 32 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0035 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.655+8248G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128790271 | |||||||
| chr11:128790313 | A | G | 71 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(68): Show |
73 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(70): 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 | a0001c0001t0001g0101 | 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 | a0001c0004t0001g0010 | 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(125): 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0161 | 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 | 64 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(61): Show |
66 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(63): 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 | a0001c0001t0002g0230 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0322 a0001c0002t0001g0001 others(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 | a0001c0001t0002g0083 a0001c0001t0002g0105 a0001c0003t0001g0218 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | 128 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(125): Show |
131 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.655+9752A>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128791775 | |||||||
| chr11:128791778 | A | G | 128 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(125): Show |
131 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(128): 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 | a0001c0001t0002g0150 | 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 | a0001c0002t0001g0204 | 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 | 127 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(124): Show |
130 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(127): 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 | a0001c0003t0001g0168 a0001c0003t0001g0303 a0001c0003t0001g0312 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0307 |
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 | a0001c0004t0003g0032 a0001c0011t0003g0100 |
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 | 127 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(124): Show |
130 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.655+10432G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792455 | |||||||
| chr11:128792675 | TC | T | 127 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(124): Show |
130 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.655+10653delC | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128792675 | |||||||
| chr11:128792684 | T | C | 187 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): 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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0322 a0001c0002t0001g0001 others(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 | a0001c0003t0001g0126 a0001c0004t0001g0176 a0001c0004t0001g0177 |
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 | a0001c0003t0001g0031 a0001c0003t0001g0112 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0002g0300 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0207 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0003t0001g0218 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 11 | a0001c0001t0002g0035 a0001c0001t0002g0041 a0001c0001t0002g0050 others(8): Show |
11 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.656-11430G>A | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128793936 | |||||||
| chr11:128794013 | G | T | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0007t0003g0057 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 135 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0079 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0244 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 31 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0035 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(28): 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 | a0001c0001t0002g0288 | 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 | a0001c0004t0001g0215 a0001c0004t0001g0221 a0001c0004t0001g0270 |
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 | 212 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(209): 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 | 43 | a0001c0001t0001g0209 a0001c0001t0001g0322 a0001c0001t0002g0011 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(41): 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 | 48 | a0001c0001t0001g0097 a0001c0001t0002g0003 a0001c0001t0002g0006 others(45): 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 | a0001c0001t0002g0088 a0001c0001t0005g0028 a0001c0001t0005g0044 others(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 | a0001c0001t0005g0280 a0001c0001t0005g0281 |
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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0003t0003g0219 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0206 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0125 | 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 | a0003c0013t0001g0086 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0003t0001g0107 a0001c0004t0003g0023 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0244 | 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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0003t0001g0107 a0001c0003t0003g0009 a0001c0003t0003g0014 others(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 | a0001c0002t0001g0216 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0002g0088 a0001c0003t0001g0073 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 5 | a0001c0001t0002g0006 a0001c0001t0002g0068 a0001c0001t0002g0129 others(2): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0002t0001g0026 a0001c0002t0001g0267 |
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 | a0001c0001t0001g0202 | 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 | a0001c0003t0001g0130 a0001c0003t0001g0196 a0001c0003t0001g0197 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0001t0017g0302 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0209 others(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 | a0001c0003t0003g0289 | 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 | a0001c0001t0002g0033 a0001c0001t0002g0035 a0001c0001t0002g0041 others(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 | a0001c0001t0002g0137 a0001c0001t0002g0241 a0001c0001t0004g0296 |
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 | a0001c0003t0007g0145 | 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 | 66 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0015 others(63): 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0002g0088 a0001c0003t0001g0031 a0001c0003t0001g0073 others(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 | 98 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0094 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.656-6323A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799043 | |||||||
| chr11:128799046 | A | T | 161 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(158): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.656-6320A>T | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 5/8 | chr11 | 128799046 | |||||||
| chr11:128799049 | A | T | 173 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(170): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): 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 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0061 others(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 | a0001c0003t0003g0014 | 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 | 225 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0019 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 35 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(32): 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 | 75 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(72): Show |
77 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(74): 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 | a0001c0001t0001g0209 a0001c0001t0010g0098 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0094 | 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 | a0001c0002t0001g0216 | 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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0002t0001g0216 | 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 | a0001c0004t0003g0096 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0004t0003g0226 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0002t0001g0066 | 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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | 183 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): 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 | a0001c0001t0001g0097 a0001c0001t0001g0322 a0001c0002t0001g0001 others(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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0101 | 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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0002t0001g0051 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0127 | 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 | a0001c0012t0015g0090 | 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 | a0001c0001t0001g0209 a0001c0001t0010g0098 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0164 a0001c0001t0001g0294 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0211 a0001c0001t0005g0213 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0004t0003g0032 a0001c0004t0003g0226 a0001c0011t0003g0100 |
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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0001g0054 | 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 | a0001c0003t0001g0073 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | 132 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0225 |
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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0001t0004g0190 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0001g0038 a0001c0003t0001g0075 a0001c0003t0001g0089 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0225 | 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 | a0001c0002t0001g0001 a0001c0002t0001g0025 a0001c0002t0001g0291 |
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 | 153 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0029 others(150): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): 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 | a0001c0001t0002g0015 a0001c0001t0002g0104 a0001c0001t0002g0137 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0008 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0001t0001g0058 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0002t0001g0216 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0001g0117 | 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 | a0001c0002t0001g0049 a0001c0002t0001g0238 |
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 | a0001c0001t0002g0253 | 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 | a0001c0002t0005g0095 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0322 a0001c0002t0001g0001 others(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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0045 | 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 | 5 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0240 others(2): 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0003t0001g0038 | 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 | a0001c0001t0002g0072 | 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 | 75 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(72): Show |
77 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(74): 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0003t0001g0168 a0001c0003t0001g0312 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0001g0012 a0001c0004t0001g0010 a0001c0004t0001g0286 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0077 | 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 | a0001c0003t0001g0012 a0001c0004t0001g0010 a0001c0004t0001g0286 others(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 | a0001c0002t0001g0285 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0004t0001g0081 | 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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0084 a0001c0001t0002g0146 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0116 |
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 | a0001c0003t0001g0012 a0001c0003t0001g0031 a0001c0003t0001g0038 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0004g0264 | 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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | 31 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0035 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(28): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0002g0072 | 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 | 94 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): 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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0209 a0001c0001t0010g0098 a0001c0003t0001g0031 others(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 | 94 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): 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 | a0001c0012t0015g0090 | 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 | a0001c0003t0001g0107 a0001c0003t0003g0009 a0001c0003t0003g0014 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0161 |
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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | 132 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): 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 | a0001c0001t0001g0138 a0001c0002t0001g0064 a0001c0002t0001g0066 others(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 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
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 | a0001c0003t0003g0289 a0001c0003t0007g0145 |
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 | a0001c0003t0001g0038 a0001c0003t0001g0075 a0001c0003t0001g0089 others(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 | a0001c0004t0003g0032 a0001c0004t0003g0226 a0001c0011t0003g0100 |
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 | 71 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(68): Show |
73 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(70): 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 | a0001c0004t0003g0191 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(65): 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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | a0001c0003t0001g0038 a0001c0003t0001g0075 a0001c0003t0001g0089 others(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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0005g0028 a0001c0001t0005g0044 a0001c0001t0005g0211 others(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 | a0001c0003t0001g0038 a0001c0003t0001g0075 a0001c0003t0001g0089 others(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 | a0001c0003t0001g0031 a0001c0003t0001g0073 a0001c0003t0001g0112 others(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 | a0001c0003t0001g0031 a0001c0003t0001g0112 |
2 | HG02572.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.830-78C>G | FLI1 | ENSG00000151702.18 | transcript | ENST00000527786.7 | protein_coding | 8/8 | chr11 | 128810381 |