Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2119 |
| ensemblid | ENSG00000244405.8 |
| hgncid | 3494 |
| symbol | ETV5 |
| name | ETS variant transcription factor 5 |
| refseq_nuc | NM_004454.3 |
| refseq_prot | NP_004445.1 |
| ensembl_nuc | ENST00000306376.10 |
| ensembl_prot | ENSP00000306894.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 186046314 |
| end | 186109089 |
| strand | - |
| ver | v1.2 |
| region | chr3:186046314-186109089 |
| region5000 | chr3:186041314-186114089 |
| regionname0 | ETV5_chr3_186046314_186109089 |
| regionname5000 | ETV5_chr3_186041314_186114089 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 510 | 335 | 84 | 58 | 153 | 12 | 26 | 122 | ETV5_chr3_186041314_186114089 | ETV5 | MDGFY others(505): Show |
chr3 | 186041314 | 186114089 |
| a0002 | 0/0 | 510 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | MDGFY others(505): Show |
chr3 | 186041314 | 186114089 |
| a0003 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | MDGFY others(505): Show |
chr3 | 186041314 | 186114089 |
| a0004 | 0/0 | 510 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | MDGFY others(505): Show |
chr3 | 186041314 | 186114089 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1530 | 330 | 81 | 56 | 153 | 12 | 26 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0001c0003 | 0/0 | 1530 | 2 | 1 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0001c0004 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0001c0005 | 0/0 | 1530 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0001c0006 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0002c0002 | 0/0 | 1530 | 3 | 3 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0003c0008 | 0/0 | 1530 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 | ||
| a0004c0007 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | ATGGA others(1525): Show |
chr3 | 186041314 | 186114089 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4083 | 83 | 24 | 19 | 28 | 6 | 6 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0002 | 0/0 | 4082 | 82 | 10 | 10 | 59 | 0 | 3 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0003 | 0/0 | 4082 | 40 | 1 | 4 | 30 | 2 | 3 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0004 | 1/0 | 4082 | 29 | 9 | 5 | 7 | 4 | 3 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0005 | 0/0 | 4083 | 27 | 2 | 8 | 16 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0006 | 0/0 | 4080 | 19 | 13 | 0 | 3 | 0 | 3 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4075): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0007 | 0/0 | 4083 | 16 | 5 | 5 | 2 | 0 | 4 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0008 | 0/0 | 4083 | 3 | 1 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0009 | 0/0 | 4083 | 4 | 0 | 0 | 4 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0010 | 0/0 | 4077 | 4 | 4 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4072): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0011 | 0/0 | 4080 | 3 | 3 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4075): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0012 | 0/0 | 4079 | 3 | 1 | 2 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4074): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0014 | 0/0 | 4083 | 2 | 0 | 1 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0015 | 0/0 | 4080 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4075): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0016 | 0/0 | 4083 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0017 | 0/0 | 4081 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4076): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0018 | 0/0 | 4083 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0019 | 0/0 | 4083 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0020 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4075): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0021 | 0/0 | 4081 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4076): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0022 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4075): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0023 | 0/0 | 4079 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4074): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0024 | 0/0 | 4082 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0025 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0027 | 0/0 | 4079 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4074): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0029 | 0/1 | 4082 | 1 | 0 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0001t0030 | 0/0 | 4082 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0003t0003 | 0/0 | 4082 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0003t0004 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0004t0013 | 0/0 | 4081 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4076): Show |
chr3 | 186041314 | 186114089 |
| a0001c0005t0003 | 0/0 | 4082 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0001c0006t0026 | 0/0 | 4083 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| a0002c0002t0013 | 0/0 | 4081 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4076): Show |
chr3 | 186041314 | 186114089 |
| a0002c0002t0028 | 0/0 | 4082 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0003c0008t0002 | 0/0 | 4082 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4077): Show |
chr3 | 186041314 | 186114089 |
| a0004c0007t0008 | 0/0 | 4083 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | AGAGT others(4078): Show |
chr3 | 186041314 | 186114089 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0012g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0012g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0014g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0016g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0017g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0020g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0021g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0022g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0024g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0027g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0029g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0001t0030g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0004t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0005t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0001c0006t0026g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0002c0002t0013g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0002c0002t0013g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0002c0002t0028g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0003c0008t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| a0004c0007t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0023 | EUR | GBR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0022 | EUR | FIN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0081 | EUR | FIN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0022 | EUR | FIN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00423 | hp1 | a0003 | c0008 | t0002 | g0240 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00735 | hp2 | a0001 | c0001 | t0012 | g0207 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01070 | hp1 | a0001 | c0005 | t0003 | g0064 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0159 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0210 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0158 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0163 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0140 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01168 | hp1 | a0001 | c0001 | t0014 | g0056 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01169 | hp1 | a0001 | c0001 | t0017 | g0057 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01261 | hp2 | a0001 | c0001 | t0024 | g0186 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0164 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0023 | EUR | IBS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0150 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0281 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02145 | hp1 | a0004 | c0007 | t0008 | g0130 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0187 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | CDX | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | CDX | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0168 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0119 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0075 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02647 | hp1 | a0001 | c0004 | t0013 | g0205 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0134 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0218 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0153 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02895 | hp2 | a0002 | c0002 | t0028 | g0227 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0167 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0295 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03130 | hp1 | a0002 | c0002 | t0013 | g0229 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0154 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0090 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0135 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | GWD | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0091 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03654 | hp2 | a0001 | c0001 | t0030 | g0254 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0160 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0198 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0117 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0202 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0162 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0199 | SAS | STU | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | STU | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | STU | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18945 | hp2 | a0001 | c0001 | t0016 | g0033 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18954 | hp2 | a0001 | c0001 | t0021 | g0097 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0060 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | LWK | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19030 | hp2 | a0001 | c0001 | t0025 | g0166 | AFR | LWK | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0049 | AFR | LWK | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | LWK | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | YRI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | YRI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | TSI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | GIH | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0018 | SAS | GIH | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02109 | hp1 | a0001 | c0006 | t0026 | g0225 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | ACB | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG06807 | hp1 | a0002 | c0002 | t0013 | g0228 | AFR | USA | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | USA | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0291 | REF | REF | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0176 | REF | REF | ETV5_chr3_186041314_186114089 | ETV5 | chr3 | 186041314 | 186114089 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:186057241 | T | C | 1 | a0004 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1043A>G | p.Lys348Arg | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/13 | 1267/4082 | 1043/1533 | 348/510 | chr3 | 186057241 | |||
| chr3:186079938 | C | A | 1 | a0003 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.529G>T | p.Ala177Ser | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/13 | 753/4082 | 529/1533 | 177/510 | chr3 | 186079938 | |||
| chr3:186080022 | G | C | 1 | a0002 | 3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.445C>G | p.Leu149Val | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/13 | 669/4082 | 445/1533 | 149/510 | chr3 | 186080022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:186048726 | C | T | 1 | a0001c0006 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1446G>A | p.Pro482Pro | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1670/4082 | 1446/1533 | 482/510 | chr3 | 186048726 | |||
| chr3:186048773 | G | A | 1 | a0001c0003 | 2 | HG01109.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.1399C>T | p.Leu467Leu | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1623/4082 | 1399/1533 | 467/510 | chr3 | 186048773 | |||
| chr3:186048777 | C | T | 1 | a0001c0003 | 2 | HG01109.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.1395G>A | p.Pro465Pro | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1619/4082 | 1395/1533 | 465/510 | chr3 | 186048777 | |||
| chr3:186057445 | A | G | 1 | a0001c0005 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.1017T>C | p.Cys339Cys | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 10/13 | 1241/4082 | 1017/1533 | 339/510 | chr3 | 186057445 | |||
| chr3:186065988 | C | T | 1 | a0001c0004 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.735G>A | p.Arg245Arg | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/13 | 959/4082 | 735/1533 | 245/510 | chr3 | 186065988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:186046539 | A | G | 1 | a0002c0002t0028 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2100T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 2100 | chr3 | 186046539 | ||||||
| chr3:186046668 | TCAA | T | 4 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0015 others(1): Show |
25 | HG00558.hp1 HG01891.hp2 HG02145.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1968_*1970delTTG | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1968 | chr3 | 186046668 | ||||||
| chr3:186046668 | TCAAA | T | 3 | a0001c0001t0012 a0001c0001t0023 a0001c0001t0027 |
5 | HG00735.hp2 HG01074.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1967_*1970delTTTG | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1967 | chr3 | 186046668 | ||||||
| chr3:186046668 | TCAAAAG | T | 1 | a0001c0001t0010 | 4 | HG02630.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1965_*1970delCTTT others(2): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1965 | chr3 | 186046668 | ||||||
| chr3:186046669 | C | CA | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(3): Show |
21 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1969dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1969 | chr3 | 186046669 | ||||||
| chr3:186046672 | AAG | A | 5 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0022 others(2): Show |
6 | HG01169.hp1 HG02647.hp1 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1965_*1966delCT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1965 | chr3 | 186046672 | ||||||
| chr3:186046673 | AG | A | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(9): Show |
39 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1965delC | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1965 | chr3 | 186046673 | ||||||
| chr3:186046674 | G | A | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1965C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1965 | chr3 | 186046674 | ||||||
| chr3:186046780 | C | T | 1 | a0001c0001t0024 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1859 | chr3 | 186046780 | ||||||
| chr3:186046887 | T | G | 1 | a0001c0001t0027 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1752A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1752 | chr3 | 186046887 | ||||||
| chr3:186047049 | C | T | 1 | a0001c0001t0009 | 4 | NA18990.hp2 NA18997.hp2 NA19001.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1590G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1590 | chr3 | 186047049 | ||||||
| chr3:186047268 | T | C | 1 | a0001c0001t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1371 | chr3 | 186047268 | ||||||
| chr3:186047602 | A | C | 2 | a0001c0001t0008 a0004c0007t0008 |
4 | HG02145.hp1 HG03540.hp2 NA18978.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1037T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 1037 | chr3 | 186047602 | ||||||
| chr3:186047779 | A | C | 1 | a0001c0001t0020 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 860 | chr3 | 186047779 | ||||||
| chr3:186047791 | G | GT | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(20): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*847dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 847 | chr3 | 186047791 | ||||||
| chr3:186047806 | T | C | 1 | a0001c0001t0025 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 833 | chr3 | 186047806 | ||||||
| chr3:186048108 | G | C | 1 | a0001c0006t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 531 | chr3 | 186048108 | ||||||
| chr3:186048128 | C | G | 1 | a0001c0001t0019 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*511G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 511 | chr3 | 186048128 | ||||||
| chr3:186048473 | T | C | 1 | a0001c0001t0022 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*166A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 166 | chr3 | 186048473 | ||||||
| chr3:186048505 | C | T | 1 | a0001c0006t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 134 | chr3 | 186048505 | ||||||
| chr3:186048577 | C | T | 1 | a0001c0001t0018 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 62 | chr3 | 186048577 | ||||||
| chr3:186048625 | C | T | 2 | a0001c0001t0014 a0001c0001t0017 |
3 | HG01168.hp1 HG01169.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 13/13 | 14 | chr3 | 186048625 | ||||||
| chr3:186108951 | T | G | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
5_prime_UTR_variant | MODIFIER | c.-86A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/13 | 3083 | chr3 | 186108951 | ||||||
| chr3:186108975 | C | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(13): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/13 | 3107 | chr3 | 186108975 | ||||||
| chr3:186109072 | C | T | 1 | a0001c0001t0016 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/13 | 3204 | chr3 | 186109072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:186048922 | G | A | 100 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(97): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1312-62C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186048922 | |||||||
| chr3:186049050 | T | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0182 others(2): Show |
7 | HG00408.hp2 HG02155.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-190A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049050 | |||||||
| chr3:186049386 | C | G | 1 | a0001c0001t0006g0206 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1312-526G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049386 | |||||||
| chr3:186049508 | C | T | 1 | a0001c0001t0005g0263 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1312-648G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049508 | |||||||
| chr3:186049525 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1312-665G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049525 | |||||||
| chr3:186049611 | G | C | 18 | a0001c0001t0006g0025 a0001c0001t0006g0192 a0001c0001t0006g0193 others(15): Show |
19 | HG00558.hp1 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1312-751C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049611 | |||||||
| chr3:186049821 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1312-961T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049821 | |||||||
| chr3:186049858 | A | G | 2 | a0001c0001t0008g0063 a0004c0007t0008g0130 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-998T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049858 | |||||||
| chr3:186049947 | T | G | 7 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312-1087A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049947 | |||||||
| chr3:186049948 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312-1088G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186049948 | |||||||
| chr3:186050403 | T | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0095 others(2): Show |
5 | HG01081.hp2 HG01106.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-1543A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186050403 | |||||||
| chr3:186051049 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1311+981C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051049 | |||||||
| chr3:186051266 | C | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0182 others(2): Show |
7 | HG00408.hp2 HG02155.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+764G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051266 | |||||||
| chr3:186051268 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0133 |
2 | HG01358.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1311+762C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051268 | |||||||
| chr3:186051636 | C | G | 16 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0023 others(13): Show |
20 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1311+394G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051636 | |||||||
| chr3:186051754 | T | C | 1 | a0001c0001t0020g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1311+276A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051754 | |||||||
| chr3:186051855 | A | G | 1 | a0001c0001t0007g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1311+175T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051855 | |||||||
| chr3:186051896 | T | A | 4 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0060 others(1): Show |
4 | NA18990.hp2 NA18997.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+134A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186051896 | |||||||
| chr3:186052003 | G | T | 3 | a0001c0004t0013g0205 a0002c0002t0013g0228 a0002c0002t0013g0229 |
3 | HG02647.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1311+27C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 12/12 | chr3 | 186052003 | |||||||
| chr3:186052307 | G | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0001g0095 others(2): Show |
5 | HG01081.hp2 HG01106.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-176C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186052307 | |||||||
| chr3:186052752 | G | A | 1 | a0001c0001t0008g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1210-621C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186052752 | |||||||
| chr3:186052891 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1210-760C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186052891 | |||||||
| chr3:186052896 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0243 a0001c0001t0002g0255 others(1): Show |
5 | NA18941.hp2 NA18947.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-765G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186052896 | |||||||
| chr3:186052965 | T | C | 24 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(21): Show |
30 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1210-834A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186052965 | |||||||
| chr3:186053078 | A | C | 4 | a0001c0001t0008g0063 a0001c0001t0008g0089 a0001c0001t0008g0105 others(1): Show |
4 | HG02145.hp1 HG03540.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-947T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053078 | |||||||
| chr3:186053425 | T | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0160 |
3 | HG03017.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1210-1294A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053425 | |||||||
| chr3:186053446 | C | CA | 34 | a0001c0001t0005g0211 a0001c0001t0006g0025 a0001c0001t0006g0189 others(31): Show |
35 | HG00558.hp1 HG00735.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1210-1316dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053446 | |||||||
| chr3:186053681 | T | C | 2 | a0001c0001t0004g0169 a0001c0001t0004g0174 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1210-1550A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053681 | |||||||
| chr3:186053849 | C | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(20): Show |
29 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1210-1718G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053849 | |||||||
| chr3:186053976 | C | G | 1 | a0001c0001t0004g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1210-1845G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186053976 | |||||||
| chr3:186054293 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0096 a0001c0001t0005g0230 |
4 | HG02015.hp2 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-2162G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186054293 | |||||||
| chr3:186054365 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1210-2234G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186054365 | |||||||
| chr3:186054386 | T | C | 7 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 others(4): Show |
7 | HG00558.hp1 HG02145.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210-2255A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186054386 | |||||||
| chr3:186054570 | G | A | 1 | a0001c0001t0007g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1210-2439C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186054570 | |||||||
| chr3:186054838 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1209+2237A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186054838 | |||||||
| chr3:186055017 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1209+2058G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055017 | |||||||
| chr3:186055028 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1209+2047C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055028 | |||||||
| chr3:186055090 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1209+1985A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055090 | |||||||
| chr3:186055147 | A | C | 1 | a0002c0002t0013g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1209+1928T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055147 | |||||||
| chr3:186055260 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1209+1815T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055260 | |||||||
| chr3:186055588 | A | G | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1209+1487T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055588 | |||||||
| chr3:186055726 | T | C | 1 | a0001c0001t0006g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1209+1349A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055726 | |||||||
| chr3:186055751 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1209+1324C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186055751 | |||||||
| chr3:186056909 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 |
4 | HG02109.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+166G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186056909 | |||||||
| chr3:186057024 | C | A | 66 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(63): Show |
79 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1209+51G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 11/12 | chr3 | 186057024 | |||||||
| chr3:186057682 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.971-191C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186057682 | |||||||
| chr3:186057834 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.971-343A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186057834 | |||||||
| chr3:186058169 | G | GAAGGC | 17 | a0001c0001t0006g0025 a0001c0001t0006g0192 a0001c0001t0006g0193 others(14): Show |
18 | HG00558.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.971-683_971-679dup others(5): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058169 | |||||||
| chr3:186058210 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0137 a0001c0001t0005g0024 |
4 | HG00140.hp1 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-719C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058210 | |||||||
| chr3:186058403 | C | T | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.971-912G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058403 | |||||||
| chr3:186058470 | T | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(67): Show |
83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.971-979A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058470 | |||||||
| chr3:186058612 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.971-1121G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058612 | |||||||
| chr3:186058702 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.971-1211A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058702 | |||||||
| chr3:186058773 | G | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-1282C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058773 | |||||||
| chr3:186058784 | T | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(67): Show |
83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.971-1293A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058784 | |||||||
| chr3:186058945 | G | A | 17 | a0001c0001t0006g0025 a0001c0001t0006g0192 a0001c0001t0006g0193 others(14): Show |
18 | HG00558.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.971-1454C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058945 | |||||||
| chr3:186058961 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.971-1470C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186058961 | |||||||
| chr3:186059012 | C | CA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
15 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-1522dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059012 | |||||||
| chr3:186059029 | A | T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0053 a0001c0001t0001g0058 others(30): Show |
36 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.971-1538T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059029 | |||||||
| chr3:186059031 | T | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.971-1540A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059031 | |||||||
| chr3:186059266 | C | T | 1 | a0001c0001t0006g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.971-1775G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059266 | |||||||
| chr3:186059518 | T | C | 6 | a0001c0001t0002g0027 a0001c0001t0002g0226 a0001c0001t0002g0235 others(3): Show |
7 | HG00642.hp1 HG01106.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.971-2027A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059518 | |||||||
| chr3:186059894 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.971-2403G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186059894 | |||||||
| chr3:186060025 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0007g0155 |
3 | HG02486.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.971-2534G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060025 | |||||||
| chr3:186060088 | C | T | 2 | a0001c0003t0003g0140 a0001c0003t0004g0153 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.971-2597G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060088 | |||||||
| chr3:186060128 | C | A | 2 | a0001c0003t0003g0140 a0001c0003t0004g0153 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.971-2637G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060128 | |||||||
| chr3:186060207 | CATTCACA others(14): Show |
C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0223 others(2): Show |
5 | HG00423.hp1 NA18960.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-2737_971-2717d others(23): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060207 | |||||||
| chr3:186060266 | G | T | 1 | a0001c0001t0002g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.971-2775C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060266 | |||||||
| chr3:186060315 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.971-2824C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060315 | |||||||
| chr3:186060341 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.971-2850C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060341 | |||||||
| chr3:186060353 | C | T | 1 | a0001c0001t0005g0269 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.971-2862G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060353 | |||||||
| chr3:186060684 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG00639.hp2 HG01891.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-3193C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060684 | |||||||
| chr3:186060866 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.971-3375A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060866 | |||||||
| chr3:186060946 | A | T | 2 | a0001c0001t0001g0147 a0001c0001t0005g0008 |
4 | NA18950.hp1 NA18971.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-3455T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186060946 | |||||||
| chr3:186061120 | G | A | 1 | a0001c0001t0015g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.970+3297C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186061120 | |||||||
| chr3:186061384 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.970+3033T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186061384 | |||||||
| chr3:186062144 | A | C | 1 | a0001c0001t0005g0264 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.970+2273T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062144 | |||||||
| chr3:186062235 | G | T | 1 | a0001c0001t0005g0263 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.970+2182C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062235 | |||||||
| chr3:186062334 | G | A | 4 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0060 others(1): Show |
4 | NA18990.hp2 NA18997.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+2083C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062334 | |||||||
| chr3:186062388 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0015g0168 |
2 | HG02257.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.970+2029G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062388 | |||||||
| chr3:186062491 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.970+1926C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062491 | |||||||
| chr3:186062508 | T | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.970+1909A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062508 | |||||||
| chr3:186062629 | A | T | 30 | a0001c0001t0006g0025 a0001c0001t0006g0189 a0001c0001t0006g0190 others(27): Show |
31 | HG00558.hp1 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.970+1788T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062629 | |||||||
| chr3:186062657 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.970+1760G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062657 | |||||||
| chr3:186062774 | C | T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0053 a0001c0001t0001g0058 others(30): Show |
36 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.970+1643G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186062774 | |||||||
| chr3:186063130 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.970+1287G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063130 | |||||||
| chr3:186063255 | G | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0099 others(12): Show |
17 | HG00140.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.970+1162C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063255 | |||||||
| chr3:186063265 | G | A | 67 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(64): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.970+1152C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063265 | |||||||
| chr3:186063437 | G | A | 2 | a0001c0003t0003g0140 a0001c0003t0004g0153 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.970+980C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063437 | |||||||
| chr3:186063640 | G | A | 67 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(64): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.970+777C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063640 | |||||||
| chr3:186063772 | C | A | 1 | a0001c0001t0002g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.970+645G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186063772 | |||||||
| chr3:186064176 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(289): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.970+241A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186064176 | |||||||
| chr3:186064211 | A | T | 1 | a0001c0001t0002g0275 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.970+206T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 9/12 | chr3 | 186064211 | |||||||
| chr3:186064696 | G | A | 2 | a0001c0001t0006g0208 a0001c0001t0012g0207 |
2 | HG00735.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.911-220C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186064696 | |||||||
| chr3:186064858 | C | T | 1 | a0001c0001t0022g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.911-382G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186064858 | |||||||
| chr3:186064910 | T | G | 1 | a0001c0001t0003g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.911-434A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186064910 | |||||||
| chr3:186064998 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0077 |
3 | NA18942.hp1 NA18989.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.911-522A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186064998 | |||||||
| chr3:186065119 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0002g0236 |
2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.911-643G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186065119 | |||||||
| chr3:186065256 | A | G | 1 | a0001c0001t0006g0201 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.910+557T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186065256 | |||||||
| chr3:186065354 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(149): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.910+459C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 8/12 | chr3 | 186065354 | |||||||
| chr3:186066262 | C | CAAAAAAA | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(52): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.651-197_651-191dup others(7): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(1): Show |
16 | a0001c0001t0002g0002 a0001c0001t0002g0212 a0001c0001t0002g0214 others(13): Show |
19 | HG01934.hp1 HG02083.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.651-198_651-191dup others(8): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0002g0213 a0001c0001t0002g0217 a0001c0001t0003g0079 others(7): Show |
10 | HG00423.hp2 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-199_651-191dup others(9): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(3): Show |
109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.651-200_651-191dup others(10): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(4): Show |
62 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0040 others(59): Show |
65 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.651-201_651-191dup others(11): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0058 others(9): Show |
12 | HG01261.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.651-202_651-191dup others(12): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066262 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0206 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.651-203_651-191dup others(13): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066262 | |||||||
| chr3:186066397 | T | C | 11 | a0001c0001t0002g0204 a0001c0001t0003g0066 a0001c0001t0003g0072 others(8): Show |
11 | HG00423.hp2 HG00639.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.651-325A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066397 | |||||||
| chr3:186066452 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.651-380A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066452 | |||||||
| chr3:186066979 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.651-907A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186066979 | |||||||
| chr3:186067027 | G | C | 1 | a0001c0001t0002g0203 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.651-955C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067027 | |||||||
| chr3:186067066 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.651-994C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067066 | |||||||
| chr3:186067110 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.651-1038G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067110 | |||||||
| chr3:186067111 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.651-1039C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067111 | |||||||
| chr3:186067159 | C | T | 1 | a0001c0001t0012g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.651-1087G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067159 | |||||||
| chr3:186067261 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.651-1189C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067261 | |||||||
| chr3:186067349 | T | C | 1 | a0001c0001t0025g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.651-1277A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067349 | |||||||
| chr3:186067388 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.651-1316G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067388 | |||||||
| chr3:186067453 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-1381G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067453 | |||||||
| chr3:186067560 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-1488G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067560 | |||||||
| chr3:186067574 | T | C | 1 | a0003c0008t0002g0240 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.651-1502A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067574 | |||||||
| chr3:186067759 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.651-1687G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067759 | |||||||
| chr3:186067903 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.651-1831T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186067903 | |||||||
| chr3:186068026 | T | C | 1 | a0001c0001t0005g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.651-1954A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068026 | |||||||
| chr3:186068207 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.651-2135A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068207 | |||||||
| chr3:186068251 | T | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(67): Show |
83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.651-2179A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068251 | |||||||
| chr3:186068432 | G | T | 2 | a0001c0001t0006g0208 a0001c0001t0012g0207 |
2 | HG00735.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.651-2360C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068432 | |||||||
| chr3:186068480 | G | GT | 67 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(64): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.651-2409dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068480 | |||||||
| chr3:186068617 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.651-2545C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068617 | |||||||
| chr3:186068952 | A | G | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.651-2880T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186068952 | |||||||
| chr3:186069085 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.651-3013T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069085 | |||||||
| chr3:186069114 | T | TCTG | 6 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-3043_651-3042i others(5): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069114 | |||||||
| chr3:186069115 | A | T | 6 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-3043T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069115 | |||||||
| chr3:186069117 | A | T | 6 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.651-3045T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069117 | |||||||
| chr3:186069326 | T | C | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.651-3254A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069326 | |||||||
| chr3:186069383 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.651-3311T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069383 | |||||||
| chr3:186069390 | T | C | 2 | a0001c0001t0007g0018 a0001c0001t0007g0160 |
3 | HG03017.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.651-3318A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069390 | |||||||
| chr3:186069494 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.651-3422G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069494 | |||||||
| chr3:186069495 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.651-3423C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069495 | |||||||
| chr3:186069501 | G | GT | 8 | a0001c0001t0001g0096 a0001c0001t0003g0085 a0001c0001t0005g0246 others(5): Show |
8 | HG00597.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.651-3430dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069501 | |||||||
| chr3:186069501 | GTT | G | 33 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(30): Show |
42 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.651-3431_651-3430d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069501 | |||||||
| chr3:186069511 | T | G | 1 | a0001c0001t0003g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.651-3439A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069511 | |||||||
| chr3:186069519 | T | A | 15 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0179 others(12): Show |
17 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.651-3447A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069519 | |||||||
| chr3:186069520 | T | A | 43 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(40): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.651-3448A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069520 | |||||||
| chr3:186069520 | T | TA | 61 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(58): Show |
74 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.651-3449dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069520 | |||||||
| chr3:186069521 | A | T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG00639.hp2 HG01891.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-3449T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069521 | |||||||
| chr3:186069522 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.651-3450T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069522 | |||||||
| chr3:186069545 | A | G | 27 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(24): Show |
33 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.651-3473T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069545 | |||||||
| chr3:186069582 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.651-3510C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069582 | |||||||
| chr3:186069963 | T | G | 1 | a0001c0001t0004g0172 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.651-3891A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186069963 | |||||||
| chr3:186070104 | G | A | 3 | a0001c0001t0014g0056 a0001c0001t0014g0117 a0001c0001t0017g0057 |
3 | HG01168.hp1 HG01169.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.651-4032C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186070104 | |||||||
| chr3:186070237 | T | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-4165A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186070237 | |||||||
| chr3:186070269 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.651-4197G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186070269 | |||||||
| chr3:186070332 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0268 |
2 | NA18968.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.651-4260G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186070332 | |||||||
| chr3:186071014 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-4942C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071014 | |||||||
| chr3:186071039 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.651-4967A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071039 | |||||||
| chr3:186071068 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.651-4996G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071068 | |||||||
| chr3:186071115 | G | A | 2 | a0001c0001t0005g0211 a0001c0001t0018g0046 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.651-5043C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071115 | |||||||
| chr3:186071683 | GGTGGCTC others(403): Show |
G | 6 | a0001c0001t0007g0018 a0001c0001t0007g0160 a0001c0001t0007g0161 others(3): Show |
7 | HG01099.hp1 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.651-6021_651-5612d others(2): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071683 | |||||||
| chr3:186071726 | G | A | 3 | a0001c0001t0004g0019 a0001c0001t0004g0170 a0001c0001t0004g0171 |
4 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.651-5654C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071726 | |||||||
| chr3:186071742 | G | A | 2 | a0001c0001t0008g0063 a0004c0007t0008g0130 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.651-5670C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071742 | |||||||
| chr3:186071743 | A | T | 2 | a0001c0001t0008g0063 a0004c0007t0008g0130 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.651-5671T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071743 | |||||||
| chr3:186071902 | A | G | 1 | a0001c0001t0004g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.651-5830T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071902 | |||||||
| chr3:186071957 | A | G | 1 | a0001c0005t0003g0064 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.651-5885T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186071957 | |||||||
| chr3:186072057 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651-5985G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072057 | |||||||
| chr3:186072117 | C | A | 1 | a0001c0001t0003g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.651-6045G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072117 | |||||||
| chr3:186072198 | C | A | 2 | a0001c0001t0001g0147 a0001c0001t0005g0008 |
4 | NA18950.hp1 NA18971.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.651-6126G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072198 | |||||||
| chr3:186072314 | G | A | 14 | a0001c0001t0001g0037 a0001c0001t0005g0200 a0001c0001t0006g0025 others(11): Show |
15 | HG00558.hp1 HG01168.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.651-6242C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072314 | |||||||
| chr3:186072360 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.651-6288T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072360 | |||||||
| chr3:186072371 | C | CA | 41 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.651-6300dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072371 | |||||||
| chr3:186072371 | C | CAA | 87 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.651-6301_651-6300d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072371 | |||||||
| chr3:186072528 | T | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.651-6456A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072528 | |||||||
| chr3:186072727 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.651-6655A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072727 | |||||||
| chr3:186072752 | T | C | 15 | a0001c0001t0005g0200 a0001c0001t0006g0025 a0001c0001t0006g0192 others(12): Show |
16 | HG00558.hp1 HG01168.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.651-6680A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072752 | |||||||
| chr3:186072803 | G | C | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.651-6731C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072803 | |||||||
| chr3:186072846 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.651-6774A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072846 | |||||||
| chr3:186072864 | G | A | 1 | a0001c0001t0007g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.651-6792C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072864 | |||||||
| chr3:186072875 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.651-6803G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072875 | |||||||
| chr3:186072984 | T | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.650+6833A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186072984 | |||||||
| chr3:186073056 | C | T | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(82): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.650+6761G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073056 | |||||||
| chr3:186073106 | T | C | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
169 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.650+6711A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073106 | |||||||
| chr3:186073245 | G | A | 1 | a0001c0001t0020g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.650+6572C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073245 | |||||||
| chr3:186073385 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.650+6432C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073385 | |||||||
| chr3:186073420 | G | A | 1 | a0001c0001t0003g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.650+6397C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073420 | |||||||
| chr3:186073555 | A | G | 2 | a0001c0001t0003g0074 a0001c0001t0003g0126 |
2 | NA18982.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.650+6262T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073555 | |||||||
| chr3:186073635 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.650+6182T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073635 | |||||||
| chr3:186073712 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650+6105C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073712 | |||||||
| chr3:186073811 | A | T | 1 | a0001c0001t0003g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.650+6006T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073811 | |||||||
| chr3:186073933 | T | C | 1 | a0001c0001t0020g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.650+5884A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073933 | |||||||
| chr3:186073987 | C | G | 1 | a0001c0001t0004g0183 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.650+5830G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186073987 | |||||||
| chr3:186074001 | A | C | 1 | a0001c0001t0002g0237 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.650+5816T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074001 | |||||||
| chr3:186074004 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.650+5813T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074004 | |||||||
| chr3:186074048 | C | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0083 |
2 | HG00544.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.650+5769G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074048 | |||||||
| chr3:186074180 | A | G | 1 | a0001c0001t0004g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.650+5637T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074180 | |||||||
| chr3:186074439 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.650+5378A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074439 | |||||||
| chr3:186074500 | G | A | 2 | a0001c0001t0003g0084 a0001c0001t0003g0086 |
2 | NA18969.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.650+5317C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074500 | |||||||
| chr3:186074508 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.650+5309T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074508 | |||||||
| chr3:186074575 | T | G | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.650+5242A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074575 | |||||||
| chr3:186074595 | C | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(109): Show |
131 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.650+5222G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074595 | |||||||
| chr3:186074714 | C | A | 1 | a0001c0006t0026g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.650+5103G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074714 | |||||||
| chr3:186074833 | C | A | 1 | a0001c0001t0022g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.650+4984G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074833 | |||||||
| chr3:186074849 | ACT | A | 3 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 |
3 | HG02630.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.650+4966_650+4967d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074849 | |||||||
| chr3:186074859 | C | CA | 85 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0061 others(82): Show |
99 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.650+4957dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074859 | |||||||
| chr3:186074859 | C | CAA | 11 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0236 others(8): Show |
13 | HG01496.hp1 HG01928.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.650+4956_650+4957d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074859 | |||||||
| chr3:186074859 | CA | C | 23 | a0001c0001t0001g0037 a0001c0001t0003g0078 a0001c0001t0004g0019 others(20): Show |
25 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.650+4957delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074859 | |||||||
| chr3:186074859 | CAAAAAAA | C | 17 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(14): Show |
17 | HG00423.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.650+4951_650+4957d others(9): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074859 | |||||||
| chr3:186074883 | G | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.650+4934C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074883 | |||||||
| chr3:186074901 | T | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
5 | NA18946.hp1 NA18955.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+4916A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074901 | |||||||
| chr3:186074917 | G | A | 1 | a0001c0001t0007g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.650+4900C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074917 | |||||||
| chr3:186074930 | T | C | 15 | a0001c0001t0005g0200 a0001c0001t0006g0025 a0001c0001t0006g0192 others(12): Show |
16 | HG00558.hp1 HG01168.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.650+4887A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186074930 | |||||||
| chr3:186075105 | A | C | 1 | a0001c0001t0004g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.650+4712T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075105 | |||||||
| chr3:186075137 | C | G | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.650+4680G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075137 | |||||||
| chr3:186075168 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.650+4649C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075168 | |||||||
| chr3:186075190 | A | T | 3 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 |
3 | HG02630.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.650+4627T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075190 | |||||||
| chr3:186075471 | G | A | 2 | a0001c0001t0005g0211 a0001c0001t0018g0046 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.650+4346C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075471 | |||||||
| chr3:186075479 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.650+4338C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075479 | |||||||
| chr3:186075663 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.650+4154T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075663 | |||||||
| chr3:186075787 | A | T | 1 | a0001c0001t0004g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.650+4030T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075787 | |||||||
| chr3:186075889 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.650+3928A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075889 | |||||||
| chr3:186075892 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.650+3925A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075892 | |||||||
| chr3:186075920 | G | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.650+3897C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186075920 | |||||||
| chr3:186076024 | A | G | 2 | a0001c0001t0010g0134 a0001c0001t0010g0136 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.650+3793T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186076024 | |||||||
| chr3:186076099 | T | C | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.650+3718A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186076099 | |||||||
| chr3:186076715 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.650+3102T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186076715 | |||||||
| chr3:186076826 | G | A | 6 | a0001c0001t0007g0018 a0001c0001t0007g0160 a0001c0001t0007g0161 others(3): Show |
7 | HG01099.hp1 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.650+2991C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186076826 | |||||||
| chr3:186077022 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.650+2795C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077022 | |||||||
| chr3:186077102 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.650+2715C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077102 | |||||||
| chr3:186077157 | G | T | 113 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(110): Show |
132 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.650+2660C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077157 | |||||||
| chr3:186077177 | A | G | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.650+2640T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077177 | |||||||
| chr3:186077228 | C | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0065 others(20): Show |
27 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.650+2589G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077228 | |||||||
| chr3:186077271 | A | G | 41 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(38): Show |
47 | HG00423.hp1 HG01496.hp1 HG01975.hp2 others(44): Show |
intron_variant | MODIFIER | c.650+2546T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077271 | |||||||
| chr3:186077360 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0108 a0001c0001t0001g0110 others(1): Show |
5 | HG01928.hp2 NA18961.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+2457A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077360 | |||||||
| chr3:186077452 | C | A | 1 | a0001c0001t0012g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.650+2365G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077452 | |||||||
| chr3:186077503 | A | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.650+2314T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077503 | |||||||
| chr3:186077544 | T | C | 154 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(151): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.650+2273A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077544 | |||||||
| chr3:186077641 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG00639.hp2 HG01891.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.650+2176A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077641 | |||||||
| chr3:186077673 | A | C | 2 | a0001c0001t0006g0208 a0001c0001t0012g0207 |
2 | HG00735.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.650+2144T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077673 | |||||||
| chr3:186077849 | C | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.650+1968G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077849 | |||||||
| chr3:186077874 | G | C | 1 | a0001c0003t0004g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.650+1943C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186077874 | |||||||
| chr3:186078066 | A | C | 142 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(139): Show |
167 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.650+1751T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078066 | |||||||
| chr3:186078350 | A | G | 123 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(120): Show |
142 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.650+1467T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078350 | |||||||
| chr3:186078830 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.650+987C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078830 | |||||||
| chr3:186078966 | C | G | 1 | a0001c0001t0006g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.650+851G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078966 | |||||||
| chr3:186078976 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(85): Show |
105 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.650+841G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078976 | |||||||
| chr3:186078996 | G | A | 24 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0023 others(21): Show |
30 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.650+821C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186078996 | |||||||
| chr3:186079173 | T | C | 16 | a0001c0001t0002g0213 a0001c0001t0005g0200 a0001c0001t0006g0025 others(13): Show |
17 | HG00558.hp1 HG01168.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.650+644A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186079173 | |||||||
| chr3:186079352 | A | G | 1 | a0001c0001t0005g0200 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650+465T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186079352 | |||||||
| chr3:186079518 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.650+299T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 7/12 | chr3 | 186079518 | |||||||
| chr3:186080236 | C | T | 27 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(24): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.363-132G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 6/12 | chr3 | 186080236 | |||||||
| chr3:186080507 | T | C | 150 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(147): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.363-403A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 6/12 | chr3 | 186080507 | |||||||
| chr3:186080939 | A | G | 16 | a0001c0001t0002g0213 a0001c0001t0005g0024 a0001c0001t0005g0200 others(13): Show |
18 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.362+107T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 6/12 | chr3 | 186080939 | |||||||
| chr3:186080968 | G | C | 1 | a0001c0001t0007g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.362+78C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 6/12 | chr3 | 186080968 | |||||||
| chr3:186081316 | C | T | 1 | a0001c0001t0005g0262 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.233-141G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186081316 | |||||||
| chr3:186081546 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233-371G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186081546 | |||||||
| chr3:186081607 | G | T | 1 | a0001c0001t0003g0066 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.233-432C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186081607 | |||||||
| chr3:186081771 | C | A | 1 | a0001c0001t0003g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.233-596G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186081771 | |||||||
| chr3:186082083 | G | A | 16 | a0001c0001t0005g0031 a0001c0001t0005g0032 a0001c0001t0005g0230 others(13): Show |
18 | HG00597.hp1 HG00673.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.233-908C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082083 | |||||||
| chr3:186082326 | A | G | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(82): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.233-1151T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082326 | |||||||
| chr3:186082392 | C | T | 1 | a0001c0001t0006g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.233-1217G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082392 | |||||||
| chr3:186082428 | C | CT | 15 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(12): Show |
18 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-1254dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082428 | |||||||
| chr3:186082428 | CT | C | 36 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0106 others(33): Show |
43 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-1254delA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082428 | |||||||
| chr3:186082430 | T | C | 1 | a0001c0001t0003g0042 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.233-1255A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082430 | |||||||
| chr3:186082447 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.233-1272T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082447 | |||||||
| chr3:186082489 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.233-1314C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082489 | |||||||
| chr3:186082751 | T | C | 4 | a0001c0001t0003g0074 a0001c0001t0003g0087 a0001c0001t0003g0126 others(1): Show |
4 | NA18982.hp2 NA18984.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-1576A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082751 | |||||||
| chr3:186082934 | T | C | 16 | a0001c0001t0002g0213 a0001c0001t0005g0024 a0001c0001t0005g0200 others(13): Show |
18 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-1759A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186082934 | |||||||
| chr3:186083510 | G | A | 1 | a0001c0005t0003g0064 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.233-2335C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186083510 | |||||||
| chr3:186083597 | C | T | 3 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG00438.hp2 HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.233-2422G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186083597 | |||||||
| chr3:186083655 | G | A | 4 | a0001c0001t0005g0246 a0001c0001t0005g0265 a0001c0001t0005g0266 others(1): Show |
4 | HG02523.hp1 NA18967.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2480C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186083655 | |||||||
| chr3:186083750 | C | T | 1 | a0001c0003t0004g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.233-2575G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186083750 | |||||||
| chr3:186083839 | A | G | 203 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(200): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.233-2664T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186083839 | |||||||
| chr3:186084084 | G | C | 2 | a0001c0001t0002g0214 a0001c0001t0005g0215 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.233-2909C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084084 | |||||||
| chr3:186084282 | TA | T | 89 | a0001c0001t0001g0106 a0001c0001t0001g0143 a0001c0001t0002g0003 others(86): Show |
103 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.233-3108delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084282 | |||||||
| chr3:186084282 | TAA | T | 30 | a0001c0001t0002g0212 a0001c0001t0002g0221 a0001c0001t0002g0294 others(27): Show |
37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.233-3109_233-3108d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084282 | |||||||
| chr3:186084282 | TAAA | T | 27 | a0001c0001t0002g0002 a0001c0001t0002g0213 a0001c0001t0002g0214 others(24): Show |
30 | HG00558.hp1 HG01167.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.233-3110_233-3108d others(5): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084282 | |||||||
| chr3:186084282 | TAAAA | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0215 a0001c0001t0006g0025 others(1): Show |
6 | HG01070.hp2 HG01071.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-3111_233-3108d others(6): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084282 | |||||||
| chr3:186084311 | C | G | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.233-3136G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084311 | |||||||
| chr3:186084461 | C | CTTCA | 16 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0115 others(13): Show |
18 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-3290_233-3287d others(6): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084461 | |||||||
| chr3:186084461 | C | CTTCATTC others(1): Show |
5 | a0001c0001t0006g0190 a0001c0001t0006g0197 a0001c0001t0006g0208 others(2): Show |
5 | HG00558.hp1 HG00735.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-3294_233-3287d others(10): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084461 | |||||||
| chr3:186084461 | CTTCA | C | 68 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0044 others(65): Show |
79 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.233-3290_233-3287d others(6): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084461 | |||||||
| chr3:186084461 | CTTCATTC others(1): Show |
C | 83 | a0001c0001t0001g0068 a0001c0001t0001g0142 a0001c0001t0002g0003 others(80): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.233-3294_233-3287d others(10): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084461 | |||||||
| chr3:186084514 | G | A | 10 | a0001c0001t0005g0211 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-3339C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084514 | |||||||
| chr3:186084727 | C | T | 1 | a0001c0001t0009g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.233-3552G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084727 | |||||||
| chr3:186084837 | G | C | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233-3662C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084837 | |||||||
| chr3:186084839 | A | C | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.233-3664T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186084839 | |||||||
| chr3:186085034 | C | T | 151 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.233-3859G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085034 | |||||||
| chr3:186085076 | T | C | 3 | a0001c0001t0002g0247 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | NA19067.hp1 NA19070.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.233-3901A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085076 | |||||||
| chr3:186085102 | CAAGGCTC others(18): Show |
C | 151 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.233-3952_233-3928d others(27): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085102 | |||||||
| chr3:186085121 | C | T | 1 | a0001c0001t0019g0091 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.233-3946G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085121 | |||||||
| chr3:186085143 | T | C | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.233-3968A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085143 | |||||||
| chr3:186085149 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0226 a0001c0001t0002g0235 others(1): Show |
5 | HG00642.hp1 HG01106.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-3974G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085149 | |||||||
| chr3:186085150 | G | A | 1 | a0001c0001t0007g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.233-3975C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085150 | |||||||
| chr3:186085180 | T | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-4005A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085180 | |||||||
| chr3:186085314 | G | C | 1 | a0001c0001t0002g0273 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.233-4139C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085314 | |||||||
| chr3:186085507 | G | GT | 97 | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0108 others(94): Show |
115 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.233-4333dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085507 | |||||||
| chr3:186085507 | G | GTT | 10 | a0001c0001t0001g0048 a0001c0001t0002g0214 a0001c0001t0002g0231 others(7): Show |
10 | HG01934.hp1 HG02071.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-4334_233-4333d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085507 | |||||||
| chr3:186085507 | GT | G | 35 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(32): Show |
43 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-4333delA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085507 | |||||||
| chr3:186085669 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.233-4494G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085669 | |||||||
| chr3:186085682 | G | C | 10 | a0001c0001t0005g0211 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-4507C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085682 | |||||||
| chr3:186085743 | C | T | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.233-4568G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085743 | |||||||
| chr3:186085799 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0038 others(1): Show |
4 | HG02486.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-4624G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085799 | |||||||
| chr3:186085805 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(147): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.233-4630G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085805 | |||||||
| chr3:186085839 | A | G | 16 | a0001c0001t0002g0213 a0001c0001t0005g0024 a0001c0001t0005g0200 others(13): Show |
18 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-4664T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085839 | |||||||
| chr3:186085972 | C | T | 1 | a0001c0001t0025g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233-4797G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186085972 | |||||||
| chr3:186086230 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.233-5055G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086230 | |||||||
| chr3:186086242 | T | C | 16 | a0001c0001t0002g0213 a0001c0001t0005g0024 a0001c0001t0005g0200 others(13): Show |
18 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-5067A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086242 | |||||||
| chr3:186086246 | T | C | 3 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG00438.hp2 HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.233-5071A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086246 | |||||||
| chr3:186086425 | C | G | 1 | a0001c0001t0003g0151 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.233-5250G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086425 | |||||||
| chr3:186086483 | T | C | 6 | a0001c0001t0006g0025 a0001c0001t0006g0192 a0001c0001t0006g0193 others(3): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-5308A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086483 | |||||||
| chr3:186086708 | C | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.233-5533G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086708 | |||||||
| chr3:186086712 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(1): Show |
5 | HG02109.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-5537A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086712 | |||||||
| chr3:186086794 | A | C | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.233-5619T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086794 | |||||||
| chr3:186086804 | G | GA | 115 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(112): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.233-5630dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186086804 | |||||||
| chr3:186087215 | A | G | 1 | a0001c0001t0004g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.233-6040T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087215 | |||||||
| chr3:186087422 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.233-6247C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087422 | |||||||
| chr3:186087448 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.233-6273A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087448 | |||||||
| chr3:186087505 | C | G | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.233-6330G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087505 | |||||||
| chr3:186087570 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0124 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.233-6395G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087570 | |||||||
| chr3:186087817 | G | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-6642C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087817 | |||||||
| chr3:186087838 | AT | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0106 a0001c0001t0002g0219 others(5): Show |
8 | HG00558.hp2 HG01515.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.233-6664delA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087838 | |||||||
| chr3:186087861 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.233-6686G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087861 | |||||||
| chr3:186087879 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-6704T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087879 | |||||||
| chr3:186087974 | T | TA | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(92): Show |
109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.233-6800dupT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186087974 | |||||||
| chr3:186088003 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.233-6828C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088003 | |||||||
| chr3:186088092 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.233-6917C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088092 | |||||||
| chr3:186088122 | T | G | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(82): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.233-6947A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088122 | |||||||
| chr3:186088204 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(147): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.233-7029G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088204 | |||||||
| chr3:186088287 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.233-7112G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088287 | |||||||
| chr3:186088360 | A | G | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.233-7185T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088360 | |||||||
| chr3:186088366 | A | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): Show |
5 | NA18939.hp1 NA18964.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-7191T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088366 | |||||||
| chr3:186088686 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.233-7511G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186088686 | |||||||
| chr3:186089401 | G | T | 8 | a0001c0001t0005g0024 a0001c0001t0005g0200 a0001c0001t0006g0196 others(5): Show |
9 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-8226C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186089401 | |||||||
| chr3:186089853 | A | G | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233-8678T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186089853 | |||||||
| chr3:186089915 | T | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-8740A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186089915 | |||||||
| chr3:186089942 | G | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-8767C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186089942 | |||||||
| chr3:186090088 | T | A | 2 | a0001c0001t0002g0280 a0001c0001t0005g0279 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.233-8913A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090088 | |||||||
| chr3:186090098 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(1): Show |
5 | HG02109.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.233-8923A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090098 | |||||||
| chr3:186090100 | T | C | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.233-8925A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090100 | |||||||
| chr3:186090107 | GA | G | 8 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-8933delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090107 | |||||||
| chr3:186090116 | T | C | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.233-8941A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090116 | |||||||
| chr3:186090505 | G | A | 1 | a0001c0001t0007g0167 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.233-9330C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090505 | |||||||
| chr3:186090854 | C | T | 2 | a0001c0001t0002g0213 a0001c0006t0026g0225 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.233-9679G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090854 | |||||||
| chr3:186090869 | G | A | 1 | a0001c0006t0026g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.233-9694C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090869 | |||||||
| chr3:186090969 | C | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0108 others(9): Show |
15 | HG00639.hp1 HG00673.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.233-9794G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186090969 | |||||||
| chr3:186091038 | T | C | 1 | a0001c0001t0004g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-9863A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186091038 | |||||||
| chr3:186091105 | G | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(80): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.233-9930C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186091105 | |||||||
| chr3:186091303 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.233-10128C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186091303 | |||||||
| chr3:186091375 | C | G | 1 | a0001c0001t0020g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233-10200G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186091375 | |||||||
| chr3:186091701 | T | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.233-10526A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186091701 | |||||||
| chr3:186092359 | A | C | 1 | a0001c0003t0003g0140 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.233-11184T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186092359 | |||||||
| chr3:186092692 | C | G | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.233-11517G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186092692 | |||||||
| chr3:186092715 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.233-11540A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186092715 | |||||||
| chr3:186092749 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.233-11574T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186092749 | |||||||
| chr3:186092773 | G | A | 1 | a0001c0001t0010g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.233-11598C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186092773 | |||||||
| chr3:186093353 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.232+11952T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093353 | |||||||
| chr3:186093359 | A | G | 2 | a0001c0001t0002g0214 a0001c0001t0005g0215 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.232+11946T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093359 | |||||||
| chr3:186093394 | G | C | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+11911C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093394 | |||||||
| chr3:186093427 | T | C | 1 | a0001c0001t0006g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.232+11878A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093427 | |||||||
| chr3:186093475 | C | T | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.232+11830G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093475 | |||||||
| chr3:186093490 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.232+11815G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093490 | |||||||
| chr3:186093512 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(147): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.232+11793G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093512 | |||||||
| chr3:186093706 | G | A | 143 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(140): Show |
169 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.232+11599C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093706 | |||||||
| chr3:186093795 | A | G | 1 | a0001c0001t0012g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.232+11510T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186093795 | |||||||
| chr3:186094173 | T | A | 2 | a0001c0001t0001g0062 a0001c0001t0007g0158 |
2 | HG01081.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.232+11132A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094173 | |||||||
| chr3:186094202 | C | T | 1 | a0001c0001t0015g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.232+11103G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094202 | |||||||
| chr3:186094361 | T | C | 1 | a0001c0006t0026g0225 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.232+10944A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094361 | |||||||
| chr3:186094380 | C | G | 27 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(24): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.232+10925G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094380 | |||||||
| chr3:186094400 | T | C | 1 | a0001c0001t0005g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.232+10905A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094400 | |||||||
| chr3:186094503 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232+10802G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094503 | |||||||
| chr3:186094680 | T | C | 1 | a0001c0001t0020g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.232+10625A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094680 | |||||||
| chr3:186094713 | A | ACGGGGCT others(4): Show |
1 | a0001c0001t0022g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+10581_232+1059 others(15): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094713 | |||||||
| chr3:186094845 | G | A | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.232+10460C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094845 | |||||||
| chr3:186094849 | C | G | 8 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0226 others(5): Show |
10 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+10456G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094849 | |||||||
| chr3:186094927 | C | T | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.232+10378G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186094927 | |||||||
| chr3:186095309 | T | A | 11 | a0001c0001t0002g0213 a0001c0001t0006g0189 a0001c0001t0006g0190 others(8): Show |
11 | HG00735.hp2 HG01074.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.232+9996A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095309 | |||||||
| chr3:186095929 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.232+9376C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095929 | |||||||
| chr3:186095943 | C | T | 5 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0034 others(2): Show |
7 | NA18939.hp1 NA18947.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+9362G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095943 | |||||||
| chr3:186095944 | G | A | 5 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0002g0289 others(2): Show |
5 | HG01496.hp1 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+9361C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095944 | |||||||
| chr3:186095952 | C | G | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.232+9353G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095952 | |||||||
| chr3:186095971 | G | A | 1 | a0001c0001t0022g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232+9334C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186095971 | |||||||
| chr3:186096749 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(80): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.232+8556G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186096749 | |||||||
| chr3:186096779 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0120 others(1): Show |
5 | HG02109.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+8526A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186096779 | |||||||
| chr3:186096853 | G | A | 31 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.232+8452C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186096853 | |||||||
| chr3:186096953 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.232+8352T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186096953 | |||||||
| chr3:186097009 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.232+8296G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097009 | |||||||
| chr3:186097021 | T | C | 1 | a0001c0001t0015g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.232+8284A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097021 | |||||||
| chr3:186097105 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+8200T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097105 | |||||||
| chr3:186097243 | GA | G | 150 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(147): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.232+8061delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097243 | |||||||
| chr3:186097302 | G | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+8003C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097302 | |||||||
| chr3:186097356 | T | C | 1 | a0001c0001t0010g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232+7949A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097356 | |||||||
| chr3:186097485 | C | T | 2 | a0001c0001t0003g0050 a0001c0005t0003g0064 |
2 | HG01070.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.232+7820G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097485 | |||||||
| chr3:186097800 | T | C | 1 | a0001c0001t0002g0284 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.232+7505A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097800 | |||||||
| chr3:186097972 | C | A | 1 | a0001c0004t0013g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.232+7333G>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186097972 | |||||||
| chr3:186098391 | T | A | 1 | a0001c0001t0003g0042 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+6914A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098391 | |||||||
| chr3:186098414 | C | G | 1 | a0001c0001t0004g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232+6891G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098414 | |||||||
| chr3:186098578 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG00639.hp2 HG01891.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+6727C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098578 | |||||||
| chr3:186098592 | T | C | 1 | a0001c0001t0012g0210 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.232+6713A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098592 | |||||||
| chr3:186098791 | G | C | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.232+6514C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098791 | |||||||
| chr3:186098799 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.232+6506G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186098799 | |||||||
| chr3:186099001 | C | T | 2 | a0001c0001t0002g0213 a0001c0006t0026g0225 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.232+6304G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099001 | |||||||
| chr3:186099041 | C | T | 1 | a0001c0001t0002g0026 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.232+6264G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099041 | |||||||
| chr3:186099285 | G | GATAGA | 84 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(81): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.232+6015_232+6019d others(7): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099285 | |||||||
| chr3:186099292 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.232+6013T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099292 | |||||||
| chr3:186099348 | A | T | 15 | a0001c0001t0005g0024 a0001c0001t0005g0200 a0001c0001t0006g0025 others(12): Show |
17 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.232+5957T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099348 | |||||||
| chr3:186099367 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.232+5938C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099367 | |||||||
| chr3:186099701 | T | A | 1 | a0001c0001t0009g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.232+5604A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186099701 | |||||||
| chr3:186100350 | T | G | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+4955A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186100350 | |||||||
| chr3:186100487 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.232+4818G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186100487 | |||||||
| chr3:186100770 | G | A | 26 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(23): Show |
33 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.232+4535C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186100770 | |||||||
| chr3:186100887 | T | C | 14 | a0001c0001t0005g0024 a0001c0001t0005g0200 a0001c0001t0006g0025 others(11): Show |
16 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+4418A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186100887 | |||||||
| chr3:186100959 | A | C | 1 | a0001c0001t0002g0234 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.232+4346T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186100959 | |||||||
| chr3:186101093 | A | G | 28 | a0001c0001t0004g0007 a0001c0001t0004g0019 a0001c0001t0004g0020 others(25): Show |
35 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.232+4212T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101093 | |||||||
| chr3:186101216 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.232+4089C>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101216 | |||||||
| chr3:186101356 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+3949C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101356 | |||||||
| chr3:186101461 | A | AT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0053 others(14): Show |
18 | HG01081.hp2 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.232+3843dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101461 | |||||||
| chr3:186101469 | C | T | 1 | a0001c0001t0009g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.232+3836G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101469 | |||||||
| chr3:186101470 | T | C | 1 | a0001c0001t0009g0122 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.232+3835A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101470 | |||||||
| chr3:186101679 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.232+3626G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101679 | |||||||
| chr3:186101698 | CTTCT | C | 5 | a0001c0001t0005g0024 a0001c0001t0005g0200 a0001c0001t0006g0198 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+3603_232+3606d others(6): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101698 | |||||||
| chr3:186101710 | T | A | 1 | a0001c0001t0002g0285 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.232+3595A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101710 | |||||||
| chr3:186101762 | C | G | 1 | a0001c0001t0025g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232+3543G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186101762 | |||||||
| chr3:186102151 | G | C | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.232+3154C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102151 | |||||||
| chr3:186102171 | A | T | 1 | a0001c0001t0002g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232+3134T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102171 | |||||||
| chr3:186102361 | A | G | 2 | a0001c0001t0007g0167 a0001c0001t0015g0168 |
2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.232+2944T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102361 | |||||||
| chr3:186102493 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232+2812G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102493 | |||||||
| chr3:186102494 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.232+2811T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102494 | |||||||
| chr3:186102496 | G | A | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.232+2809C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102496 | |||||||
| chr3:186102526 | G | A | 1 | a0001c0001t0005g0200 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.232+2779C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102526 | |||||||
| chr3:186102586 | G | A | 1 | a0001c0001t0015g0168 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.232+2719C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102586 | |||||||
| chr3:186102636 | CA | C | 126 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0123 others(123): Show |
144 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.232+2668delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102636 | |||||||
| chr3:186102636 | CAA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.232+2667_232+2668d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102636 | |||||||
| chr3:186102657 | AG | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+2647delC | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186102657 | |||||||
| chr3:186103168 | TA | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(4): Show |
10 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+2136delT | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103168 | |||||||
| chr3:186103525 | G | A | 1 | a0001c0001t0005g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.232+1780C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103525 | |||||||
| chr3:186103570 | T | C | 3 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 |
3 | HG02630.hp1 HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.232+1735A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103570 | |||||||
| chr3:186103619 | AAACACAC others(8): Show |
A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0226 a0001c0001t0002g0290 |
3 | HG02004.hp1 NA18945.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.232+1671_232+1685d others(17): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103619 | |||||||
| chr3:186103619 | AAACACAC others(10): Show |
A | 1 | a0001c0001t0002g0292 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.232+1669_232+1685d others(19): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103619 | |||||||
| chr3:186103620 | A | AAC | 8 | a0001c0001t0004g0169 a0001c0001t0004g0174 a0001c0001t0004g0180 others(5): Show |
8 | HG02647.hp1 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+1683_232+1684d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACAC | 11 | a0001c0001t0004g0019 a0001c0001t0004g0022 a0001c0001t0004g0170 others(8): Show |
11 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+1681_232+1684d others(6): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACACAC | 5 | a0001c0001t0004g0020 a0001c0001t0004g0023 a0001c0001t0004g0172 others(2): Show |
5 | HG00099.hp2 HG01884.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+1679_232+1684d others(8): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACACACA others(3): Show |
4 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(1): Show |
4 | HG00280.hp1 HG02055.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+1675_232+1684d others(12): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACACACA others(5): Show |
2 | a0001c0001t0004g0007 a0001c0001t0004g0182 |
3 | HG00408.hp2 NA19060.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.232+1673_232+1684d others(14): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACACACA others(7): Show |
3 | a0001c0001t0004g0023 a0001c0001t0004g0183 a0001c0001t0007g0021 |
3 | HG01515.hp1 HG02155.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.232+1671_232+1684d others(16): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | AACACACA others(9): Show |
2 | a0001c0001t0004g0188 a0001c0001t0007g0021 |
2 | HG04228.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.232+1669_232+1684d others(18): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | A | ACACACAC others(4): Show |
1 | a0001c0001t0004g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.232+1684_232+1685i others(13): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AAC | A | 8 | a0001c0001t0005g0024 a0001c0001t0005g0211 a0001c0001t0006g0193 others(5): Show |
9 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+1683_232+1684d others(4): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACAC | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0214 a0001c0001t0002g0216 others(7): Show |
13 | HG00735.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.232+1679_232+1684d others(8): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0005 a0001c0001t0003g0009 a0001c0001t0003g0011 others(5): Show |
10 | HG01109.hp2 HG02559.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.232+1677_232+1684d others(10): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(3): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(15): Show |
19 | HG00642.hp2 HG02109.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.232+1675_232+1684d others(12): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(5): Show |
A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(118): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.232+1673_232+1684d others(14): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(7): Show |
A | 34 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0068 others(31): Show |
38 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(35): Show |
intron_variant | MODIFIER | c.232+1671_232+1684d others(16): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(9): Show |
A | 47 | a0001c0001t0002g0004 a0001c0001t0002g0026 a0001c0001t0002g0027 others(44): Show |
54 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.232+1669_232+1684d others(18): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(11): Show |
A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01496.hp1 HG02109.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+1667_232+1684d others(20): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186103620 | AACACACA others(13): Show |
A | 1 | a0001c0001t0002g0213 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232+1665_232+1684d others(22): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186103620 | |||||||
| chr3:186104139 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.232+1166C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104139 | |||||||
| chr3:186104154 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+1151T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104154 | |||||||
| chr3:186104233 | G | A | 1 | a0001c0001t0025g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232+1072C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104233 | |||||||
| chr3:186104564 | T | G | 16 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0023 others(13): Show |
21 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.232+741A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104564 | |||||||
| chr3:186104741 | T | C | 1 | a0001c0001t0003g0138 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.232+564A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104741 | |||||||
| chr3:186104742 | C | CT | 20 | a0001c0001t0001g0051 a0001c0001t0005g0024 a0001c0001t0005g0200 others(17): Show |
22 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.232+562dupA | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104742 | |||||||
| chr3:186104742 | C | CTT | 12 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.232+561_232+562dup others(2): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104742 | |||||||
| chr3:186104816 | A | G | 1 | a0001c0001t0025g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232+489T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104816 | |||||||
| chr3:186104917 | T | C | 3 | a0001c0001t0002g0293 a0001c0001t0003g0017 a0001c0001t0003g0151 |
4 | HG00438.hp1 HG02071.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.232+388A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104917 | |||||||
| chr3:186104930 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.232+375G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104930 | |||||||
| chr3:186104984 | C | G | 1 | a0001c0001t0003g0050 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.232+321G>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104984 | |||||||
| chr3:186104985 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.232+320T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186104985 | |||||||
| chr3:186105193 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.232+112A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186105193 | |||||||
| chr3:186105237 | T | G | 1 | a0001c0003t0003g0140 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.232+68A>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 5/12 | chr3 | 186105237 | |||||||
| chr3:186105983 | A | T | 3 | a0002c0002t0013g0228 a0002c0002t0013g0229 a0002c0002t0028g0227 |
3 | HG02895.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-74-41T>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186105983 | |||||||
| chr3:186106153 | C | T | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(83): Show |
100 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-74-211G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106153 | |||||||
| chr3:186106184 | T | C | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
11 | HG00323.hp2 HG01257.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-74-242A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106184 | |||||||
| chr3:186106215 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.-74-273A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106215 | |||||||
| chr3:186106239 | A | C | 1 | a0001c0001t0002g0226 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-74-297T>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106239 | |||||||
| chr3:186106362 | G | C | 6 | a0001c0001t0007g0018 a0001c0001t0007g0160 a0001c0001t0007g0161 others(3): Show |
7 | HG01099.hp1 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74-420C>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106362 | |||||||
| chr3:186106380 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-74-438A>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106380 | |||||||
| chr3:186106485 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-74-543T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106485 | |||||||
| chr3:186106562 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-74-620A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106562 | |||||||
| chr3:186106710 | A | G | 5 | a0001c0001t0006g0192 a0001c0001t0006g0193 a0001c0001t0006g0194 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74-768T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106710 | |||||||
| chr3:186106855 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-74-913G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186106855 | |||||||
| chr3:186107114 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-74-1172G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107114 | |||||||
| chr3:186107426 | A | G | 4 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0222 others(1): Show |
4 | NA18960.hp1 NA18992.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74-1484T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107426 | |||||||
| chr3:186107525 | T | C | 87 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0026 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-75+1415A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107525 | |||||||
| chr3:186107545 | TAAACGAA others(3): Show |
T | 1 | a0001c0001t0002g0212 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-75+1385_-75+1394d others(12): Show |
ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107545 | |||||||
| chr3:186107884 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-75+1056A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107884 | |||||||
| chr3:186107936 | TC | T | 10 | a0001c0001t0005g0211 a0001c0001t0006g0189 a0001c0001t0006g0190 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-75+1003delG | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186107936 | |||||||
| chr3:186108239 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-75+701T>C | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108239 | |||||||
| chr3:186108329 | C | T | 2 | a0001c0001t0023g0154 a0001c0003t0004g0153 |
2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-75+611G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108329 | |||||||
| chr3:186108485 | T | C | 1 | a0001c0001t0006g0025 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-75+455A>G | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108485 | |||||||
| chr3:186108757 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-75+183C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108757 | |||||||
| chr3:186108788 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-75+152C>T | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108788 | |||||||
| chr3:186108801 | C | CG | 18 | a0001c0001t0002g0203 a0001c0001t0003g0034 a0001c0001t0005g0024 others(15): Show |
20 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-75+138dupC | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108801 | |||||||
| chr3:186108910 | C | T | 4 | a0001c0001t0003g0009 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): Show |
5 | NA18939.hp1 NA18964.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-75+30G>A | ETV5 | ENSG00000244405.8 | transcript | ENST00000306376.10 | protein_coding | 1/12 | chr3 | 186108910 |