Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2115 |
| ensemblid | ENSG00000006468.15 |
| hgncid | 3490 |
| symbol | ETV1 |
| name | ETS variant transcription factor 1 |
| refseq_nuc | NM_004956.5 |
| refseq_prot | NP_004947.2 |
| ensembl_nuc | ENST00000430479.6 |
| ensembl_prot | ENSP00000405327.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 13891229 |
| end | 13989666 |
| strand | - |
| ver | v1.2 |
| region | chr7:13891229-13989666 |
| region5000 | chr7:13886229-13994666 |
| regionname0 | ETV1_chr7_13891229_13989666 |
| regionname5000 | ETV1_chr7_13886229_13994666 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 477 | 219 | 63 | 41 | 79 | 12 | 22 | 59 | ETV1_chr7_13886229_13994666 | ETV1 | MDGFY others(472): Show |
chr7 | 13886229 | 13994666 |
| a0002 | 0/0 | 477 | 101 | 17 | 17 | 49 | 6 | 12 | 35 | ETV1_chr7_13886229_13994666 | ETV1 | MDGFY others(472): Show |
chr7 | 13886229 | 13994666 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1431 | 216 | 62 | 41 | 79 | 11 | 21 | ETV1_chr7_13886229_13994666 | ETV1 | ATGGA others(1426): Show |
chr7 | 13886229 | 13994666 | ||
| a0001c0003 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | ATGGA others(1426): Show |
chr7 | 13886229 | 13994666 | ||
| a0001c0004 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | ATGGA others(1426): Show |
chr7 | 13886229 | 13994666 | ||
| a0001c0005 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | ATGGA others(1426): Show |
chr7 | 13886229 | 13994666 | ||
| a0002c0002 | 0/0 | 1431 | 101 | 17 | 17 | 49 | 6 | 12 | ETV1_chr7_13886229_13994666 | ETV1 | ATGGA others(1426): Show |
chr7 | 13886229 | 13994666 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6459 | 16 | 1 | 3 | 6 | 1 | 5 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0002 | 0/0 | 6458 | 26 | 5 | 6 | 15 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0003 | 0/0 | 6458 | 24 | 0 | 1 | 19 | 2 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0004 | 0/0 | 6460 | 15 | 3 | 0 | 6 | 0 | 6 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0005 | 0/0 | 6459 | 9 | 0 | 3 | 5 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0006 | 0/0 | 6458 | 17 | 8 | 2 | 7 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0007 | 0/0 | 6459 | 10 | 2 | 3 | 4 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0008 | 0/0 | 6459 | 4 | 0 | 1 | 3 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0009 | 0/0 | 6459 | 5 | 2 | 0 | 0 | 0 | 3 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0010 | 0/0 | 6459 | 8 | 4 | 3 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0011 | 0/0 | 6458 | 10 | 0 | 9 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0012 | 0/0 | 6458 | 5 | 0 | 0 | 5 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0013 | 0/0 | 6458 | 4 | 1 | 2 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0014 | 0/0 | 6458 | 4 | 4 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0015 | 0/0 | 6459 | 5 | 5 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0016 | 0/0 | 6459 | 4 | 0 | 0 | 4 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0017 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0018 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0019 | 0/1 | 6459 | 3 | 0 | 0 | 0 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0020 | 0/0 | 6460 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0021 | 0/0 | 6460 | 3 | 2 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0023 | 0/0 | 6459 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0024 | 0/0 | 6458 | 2 | 0 | 2 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0025 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0026 | 0/0 | 6458 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0027 | 0/0 | 6460 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0028 | 0/0 | 6456 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6451): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0029 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0030 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0032 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0035 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0036 | 0/0 | 6458 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0038 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0039 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0040 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0041 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0042 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0043 | 0/0 | 6458 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0044 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0045 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6450): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0046 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0047 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0048 | 0/0 | 6460 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0050 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0051 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0053 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0054 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0055 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0056 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0057 | 0/0 | 6460 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0058 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0059 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0001t0060 | 1/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0003t0002 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0001c0004t0001 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0001c0005t0010 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0001 | 0/0 | 6459 | 22 | 0 | 4 | 9 | 3 | 6 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0002 | 0/0 | 6458 | 3 | 0 | 1 | 2 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0003 | 0/0 | 6458 | 5 | 0 | 0 | 5 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0004 | 0/0 | 6460 | 12 | 1 | 1 | 8 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0005 | 0/0 | 6459 | 13 | 0 | 0 | 9 | 0 | 4 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0006 | 0/0 | 6458 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0007 | 0/0 | 6459 | 7 | 1 | 1 | 4 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0008 | 0/0 | 6459 | 7 | 0 | 1 | 6 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0009 | 0/0 | 6459 | 6 | 0 | 6 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0010 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0012 | 0/0 | 6458 | 3 | 0 | 0 | 3 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0013 | 0/0 | 6458 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0014 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0016 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0017 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0018 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0022 | 0/0 | 6459 | 2 | 0 | 0 | 0 | 2 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0027 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0029 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0031 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0033 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0034 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0037 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0049 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0052 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6455): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0061 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6454): Show |
chr7 | 13886229 | 13994666 |
| a0002c0002t0062 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | AGAGG others(6453): Show |
chr7 | 13886229 | 13994666 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0023g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0024g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0024g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0025g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0025g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0026g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0026g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0027g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0028g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0028g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0029g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0030g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0035g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0036g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0038g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0039g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0040g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0041g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0042g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0043g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0044g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0045g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0046g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0047g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0048g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0050g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0051g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0053g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0054g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0055g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0056g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0057g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0058g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0059g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0060g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0005t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0014g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0016g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0017g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0017g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0018g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0022g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0027g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0029g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0031g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0033g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0034g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0037g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0049g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0052g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0061g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0062g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00099 | hp2 | a0001 | c0001 | t0035 | g0124 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00140 | hp1 | a0001 | c0001 | t0019 | g0152 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0066 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00280 | hp1 | a0001 | c0001 | t0029 | g0257 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0072 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0258 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00323 | hp2 | a0001 | c0001 | t0032 | g0005 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00408 | hp1 | a0002 | c0002 | t0007 | g0020 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0180 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00438 | hp1 | a0002 | c0002 | t0037 | g0060 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00438 | hp2 | a0001 | c0001 | t0054 | g0188 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0241 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0296 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0067 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00735 | hp1 | a0002 | c0002 | t0007 | g0050 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00738 | hp2 | a0001 | c0001 | t0023 | g0008 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0209 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0074 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01070 | hp2 | a0002 | c0002 | t0009 | g0225 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01071 | hp1 | a0002 | c0002 | t0009 | g0226 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0068 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0097 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0018 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01081 | hp2 | a0001 | c0001 | t0021 | g0140 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0065 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01109 | hp1 | a0001 | c0001 | t0058 | g0135 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01109 | hp2 | a0002 | c0002 | t0029 | g0163 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0122 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01167 | hp2 | a0001 | c0001 | t0011 | g0081 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0260 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0121 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0116 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01175 | hp2 | a0001 | c0001 | t0024 | g0028 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01192 | hp2 | a0001 | c0001 | t0024 | g0029 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0010 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01255 | hp1 | a0001 | c0001 | t0026 | g0094 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0063 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01258 | hp2 | a0002 | c0002 | t0008 | g0262 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01261 | hp1 | a0001 | c0001 | t0036 | g0103 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01261 | hp2 | a0002 | c0002 | t0031 | g0006 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0245 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01346 | hp2 | a0001 | c0001 | t0011 | g0101 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0098 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01515 | hp2 | a0002 | c0002 | t0022 | g0001 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0205 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01516 | hp2 | a0001 | c0001 | t0044 | g0127 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0204 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01517 | hp2 | a0002 | c0002 | t0022 | g0001 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0263 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01891 | hp2 | a0002 | c0002 | t0049 | g0197 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01928 | hp1 | a0002 | c0002 | t0009 | g0194 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0086 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01981 | hp1 | a0002 | c0002 | t0009 | g0219 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0087 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01993 | hp1 | a0002 | c0002 | t0009 | g0198 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01993 | hp2 | a0001 | c0001 | t0011 | g0129 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02015 | hp1 | a0001 | c0001 | t0057 | g0171 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02055 | hp2 | a0001 | c0001 | t0038 | g0304 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02071 | hp1 | a0002 | c0002 | t0005 | g0267 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0130 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0191 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0284 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02129 | hp1 | a0002 | c0002 | t0008 | g0206 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02132 | hp1 | a0002 | c0002 | t0005 | g0176 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02135 | hp2 | a0002 | c0002 | t0004 | g0270 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0133 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0007 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02155 | hp1 | a0002 | c0002 | t0008 | g0172 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02155 | hp2 | a0002 | c0002 | t0005 | g0202 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0115 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02257 | hp2 | a0001 | c0001 | t0040 | g0011 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02258 | hp1 | a0002 | c0002 | t0027 | g0240 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0274 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02273 | hp1 | a0001 | c0001 | t0011 | g0092 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02280 | hp1 | a0002 | c0002 | t0033 | g0022 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0306 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02300 | hp1 | a0002 | c0002 | t0009 | g0201 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02300 | hp2 | a0001 | c0001 | t0043 | g0125 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02622 | hp1 | a0001 | c0001 | t0020 | g0237 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02630 | hp1 | a0002 | c0002 | t0062 | g0317 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0305 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0025 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0080 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02723 | hp1 | a0001 | c0001 | t0051 | g0235 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02723 | hp2 | a0002 | c0002 | t0006 | g0078 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0179 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0213 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0153 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02809 | hp1 | a0001 | c0001 | t0028 | g0239 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02809 | hp2 | a0001 | c0005 | t0010 | g0113 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02818 | hp2 | a0002 | c0002 | t0010 | g0114 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02886 | hp1 | a0002 | c0002 | t0052 | g0256 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02895 | hp1 | a0002 | c0002 | t0013 | g0302 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0096 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02896 | hp2 | a0001 | c0001 | t0026 | g0039 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02897 | hp1 | a0002 | c0002 | t0013 | g0303 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02965 | hp2 | a0001 | c0001 | t0028 | g0238 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0264 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0083 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02976 | hp2 | a0002 | c0002 | t0017 | g0043 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0110 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0300 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0298 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03195 | hp1 | a0001 | c0001 | t0046 | g0071 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0139 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03209 | hp2 | a0002 | c0002 | t0007 | g0311 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0040 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0250 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03453 | hp2 | a0002 | c0002 | t0013 | g0313 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03540 | hp2 | a0002 | c0002 | t0014 | g0308 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0041 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0265 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0196 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03710 | hp2 | a0002 | c0002 | t0005 | g0151 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03831 | hp2 | a0001 | c0001 | t0059 | g0249 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03834 | hp2 | a0002 | c0002 | t0005 | g0150 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03927 | hp1 | a0001 | c0001 | t0027 | g0252 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04115 | hp1 | a0002 | c0002 | t0005 | g0234 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04115 | hp2 | a0001 | c0001 | t0019 | g0221 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04199 | hp2 | a0002 | c0002 | t0007 | g0112 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0073 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18522 | hp1 | a0001 | c0001 | t0055 | g0253 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18522 | hp2 | a0001 | c0001 | t0042 | g0301 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0309 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18941 | hp2 | a0001 | c0001 | t0016 | g0189 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18946 | hp2 | a0002 | c0002 | t0012 | g0047 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18953 | hp1 | a0002 | c0002 | t0004 | g0168 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18957 | hp1 | a0002 | c0002 | t0008 | g0175 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18960 | hp1 | a0002 | c0002 | t0016 | g0273 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18963 | hp1 | a0002 | c0002 | t0005 | g0155 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18964 | hp2 | a0002 | c0002 | t0007 | g0118 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18967 | hp2 | a0001 | c0001 | t0008 | g0146 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18972 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18977 | hp2 | a0002 | c0002 | t0004 | g0141 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18978 | hp1 | a0002 | c0002 | t0005 | g0145 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18978 | hp2 | a0002 | c0002 | t0007 | g0062 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18988 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18988 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18991 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18992 | hp2 | a0002 | c0002 | t0012 | g0059 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18995 | hp2 | a0001 | c0001 | t0053 | g0224 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0295 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19004 | hp1 | a0002 | c0002 | t0005 | g0174 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19007 | hp1 | a0002 | c0002 | t0005 | g0195 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0294 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0144 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19009 | hp2 | a0002 | c0002 | t0012 | g0033 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19011 | hp1 | a0002 | c0002 | t0004 | g0223 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19043 | hp1 | a0002 | c0002 | t0034 | g0312 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19043 | hp2 | a0001 | c0001 | t0045 | g0111 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19058 | hp1 | a0002 | c0002 | t0005 | g0272 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19058 | hp2 | a0001 | c0001 | t0016 | g0266 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19063 | hp1 | a0002 | c0002 | t0008 | g0156 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19065 | hp2 | a0002 | c0002 | t0008 | g0160 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19068 | hp1 | a0002 | c0002 | t0005 | g0269 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19072 | hp1 | a0001 | c0001 | t0016 | g0165 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19072 | hp2 | a0002 | c0002 | t0008 | g0162 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0210 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19085 | hp2 | a0001 | c0001 | t0012 | g0283 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19087 | hp2 | a0001 | c0001 | t0048 | g0229 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19091 | hp1 | a0002 | c0002 | t0061 | g0316 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0314 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19240 | hp2 | a0002 | c0002 | t0018 | g0297 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0126 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0244 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0030 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0076 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02109 | hp1 | a0001 | c0001 | t0039 | g0084 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0307 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02486 | hp2 | a0002 | c0002 | t0017 | g0036 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0138 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03471 | hp1 | a0001 | c0001 | t0041 | g0310 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03471 | hp2 | a0001 | c0001 | t0056 | g0259 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG06807 | hp1 | a0001 | c0001 | t0030 | g0004 | AFR | USA | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0143 | AFR | USA | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18955 | hp2 | a0001 | c0001 | t0047 | g0212 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA21309 | hp2 | a0001 | c0001 | t0050 | g0142 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0161 | REF | REF | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0060 | g0207 | REF | REF | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13939184 | T | C | 1 | a0002 | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
missense_variant | MODERATE | c.298A>G | p.Ser100Gly | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/14 | 686/6459 | 298/1434 | 100/477 | chr7 | 13939184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13895917 | C | T | 1 | a0001c0005 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1383G>A | p.Pro461Pro | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1771/6459 | 1383/1434 | 461/477 | chr7 | 13895917 | |||
| chr7:13906439 | C | T | 1 | a0001c0004 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1101G>A | p.Glu367Glu | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/14 | 1489/6459 | 1101/1434 | 367/477 | chr7 | 13906439 | |||
| chr7:13977479 | A | T | 1 | a0001c0003 | 1 | HG00280.hp2 | splice_region_variant&synonymous_variant | LOW | c.183T>A | p.Ala61Ala | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/14 | 571/6459 | 183/1434 | 61/477 | chr7 | 13977479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13891292 | T | C | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4574A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4574 | chr7 | 13891292 | ||||||
| chr7:13891347 | G | A | 2 | a0001c0001t0028 a0001c0001t0045 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4519C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4519 | chr7 | 13891347 | ||||||
| chr7:13891557 | G | A | 68 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(65): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*4309C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4309 | chr7 | 13891557 | ||||||
| chr7:13891610 | T | C | 5 | a0001c0001t0010 a0001c0001t0020 a0001c0001t0039 others(2): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4256 | chr7 | 13891610 | ||||||
| chr7:13891611 | A | G | 2 | a0001c0001t0028 a0001c0001t0045 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4255T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4255 | chr7 | 13891611 | ||||||
| chr7:13891678 | T | C | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4188A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4188 | chr7 | 13891678 | ||||||
| chr7:13891836 | G | A | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4030C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4030 | chr7 | 13891836 | ||||||
| chr7:13891838 | A | T | 1 | a0001c0001t0056 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4028T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4028 | chr7 | 13891838 | ||||||
| chr7:13891971 | A | G | 1 | a0001c0001t0036 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3895T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3895 | chr7 | 13891971 | ||||||
| chr7:13892043 | T | C | 2 | a0001c0001t0028 a0001c0001t0045 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3823A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3823 | chr7 | 13892043 | ||||||
| chr7:13892045 | C | T | 1 | a0001c0001t0055 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3821G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3821 | chr7 | 13892045 | ||||||
| chr7:13892111 | A | T | 1 | a0001c0001t0038 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3755T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3755 | chr7 | 13892111 | ||||||
| chr7:13892142 | T | A | 2 | a0001c0001t0053 a0002c0002t0037 |
2 | HG00438.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3724A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3724 | chr7 | 13892142 | ||||||
| chr7:13892151 | A | G | 4 | a0001c0001t0012 a0001c0001t0016 a0002c0002t0012 others(1): Show |
13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3715T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3715 | chr7 | 13892151 | ||||||
| chr7:13892273 | T | C | 1 | a0001c0001t0054 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3593 | chr7 | 13892273 | ||||||
| chr7:13892353 | A | G | 2 | a0001c0001t0028 a0001c0001t0045 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3513T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3513 | chr7 | 13892353 | ||||||
| chr7:13892357 | T | A | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(67): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*3509A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3509 | chr7 | 13892357 | ||||||
| chr7:13892431 | G | A | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3435C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3435 | chr7 | 13892431 | ||||||
| chr7:13892532 | G | A | 2 | a0001c0001t0026 a0001c0001t0059 |
3 | HG01255.hp1 HG02896.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3334C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3334 | chr7 | 13892532 | ||||||
| chr7:13892693 | A | G | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3173 | chr7 | 13892693 | ||||||
| chr7:13892790 | C | G | 4 | a0001c0001t0029 a0001c0001t0032 a0002c0002t0029 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3076G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3076 | chr7 | 13892790 | ||||||
| chr7:13892863 | C | G | 1 | a0001c0001t0058 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3003G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3003 | chr7 | 13892863 | ||||||
| chr7:13892976 | C | T | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(41): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*2890G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2890 | chr7 | 13892976 | ||||||
| chr7:13893000 | G | A | 4 | a0001c0001t0012 a0001c0001t0016 a0002c0002t0012 others(1): Show |
13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2866C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2866 | chr7 | 13893000 | ||||||
| chr7:13893064 | T | C | 5 | a0001c0001t0009 a0001c0001t0013 a0002c0002t0009 others(2): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2802A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2802 | chr7 | 13893064 | ||||||
| chr7:13893068 | G | A | 4 | a0001c0001t0029 a0001c0001t0032 a0002c0002t0029 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2798C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2798 | chr7 | 13893068 | ||||||
| chr7:13893088 | T | C | 1 | a0001c0001t0044 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2778A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2778 | chr7 | 13893088 | ||||||
| chr7:13893281 | A | G | 2 | a0001c0001t0019 a0001c0001t0035 |
3 | HG00099.hp2 HG00140.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2585T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2585 | chr7 | 13893281 | ||||||
| chr7:13893341 | A | C | 4 | a0001c0001t0012 a0001c0001t0016 a0002c0002t0012 others(1): Show |
13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2525T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2525 | chr7 | 13893341 | ||||||
| chr7:13893466 | C | T | 1 | a0001c0001t0042 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2400 | chr7 | 13893466 | ||||||
| chr7:13893557 | C | T | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2309 | chr7 | 13893557 | ||||||
| chr7:13893613 | AAGG | A | 2 | a0001c0001t0028 a0001c0001t0045 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2250_*2252delCCT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2250 | chr7 | 13893613 | ||||||
| chr7:13893745 | T | C | 18 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0015 others(15): Show |
37 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2121A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2121 | chr7 | 13893745 | ||||||
| chr7:13893926 | C | T | 1 | a0001c0001t0057 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1940G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1940 | chr7 | 13893926 | ||||||
| chr7:13894049 | G | T | 1 | a0001c0001t0041 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1817C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1817 | chr7 | 13894049 | ||||||
| chr7:13894147 | G | T | 9 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0027 others(6): Show |
12 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1719 | chr7 | 13894147 | ||||||
| chr7:13894154 | A | AT | 25 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(22): Show |
80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1711dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1711 | chr7 | 13894154 | ||||||
| chr7:13894186 | T | A | 4 | a0001c0001t0029 a0001c0001t0032 a0002c0002t0029 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1680A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1680 | chr7 | 13894186 | ||||||
| chr7:13894261 | C | T | 2 | a0001c0001t0021 a0001c0001t0025 |
5 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1605G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1605 | chr7 | 13894261 | ||||||
| chr7:13894536 | A | C | 2 | a0001c0001t0040 a0001c0001t0055 |
2 | HG02257.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1330 | chr7 | 13894536 | ||||||
| chr7:13894613 | T | C | 4 | a0001c0001t0012 a0001c0001t0016 a0002c0002t0012 others(1): Show |
13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1253A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1253 | chr7 | 13894613 | ||||||
| chr7:13894733 | A | T | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0019 others(13): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1133 | chr7 | 13894733 | ||||||
| chr7:13895063 | A | G | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(22): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 803 | chr7 | 13895063 | ||||||
| chr7:13895087 | C | T | 1 | a0001c0001t0024 | 2 | HG01175.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*779G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 779 | chr7 | 13895087 | ||||||
| chr7:13895107 | G | A | 1 | a0001c0001t0046 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*759C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 759 | chr7 | 13895107 | ||||||
| chr7:13895382 | A | G | 3 | a0001c0001t0017 a0001c0001t0051 a0002c0002t0017 |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*484T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 484 | chr7 | 13895382 | ||||||
| chr7:13895446 | A | G | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 420 | chr7 | 13895446 | ||||||
| chr7:13895511 | C | T | 1 | a0001c0001t0047 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*355G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 355 | chr7 | 13895511 | ||||||
| chr7:13895557 | A | T | 1 | a0002c0002t0049 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 309 | chr7 | 13895557 | ||||||
| chr7:13895682 | C | T | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0024 others(6): Show |
58 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*184G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 184 | chr7 | 13895682 | ||||||
| chr7:13895683 | C | G | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 183 | chr7 | 13895683 | ||||||
| chr7:13989082 | TA | T | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(39): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-31delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/14 | 31 | chr7 | 13989082 | ||||||
| chr7:13989340 | C | T | 4 | a0001c0001t0023 a0001c0001t0032 a0002c0002t0022 others(1): Show |
6 | HG00323.hp2 HG00738.hp2 HG01261.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-160G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 288 | chr7 | 13989340 | ||||||
| chr7:13989351 | T | A | 1 | a0002c0002t0061 | 1 | NA19091.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 299 | chr7 | 13989351 | ||||||
| chr7:13989406 | G | A | 1 | a0002c0002t0062 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-226C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 354 | chr7 | 13989406 | ||||||
| chr7:13989624 | A | C | 1 | a0001c0001t0030 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-346T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 1/14 | 572 | chr7 | 13989624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13896189 | T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1213-102A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896189 | |||||||
| chr7:13896236 | T | TA | 115 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1213-150dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896236 | |||||||
| chr7:13896362 | C | T | 118 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1213-275G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896362 | |||||||
| chr7:13896431 | T | C | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-344A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896431 | |||||||
| chr7:13896437 | G | C | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1213-350C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896437 | |||||||
| chr7:13896438 | C | T | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213-351G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896438 | |||||||
| chr7:13896494 | T | G | 80 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.1213-407A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896494 | |||||||
| chr7:13896523 | G | A | 10 | a0001c0001t0004g0236 a0001c0001t0004g0261 a0001c0001t0007g0061 others(7): Show |
10 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1213-436C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896523 | |||||||
| chr7:13896538 | T | C | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1213-451A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896538 | |||||||
| chr7:13896552 | G | T | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1213-465C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896552 | |||||||
| chr7:13896605 | G | A | 3 | a0001c0001t0018g0096 a0001c0001t0027g0252 a0001c0001t0056g0259 |
3 | HG02895.hp2 HG03471.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1213-518C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896605 | |||||||
| chr7:13896675 | T | G | 1 | a0001c0001t0003g0287 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1213-588A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896675 | |||||||
| chr7:13896681 | A | AAGAC | 242 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(239): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1213-595_1213-594i others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896681 | |||||||
| chr7:13896693 | A | AGAGAGAG others(12): Show |
84 | a0001c0001t0001g0159 a0001c0001t0001g0182 a0001c0001t0001g0183 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1213-625_1213-607d others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896693 | |||||||
| chr7:13896700 | G | GAAAGAAA others(12): Show |
1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1213-614_1213-613i others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896700 | |||||||
| chr7:13896710 | A | G | 1 | a0001c0001t0026g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1213-623T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896710 | |||||||
| chr7:13896725 | A | AAGAAAGG others(6): Show |
1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-639_1213-638i others(15): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | |||||||
| chr7:13896725 | A | AAGAAAGG others(22): Show |
30 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0002g0014 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1213-639_1213-638i others(31): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | |||||||
| chr7:13896725 | A | AAGAAAGG others(31): Show |
17 | a0001c0001t0001g0167 a0001c0001t0001g0220 a0001c0001t0001g0254 others(14): Show |
17 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1213-639_1213-638i others(40): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | |||||||
| chr7:13896725 | A | AAGAAAGG others(35): Show |
2 | a0001c0001t0002g0104 a0002c0002t0001g0228 |
2 | NA18956.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1213-639_1213-638i others(44): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | |||||||
| chr7:13896731 | A | AAG | 19 | a0001c0001t0001g0167 a0001c0001t0001g0220 a0001c0001t0001g0254 others(16): Show |
19 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1213-645_1213-644i others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896731 | |||||||
| chr7:13896731 | A | AAGG | 30 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0002g0014 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1213-645_1213-644i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896731 | |||||||
| chr7:13896742 | AG | A | 12 | a0001c0001t0001g0254 a0001c0001t0002g0013 a0001c0001t0014g0080 others(9): Show |
12 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1213-656delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896742 | |||||||
| chr7:13896743 | G | GAAA | 37 | a0001c0001t0001g0167 a0001c0001t0001g0217 a0001c0001t0001g0218 others(34): Show |
37 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1213-657_1213-656i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GAAAGAAA others(16): Show |
1 | a0001c0001t0008g0170 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1213-657_1213-656i others(25): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAA | 39 | a0001c0001t0002g0107 a0001c0001t0003g0046 a0001c0001t0003g0288 others(36): Show |
39 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1213-660_1213-657d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAAGAA others(1): Show |
82 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0242 others(79): Show |
82 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1213-664_1213-657d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAAGAA others(5): Show |
72 | a0001c0001t0001g0159 a0001c0001t0001g0183 a0001c0001t0001g0184 others(69): Show |
74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1213-668_1213-657d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAAGAA others(9): Show |
16 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0286 others(13): Show |
16 | HG00423.hp2 HG01123.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1213-672_1213-657d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAAGAA others(13): Show |
10 | a0001c0001t0003g0090 a0001c0001t0003g0279 a0001c0001t0006g0282 others(7): Show |
10 | HG00738.hp1 HG02071.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1213-676_1213-657d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAAGAA others(17): Show |
4 | a0001c0001t0004g0248 a0001c0001t0006g0086 a0001c0001t0006g0278 others(1): Show |
4 | HG01192.hp2 HG01978.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-680_1213-657d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | G | GGAAGAAA others(4): Show |
1 | a0002c0002t0007g0284 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1213-657_1213-656i others(13): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | GGAAA | G | 7 | a0001c0001t0004g0179 a0001c0001t0013g0010 a0001c0001t0023g0007 others(4): Show |
7 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-660_1213-657d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | GGAAAGAA others(1): Show |
G | 4 | a0001c0001t0004g0187 a0002c0002t0004g0144 a0002c0002t0007g0118 others(1): Show |
4 | HG01891.hp2 NA18946.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-664_1213-657d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | GGAAAGAA others(5): Show |
G | 2 | a0001c0001t0029g0257 a0001c0001t0032g0005 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1213-668_1213-657d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896743 | GGAAAGAA others(9): Show |
G | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1213-672_1213-657d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | |||||||
| chr7:13896744 | G | A | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-657C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896744 | |||||||
| chr7:13896747 | A | G | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-660T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896747 | |||||||
| chr7:13896768 | G | GAA | 5 | a0001c0001t0021g0140 a0001c0001t0021g0263 a0001c0001t0021g0264 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213-683_1213-682d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896768 | |||||||
| chr7:13896789 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0030g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1213-703_1213-702i others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896789 | |||||||
| chr7:13896790 | A | AAGAAAGA others(11): Show |
1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1213-704_1213-703i others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896790 | |||||||
| chr7:13896792 | G | GAAAGAAA others(8): Show |
1 | a0001c0001t0005g0260 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1213-706_1213-705i others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896792 | |||||||
| chr7:13896802 | C | G | 1 | a0001c0001t0042g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1213-715G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896802 | |||||||
| chr7:13896887 | T | A | 1 | a0002c0002t0001g0131 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1213-800A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896887 | |||||||
| chr7:13896921 | G | A | 1 | a0002c0002t0004g0223 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1213-834C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896921 | |||||||
| chr7:13896941 | G | T | 1 | a0001c0001t0003g0019 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1213-854C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896941 | |||||||
| chr7:13896995 | T | C | 114 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.1213-908A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896995 | |||||||
| chr7:13897015 | C | T | 114 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.1213-928G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897015 | |||||||
| chr7:13897020 | T | G | 1 | a0002c0002t0004g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1213-933A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897020 | |||||||
| chr7:13897038 | C | A | 12 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0018g0096 others(9): Show |
12 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1213-951G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897038 | |||||||
| chr7:13897131 | G | A | 3 | a0002c0002t0003g0120 a0002c0002t0005g0267 a0002c0002t0005g0269 |
3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1213-1044C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897131 | |||||||
| chr7:13897189 | C | T | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1213-1102G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897189 | |||||||
| chr7:13897325 | C | T | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1213-1238G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897325 | |||||||
| chr7:13897364 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213-1277A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897364 | |||||||
| chr7:13897511 | T | C | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1213-1424A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897511 | |||||||
| chr7:13897538 | G | C | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1213-1451C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897538 | |||||||
| chr7:13897641 | C | T | 1 | a0001c0001t0007g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1213-1554G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897641 | |||||||
| chr7:13897788 | CT | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1213-1702delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897788 | |||||||
| chr7:13897887 | G | A | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1213-1800C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897887 | |||||||
| chr7:13897904 | T | G | 122 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1213-1817A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897904 | |||||||
| chr7:13898040 | T | C | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1213-1953A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898040 | |||||||
| chr7:13898239 | C | G | 1 | a0001c0001t0013g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1213-2152G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898239 | |||||||
| chr7:13898251 | G | T | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1213-2164C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898251 | |||||||
| chr7:13898412 | A | C | 1 | a0002c0002t0004g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1213-2325T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898412 | |||||||
| chr7:13898431 | T | G | 15 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(12): Show |
15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+2307A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898431 | |||||||
| chr7:13898442 | A | G | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1212+2296T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898442 | |||||||
| chr7:13898454 | A | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1212+2284T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898454 | |||||||
| chr7:13898476 | G | T | 1 | a0001c0001t0003g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1212+2262C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898476 | |||||||
| chr7:13898534 | A | G | 136 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1212+2204T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898534 | |||||||
| chr7:13898560 | C | T | 116 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1212+2178G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898560 | |||||||
| chr7:13898664 | A | C | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212+2074T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898664 | |||||||
| chr7:13898708 | A | G | 1 | a0001c0001t0011g0063 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1212+2030T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898708 | |||||||
| chr7:13898839 | C | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1899G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898839 | |||||||
| chr7:13898839 | C | T | 54 | a0001c0001t0004g0003 a0001c0001t0004g0137 a0001c0001t0004g0177 others(51): Show |
55 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1212+1899G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898839 | |||||||
| chr7:13898967 | G | A | 1 | a0002c0002t0008g0262 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1212+1771C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898967 | |||||||
| chr7:13899074 | G | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1664C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899074 | |||||||
| chr7:13899214 | T | C | 3 | a0001c0001t0003g0291 a0001c0001t0005g0173 a0002c0002t0003g0055 |
3 | HG00544.hp2 HG00609.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1212+1524A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899214 | |||||||
| chr7:13899277 | G | C | 1 | a0001c0001t0006g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1212+1461C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899277 | |||||||
| chr7:13899328 | T | C | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1212+1410A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899328 | |||||||
| chr7:13899434 | G | A | 1 | a0002c0002t0001g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1212+1304C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899434 | |||||||
| chr7:13899555 | T | G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1183A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899555 | |||||||
| chr7:13899591 | A | G | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212+1147T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899591 | |||||||
| chr7:13899742 | G | A | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1212+996C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899742 | |||||||
| chr7:13899818 | T | C | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+920A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899818 | |||||||
| chr7:13899921 | G | C | 7 | a0001c0001t0015g0132 a0001c0001t0015g0139 a0001c0001t0021g0140 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+817C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899921 | |||||||
| chr7:13899958 | A | G | 101 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1212+780T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899958 | |||||||
| chr7:13899969 | G | T | 2 | a0001c0001t0002g0106 a0002c0002t0001g0192 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1212+769C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899969 | |||||||
| chr7:13900037 | G | A | 8 | a0001c0001t0004g0261 a0001c0001t0014g0042 a0001c0001t0018g0096 others(5): Show |
8 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212+701C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900037 | |||||||
| chr7:13900129 | AAAAC | A | 7 | a0001c0001t0014g0025 a0001c0001t0014g0080 a0001c0001t0014g0110 others(4): Show |
7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212+605_1212+608d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900129 | |||||||
| chr7:13900147 | A | C | 1 | a0001c0001t0026g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1212+591T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900147 | |||||||
| chr7:13900207 | A | C | 101 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1212+531T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900207 | |||||||
| chr7:13900241 | A | G | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+497T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900241 | |||||||
| chr7:13900251 | A | T | 3 | a0001c0001t0004g0187 a0002c0002t0004g0144 a0002c0002t0007g0118 |
3 | NA18946.hp1 NA18964.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1212+487T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900251 | |||||||
| chr7:13900333 | T | A | 101 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1212+405A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900333 | |||||||
| chr7:13900363 | C | A | 2 | a0001c0001t0004g0236 a0001c0001t0007g0315 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1212+375G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900363 | |||||||
| chr7:13900493 | T | C | 1 | a0002c0002t0005g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1212+245A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900493 | |||||||
| chr7:13900666 | G | A | 7 | a0001c0001t0012g0115 a0001c0001t0012g0295 a0001c0001t0012g0296 others(4): Show |
7 | HG00597.hp2 HG02165.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+72C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900666 | |||||||
| chr7:13900669 | G | A | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212+69C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900669 | |||||||
| chr7:13900989 | C | G | 1 | a0001c0001t0003g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1111-150G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13900989 | |||||||
| chr7:13901005 | CT | C | 237 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1111-167delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901005 | |||||||
| chr7:13901030 | G | C | 16 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(13): Show |
16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111-191C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901030 | |||||||
| chr7:13901106 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1111-267C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901106 | |||||||
| chr7:13901109 | A | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-270T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901109 | |||||||
| chr7:13901204 | C | A | 7 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0018g0314 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-365G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901204 | |||||||
| chr7:13901215 | G | C | 1 | a0001c0001t0005g0169 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1111-376C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901215 | |||||||
| chr7:13901296 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1111-457G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901296 | |||||||
| chr7:13901297 | G | C | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-458C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901297 | |||||||
| chr7:13901325 | G | T | 1 | a0001c0001t0005g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1111-486C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901325 | |||||||
| chr7:13901428 | A | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0056 a0001c0001t0003g0100 |
3 | HG02135.hp1 NA18971.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1111-589T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901428 | |||||||
| chr7:13901498 | G | C | 84 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.1111-659C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901498 | |||||||
| chr7:13901577 | C | G | 1 | a0002c0002t0008g0156 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1111-738G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901577 | |||||||
| chr7:13901762 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG03540.hp2 HG03834.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-923G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901762 | |||||||
| chr7:13901913 | T | G | 14 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1074A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901913 | |||||||
| chr7:13901929 | T | C | 1 | a0001c0001t0054g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1111-1090A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901929 | |||||||
| chr7:13902083 | T | C | 1 | a0002c0002t0012g0047 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1111-1244A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902083 | |||||||
| chr7:13902210 | T | A | 100 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1111-1371A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902210 | |||||||
| chr7:13902374 | G | A | 1 | a0002c0002t0003g0120 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1111-1535C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902374 | |||||||
| chr7:13902420 | T | C | 1 | a0001c0001t0003g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1111-1581A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902420 | |||||||
| chr7:13902515 | C | T | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-1676G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902515 | |||||||
| chr7:13902521 | T | TG | 14 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1683dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902521 | |||||||
| chr7:13902562 | C | G | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1723G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902562 | |||||||
| chr7:13902716 | G | T | 117 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0004g0003 others(114): Show |
119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1111-1877C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902716 | |||||||
| chr7:13902963 | T | C | 1 | a0001c0001t0006g0058 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1111-2124A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902963 | |||||||
| chr7:13903058 | A | G | 1 | a0001c0001t0012g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1111-2219T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903058 | |||||||
| chr7:13903089 | G | A | 84 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.1111-2250C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903089 | |||||||
| chr7:13903124 | C | G | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1111-2285G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903124 | |||||||
| chr7:13903256 | C | A | 12 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111-2417G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903256 | |||||||
| chr7:13903283 | A | C | 1 | a0002c0002t0001g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1111-2444T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903283 | |||||||
| chr7:13903365 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1111-2526G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903365 | |||||||
| chr7:13903460 | C | G | 1 | a0002c0002t0031g0006 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1111-2621G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903460 | |||||||
| chr7:13903481 | G | A | 1 | a0001c0001t0009g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-2642C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903481 | |||||||
| chr7:13903509 | T | A | 1 | a0002c0002t0005g0272 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1111-2670A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903509 | |||||||
| chr7:13903554 | G | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1111-2715C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903554 | |||||||
| chr7:13903613 | A | G | 3 | a0001c0001t0019g0152 a0001c0001t0019g0221 a0001c0001t0035g0124 |
3 | HG00099.hp2 HG00140.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1111-2774T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903613 | |||||||
| chr7:13903762 | C | CA | 10 | a0001c0001t0002g0024 a0001c0001t0002g0049 a0001c0001t0002g0057 others(7): Show |
10 | HG00597.hp1 HG01192.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+2667dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | |||||||
| chr7:13903762 | CA | C | 62 | a0001c0001t0001g0185 a0001c0001t0002g0026 a0001c0001t0002g0281 others(59): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1110+2667delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | |||||||
| chr7:13903762 | CAA | C | 91 | a0001c0001t0004g0003 a0001c0001t0004g0137 a0001c0001t0004g0177 others(88): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1110+2666_1110+266 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | |||||||
| chr7:13903787 | T | C | 1 | a0001c0001t0007g0102 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1110+2643A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903787 | |||||||
| chr7:13903829 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+2601A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903829 | |||||||
| chr7:13903896 | C | T | 3 | a0001c0001t0015g0139 a0001c0001t0021g0140 a0001c0001t0025g0307 |
3 | HG01081.hp2 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1110+2534G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903896 | |||||||
| chr7:13904069 | T | C | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+2361A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904069 | |||||||
| chr7:13904154 | G | T | 7 | a0001c0001t0015g0132 a0001c0001t0015g0139 a0001c0001t0021g0140 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2276C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904154 | |||||||
| chr7:13904291 | C | T | 1 | a0001c0001t0055g0253 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+2139G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904291 | |||||||
| chr7:13904496 | G | T | 2 | a0001c0001t0053g0224 a0002c0002t0037g0060 |
2 | HG00438.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1110+1934C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904496 | |||||||
| chr7:13904523 | A | C | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1110+1907T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904523 | |||||||
| chr7:13904668 | T | C | 115 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0004g0003 others(112): Show |
117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1110+1762A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904668 | |||||||
| chr7:13904672 | T | G | 17 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0037 others(14): Show |
17 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1110+1758A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904672 | |||||||
| chr7:13904697 | G | A | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+1733C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904697 | |||||||
| chr7:13904771 | C | A | 3 | a0001c0001t0006g0031 a0001c0001t0006g0123 a0001c0001t0006g0309 |
3 | HG02486.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1110+1659G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904771 | |||||||
| chr7:13904893 | A | C | 2 | a0001c0001t0018g0096 a0001c0001t0056g0259 |
2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1110+1537T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904893 | |||||||
| chr7:13904919 | T | G | 1 | a0001c0004t0001g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+1511A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904919 | |||||||
| chr7:13904966 | G | A | 13 | a0001c0001t0004g0261 a0001c0001t0018g0096 a0001c0001t0018g0314 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110+1464C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904966 | |||||||
| chr7:13905217 | G | A | 17 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(14): Show |
17 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1110+1213C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905217 | |||||||
| chr7:13905226 | G | A | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+1204C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905226 | |||||||
| chr7:13905271 | C | T | 24 | a0001c0001t0004g0166 a0001c0001t0004g0187 a0001c0001t0004g0248 others(21): Show |
24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1110+1159G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905271 | |||||||
| chr7:13905288 | A | C | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+1142T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905288 | |||||||
| chr7:13905379 | T | C | 1 | a0001c0001t0003g0289 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1110+1051A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905379 | |||||||
| chr7:13905433 | T | A | 1 | a0001c0001t0004g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1110+997A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905433 | |||||||
| chr7:13905502 | T | C | 108 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1110+928A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905502 | |||||||
| chr7:13905693 | C | T | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1110+737G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905693 | |||||||
| chr7:13905718 | G | C | 13 | a0001c0001t0004g0261 a0001c0001t0017g0023 a0001c0001t0017g0040 others(10): Show |
13 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+712C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905718 | |||||||
| chr7:13905787 | C | A | 1 | a0001c0001t0046g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1110+643G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905787 | |||||||
| chr7:13905833 | C | G | 141 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1110+597G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905833 | |||||||
| chr7:13905941 | C | T | 1 | a0001c0001t0011g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1110+489G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905941 | |||||||
| chr7:13906050 | A | G | 216 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1110+380T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906050 | |||||||
| chr7:13906081 | G | A | 2 | a0001c0001t0002g0106 a0002c0002t0001g0192 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1110+349C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906081 | |||||||
| chr7:13906155 | T | G | 14 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+275A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906155 | |||||||
| chr7:13906239 | C | T | 24 | a0001c0001t0004g0166 a0001c0001t0004g0187 a0001c0001t0004g0248 others(21): Show |
24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1110+191G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906239 | |||||||
| chr7:13906250 | C | T | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+180G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906250 | |||||||
| chr7:13906251 | G | C | 1 | a0001c0001t0003g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1110+179C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906251 | |||||||
| chr7:13906298 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1110+132G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906298 | |||||||
| chr7:13906306 | T | C | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+124A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906306 | |||||||
| chr7:13906364 | C | G | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1110+66G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906364 | |||||||
| chr7:13906623 | T | C | 1 | a0002c0002t0003g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.941-24A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906623 | |||||||
| chr7:13906658 | A | G | 16 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(13): Show |
16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-59T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906658 | |||||||
| chr7:13906691 | C | T | 55 | a0001c0001t0002g0013 a0001c0001t0002g0052 a0001c0001t0004g0003 others(52): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.941-92G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906691 | |||||||
| chr7:13906790 | C | T | 1 | a0002c0002t0005g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.941-191G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906790 | |||||||
| chr7:13906879 | G | A | 2 | a0002c0002t0007g0020 a0002c0002t0007g0050 |
2 | HG00408.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.941-280C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906879 | |||||||
| chr7:13906889 | C | CT | 14 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.941-291dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906889 | |||||||
| chr7:13907014 | G | A | 16 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(13): Show |
16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-415C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907014 | |||||||
| chr7:13907028 | T | C | 5 | a0001c0001t0026g0039 a0001c0001t0026g0094 a0001c0001t0028g0238 others(2): Show |
5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-429A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907028 | |||||||
| chr7:13907062 | T | C | 7 | a0001c0001t0007g0067 a0001c0001t0007g0076 a0001c0001t0007g0077 others(4): Show |
7 | HG00642.hp1 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-463A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907062 | |||||||
| chr7:13907069 | T | A | 55 | a0001c0001t0002g0013 a0001c0001t0002g0052 a0001c0001t0004g0003 others(52): Show |
56 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.941-470A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907069 | |||||||
| chr7:13907187 | G | C | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-588C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907187 | |||||||
| chr7:13907306 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.941-707T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907306 | |||||||
| chr7:13907486 | A | G | 1 | a0002c0002t0005g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.941-887T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907486 | |||||||
| chr7:13907545 | C | CA | 49 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0017 others(46): Show |
50 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.941-947dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907545 | |||||||
| chr7:13907545 | C | CAA | 11 | a0001c0001t0004g0236 a0001c0001t0007g0061 a0001c0001t0007g0315 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.941-948_941-947dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907545 | |||||||
| chr7:13907664 | G | A | 118 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(115): Show |
120 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.941-1065C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907664 | |||||||
| chr7:13907980 | G | GT | 82 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.941-1382dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907980 | |||||||
| chr7:13908043 | A | G | 1 | a0002c0002t0003g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.941-1444T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908043 | |||||||
| chr7:13908094 | G | A | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-1495C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908094 | |||||||
| chr7:13908151 | T | C | 6 | a0001c0001t0003g0019 a0001c0001t0003g0095 a0001c0001t0005g0245 others(3): Show |
6 | HG00280.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1481A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908151 | |||||||
| chr7:13908221 | T | C | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.940+1411A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908221 | |||||||
| chr7:13908401 | C | G | 24 | a0001c0001t0004g0166 a0001c0001t0004g0187 a0001c0001t0004g0248 others(21): Show |
24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.940+1231G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908401 | |||||||
| chr7:13908503 | C | T | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.940+1129G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908503 | |||||||
| chr7:13908554 | G | A | 209 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.940+1078C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908554 | |||||||
| chr7:13908604 | T | C | 1 | a0001c0001t0013g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.940+1028A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908604 | |||||||
| chr7:13908662 | G | A | 2 | a0001c0001t0002g0106 a0002c0002t0001g0192 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.940+970C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908662 | |||||||
| chr7:13908879 | T | C | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.940+753A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908879 | |||||||
| chr7:13908892 | T | C | 99 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0017 others(96): Show |
101 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.940+740A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908892 | |||||||
| chr7:13909058 | A | G | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.940+574T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909058 | |||||||
| chr7:13909094 | T | C | 111 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.940+538A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909094 | |||||||
| chr7:13909136 | TA | T | 180 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.940+495delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909136 | |||||||
| chr7:13909136 | TAA | T | 21 | a0001c0001t0002g0117 a0001c0001t0007g0076 a0001c0001t0010g0037 others(18): Show |
21 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+494_940+495del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909136 | |||||||
| chr7:13909172 | C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.940+460G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909172 | |||||||
| chr7:13909210 | C | T | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.940+422G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909210 | |||||||
| chr7:13909300 | A | T | 1 | a0002c0002t0003g0119 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.940+332T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909300 | |||||||
| chr7:13909587 | C | G | 1 | a0001c0001t0002g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.940+45G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909587 | |||||||
| chr7:13909810 | C | G | 5 | a0001c0001t0014g0080 a0001c0001t0014g0110 a0001c0001t0015g0136 others(2): Show |
5 | HG02055.hp2 HG02717.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-110G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13909810 | |||||||
| chr7:13910036 | T | G | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-336A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910036 | |||||||
| chr7:13910040 | A | T | 3 | a0001c0001t0003g0293 a0002c0002t0003g0070 a0002c0002t0005g0272 |
3 | NA18956.hp1 NA18972.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.872-340T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910040 | |||||||
| chr7:13910228 | C | CT | 109 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.872-529dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | |||||||
| chr7:13910228 | C | CTT | 16 | a0001c0001t0001g0254 a0001c0001t0004g0137 a0001c0001t0004g0261 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.872-530_872-529dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | |||||||
| chr7:13910228 | C | CTTT | 52 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0052 others(49): Show |
53 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.872-531_872-529dup others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | |||||||
| chr7:13910228 | C | CTTTT | 29 | a0001c0001t0002g0013 a0001c0001t0002g0024 a0001c0001t0004g0265 others(26): Show |
30 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.872-532_872-529dup others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | |||||||
| chr7:13910228 | CTTTT | C | 12 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.872-532_872-529del others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | |||||||
| chr7:13910339 | T | G | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-639A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910339 | |||||||
| chr7:13910429 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.872-729A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910429 | |||||||
| chr7:13910578 | T | C | 1 | a0001c0001t0057g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.871+661A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910578 | |||||||
| chr7:13910579 | G | A | 2 | a0001c0001t0006g0298 a0001c0001t0042g0301 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.871+660C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910579 | |||||||
| chr7:13910613 | T | G | 2 | a0001c0001t0006g0035 a0001c0001t0006g0306 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+626A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910613 | |||||||
| chr7:13910673 | C | T | 12 | a0001c0001t0009g0002 a0001c0001t0009g0196 a0001c0001t0009g0227 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.871+566G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910673 | |||||||
| chr7:13910735 | C | G | 46 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(43): Show |
47 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.871+504G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910735 | |||||||
| chr7:13910738 | G | A | 16 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(13): Show |
16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+501C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910738 | |||||||
| chr7:13910970 | G | A | 16 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(13): Show |
16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+269C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910970 | |||||||
| chr7:13911034 | T | G | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+205A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13911034 | |||||||
| chr7:13911213 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.871+26G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13911213 | |||||||
| chr7:13911359 | G | A | 1 | a0001c0001t0012g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.803-52C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911359 | |||||||
| chr7:13911457 | G | C | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-150C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911457 | |||||||
| chr7:13911566 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.803-259T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911566 | |||||||
| chr7:13911693 | T | C | 2 | a0001c0001t0026g0039 a0001c0001t0026g0094 |
2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.803-386A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911693 | |||||||
| chr7:13911774 | T | G | 60 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0017 others(57): Show |
61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.803-467A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911774 | |||||||
| chr7:13911775 | T | C | 60 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0017 others(57): Show |
61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.803-468A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911775 | |||||||
| chr7:13911820 | A | G | 3 | a0001c0001t0001g0242 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | HG03834.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.803-513T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911820 | |||||||
| chr7:13911850 | G | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-543C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911850 | |||||||
| chr7:13912048 | C | T | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-741G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912048 | |||||||
| chr7:13912113 | T | G | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.803-806A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912113 | |||||||
| chr7:13912172 | G | A | 1 | a0001c0001t0026g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.803-865C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912172 | |||||||
| chr7:13912181 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-874A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912181 | |||||||
| chr7:13912183 | G | A | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-876C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912183 | |||||||
| chr7:13912223 | T | C | 7 | a0001c0001t0013g0098 a0002c0002t0009g0194 a0002c0002t0009g0198 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-916A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912223 | |||||||
| chr7:13912286 | C | T | 1 | a0001c0001t0016g0191 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.803-979G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912286 | |||||||
| chr7:13912370 | T | A | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-1063A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912370 | |||||||
| chr7:13912442 | ATTTAC | A | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1140_803-1136d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912442 | |||||||
| chr7:13912479 | G | A | 3 | a0001c0001t0019g0152 a0001c0001t0019g0221 a0001c0001t0035g0124 |
3 | HG00099.hp2 HG00140.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.803-1172C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912479 | |||||||
| chr7:13912644 | C | T | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-1337G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912644 | |||||||
| chr7:13912758 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.803-1451T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912758 | |||||||
| chr7:13912813 | G | C | 2 | a0001c0001t0040g0011 a0001c0001t0055g0253 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.803-1506C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912813 | |||||||
| chr7:13913169 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.803-1862A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913169 | |||||||
| chr7:13913218 | C | T | 2 | a0001c0001t0002g0064 a0002c0002t0001g0216 |
2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.803-1911G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913218 | |||||||
| chr7:13913363 | T | C | 7 | a0001c0001t0004g0261 a0001c0001t0014g0042 a0001c0001t0018g0096 others(4): Show |
7 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2056A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913363 | |||||||
| chr7:13913484 | C | T | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2177G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913484 | |||||||
| chr7:13913510 | C | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2203G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913510 | |||||||
| chr7:13913536 | C | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2229G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913536 | |||||||
| chr7:13913579 | A | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2272T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913579 | |||||||
| chr7:13913775 | T | G | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-2468A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913775 | |||||||
| chr7:13913776 | A | G | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-2469T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913776 | |||||||
| chr7:13913869 | GGGGTACC others(5): Show |
G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-2574_803-2563d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913869 | |||||||
| chr7:13913872 | G | T | 3 | a0001c0001t0051g0235 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.803-2565C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913872 | |||||||
| chr7:13913878 | C | CT | 34 | a0001c0001t0001g0242 a0001c0001t0001g0254 a0001c0001t0001g0255 others(31): Show |
34 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.803-2572dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913878 | C | CTT | 65 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.803-2573_803-2572d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913878 | CT | C | 20 | a0001c0001t0004g0166 a0001c0001t0006g0298 a0001c0001t0006g0300 others(17): Show |
21 | HG01071.hp1 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.803-2572delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913878 | CTT | C | 77 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(74): Show |
78 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.803-2573_803-2572d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913878 | CTTT | C | 12 | a0001c0001t0004g0236 a0001c0001t0007g0315 a0001c0001t0010g0044 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-2574_803-2572d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913878 | CTTTT | C | 14 | a0001c0001t0010g0037 a0001c0001t0010g0068 a0001c0001t0010g0083 others(11): Show |
14 | HG01071.hp2 HG01081.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-2575_803-2572d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | |||||||
| chr7:13913883 | T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-2576A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913883 | |||||||
| chr7:13913915 | C | T | 7 | a0001c0001t0013g0098 a0002c0002t0009g0194 a0002c0002t0009g0198 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2608G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913915 | |||||||
| chr7:13914008 | T | C | 93 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0017 others(90): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.803-2701A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914008 | |||||||
| chr7:13914033 | G | A | 7 | a0001c0001t0013g0098 a0002c0002t0009g0194 a0002c0002t0009g0198 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2726C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914033 | |||||||
| chr7:13914066 | G | C | 1 | a0002c0002t0005g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.803-2759C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914066 | |||||||
| chr7:13914203 | C | T | 1 | a0001c0001t0044g0127 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.803-2896G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914203 | |||||||
| chr7:13914211 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.803-2904A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914211 | |||||||
| chr7:13914244 | C | G | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2937G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914244 | |||||||
| chr7:13914251 | G | A | 1 | a0001c0001t0013g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.803-2944C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914251 | |||||||
| chr7:13914440 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG00099.hp1 HG01361.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.803-3133A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914440 | |||||||
| chr7:13914505 | C | T | 2 | a0001c0001t0006g0298 a0001c0001t0042g0301 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-3198G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914505 | |||||||
| chr7:13914614 | A | G | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-3307T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914614 | |||||||
| chr7:13914618 | TA | T | 103 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.803-3312delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914618 | |||||||
| chr7:13914618 | TAA | T | 23 | a0001c0001t0004g0179 a0001c0001t0004g0265 a0001c0001t0006g0053 others(20): Show |
23 | HG00408.hp1 HG00735.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-3313_803-3312d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914618 | |||||||
| chr7:13914653 | G | A | 1 | a0002c0002t0005g0272 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.803-3346C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914653 | |||||||
| chr7:13914740 | A | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3433T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914740 | |||||||
| chr7:13914741 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.803-3434A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914741 | |||||||
| chr7:13914784 | A | G | 1 | a0001c0001t0012g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.803-3477T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914784 | |||||||
| chr7:13914867 | G | A | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-3560C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914867 | |||||||
| chr7:13914895 | C | T | 205 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.803-3588G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914895 | |||||||
| chr7:13914915 | C | A | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3608G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914915 | |||||||
| chr7:13914937 | C | G | 2 | a0001c0001t0026g0039 a0001c0001t0026g0094 |
2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.803-3630G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914937 | |||||||
| chr7:13915006 | C | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3699G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915006 | |||||||
| chr7:13915483 | C | T | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-4176G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915483 | |||||||
| chr7:13915485 | T | A | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-4178A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915485 | |||||||
| chr7:13915508 | C | A | 1 | a0001c0001t0012g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.803-4201G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915508 | |||||||
| chr7:13915530 | T | C | 76 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(73): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.803-4223A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915530 | |||||||
| chr7:13915591 | G | A | 33 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0010g0037 others(30): Show |
33 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.803-4284C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915591 | |||||||
| chr7:13915599 | G | T | 1 | a0002c0002t0004g0210 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-4292C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915599 | |||||||
| chr7:13915693 | T | G | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-4386A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915693 | |||||||
| chr7:13915699 | C | T | 23 | a0001c0001t0004g0166 a0001c0001t0004g0187 a0001c0001t0004g0248 others(20): Show |
23 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-4392G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915699 | |||||||
| chr7:13915701 | C | G | 119 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(116): Show |
121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-4394G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915701 | |||||||
| chr7:13915743 | T | C | 9 | a0001c0001t0014g0025 a0001c0001t0014g0042 a0001c0001t0014g0080 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-4436A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915743 | |||||||
| chr7:13915744 | G | C | 3 | a0001c0001t0051g0235 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.803-4437C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915744 | |||||||
| chr7:13915757 | A | AT | 6 | a0001c0001t0003g0285 a0001c0001t0003g0288 a0001c0001t0005g0190 others(3): Show |
6 | HG02965.hp1 HG03225.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4451dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915757 | |||||||
| chr7:13915757 | AT | A | 23 | a0001c0001t0002g0017 a0001c0001t0003g0291 a0001c0001t0004g0187 others(20): Show |
24 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.803-4451delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915757 | |||||||
| chr7:13915780 | A | G | 2 | a0001c0001t0010g0068 a0001c0001t0010g0126 |
2 | HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.803-4473T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915780 | |||||||
| chr7:13915980 | G | A | 1 | a0001c0004t0001g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.803-4673C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915980 | |||||||
| chr7:13916012 | G | T | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4705C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916012 | |||||||
| chr7:13916013 | G | C | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4706C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916013 | |||||||
| chr7:13916015 | T | C | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4708A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916015 | |||||||
| chr7:13916016 | G | A | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4709C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916016 | |||||||
| chr7:13916017 | C | T | 213 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.803-4710G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916017 | |||||||
| chr7:13916037 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.803-4730G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916037 | |||||||
| chr7:13916093 | C | T | 1 | a0001c0001t0006g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.803-4786G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916093 | |||||||
| chr7:13916110 | T | G | 1 | a0001c0001t0041g0310 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-4803A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916110 | |||||||
| chr7:13916152 | A | G | 2 | a0001c0001t0003g0090 a0002c0002t0022g0001 |
3 | HG00738.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.803-4845T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916152 | |||||||
| chr7:13916154 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.803-4847T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916154 | |||||||
| chr7:13916307 | T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-5000A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916307 | |||||||
| chr7:13916364 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.803-5057C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916364 | |||||||
| chr7:13916475 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.803-5168A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916475 | |||||||
| chr7:13916552 | C | T | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.803-5245G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916552 | |||||||
| chr7:13916569 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.803-5262G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916569 | |||||||
| chr7:13916586 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-5279G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916586 | |||||||
| chr7:13916672 | T | C | 1 | a0001c0001t0006g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.803-5365A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916672 | |||||||
| chr7:13916729 | G | T | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-5422C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916729 | |||||||
| chr7:13916819 | C | A | 107 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(104): Show |
109 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.803-5512G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916819 | |||||||
| chr7:13916827 | G | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-5520C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916827 | |||||||
| chr7:13916859 | G | A | 1 | a0001c0001t0006g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.803-5552C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916859 | |||||||
| chr7:13916906 | T | G | 1 | a0002c0002t0001g0131 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.803-5599A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916906 | |||||||
| chr7:13916930 | CA | C | 121 | a0001c0001t0001g0159 a0001c0001t0002g0024 a0001c0001t0002g0026 others(118): Show |
123 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.803-5624delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916930 | |||||||
| chr7:13916961 | G | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-5654C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916961 | |||||||
| chr7:13916973 | A | G | 1 | a0001c0001t0041g0310 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-5666T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916973 | |||||||
| chr7:13916980 | G | A | 121 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(118): Show |
123 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.803-5673C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916980 | |||||||
| chr7:13916988 | A | G | 14 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(11): Show |
14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-5681T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916988 | |||||||
| chr7:13917004 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0018g0314 |
3 | NA18949.hp2 NA18953.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-5697C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917004 | |||||||
| chr7:13917107 | C | T | 1 | a0002c0002t0017g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.803-5800G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917107 | |||||||
| chr7:13917152 | T | C | 1 | a0001c0005t0010g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803-5845A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917152 | |||||||
| chr7:13917168 | T | C | 2 | a0001c0001t0017g0023 a0001c0001t0017g0040 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803-5861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917168 | |||||||
| chr7:13917175 | A | C | 1 | a0001c0001t0038g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.803-5868T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917175 | |||||||
| chr7:13917273 | C | T | 1 | a0002c0002t0009g0219 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-5966G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917273 | |||||||
| chr7:13917288 | G | GTATT | 35 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0003g0009 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.803-5985_803-5982d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | G | GTATTTAT others(1): Show |
6 | a0001c0001t0001g0184 a0001c0001t0002g0038 a0001c0001t0019g0221 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-5989_803-5982d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | G | GTATTTAT others(5): Show |
1 | a0002c0002t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.803-5993_803-5982d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | GTATT | G | 45 | a0001c0001t0001g0167 a0001c0001t0003g0293 a0001c0001t0004g0166 others(42): Show |
45 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.803-5985_803-5982d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | GTATTTAT others(1): Show |
G | 8 | a0001c0001t0006g0298 a0001c0001t0011g0081 a0001c0001t0011g0097 others(5): Show |
8 | HG01074.hp1 HG01167.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-5989_803-5982d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | GTATTTAT others(5): Show |
G | 3 | a0001c0001t0010g0068 a0001c0001t0010g0126 a0001c0001t0039g0084 |
3 | HG01071.hp2 HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.803-5993_803-5982d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917288 | GTATTTAT others(13): Show |
G | 1 | a0001c0001t0017g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803-6001_803-5982d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | |||||||
| chr7:13917340 | G | A | 81 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.803-6033C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917340 | |||||||
| chr7:13917411 | G | A | 81 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.803-6104C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917411 | |||||||
| chr7:13917420 | T | C | 74 | a0001c0001t0001g0159 a0001c0001t0002g0017 a0001c0001t0002g0024 others(71): Show |
76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.803-6113A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917420 | |||||||
| chr7:13917429 | C | T | 1 | a0001c0001t0005g0190 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.803-6122G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917429 | |||||||
| chr7:13917563 | C | T | 1 | a0001c0001t0004g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.803-6256G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917563 | |||||||
| chr7:13917693 | G | A | 93 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.803-6386C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917693 | |||||||
| chr7:13917781 | G | A | 1 | a0002c0002t0004g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.803-6474C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917781 | |||||||
| chr7:13917819 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-6512G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917819 | |||||||
| chr7:13917833 | G | A | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-6526C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917833 | |||||||
| chr7:13917874 | A | G | 2 | a0001c0001t0029g0257 a0001c0001t0032g0005 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.803-6567T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917874 | |||||||
| chr7:13918075 | A | G | 3 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0002c0002t0006g0078 |
3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.803-6768T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918075 | |||||||
| chr7:13918181 | CT | C | 13 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(10): Show |
13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-6875delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918181 | |||||||
| chr7:13918183 | T | A | 13 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(10): Show |
13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-6876A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918183 | |||||||
| chr7:13918230 | G | C | 1 | a0001c0001t0041g0310 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-6923C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918230 | |||||||
| chr7:13918388 | G | C | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.803-7081C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918388 | |||||||
| chr7:13918430 | A | C | 50 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(47): Show |
51 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.803-7123T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918430 | |||||||
| chr7:13918470 | G | C | 1 | a0001c0001t0006g0099 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.803-7163C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918470 | |||||||
| chr7:13918540 | C | G | 9 | a0001c0001t0001g0251 a0001c0001t0002g0064 a0001c0001t0002g0107 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-7233G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918540 | |||||||
| chr7:13918544 | G | GCAGC | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-7241_803-7238d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918544 | |||||||
| chr7:13918578 | T | C | 1 | a0002c0002t0007g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.803-7271A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918578 | |||||||
| chr7:13918600 | AATC | A | 27 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7296_803-7294d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918600 | |||||||
| chr7:13918688 | C | T | 2 | a0002c0002t0002g0075 a0002c0002t0008g0206 |
2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.803-7381G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918688 | |||||||
| chr7:13918729 | T | TG | 18 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0200 others(15): Show |
18 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-7423dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918729 | |||||||
| chr7:13918734 | G | GA | 3 | a0001c0001t0011g0074 a0001c0001t0017g0040 a0002c0002t0017g0036 |
3 | HG00741.hp2 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.803-7428_803-7427i others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918734 | |||||||
| chr7:13918737 | C | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-7430G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918737 | |||||||
| chr7:13918738 | G | A | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.803-7431C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918738 | |||||||
| chr7:13918741 | G | A | 1 | a0001c0001t0027g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-7434C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918741 | |||||||
| chr7:13918754 | T | C | 27 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7447A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918754 | |||||||
| chr7:13918765 | C | G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-7458G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918765 | |||||||
| chr7:13918776 | A | C | 1 | a0001c0001t0047g0212 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.803-7469T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918776 | |||||||
| chr7:13918798 | G | A | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.803-7491C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918798 | |||||||
| chr7:13918798 | G | T | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803-7491C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918798 | |||||||
| chr7:13918843 | G | A | 27 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(24): Show |
27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7536C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918843 | |||||||
| chr7:13918847 | A | T | 8 | a0001c0001t0014g0025 a0001c0001t0014g0080 a0001c0001t0014g0110 others(5): Show |
8 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-7540T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918847 | |||||||
| chr7:13918853 | AC | A | 19 | a0001c0001t0002g0117 a0001c0001t0002g0281 a0001c0001t0004g0181 others(16): Show |
19 | HG00621.hp2 HG02074.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.803-7547delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918853 | |||||||
| chr7:13918874 | T | TA | 94 | a0001c0001t0001g0159 a0001c0001t0001g0183 a0001c0001t0002g0017 others(91): Show |
95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.803-7568dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | |||||||
| chr7:13918874 | T | TAA | 100 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0184 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.803-7569_803-7568d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | |||||||
| chr7:13918874 | T | TAAA | 11 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(8): Show |
11 | HG01070.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.803-7570_803-7568d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | |||||||
| chr7:13918874 | T | TAAAA | 25 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(22): Show |
26 | HG00280.hp1 HG00323.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.803-7571_803-7568d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | |||||||
| chr7:13918874 | T | TAAAAA | 6 | a0001c0001t0010g0068 a0001c0001t0010g0126 a0001c0001t0028g0238 others(3): Show |
6 | HG01071.hp2 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-7572_803-7568d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | |||||||
| chr7:13918910 | C | T | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-7603G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918910 | |||||||
| chr7:13918949 | T | C | 2 | a0001c0001t0017g0023 a0001c0001t0017g0040 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803-7642A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918949 | |||||||
| chr7:13918988 | C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.803-7681G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918988 | |||||||
| chr7:13919037 | G | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-7730C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919037 | |||||||
| chr7:13919145 | A | C | 25 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-7838T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919145 | |||||||
| chr7:13919289 | C | G | 48 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.803-7982G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919289 | |||||||
| chr7:13919310 | G | A | 48 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.803-8003C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919310 | |||||||
| chr7:13919311 | T | C | 214 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.803-8004A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919311 | |||||||
| chr7:13919316 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0040 a0001c0001t0051g0235 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-8009A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919316 | |||||||
| chr7:13919369 | C | T | 2 | a0001c0001t0004g0181 a0001c0001t0004g0186 |
2 | NA18972.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.803-8062G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919369 | |||||||
| chr7:13919398 | C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-8091G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919398 | |||||||
| chr7:13919463 | G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-8156C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919463 | |||||||
| chr7:13919475 | G | GT | 7 | a0001c0001t0026g0039 a0001c0001t0026g0094 a0001c0001t0028g0238 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-8169dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919475 | |||||||
| chr7:13919475 | GT | G | 6 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0013g0032 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-8169delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919475 | |||||||
| chr7:13919510 | G | C | 12 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-8203C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919510 | |||||||
| chr7:13919548 | CAACT | C | 23 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(20): Show |
24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-8245_803-8242d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919548 | |||||||
| chr7:13919565 | T | TAC | 17 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0057 others(14): Show |
17 | HG00642.hp2 HG00741.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-8260_803-8259d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | T | TACAC | 9 | a0001c0001t0003g0051 a0001c0001t0006g0298 a0001c0001t0009g0143 others(6): Show |
9 | HG01243.hp2 HG02135.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-8262_803-8259d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | T | TACACAC | 20 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0009g0002 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-8264_803-8259d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | T | TACACACA others(3): Show |
18 | a0001c0001t0003g0287 a0001c0001t0012g0108 a0001c0001t0012g0115 others(15): Show |
18 | HG00597.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-8268_803-8259d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | T | TACACACA others(5): Show |
2 | a0001c0001t0002g0026 a0001c0001t0012g0283 |
2 | NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.803-8270_803-8259d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | T | TACACACA others(7): Show |
1 | a0002c0002t0009g0198 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.803-8272_803-8259d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | TAC | T | 111 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(108): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.803-8260_803-8259d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | TACAC | T | 6 | a0001c0001t0004g0236 a0001c0001t0006g0309 a0002c0002t0001g0157 others(3): Show |
6 | HG02080.hp1 HG02886.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-8262_803-8259d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | TACACACA others(7): Show |
T | 4 | a0001c0001t0026g0094 a0001c0001t0028g0238 a0001c0001t0028g0239 others(1): Show |
4 | HG01255.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-8272_803-8259d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919565 | TACACACA others(9): Show |
T | 2 | a0001c0001t0018g0314 a0001c0001t0026g0039 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-8274_803-8259d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | |||||||
| chr7:13919593 | CACACACA others(3): Show |
C | 1 | a0001c0001t0002g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-8296_803-8287d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919593 | |||||||
| chr7:13919602 | A | AC | 3 | a0001c0001t0006g0058 a0001c0001t0059g0249 a0002c0002t0005g0213 |
3 | HG00423.hp1 HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.803-8296_803-8295i others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919602 | |||||||
| chr7:13919632 | T | C | 2 | a0001c0001t0006g0298 a0001c0001t0042g0301 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-8325A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919632 | |||||||
| chr7:13919685 | G | A | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-8378C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919685 | |||||||
| chr7:13919764 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.803-8457T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919764 | |||||||
| chr7:13919781 | G | A | 84 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.803-8474C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919781 | |||||||
| chr7:13919873 | A | G | 1 | a0001c0001t0012g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.803-8566T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919873 | |||||||
| chr7:13919880 | G | GAC | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-8575_803-8574d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919880 | |||||||
| chr7:13919886 | C | A | 5 | a0001c0001t0026g0039 a0001c0001t0026g0094 a0001c0001t0028g0238 others(2): Show |
5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-8579G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919886 | |||||||
| chr7:13919890 | C | G | 1 | a0001c0001t0002g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.803-8583G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919890 | |||||||
| chr7:13919892 | G | C | 19 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(16): Show |
19 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-8585C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919892 | |||||||
| chr7:13919900 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.803-8593C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919900 | |||||||
| chr7:13920093 | C | G | 1 | a0001c0001t0005g0233 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.803-8786G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920093 | |||||||
| chr7:13920129 | C | G | 25 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-8822G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920129 | |||||||
| chr7:13920209 | T | C | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803-8902A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920209 | |||||||
| chr7:13920300 | G | C | 5 | a0001c0001t0026g0039 a0001c0001t0026g0094 a0001c0001t0028g0238 others(2): Show |
5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-8993C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920300 | |||||||
| chr7:13920417 | T | C | 6 | a0001c0001t0014g0042 a0001c0001t0018g0096 a0001c0001t0027g0252 others(3): Show |
6 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-9110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920417 | |||||||
| chr7:13920441 | A | AGT | 64 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(61): Show |
64 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-9136_803-9135d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGT | 57 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0002g0017 others(54): Show |
58 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.803-9138_803-9135d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGT | 28 | a0001c0001t0002g0026 a0001c0001t0002g0117 a0001c0001t0002g0281 others(25): Show |
28 | HG00597.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.803-9140_803-9135d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGTG others(1): Show |
10 | a0001c0001t0004g0268 a0001c0001t0006g0130 a0001c0001t0006g0282 others(7): Show |
10 | HG00544.hp1 HG00621.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-9142_803-9135d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGTG others(3): Show |
4 | a0001c0001t0007g0294 a0001c0001t0029g0257 a0001c0001t0032g0005 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-9144_803-9135d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGTG others(5): Show |
1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.803-9146_803-9135d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0051g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.803-9148_803-9135d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920441 | A | AGTGTGTG others(9): Show |
2 | a0002c0002t0017g0036 a0002c0002t0017g0043 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.803-9150_803-9135d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | |||||||
| chr7:13920511 | A | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-9204T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920511 | |||||||
| chr7:13920628 | T | C | 2 | a0001c0001t0006g0298 a0001c0001t0042g0301 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-9321A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920628 | |||||||
| chr7:13920696 | C | T | 56 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(53): Show |
57 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.803-9389G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920696 | |||||||
| chr7:13920776 | C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-9469G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920776 | |||||||
| chr7:13920782 | T | C | 15 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(12): Show |
15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-9475A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920782 | |||||||
| chr7:13920808 | G | T | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-9501C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920808 | |||||||
| chr7:13920894 | A | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.803-9587T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920894 | |||||||
| chr7:13920955 | A | G | 57 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-9648T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920955 | |||||||
| chr7:13921050 | A | C | 57 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-9743T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921050 | |||||||
| chr7:13921080 | T | C | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-9773A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921080 | |||||||
| chr7:13921348 | T | G | 57 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(54): Show |
58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-10041A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921348 | |||||||
| chr7:13921419 | G | A | 54 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+10083C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921419 | |||||||
| chr7:13921474 | G | GA | 6 | a0001c0001t0007g0048 a0001c0005t0010g0113 a0002c0002t0001g0158 others(3): Show |
6 | HG02080.hp1 HG02809.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+10027dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921474 | |||||||
| chr7:13921526 | G | T | 23 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(20): Show |
23 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.802+9976C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921526 | |||||||
| chr7:13921601 | G | A | 3 | a0001c0001t0051g0235 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9901C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921601 | |||||||
| chr7:13921645 | G | A | 3 | a0002c0002t0003g0120 a0002c0002t0005g0267 a0002c0002t0005g0269 |
3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.802+9857C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921645 | |||||||
| chr7:13921660 | G | A | 1 | a0001c0001t0004g0268 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.802+9842C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921660 | |||||||
| chr7:13921680 | C | T | 3 | a0001c0001t0051g0235 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9822G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921680 | |||||||
| chr7:13921681 | C | T | 54 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9821G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921681 | |||||||
| chr7:13921737 | G | A | 52 | a0001c0001t0003g0287 a0001c0001t0006g0300 a0001c0001t0006g0305 others(49): Show |
53 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.802+9765C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921737 | |||||||
| chr7:13921834 | G | A | 1 | a0002c0002t0007g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.802+9668C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921834 | |||||||
| chr7:13921837 | A | T | 29 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(26): Show |
30 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.802+9665T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921837 | |||||||
| chr7:13921839 | C | T | 11 | a0001c0001t0014g0025 a0001c0001t0014g0080 a0001c0001t0014g0110 others(8): Show |
11 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+9663G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921839 | |||||||
| chr7:13921846 | C | T | 54 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9656G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921846 | |||||||
| chr7:13921863 | G | C | 3 | a0001c0001t0051g0235 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9639C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921863 | |||||||
| chr7:13921970 | T | C | 12 | a0001c0001t0003g0290 a0001c0001t0009g0002 a0001c0001t0009g0196 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+9532A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921970 | |||||||
| chr7:13922072 | A | C | 30 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.802+9430T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922072 | |||||||
| chr7:13922257 | C | T | 19 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0012g0108 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.802+9245G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922257 | |||||||
| chr7:13922337 | C | A | 1 | a0002c0002t0005g0272 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.802+9165G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922337 | |||||||
| chr7:13922363 | TG | T | 54 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9138delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922363 | |||||||
| chr7:13922390 | C | T | 13 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0068 others(10): Show |
13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+9112G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922390 | |||||||
| chr7:13922618 | A | G | 7 | a0001c0001t0004g0261 a0001c0001t0014g0042 a0001c0001t0018g0096 others(4): Show |
7 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+8884T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922618 | |||||||
| chr7:13922741 | C | T | 1 | a0001c0001t0013g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.802+8761G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922741 | |||||||
| chr7:13922801 | C | T | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+8701G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922801 | |||||||
| chr7:13922893 | A | G | 1 | a0001c0001t0026g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.802+8609T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922893 | |||||||
| chr7:13922995 | T | C | 69 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(66): Show |
70 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+8507A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922995 | |||||||
| chr7:13923030 | T | C | 1 | a0001c0001t0006g0278 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.802+8472A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923030 | |||||||
| chr7:13923048 | T | C | 2 | a0002c0002t0005g0151 a0002c0002t0005g0213 |
2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.802+8454A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923048 | |||||||
| chr7:13923079 | T | C | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.802+8423A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923079 | |||||||
| chr7:13923191 | T | C | 12 | a0001c0001t0014g0025 a0001c0001t0014g0080 a0001c0001t0014g0110 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+8311A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923191 | |||||||
| chr7:13923217 | C | A | 11 | a0001c0001t0014g0025 a0001c0001t0014g0080 a0001c0001t0014g0110 others(8): Show |
11 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+8285G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923217 | |||||||
| chr7:13923237 | G | C | 117 | a0001c0001t0001g0159 a0001c0001t0001g0243 a0001c0001t0002g0017 others(114): Show |
119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.802+8265C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923237 | |||||||
| chr7:13923353 | T | C | 18 | a0001c0001t0009g0002 a0001c0001t0009g0143 a0001c0001t0009g0196 others(15): Show |
19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.802+8149A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923353 | |||||||
| chr7:13923375 | T | C | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+8127A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923375 | |||||||
| chr7:13923392 | T | C | 25 | a0001c0001t0003g0276 a0001c0001t0004g0166 a0001c0001t0004g0187 others(22): Show |
25 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+8110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923392 | |||||||
| chr7:13923534 | G | A | 58 | a0001c0001t0002g0026 a0001c0001t0002g0034 a0001c0001t0003g0287 others(55): Show |
59 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.802+7968C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923534 | |||||||
| chr7:13923560 | T | C | 1 | a0002c0002t0005g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802+7942A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923560 | |||||||
| chr7:13923603 | G | A | 1 | a0001c0001t0002g0026 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.802+7899C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923603 | |||||||
| chr7:13923625 | G | A | 25 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+7877C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923625 | |||||||
| chr7:13923804 | G | A | 5 | a0001c0001t0018g0096 a0001c0001t0027g0252 a0001c0001t0056g0259 others(2): Show |
5 | HG02258.hp1 HG02895.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+7698C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923804 | |||||||
| chr7:13923804 | G | T | 4 | a0001c0001t0003g0285 a0001c0001t0003g0288 a0001c0001t0005g0190 others(1): Show |
4 | NA18967.hp1 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+7698C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923804 | |||||||
| chr7:13923808 | G | A | 2 | a0001c0001t0003g0019 a0001c0003t0002g0072 |
2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.802+7694C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923808 | |||||||
| chr7:13923966 | C | T | 198 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.802+7536G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923966 | |||||||
| chr7:13923990 | G | A | 37 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+7512C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923990 | |||||||
| chr7:13924008 | C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+7494G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924008 | |||||||
| chr7:13924048 | A | T | 2 | a0001c0001t0026g0039 a0001c0001t0026g0094 |
2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.802+7454T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924048 | |||||||
| chr7:13924178 | A | G | 2 | a0002c0002t0034g0312 a0002c0002t0052g0256 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.802+7324T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924178 | |||||||
| chr7:13924336 | C | G | 1 | a0001c0001t0003g0289 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.802+7166G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924336 | |||||||
| chr7:13924447 | T | A | 19 | a0001c0001t0002g0034 a0001c0001t0009g0002 a0001c0001t0009g0196 others(16): Show |
20 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+7055A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924447 | |||||||
| chr7:13924491 | C | G | 11 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+7011G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924491 | |||||||
| chr7:13924528 | C | T | 38 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6974G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924528 | |||||||
| chr7:13924578 | G | A | 37 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6924C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924578 | |||||||
| chr7:13924578 | G | C | 2 | a0001c0001t0058g0135 a0002c0002t0004g0223 |
2 | HG01109.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.802+6924C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924578 | |||||||
| chr7:13924665 | T | C | 1 | a0001c0001t0028g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.802+6837A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924665 | |||||||
| chr7:13924724 | G | A | 4 | a0001c0001t0029g0257 a0001c0001t0032g0005 a0002c0002t0029g0163 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+6778C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924724 | |||||||
| chr7:13924763 | A | G | 38 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6739T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924763 | |||||||
| chr7:13924901 | G | A | 38 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6601C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924901 | |||||||
| chr7:13924930 | T | C | 38 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6572A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924930 | |||||||
| chr7:13924931 | CAAAG | C | 38 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6567_802+6570d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924931 | |||||||
| chr7:13924964 | C | T | 16 | a0001c0001t0014g0025 a0001c0001t0014g0042 a0001c0001t0014g0080 others(13): Show |
16 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+6538G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924964 | |||||||
| chr7:13925013 | C | G | 2 | a0001c0001t0011g0081 a0001c0001t0011g0097 |
2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.802+6489G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925013 | |||||||
| chr7:13925219 | A | G | 1 | a0001c0004t0001g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.802+6283T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925219 | |||||||
| chr7:13925255 | C | A | 37 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6247G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925255 | |||||||
| chr7:13925256 | A | T | 1 | a0001c0001t0042g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.802+6246T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925256 | |||||||
| chr7:13925306 | A | G | 37 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6196T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925306 | |||||||
| chr7:13925327 | G | A | 37 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0006g0300 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6175C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925327 | |||||||
| chr7:13925348 | C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+6154G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925348 | |||||||
| chr7:13925362 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.802+6140A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925362 | |||||||
| chr7:13925375 | G | A | 12 | a0001c0001t0014g0025 a0001c0001t0014g0042 a0001c0001t0014g0080 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+6127C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925375 | |||||||
| chr7:13925552 | A | G | 1 | a0001c0001t0014g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.802+5950T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925552 | |||||||
| chr7:13925558 | C | A | 25 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0003g0291 others(22): Show |
25 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.802+5944G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925558 | |||||||
| chr7:13925567 | A | AT | 12 | a0001c0001t0004g0261 a0001c0001t0006g0305 a0001c0001t0007g0102 others(9): Show |
12 | HG01243.hp2 HG01517.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+5934dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925567 | |||||||
| chr7:13925567 | AT | A | 81 | a0001c0001t0001g0159 a0001c0001t0001g0182 a0001c0001t0001g0183 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.802+5934delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925567 | |||||||
| chr7:13925628 | C | T | 1 | a0002c0002t0008g0156 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.802+5874G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925628 | |||||||
| chr7:13925690 | A | C | 50 | a0001c0001t0001g0251 a0001c0001t0002g0021 a0001c0001t0002g0026 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.802+5812T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925690 | |||||||
| chr7:13925716 | C | T | 1 | a0002c0002t0005g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.802+5786G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925716 | |||||||
| chr7:13925726 | C | T | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+5776G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925726 | |||||||
| chr7:13925728 | G | A | 18 | a0001c0001t0002g0026 a0001c0001t0003g0287 a0001c0001t0003g0291 others(15): Show |
18 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+5774C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925728 | |||||||
| chr7:13925741 | A | AT | 141 | a0001c0001t0001g0183 a0001c0001t0001g0200 a0001c0001t0001g0217 others(138): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.802+5760dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925741 | |||||||
| chr7:13925750 | A | T | 2 | a0001c0001t0003g0293 a0002c0002t0005g0272 |
2 | NA18956.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.802+5752T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925750 | |||||||
| chr7:13925859 | C | T | 11 | a0001c0001t0010g0037 a0001c0001t0010g0044 a0001c0001t0010g0083 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+5643G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925859 | |||||||
| chr7:13925862 | A | ATTTTTTT others(6077): Show |
1 | a0001c0001t0014g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+5639_802+5640i others(6086): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925862 | |||||||
| chr7:13925994 | T | A | 1 | a0001c0001t0007g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+5508A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925994 | |||||||
| chr7:13926000 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.802+5502A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926000 | |||||||
| chr7:13926390 | T | A | 95 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.802+5112A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926390 | |||||||
| chr7:13926549 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0002g0091 |
2 | HG01978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.802+4953G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926549 | |||||||
| chr7:13926552 | A | T | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+4950T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926552 | |||||||
| chr7:13926578 | C | G | 26 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(23): Show |
26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4924G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926578 | |||||||
| chr7:13926743 | T | C | 60 | a0001c0001t0001g0167 a0001c0001t0003g0019 a0001c0001t0003g0046 others(57): Show |
60 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.802+4759A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926743 | |||||||
| chr7:13926785 | C | G | 1 | a0001c0001t0027g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.802+4717G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926785 | |||||||
| chr7:13927174 | T | C | 26 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(23): Show |
26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4328A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927174 | |||||||
| chr7:13927243 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.802+4259C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927243 | |||||||
| chr7:13927276 | C | T | 26 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(23): Show |
26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4226G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927276 | |||||||
| chr7:13927338 | A | G | 2 | a0002c0002t0013g0302 a0002c0002t0013g0303 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.802+4164T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927338 | |||||||
| chr7:13927466 | A | G | 2 | a0001c0001t0007g0294 a0002c0002t0007g0062 |
2 | NA18978.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.802+4036T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927466 | |||||||
| chr7:13927512 | T | C | 27 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(24): Show |
27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3990A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927512 | |||||||
| chr7:13927594 | T | TCC | 27 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(24): Show |
27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3906_802+3907d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927594 | |||||||
| chr7:13927752 | C | T | 27 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(24): Show |
27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3750G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927752 | |||||||
| chr7:13927899 | G | A | 27 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0006g0300 others(24): Show |
27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3603C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927899 | |||||||
| chr7:13927922 | T | A | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+3580A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927922 | |||||||
| chr7:13928037 | A | G | 1 | a0002c0002t0008g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.802+3465T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928037 | |||||||
| chr7:13928152 | T | G | 70 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(67): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+3350A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928152 | |||||||
| chr7:13928154 | A | G | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.802+3348T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928154 | |||||||
| chr7:13928243 | C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+3259G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928243 | |||||||
| chr7:13928388 | A | G | 71 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(68): Show |
71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.802+3114T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928388 | |||||||
| chr7:13928399 | G | T | 70 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(67): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+3103C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928399 | |||||||
| chr7:13928430 | C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+3072G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928430 | |||||||
| chr7:13928482 | C | T | 69 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(66): Show |
69 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+3020G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928482 | |||||||
| chr7:13928508 | G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+2994C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928508 | |||||||
| chr7:13928528 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.802+2974G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928528 | |||||||
| chr7:13928555 | G | A | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.802+2947C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928555 | |||||||
| chr7:13928600 | G | A | 12 | a0001c0001t0002g0088 a0001c0001t0010g0037 a0001c0001t0010g0044 others(9): Show |
12 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+2902C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928600 | |||||||
| chr7:13928629 | G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+2873C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928629 | |||||||
| chr7:13928635 | G | C | 1 | a0001c0001t0036g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+2867C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928635 | |||||||
| chr7:13928819 | G | A | 1 | a0001c0001t0007g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.802+2683C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928819 | |||||||
| chr7:13928847 | A | G | 4 | a0002c0002t0013g0302 a0002c0002t0013g0303 a0002c0002t0013g0313 others(1): Show |
4 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+2655T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928847 | |||||||
| chr7:13928936 | C | T | 1 | a0002c0002t0003g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.802+2566G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928936 | |||||||
| chr7:13929204 | G | C | 1 | a0002c0002t0004g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.802+2298C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929204 | |||||||
| chr7:13929241 | G | A | 17 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0007g0315 others(14): Show |
17 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+2261C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929241 | |||||||
| chr7:13929344 | T | C | 66 | a0001c0001t0002g0117 a0001c0001t0002g0281 a0001c0001t0003g0090 others(63): Show |
69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+2158A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929344 | |||||||
| chr7:13929378 | A | G | 16 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0007g0315 others(13): Show |
16 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.802+2124T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929378 | |||||||
| chr7:13929460 | A | C | 69 | a0001c0001t0001g0167 a0001c0001t0002g0034 a0001c0001t0003g0019 others(66): Show |
69 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+2042T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929460 | |||||||
| chr7:13929521 | A | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+1981T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929521 | |||||||
| chr7:13929522 | C | T | 2 | a0001c0001t0024g0028 a0001c0001t0024g0029 |
2 | HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.802+1980G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929522 | |||||||
| chr7:13929564 | G | C | 9 | a0001c0001t0004g0236 a0001c0001t0006g0123 a0001c0001t0015g0132 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+1938C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929564 | |||||||
| chr7:13929735 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.802+1767A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929735 | |||||||
| chr7:13929894 | C | G | 13 | a0001c0001t0002g0026 a0001c0001t0003g0291 a0001c0001t0005g0173 others(10): Show |
13 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+1608G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929894 | |||||||
| chr7:13930329 | A | T | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+1173T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930329 | |||||||
| chr7:13930444 | A | T | 3 | a0001c0001t0015g0138 a0001c0001t0050g0142 a0001c0001t0055g0253 |
3 | HG02559.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.802+1058T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930444 | |||||||
| chr7:13930507 | C | G | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.802+995G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930507 | |||||||
| chr7:13930512 | A | G | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.802+990T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930512 | |||||||
| chr7:13930515 | G | T | 12 | a0001c0001t0003g0291 a0001c0001t0005g0173 a0001c0001t0012g0115 others(9): Show |
12 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+987C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930515 | |||||||
| chr7:13930564 | G | A | 1 | a0001c0001t0059g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+938C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930564 | |||||||
| chr7:13930601 | G | A | 2 | a0001c0001t0019g0152 a0001c0001t0035g0124 |
2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.802+901C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930601 | |||||||
| chr7:13930606 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.802+896G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930606 | |||||||
| chr7:13930608 | A | G | 1 | a0002c0002t0001g0216 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.802+894T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930608 | |||||||
| chr7:13930641 | T | C | 4 | a0001c0001t0004g0137 a0001c0001t0006g0309 a0001c0001t0039g0084 others(1): Show |
4 | HG02109.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930641 | |||||||
| chr7:13930672 | G | A | 4 | a0001c0001t0006g0123 a0001c0001t0038g0304 a0002c0002t0007g0311 others(1): Show |
4 | HG02055.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+830C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930672 | |||||||
| chr7:13930693 | G | A | 1 | a0002c0002t0013g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+809C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930693 | |||||||
| chr7:13930705 | A | G | 8 | a0001c0001t0007g0061 a0001c0001t0009g0143 a0001c0001t0014g0042 others(5): Show |
8 | HG02559.hp1 HG02818.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+797T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930705 | |||||||
| chr7:13930789 | A | AAT | 11 | a0001c0001t0002g0013 a0001c0001t0002g0052 a0001c0001t0003g0291 others(8): Show |
11 | HG00544.hp1 HG00544.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+711_802+712dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930789 | |||||||
| chr7:13930797 | T | TA | 123 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(120): Show |
124 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.802+704_802+705ins others(1): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930797 | |||||||
| chr7:13930798 | T | A | 124 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.802+704A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930798 | |||||||
| chr7:13930799 | T | A | 113 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(110): Show |
114 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.802+703A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930799 | |||||||
| chr7:13930800 | T | A | 124 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.802+702A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930800 | |||||||
| chr7:13930801 | T | A | 2 | a0001c0001t0005g0230 a0001c0001t0007g0294 |
2 | HG00408.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.802+701A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930801 | |||||||
| chr7:13930802 | T | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+700A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930802 | |||||||
| chr7:13930805 | T | C | 9 | a0001c0001t0002g0034 a0001c0001t0028g0238 a0001c0001t0028g0239 others(6): Show |
9 | HG01109.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+697A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930805 | |||||||
| chr7:13930823 | C | T | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.802+679G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930823 | |||||||
| chr7:13930847 | C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+655G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930847 | |||||||
| chr7:13930870 | G | A | 2 | a0001c0001t0053g0224 a0002c0002t0001g0192 |
2 | NA18965.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.802+632C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930870 | |||||||
| chr7:13930927 | A | T | 6 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0010g0299 others(3): Show |
6 | HG02257.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+575T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930927 | |||||||
| chr7:13930975 | T | C | 4 | a0001c0001t0008g0247 a0001c0001t0019g0152 a0001c0001t0019g0221 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+527A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930975 | |||||||
| chr7:13931040 | C | T | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+462G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931040 | |||||||
| chr7:13931114 | C | T | 298 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.802+388G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931114 | |||||||
| chr7:13931126 | TTCAGAAG others(4): Show |
T | 2 | a0001c0001t0006g0278 a0001c0001t0053g0224 |
2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.802+365_802+375del others(11): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931126 | |||||||
| chr7:13931174 | A | G | 8 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0005g0173 others(5): Show |
8 | HG00544.hp2 HG00597.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+328T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931174 | |||||||
| chr7:13931201 | A | G | 17 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0010g0299 others(14): Show |
17 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+301T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931201 | |||||||
| chr7:13931211 | G | GA | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0010g0299 others(10): Show |
13 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.802+290dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931211 | |||||||
| chr7:13931300 | C | G | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+202G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931300 | |||||||
| chr7:13931492 | G | A | 13 | a0001c0001t0006g0123 a0001c0001t0015g0136 a0002c0002t0006g0078 others(10): Show |
13 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+10C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931492 | |||||||
| chr7:13931798 | T | C | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-49A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931798 | |||||||
| chr7:13931822 | C | T | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-73G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931822 | |||||||
| chr7:13931886 | G | A | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-137C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931886 | |||||||
| chr7:13931977 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.555-228A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931977 | |||||||
| chr7:13931982 | G | A | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-233C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931982 | |||||||
| chr7:13932037 | T | TAC | 3 | a0001c0001t0004g0137 a0001c0001t0039g0084 a0001c0001t0042g0301 |
3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.555-290_555-289dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932037 | |||||||
| chr7:13932042 | ACC | A | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.555-295_555-294del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932042 | |||||||
| chr7:13932044 | C | A | 4 | a0001c0001t0004g0137 a0001c0001t0020g0237 a0001c0001t0039g0084 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-295G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932044 | C | CCA | 96 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(93): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.555-297_555-296dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932044 | C | CCACA | 51 | a0001c0001t0002g0012 a0001c0001t0002g0021 a0001c0001t0002g0027 others(48): Show |
51 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.555-299_555-296dup others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932044 | C | CCACACA | 11 | a0001c0001t0004g0166 a0001c0001t0015g0132 a0001c0001t0015g0139 others(8): Show |
11 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-301_555-296dup others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932044 | C | CCACACAC others(3): Show |
5 | a0002c0002t0006g0078 a0002c0002t0013g0313 a0002c0002t0018g0297 others(2): Show |
5 | HG02630.hp1 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-305_555-296dup others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932044 | CCACA | C | 4 | a0001c0001t0006g0130 a0001c0001t0028g0238 a0001c0001t0028g0239 others(1): Show |
4 | HG02074.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-299_555-296del others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | |||||||
| chr7:13932115 | G | T | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-366C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932115 | |||||||
| chr7:13932246 | A | G | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-497T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932246 | |||||||
| chr7:13932367 | C | T | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-618G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932367 | |||||||
| chr7:13932573 | G | C | 1 | a0001c0001t0006g0089 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.555-824C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932573 | |||||||
| chr7:13932584 | G | T | 1 | a0002c0002t0016g0273 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.555-835C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932584 | |||||||
| chr7:13932682 | C | T | 122 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(119): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.555-933G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932682 | |||||||
| chr7:13932730 | C | A | 1 | a0001c0001t0002g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.555-981G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932730 | |||||||
| chr7:13932785 | A | T | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1036T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932785 | |||||||
| chr7:13932833 | G | C | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1084C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932833 | |||||||
| chr7:13932836 | T | A | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1087A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932836 | |||||||
| chr7:13932845 | G | A | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.555-1096C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932845 | |||||||
| chr7:13932858 | A | G | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1109T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932858 | |||||||
| chr7:13933281 | T | C | 12 | a0001c0001t0015g0136 a0002c0002t0006g0078 a0002c0002t0007g0311 others(9): Show |
12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1532A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933281 | |||||||
| chr7:13933460 | T | C | 1 | a0001c0001t0003g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.555-1711A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933460 | |||||||
| chr7:13933512 | G | C | 1 | a0002c0002t0004g0274 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.555-1763C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933512 | |||||||
| chr7:13933759 | T | C | 1 | a0001c0001t0011g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.554+1949A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933759 | |||||||
| chr7:13933826 | G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.554+1882C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933826 | |||||||
| chr7:13933847 | T | C | 1 | a0001c0005t0010g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.554+1861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933847 | |||||||
| chr7:13933848 | C | T | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+1860G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933848 | |||||||
| chr7:13933852 | C | T | 8 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0013g0302 others(5): Show |
8 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+1856G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933852 | |||||||
| chr7:13933936 | G | T | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+1772C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933936 | |||||||
| chr7:13934138 | A | C | 1 | a0002c0002t0002g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.554+1570T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934138 | |||||||
| chr7:13934298 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.554+1410T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934298 | |||||||
| chr7:13934509 | C | T | 2 | a0001c0001t0006g0035 a0001c0001t0006g0306 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+1199G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934509 | |||||||
| chr7:13934522 | C | A | 1 | a0001c0001t0007g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.554+1186G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934522 | |||||||
| chr7:13934756 | C | G | 19 | a0001c0001t0002g0034 a0001c0001t0006g0123 a0001c0001t0006g0300 others(16): Show |
19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+952G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934756 | |||||||
| chr7:13934756 | C | T | 2 | a0001c0001t0015g0134 a0001c0001t0058g0135 |
2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.554+952G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934756 | |||||||
| chr7:13934824 | A | G | 2 | a0001c0001t0015g0134 a0001c0001t0058g0135 |
2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.554+884T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934824 | |||||||
| chr7:13934836 | C | T | 92 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(89): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.554+872G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934836 | |||||||
| chr7:13934937 | A | G | 12 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(9): Show |
13 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+771T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934937 | |||||||
| chr7:13934938 | G | A | 91 | a0002c0002t0001g0131 a0002c0002t0001g0148 a0002c0002t0001g0149 others(88): Show |
92 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.554+770C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934938 | |||||||
| chr7:13934969 | T | C | 2 | a0002c0002t0013g0302 a0002c0002t0013g0303 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.554+739A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934969 | |||||||
| chr7:13934991 | G | A | 2 | a0002c0002t0007g0062 a0002c0002t0016g0273 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.554+717C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934991 | |||||||
| chr7:13935161 | T | C | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.554+547A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935161 | |||||||
| chr7:13935251 | T | C | 19 | a0001c0001t0002g0034 a0001c0001t0006g0123 a0001c0001t0006g0300 others(16): Show |
19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+457A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935251 | |||||||
| chr7:13935441 | C | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.554+267G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935441 | |||||||
| chr7:13935454 | C | T | 2 | a0001c0001t0039g0084 a0001c0001t0042g0301 |
2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.554+254G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935454 | |||||||
| chr7:13935603 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.554+105A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935603 | |||||||
| chr7:13935675 | A | G | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+33T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935675 | |||||||
| chr7:13935949 | T | A | 20 | a0001c0001t0002g0034 a0001c0001t0006g0123 a0001c0001t0006g0300 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-53A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935949 | |||||||
| chr7:13935950 | A | T | 11 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0010g0114 others(8): Show |
11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.366-54T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935950 | |||||||
| chr7:13935968 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.366-72T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935968 | |||||||
| chr7:13936070 | C | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-174G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936070 | |||||||
| chr7:13936144 | A | G | 99 | a0002c0002t0001g0131 a0002c0002t0001g0148 a0002c0002t0001g0149 others(96): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.366-248T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936144 | |||||||
| chr7:13936287 | A | G | 1 | a0002c0002t0007g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.366-391T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936287 | |||||||
| chr7:13936294 | G | A | 1 | a0001c0001t0003g0285 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.366-398C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936294 | |||||||
| chr7:13936407 | T | G | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.366-511A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936407 | |||||||
| chr7:13936633 | G | T | 96 | a0002c0002t0001g0131 a0002c0002t0001g0148 a0002c0002t0001g0149 others(93): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-737C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936633 | |||||||
| chr7:13936766 | C | T | 3 | a0002c0002t0003g0120 a0002c0002t0005g0267 a0002c0002t0005g0269 |
3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.366-870G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936766 | |||||||
| chr7:13936939 | G | T | 2 | a0002c0002t0007g0062 a0002c0002t0016g0273 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.366-1043C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936939 | |||||||
| chr7:13936966 | C | T | 1 | a0001c0001t0041g0310 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366-1070G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936966 | |||||||
| chr7:13937041 | CA | C | 96 | a0002c0002t0001g0131 a0002c0002t0001g0148 a0002c0002t0001g0149 others(93): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-1146delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937041 | |||||||
| chr7:13937139 | A | C | 1 | a0001c0001t0003g0100 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.366-1243T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937139 | |||||||
| chr7:13937200 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.366-1304A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937200 | |||||||
| chr7:13937208 | T | G | 89 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.366-1312A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937208 | |||||||
| chr7:13937234 | T | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.366-1338A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937234 | |||||||
| chr7:13937276 | T | C | 1 | a0001c0001t0002g0026 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.366-1380A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937276 | |||||||
| chr7:13937370 | C | A | 96 | a0002c0002t0001g0131 a0002c0002t0001g0148 a0002c0002t0001g0149 others(93): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-1474G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937370 | |||||||
| chr7:13937390 | T | A | 3 | a0001c0001t0015g0134 a0001c0001t0017g0023 a0001c0001t0017g0040 |
3 | HG02717.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.366-1494A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937390 | |||||||
| chr7:13937442 | TTATTGCA others(7): Show |
T | 3 | a0001c0001t0004g0137 a0001c0001t0039g0084 a0001c0001t0042g0301 |
3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.366-1560_366-1547d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937442 | |||||||
| chr7:13937461 | T | G | 1 | a0002c0002t0001g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.366-1565A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937461 | |||||||
| chr7:13937484 | C | T | 1 | a0001c0001t0010g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.366-1588G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937484 | |||||||
| chr7:13937678 | C | G | 1 | a0002c0002t0016g0273 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.365+1439G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937678 | |||||||
| chr7:13937688 | G | A | 1 | a0001c0001t0003g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.365+1429C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937688 | |||||||
| chr7:13937767 | A | C | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+1350T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937767 | |||||||
| chr7:13938008 | C | T | 7 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0157 others(4): Show |
7 | HG02080.hp1 NA18973.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+1109G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938008 | |||||||
| chr7:13938069 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0004g0261 a0001c0001t0007g0315 others(3): Show |
6 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+1048A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938069 | |||||||
| chr7:13938236 | C | A | 1 | a0002c0002t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.365+881G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938236 | |||||||
| chr7:13938264 | A | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.365+853T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938264 | |||||||
| chr7:13938280 | C | T | 1 | a0002c0002t0022g0001 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.365+837G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938280 | |||||||
| chr7:13938381 | A | C | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+736T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938381 | |||||||
| chr7:13938470 | GAC | G | 22 | a0001c0001t0002g0034 a0001c0001t0006g0123 a0001c0001t0006g0300 others(19): Show |
22 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.365+645_365+646del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938470 | |||||||
| chr7:13938488 | T | G | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365+629A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938488 | |||||||
| chr7:13938520 | T | C | 6 | a0001c0001t0009g0143 a0001c0001t0014g0042 a0001c0001t0015g0138 others(3): Show |
6 | HG02559.hp1 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+597A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938520 | |||||||
| chr7:13938632 | C | A | 5 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0006g0089 others(2): Show |
5 | NA18988.hp1 NA18991.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+485G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938632 | |||||||
| chr7:13938663 | G | T | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.365+454C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938663 | |||||||
| chr7:13938682 | T | A | 1 | a0002c0002t0027g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.365+435A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938682 | |||||||
| chr7:13939020 | C | T | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+97G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939020 | |||||||
| chr7:13939023 | T | A | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+94A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939023 | |||||||
| chr7:13939058 | C | G | 4 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0214 others(1): Show |
4 | HG01074.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+59G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939058 | |||||||
| chr7:13939419 | T | C | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-173A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939419 | |||||||
| chr7:13939539 | A | G | 19 | a0001c0001t0002g0034 a0001c0001t0006g0123 a0001c0001t0006g0300 others(16): Show |
19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.236-293T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939539 | |||||||
| chr7:13939600 | G | A | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-354C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939600 | |||||||
| chr7:13939601 | A | C | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-355T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939601 | |||||||
| chr7:13939645 | C | A | 1 | a0001c0001t0009g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.236-399G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939645 | |||||||
| chr7:13939669 | A | G | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-423T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939669 | |||||||
| chr7:13939730 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.236-484G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939730 | |||||||
| chr7:13939760 | G | C | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236-514C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939760 | |||||||
| chr7:13939842 | T | C | 1 | a0001c0001t0010g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.236-596A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939842 | |||||||
| chr7:13939953 | C | T | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-707G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939953 | |||||||
| chr7:13939985 | C | T | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-739G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939985 | |||||||
| chr7:13939986 | G | A | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-740C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939986 | |||||||
| chr7:13940104 | G | A | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-858C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940104 | |||||||
| chr7:13940245 | C | G | 3 | a0001c0001t0004g0137 a0001c0001t0039g0084 a0001c0001t0042g0301 |
3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.236-999G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940245 | |||||||
| chr7:13940278 | C | T | 1 | a0002c0002t0018g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-1032G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940278 | |||||||
| chr7:13940351 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0020g0237 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.236-1105C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940351 | |||||||
| chr7:13940363 | AAAAAAAA others(2): Show |
A | 101 | a0001c0001t0001g0251 a0002c0002t0001g0131 a0002c0002t0001g0147 others(98): Show |
102 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.236-1126_236-1118d others(11): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940363 | |||||||
| chr7:13940441 | C | A | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.236-1195G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940441 | |||||||
| chr7:13940530 | C | T | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-1284G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940530 | |||||||
| chr7:13940574 | T | A | 8 | a0001c0001t0007g0067 a0001c0001t0010g0068 a0001c0001t0010g0126 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-1328A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940574 | |||||||
| chr7:13940793 | T | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-1547A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940793 | |||||||
| chr7:13940814 | G | C | 1 | a0002c0002t0027g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.236-1568C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940814 | |||||||
| chr7:13940924 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.236-1678G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940924 | |||||||
| chr7:13941037 | G | C | 2 | a0002c0002t0007g0062 a0002c0002t0016g0273 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.236-1791C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941037 | |||||||
| chr7:13941045 | C | T | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-1799G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941045 | |||||||
| chr7:13941193 | G | T | 1 | a0001c0001t0042g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.236-1947C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941193 | |||||||
| chr7:13941223 | T | G | 2 | a0002c0002t0007g0062 a0002c0002t0016g0273 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.236-1977A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941223 | |||||||
| chr7:13941638 | A | G | 108 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(105): Show |
109 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.236-2392T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941638 | |||||||
| chr7:13941863 | G | GAATA | 3 | a0001c0001t0001g0217 a0001c0001t0002g0088 a0001c0001t0011g0128 |
3 | HG00735.hp2 HG01123.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.236-2621_236-2618d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941863 | GAATA | G | 76 | a0001c0001t0001g0159 a0001c0001t0001g0182 a0001c0001t0001g0183 others(73): Show |
76 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.236-2621_236-2618d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941863 | GAATAAAT others(1): Show |
G | 63 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0254 others(60): Show |
64 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.236-2625_236-2618d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941863 | GAATAAAT others(5): Show |
G | 21 | a0001c0001t0003g0046 a0001c0001t0004g0003 a0001c0001t0004g0137 others(18): Show |
22 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.236-2629_236-2618d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941863 | GAATAAAT others(9): Show |
G | 1 | a0001c0001t0012g0295 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.236-2633_236-2618d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941863 | GAATAAAT others(17): Show |
G | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2641_236-2618d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | |||||||
| chr7:13941948 | C | G | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2702G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941948 | |||||||
| chr7:13941957 | G | C | 100 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2711C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941957 | |||||||
| chr7:13942020 | CT | C | 154 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(151): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.236-2775delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942020 | |||||||
| chr7:13942020 | CTTTTT | C | 94 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(91): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.236-2779_236-2775d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942020 | |||||||
| chr7:13942060 | T | G | 7 | a0002c0002t0006g0078 a0002c0002t0007g0311 a0002c0002t0013g0302 others(4): Show |
7 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2814A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942060 | |||||||
| chr7:13942061 | T | C | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-2815A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942061 | |||||||
| chr7:13942062 | C | T | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2816G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942062 | |||||||
| chr7:13942115 | C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-2869G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942115 | |||||||
| chr7:13942123 | A | G | 99 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(96): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-2877T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942123 | |||||||
| chr7:13942140 | C | T | 7 | a0001c0001t0003g0276 a0001c0001t0003g0291 a0001c0001t0003g0293 others(4): Show |
7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2894G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942140 | |||||||
| chr7:13942176 | A | G | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-2930T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942176 | |||||||
| chr7:13942180 | C | T | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2934G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942180 | |||||||
| chr7:13942248 | C | G | 1 | a0002c0002t0003g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236-3002G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942248 | |||||||
| chr7:13942262 | A | G | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-3016T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942262 | |||||||
| chr7:13942317 | C | T | 2 | a0001c0001t0015g0134 a0001c0001t0058g0135 |
2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.236-3071G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942317 | |||||||
| chr7:13942357 | TA | T | 97 | a0002c0002t0001g0131 a0002c0002t0001g0147 a0002c0002t0001g0148 others(94): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.236-3112delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942357 | |||||||
| chr7:13942410 | T | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-3164A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942410 | |||||||
| chr7:13942421 | C | T | 106 | a0001c0001t0003g0051 a0001c0001t0003g0056 a0001c0001t0003g0276 others(103): Show |
107 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.236-3175G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942421 | |||||||
| chr7:13942435 | A | G | 99 | a0001c0001t0003g0051 a0001c0001t0003g0056 a0002c0002t0001g0131 others(96): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-3189T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942435 | |||||||
| chr7:13942613 | C | G | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.236-3367G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942613 | |||||||
| chr7:13942628 | C | G | 2 | a0001c0001t0028g0239 a0001c0001t0039g0084 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.236-3382G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942628 | |||||||
| chr7:13942795 | A | C | 120 | a0001c0001t0003g0016 a0001c0001t0003g0051 a0001c0001t0003g0056 others(117): Show |
121 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3549T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942795 | |||||||
| chr7:13942991 | A | G | 2 | a0001c0001t0029g0257 a0001c0001t0032g0005 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.236-3745T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942991 | |||||||
| chr7:13943108 | A | G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0186 |
2 | NA18972.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.236-3862T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943108 | |||||||
| chr7:13943163 | G | C | 1 | a0001c0001t0003g0285 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.236-3917C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943163 | |||||||
| chr7:13943420 | G | A | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4174C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943420 | |||||||
| chr7:13943549 | T | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4303A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943549 | |||||||
| chr7:13943587 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.236-4341A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943587 | |||||||
| chr7:13943662 | A | G | 1 | a0002c0002t0004g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.236-4416T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943662 | |||||||
| chr7:13943737 | G | A | 2 | a0001c0001t0028g0238 a0001c0001t0045g0111 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-4491C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943737 | |||||||
| chr7:13943744 | T | A | 253 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(250): Show |
256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.236-4498A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943744 | |||||||
| chr7:13943783 | T | G | 14 | a0002c0002t0001g0148 a0002c0002t0001g0149 a0002c0002t0001g0154 others(11): Show |
14 | HG02027.hp1 HG02080.hp1 NA18960.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-4537A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943783 | |||||||
| chr7:13943791 | T | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4545A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943791 | |||||||
| chr7:13943826 | C | T | 2 | a0001c0001t0028g0238 a0001c0001t0045g0111 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-4580G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943826 | |||||||
| chr7:13943862 | A | G | 7 | a0001c0001t0003g0276 a0001c0001t0003g0291 a0001c0001t0003g0293 others(4): Show |
7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4616T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943862 | |||||||
| chr7:13944075 | C | T | 7 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(4): Show |
7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4829G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944075 | |||||||
| chr7:13944100 | C | T | 7 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(4): Show |
7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4854G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944100 | |||||||
| chr7:13944110 | A | G | 4 | a0002c0002t0001g0154 a0002c0002t0005g0155 a0002c0002t0008g0156 others(1): Show |
4 | NA18963.hp1 NA19063.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-4864T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944110 | |||||||
| chr7:13944217 | T | A | 15 | a0001c0001t0002g0049 a0001c0001t0003g0100 a0001c0001t0007g0067 others(12): Show |
15 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-4971A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944217 | |||||||
| chr7:13944250 | C | T | 291 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(288): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.236-5004G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944250 | |||||||
| chr7:13944420 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236-5174G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944420 | |||||||
| chr7:13944420 | C | G | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5174G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944420 | |||||||
| chr7:13944445 | G | A | 1 | a0001c0001t0025g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236-5199C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944445 | |||||||
| chr7:13944564 | A | G | 9 | a0001c0001t0002g0012 a0001c0001t0002g0027 a0001c0001t0007g0061 others(6): Show |
9 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-5318T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944564 | |||||||
| chr7:13944567 | C | T | 1 | a0001c0001t0025g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236-5321G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944567 | |||||||
| chr7:13944634 | ATCCCTGA others(18): Show |
A | 4 | a0001c0001t0004g0137 a0001c0001t0006g0309 a0001c0001t0014g0080 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-5413_236-5389d others(27): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944634 | |||||||
| chr7:13944771 | A | C | 1 | a0001c0001t0055g0253 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236-5525T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944771 | |||||||
| chr7:13944787 | T | C | 4 | a0001c0001t0006g0031 a0001c0001t0013g0032 a0001c0001t0024g0028 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-5541A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944787 | |||||||
| chr7:13944944 | G | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5698C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944944 | |||||||
| chr7:13944973 | A | G | 1 | a0001c0001t0004g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.236-5727T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944973 | |||||||
| chr7:13945069 | A | AAAC | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5826_236-5824d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945069 | |||||||
| chr7:13945270 | C | T | 3 | a0002c0002t0004g0180 a0002c0002t0012g0033 a0002c0002t0012g0047 |
3 | HG00423.hp2 NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.236-6024G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945270 | |||||||
| chr7:13945293 | T | A | 138 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(135): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.236-6047A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945293 | |||||||
| chr7:13945294 | A | T | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-6048T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945294 | |||||||
| chr7:13945392 | A | C | 2 | a0001c0001t0014g0080 a0001c0001t0042g0301 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-6146T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945392 | |||||||
| chr7:13945443 | A | AT | 7 | a0001c0001t0003g0286 a0001c0001t0009g0143 a0001c0001t0010g0044 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-6198dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945443 | |||||||
| chr7:13945443 | AT | A | 108 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(105): Show |
109 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.236-6198delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945443 | |||||||
| chr7:13945506 | A | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-6260T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945506 | |||||||
| chr7:13945506 | A | T | 4 | a0001c0001t0008g0247 a0001c0001t0019g0152 a0001c0001t0019g0221 others(1): Show |
4 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-6260T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945506 | |||||||
| chr7:13945507 | T | A | 3 | a0001c0001t0014g0080 a0001c0001t0015g0134 a0001c0001t0058g0135 |
3 | HG01109.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.236-6261A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945507 | |||||||
| chr7:13945543 | G | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-6297C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945543 | |||||||
| chr7:13945841 | A | T | 10 | a0001c0001t0002g0088 a0001c0001t0005g0245 a0001c0001t0005g0246 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-6595T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945841 | |||||||
| chr7:13946265 | G | A | 7 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(4): Show |
7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7019C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946265 | |||||||
| chr7:13946415 | C | T | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.236-7169G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946415 | |||||||
| chr7:13946617 | A | C | 1 | a0002c0002t0008g0262 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.236-7371T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946617 | |||||||
| chr7:13946623 | A | C | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-7377T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946623 | |||||||
| chr7:13946670 | G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-7424C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946670 | |||||||
| chr7:13946725 | T | C | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-7479A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946725 | |||||||
| chr7:13946881 | C | T | 27 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0088 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.236-7635G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946881 | |||||||
| chr7:13947008 | C | T | 1 | a0001c0001t0020g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.236-7762G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947008 | |||||||
| chr7:13947023 | G | A | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-7777C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947023 | |||||||
| chr7:13947031 | C | G | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-7785G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947031 | |||||||
| chr7:13947100 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0026g0094 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.236-7854G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947100 | |||||||
| chr7:13947294 | AAAGAT | A | 7 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(4): Show |
7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-8053_236-8049d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947294 | |||||||
| chr7:13947392 | C | CA | 99 | a0001c0001t0001g0200 a0001c0001t0001g0218 a0001c0001t0002g0013 others(96): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-8147dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947392 | |||||||
| chr7:13947392 | CA | C | 26 | a0001c0001t0001g0217 a0001c0001t0003g0016 a0001c0001t0003g0276 others(23): Show |
26 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-8147delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947392 | |||||||
| chr7:13947402 | A | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0001c0001t0045g0111 |
3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-8156T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947402 | |||||||
| chr7:13947405 | A | C | 1 | a0001c0001t0006g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.236-8159T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947405 | |||||||
| chr7:13947408 | AC | A | 11 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0037 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-8163delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947408 | |||||||
| chr7:13947409 | C | A | 7 | a0001c0001t0006g0123 a0001c0001t0015g0132 a0001c0001t0015g0139 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-8163G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947409 | |||||||
| chr7:13947497 | T | C | 1 | a0002c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.236-8251A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947497 | |||||||
| chr7:13947601 | C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-8355G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947601 | |||||||
| chr7:13947864 | A | G | 1 | a0002c0002t0003g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236-8618T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947864 | |||||||
| chr7:13948019 | C | T | 10 | a0001c0001t0002g0088 a0001c0001t0005g0245 a0001c0001t0005g0246 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-8773G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948019 | |||||||
| chr7:13948153 | G | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-8907C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948153 | |||||||
| chr7:13948238 | G | A | 16 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(13): Show |
16 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.236-8992C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948238 | |||||||
| chr7:13948320 | G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-9074C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948320 | |||||||
| chr7:13948356 | T | C | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-9110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948356 | |||||||
| chr7:13948484 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-9238A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948484 | |||||||
| chr7:13948501 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.236-9255G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948501 | |||||||
| chr7:13948545 | G | A | 15 | a0001c0001t0002g0049 a0001c0001t0003g0100 a0001c0001t0007g0067 others(12): Show |
15 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-9299C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948545 | |||||||
| chr7:13948622 | G | C | 283 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0182 others(280): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.236-9376C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948622 | |||||||
| chr7:13948697 | A | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-9451T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948697 | |||||||
| chr7:13948888 | T | A | 41 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0088 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.236-9642A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948888 | |||||||
| chr7:13948898 | C | A | 86 | a0001c0001t0002g0281 a0001c0001t0004g0265 a0001c0001t0004g0268 others(83): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.236-9652G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948898 | |||||||
| chr7:13948943 | C | G | 21 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0003g0276 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.236-9697G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948943 | |||||||
| chr7:13949075 | A | G | 1 | a0002c0002t0008g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.236-9829T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949075 | |||||||
| chr7:13949097 | A | C | 1 | a0001c0001t0003g0277 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.236-9851T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949097 | |||||||
| chr7:13949108 | T | C | 3 | a0002c0002t0010g0114 a0002c0002t0017g0036 a0002c0002t0017g0043 |
3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-9862A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949108 | |||||||
| chr7:13949110 | G | T | 4 | a0002c0002t0001g0154 a0002c0002t0005g0155 a0002c0002t0008g0156 others(1): Show |
4 | NA18963.hp1 NA19063.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-9864C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949110 | |||||||
| chr7:13949117 | T | C | 12 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0003g0019 others(9): Show |
12 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-9871A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949117 | |||||||
| chr7:13949165 | T | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-9919A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949165 | |||||||
| chr7:13949165 | TA | T | 27 | a0001c0001t0002g0013 a0001c0001t0002g0021 a0001c0001t0002g0034 others(24): Show |
27 | HG00544.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.236-9920delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949165 | |||||||
| chr7:13949261 | C | T | 7 | a0001c0001t0003g0276 a0001c0001t0003g0291 a0001c0001t0003g0293 others(4): Show |
7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-10015G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949261 | |||||||
| chr7:13949550 | C | T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0205 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.236-10304G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949550 | |||||||
| chr7:13949615 | G | C | 1 | a0001c0001t0013g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.236-10369C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949615 | |||||||
| chr7:13949696 | G | T | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236-10450C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949696 | |||||||
| chr7:13949720 | C | A | 1 | a0002c0002t0022g0001 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.236-10474G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949720 | |||||||
| chr7:13949839 | A | G | 8 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(5): Show |
8 | HG00140.hp2 HG01099.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-10593T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949839 | |||||||
| chr7:13949885 | T | A | 1 | a0001c0001t0016g0191 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.236-10639A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949885 | |||||||
| chr7:13949902 | T | A | 10 | a0001c0001t0004g0137 a0001c0001t0009g0143 a0001c0001t0010g0044 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-10656A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949902 | |||||||
| chr7:13949918 | G | A | 7 | a0001c0001t0019g0152 a0002c0002t0004g0244 a0002c0002t0005g0150 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-10672C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949918 | |||||||
| chr7:13950049 | T | A | 19 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0003g0046 others(16): Show |
19 | HG01070.hp1 HG02015.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.236-10803A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950049 | |||||||
| chr7:13950065 | G | C | 12 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(9): Show |
12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-10819C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950065 | |||||||
| chr7:13950066 | G | A | 1 | a0001c0001t0004g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.236-10820C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950066 | |||||||
| chr7:13950102 | G | T | 12 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(9): Show |
12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-10856C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950102 | |||||||
| chr7:13950124 | T | C | 8 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(5): Show |
8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-10878A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950124 | |||||||
| chr7:13950317 | G | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.236-11071C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950317 | |||||||
| chr7:13950408 | C | T | 5 | a0001c0001t0007g0061 a0001c0001t0038g0304 a0001c0001t0041g0310 others(2): Show |
5 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11162G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950408 | |||||||
| chr7:13950645 | T | G | 1 | a0002c0002t0007g0050 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.236-11399A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950645 | |||||||
| chr7:13950713 | G | C | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-11467C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950713 | |||||||
| chr7:13950789 | C | T | 1 | a0001c0001t0007g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236-11543G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950789 | |||||||
| chr7:13950899 | A | AAC | 26 | a0001c0001t0002g0026 a0001c0001t0004g0215 a0001c0001t0004g0268 others(23): Show |
26 | HG00621.hp2 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-11655_236-1165 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACAC | 21 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(18): Show |
21 | HG00597.hp2 HG00609.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.236-11657_236-1165 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACAC | 23 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0254 others(20): Show |
23 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-11659_236-1165 others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(1): Show |
7 | a0001c0001t0003g0009 a0001c0001t0007g0076 a0001c0001t0046g0071 others(4): Show |
7 | HG02258.hp1 HG03195.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-11661_236-1165 others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(3): Show |
9 | a0001c0001t0002g0091 a0001c0001t0007g0077 a0001c0001t0019g0152 others(6): Show |
9 | HG00140.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-11663_236-1165 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(5): Show |
2 | a0001c0001t0002g0012 a0002c0002t0017g0036 |
2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.236-11665_236-1165 others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(7): Show |
1 | a0002c0002t0017g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.236-11667_236-1165 others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(9): Show |
1 | a0001c0001t0024g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.236-11669_236-1165 others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | A | AACACACA others(11): Show |
1 | a0002c0002t0010g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.236-11671_236-1165 others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AAC | A | 5 | a0001c0001t0006g0123 a0001c0001t0015g0132 a0001c0001t0021g0263 others(2): Show |
5 | HG01891.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11655_236-1165 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AACAC | A | 5 | a0001c0001t0004g0137 a0001c0001t0013g0098 a0001c0001t0014g0080 others(2): Show |
5 | HG01361.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11657_236-1165 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AACACACA others(1): Show |
A | 23 | a0001c0001t0002g0281 a0001c0001t0003g0051 a0001c0001t0003g0056 others(20): Show |
23 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.236-11661_236-1165 others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AACACACA others(3): Show |
A | 78 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.236-11663_236-1165 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AACACACA others(5): Show |
A | 1 | a0001c0001t0023g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236-11665_236-1165 others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950899 | AACACACA others(11): Show |
A | 9 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(6): Show |
9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-11671_236-1165 others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | |||||||
| chr7:13950941 | C | A | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-11695G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | |||||||
| chr7:13950941 | C | CACAA | 7 | a0001c0001t0002g0038 a0001c0001t0008g0247 a0001c0001t0009g0002 others(4): Show |
8 | HG01070.hp1 HG02602.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-11696_236-1169 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | |||||||
| chr7:13950941 | C | CACACAA | 7 | a0001c0001t0002g0034 a0001c0001t0004g0261 a0001c0001t0007g0315 others(4): Show |
7 | HG02257.hp2 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-11696_236-1169 others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | |||||||
| chr7:13950941 | C | CACACACA others(3): Show |
2 | a0001c0001t0002g0021 a0001c0001t0014g0025 |
2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.236-11696_236-1169 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | |||||||
| chr7:13951129 | C | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-11883G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951129 | |||||||
| chr7:13951132 | C | T | 1 | a0001c0001t0003g0287 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.236-11886G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951132 | |||||||
| chr7:13951255 | T | C | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-12009A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951255 | |||||||
| chr7:13951294 | G | A | 9 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(6): Show |
9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-12048C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951294 | |||||||
| chr7:13951318 | C | T | 148 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.236-12072G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951318 | |||||||
| chr7:13951367 | A | G | 128 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-12121T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951367 | |||||||
| chr7:13951560 | G | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0042g0301 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-12314C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951560 | |||||||
| chr7:13951596 | T | C | 149 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(146): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.236-12350A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951596 | |||||||
| chr7:13951730 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.236-12484A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951730 | |||||||
| chr7:13951753 | T | A | 8 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(5): Show |
8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-12507A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951753 | |||||||
| chr7:13951839 | G | A | 44 | a0001c0001t0003g0016 a0001c0001t0003g0276 a0001c0001t0003g0277 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.236-12593C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951839 | |||||||
| chr7:13951972 | C | A | 1 | a0002c0002t0052g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236-12726G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951972 | |||||||
| chr7:13952046 | AAAAT | A | 44 | a0001c0001t0003g0016 a0001c0001t0003g0276 a0001c0001t0003g0277 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.236-12804_236-1280 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952046 | |||||||
| chr7:13952069 | A | G | 12 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(9): Show |
12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-12823T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952069 | |||||||
| chr7:13952080 | G | A | 1 | a0001c0001t0051g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.236-12834C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952080 | |||||||
| chr7:13952117 | C | T | 3 | a0001c0001t0005g0245 a0001c0001t0005g0260 a0002c0002t0008g0262 |
3 | HG01168.hp1 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.236-12871G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952117 | |||||||
| chr7:13952139 | A | G | 1 | a0001c0001t0006g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236-12893T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952139 | |||||||
| chr7:13952203 | T | G | 128 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-12957A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952203 | |||||||
| chr7:13952204 | G | A | 19 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(16): Show |
20 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.236-12958C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952204 | |||||||
| chr7:13952228 | C | G | 173 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.236-12982G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952228 | |||||||
| chr7:13952303 | C | T | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.236-13057G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952303 | |||||||
| chr7:13952608 | T | A | 183 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.236-13362A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952608 | |||||||
| chr7:13952641 | G | A | 1 | a0002c0002t0007g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.236-13395C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952641 | |||||||
| chr7:13952732 | G | T | 1 | a0001c0001t0002g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-13486C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952732 | |||||||
| chr7:13952804 | C | T | 1 | a0002c0002t0001g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.236-13558G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952804 | |||||||
| chr7:13952835 | A | G | 182 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.236-13589T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952835 | |||||||
| chr7:13952986 | A | G | 4 | a0001c0001t0002g0034 a0001c0001t0010g0083 a0001c0001t0020g0133 others(1): Show |
4 | HG02145.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-13740T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952986 | |||||||
| chr7:13953065 | A | G | 1 | a0001c0001t0051g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.236-13819T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953065 | |||||||
| chr7:13953085 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0009g0227 a0001c0003t0002g0072 |
3 | HG00280.hp2 HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.236-13839T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953085 | |||||||
| chr7:13953111 | C | T | 6 | a0002c0002t0001g0199 a0002c0002t0001g0214 a0002c0002t0009g0198 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-13865G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953111 | |||||||
| chr7:13953246 | C | T | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14000G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953246 | |||||||
| chr7:13953357 | C | T | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14111G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953357 | |||||||
| chr7:13953389 | C | T | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.236-14143G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953389 | |||||||
| chr7:13953400 | C | T | 2 | a0002c0002t0004g0144 a0002c0002t0005g0145 |
2 | NA18978.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.236-14154G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953400 | |||||||
| chr7:13953439 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0059g0249 |
2 | HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.236-14193C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953439 | |||||||
| chr7:13953445 | T | G | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236-14199A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953445 | |||||||
| chr7:13953464 | A | T | 1 | a0002c0002t0004g0168 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.236-14218T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953464 | |||||||
| chr7:13953501 | G | A | 1 | a0001c0001t0006g0089 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.236-14255C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953501 | |||||||
| chr7:13953623 | C | G | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14377G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953623 | |||||||
| chr7:13953669 | G | T | 8 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(5): Show |
8 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-14423C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953669 | |||||||
| chr7:13953672 | A | T | 8 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(5): Show |
8 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-14426T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953672 | |||||||
| chr7:13953684 | A | G | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14438T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953684 | |||||||
| chr7:13953770 | T | A | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-14524A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953770 | |||||||
| chr7:13954144 | C | T | 1 | a0001c0001t0006g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.236-14898G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954144 | |||||||
| chr7:13954145 | A | T | 7 | a0001c0001t0010g0037 a0001c0001t0010g0121 a0001c0001t0010g0122 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-14899T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954145 | |||||||
| chr7:13954162 | C | A | 2 | a0001c0001t0039g0084 a0001c0001t0046g0071 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-14916G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954162 | |||||||
| chr7:13954163 | A | T | 2 | a0001c0001t0039g0084 a0001c0001t0046g0071 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-14917T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954163 | |||||||
| chr7:13954288 | C | T | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-15042G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954288 | |||||||
| chr7:13954332 | A | G | 1 | a0001c0001t0006g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236-15086T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954332 | |||||||
| chr7:13954475 | G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-15229C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954475 | |||||||
| chr7:13954640 | C | T | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-15394G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954640 | |||||||
| chr7:13954758 | C | T | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-15512G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954758 | |||||||
| chr7:13955033 | C | T | 18 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0003g0046 others(15): Show |
19 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.236-15787G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955033 | |||||||
| chr7:13955264 | G | A | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-16018C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955264 | |||||||
| chr7:13955368 | G | C | 2 | a0001c0001t0039g0084 a0001c0001t0046g0071 |
2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-16122C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955368 | |||||||
| chr7:13955519 | G | C | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-16273C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955519 | |||||||
| chr7:13955584 | G | T | 69 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(66): Show |
70 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.236-16338C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955584 | |||||||
| chr7:13955835 | AT | A | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-16590delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955835 | |||||||
| chr7:13955899 | A | T | 22 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0003g0046 others(19): Show |
23 | HG01070.hp1 HG01243.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-16653T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955899 | |||||||
| chr7:13955944 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | NA18960.hp2 NA19006.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.236-16698T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955944 | |||||||
| chr7:13956048 | G | A | 13 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0004g0261 others(10): Show |
13 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-16802C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956048 | |||||||
| chr7:13956162 | T | G | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.236-16916A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956162 | |||||||
| chr7:13956193 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-16947A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956193 | |||||||
| chr7:13956257 | T | G | 3 | a0001c0001t0006g0278 a0001c0001t0012g0115 a0001c0001t0053g0224 |
3 | HG02165.hp2 NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.236-17011A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956257 | |||||||
| chr7:13956258 | C | T | 2 | a0001c0001t0014g0080 a0001c0001t0042g0301 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-17012G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956258 | |||||||
| chr7:13956305 | G | T | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-17059C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956305 | |||||||
| chr7:13956321 | A | AT | 31 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0003g0016 others(28): Show |
32 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.236-17076dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956321 | |||||||
| chr7:13956373 | T | G | 1 | a0002c0002t0027g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.236-17127A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956373 | |||||||
| chr7:13956386 | A | G | 2 | a0001c0001t0028g0238 a0001c0001t0028g0239 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.236-17140T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956386 | |||||||
| chr7:13956399 | G | C | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-17153C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956399 | |||||||
| chr7:13956538 | G | A | 13 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(10): Show |
13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-17292C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956538 | |||||||
| chr7:13956787 | A | G | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.236-17541T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956787 | |||||||
| chr7:13956795 | G | A | 1 | a0002c0002t0007g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.236-17549C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956795 | |||||||
| chr7:13956927 | CA | C | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17682delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956927 | |||||||
| chr7:13957156 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.236-17910C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957156 | |||||||
| chr7:13957171 | C | T | 11 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0019g0152 others(8): Show |
11 | HG00140.hp1 HG02258.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-17925G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957171 | |||||||
| chr7:13957175 | T | G | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17929A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957175 | |||||||
| chr7:13957179 | A | C | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.236-17933T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957179 | |||||||
| chr7:13957203 | A | C | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17957T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957203 | |||||||
| chr7:13957234 | C | T | 4 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0039g0084 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-17988G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957234 | |||||||
| chr7:13957277 | G | A | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-18031C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957277 | |||||||
| chr7:13957322 | G | A | 9 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(6): Show |
9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-18076C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957322 | |||||||
| chr7:13957526 | A | G | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(12): Show |
15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-18280T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957526 | |||||||
| chr7:13957534 | T | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(36): Show |
40 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.236-18288A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957534 | |||||||
| chr7:13957539 | T | C | 3 | a0001c0001t0041g0310 a0001c0001t0045g0111 a0001c0001t0051g0235 |
3 | HG02723.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.236-18293A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957539 | |||||||
| chr7:13957917 | G | A | 1 | a0001c0001t0012g0296 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.236-18671C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957917 | |||||||
| chr7:13957919 | T | C | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-18673A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957919 | |||||||
| chr7:13957948 | C | T | 2 | a0001c0001t0003g0095 a0001c0001t0007g0116 |
2 | HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.236-18702G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957948 | |||||||
| chr7:13958020 | C | A | 14 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0006g0305 others(11): Show |
14 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-18774G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958020 | |||||||
| chr7:13958154 | G | C | 1 | a0002c0002t0009g0194 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.236-18908C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958154 | |||||||
| chr7:13958272 | C | G | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.236-19026G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958272 | |||||||
| chr7:13958306 | C | T | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-19060G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958306 | |||||||
| chr7:13958415 | T | C | 1 | a0001c0001t0004g0248 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235+19012A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958415 | |||||||
| chr7:13958416 | G | T | 7 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(4): Show |
7 | HG00597.hp2 HG00609.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+19011C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958416 | |||||||
| chr7:13958612 | C | T | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+18815G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958612 | |||||||
| chr7:13958657 | G | C | 1 | a0001c0001t0002g0064 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+18770C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958657 | |||||||
| chr7:13958913 | T | G | 2 | a0001c0001t0028g0238 a0001c0001t0028g0239 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.235+18514A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958913 | |||||||
| chr7:13958947 | A | G | 7 | a0001c0001t0019g0152 a0001c0004t0001g0153 a0002c0002t0004g0244 others(4): Show |
7 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+18480T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958947 | |||||||
| chr7:13959043 | T | TA | 18 | a0001c0001t0003g0016 a0001c0001t0003g0277 a0001c0001t0003g0279 others(15): Show |
18 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+18383dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959043 | |||||||
| chr7:13959043 | TA | T | 28 | a0001c0001t0003g0046 a0001c0001t0004g0179 a0001c0001t0006g0123 others(25): Show |
29 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.235+18383delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959043 | |||||||
| chr7:13959152 | T | C | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0056g0259 |
3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+18275A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959152 | |||||||
| chr7:13959169 | T | C | 6 | a0001c0001t0004g0181 a0001c0001t0004g0186 a0001c0001t0005g0190 others(3): Show |
6 | NA18941.hp2 NA18965.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+18258A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959169 | |||||||
| chr7:13959203 | T | G | 22 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(19): Show |
23 | HG01070.hp1 HG01243.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.235+18224A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959203 | |||||||
| chr7:13959415 | A | C | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.235+18012T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959415 | |||||||
| chr7:13959638 | C | G | 8 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(5): Show |
8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+17789G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959638 | |||||||
| chr7:13959846 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.235+17581C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959846 | |||||||
| chr7:13959882 | C | CA | 69 | a0001c0001t0001g0159 a0001c0001t0001g0220 a0001c0001t0001g0243 others(66): Show |
69 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.235+17544dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | |||||||
| chr7:13959882 | CA | C | 25 | a0001c0001t0002g0027 a0001c0001t0003g0016 a0001c0001t0003g0276 others(22): Show |
25 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+17544delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | |||||||
| chr7:13959882 | CAAAAAAA others(6): Show |
C | 20 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(17): Show |
21 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.235+17532_235+1754 others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | |||||||
| chr7:13959882 | CAAAAAAA others(7): Show |
C | 15 | a0001c0001t0006g0123 a0001c0001t0006g0300 a0001c0001t0010g0044 others(12): Show |
15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+17531_235+1754 others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | |||||||
| chr7:13960033 | C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235+17394G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960033 | |||||||
| chr7:13960069 | CTAAAG | C | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0056g0259 |
3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+17353_235+1735 others(9): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960069 | |||||||
| chr7:13960102 | A | G | 1 | a0001c0001t0005g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.235+17325T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960102 | |||||||
| chr7:13960134 | T | C | 24 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0254 others(21): Show |
24 | HG00438.hp1 HG01106.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.235+17293A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960134 | |||||||
| chr7:13960137 | G | C | 3 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0056g0259 |
3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+17290C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960137 | |||||||
| chr7:13960182 | G | A | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+17245C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960182 | |||||||
| chr7:13960229 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0034 a0001c0001t0002g0038 others(28): Show |
32 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235+17198T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960229 | |||||||
| chr7:13960477 | C | G | 10 | a0001c0001t0004g0137 a0001c0001t0019g0152 a0001c0001t0050g0142 others(7): Show |
10 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+16950G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960477 | |||||||
| chr7:13960557 | C | T | 57 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0003g0276 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.235+16870G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960557 | |||||||
| chr7:13960614 | G | A | 16 | a0001c0001t0006g0035 a0001c0001t0006g0123 a0001c0001t0006g0300 others(13): Show |
16 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+16813C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960614 | |||||||
| chr7:13960786 | T | C | 1 | a0001c0001t0028g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235+16641A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960786 | |||||||
| chr7:13960796 | T | G | 21 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0254 others(18): Show |
21 | HG00544.hp1 HG01070.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.235+16631A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960796 | |||||||
| chr7:13961010 | T | C | 7 | a0001c0001t0003g0276 a0001c0001t0003g0291 a0001c0001t0003g0292 others(4): Show |
7 | HG00597.hp2 HG00609.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+16417A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961010 | |||||||
| chr7:13961016 | C | T | 1 | a0001c0001t0006g0278 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.235+16411G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961016 | |||||||
| chr7:13961084 | T | TG | 104 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.235+16342dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961084 | |||||||
| chr7:13961108 | T | C | 14 | a0001c0001t0003g0276 a0001c0001t0003g0280 a0001c0001t0003g0285 others(11): Show |
14 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+16319A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961108 | |||||||
| chr7:13961110 | C | T | 14 | a0001c0001t0003g0276 a0001c0001t0003g0280 a0001c0001t0003g0285 others(11): Show |
14 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+16317G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961110 | |||||||
| chr7:13961145 | C | CA | 6 | a0001c0001t0002g0017 a0001c0001t0002g0024 a0001c0001t0002g0117 others(3): Show |
6 | HG00597.hp1 HG02074.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+16281dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961145 | |||||||
| chr7:13961145 | CA | C | 36 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0254 others(33): Show |
36 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.235+16281delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961145 | |||||||
| chr7:13961146 | AAAAAAAA others(3): Show |
A | 23 | a0001c0001t0001g0159 a0001c0001t0015g0136 a0001c0001t0019g0152 others(20): Show |
23 | HG00140.hp1 HG02080.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.235+16271_235+1628 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961146 | |||||||
| chr7:13961191 | A | G | 61 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0251 others(58): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.235+16236T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961191 | |||||||
| chr7:13961210 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.235+16217A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961210 | |||||||
| chr7:13961224 | G | C | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+16203C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961224 | |||||||
| chr7:13961278 | A | C | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.235+16149T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961278 | |||||||
| chr7:13961441 | T | A | 9 | a0001c0001t0003g0276 a0001c0001t0003g0290 a0001c0001t0003g0291 others(6): Show |
9 | HG00597.hp2 HG00609.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+15986A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961441 | |||||||
| chr7:13961504 | G | C | 47 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(44): Show |
47 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.235+15923C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961504 | |||||||
| chr7:13961549 | T | C | 1 | a0002c0002t0013g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+15878A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961549 | |||||||
| chr7:13961553 | T | C | 1 | a0001c0001t0003g0046 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.235+15874A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961553 | |||||||
| chr7:13961720 | C | A | 6 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0018g0314 others(3): Show |
6 | HG02280.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+15707G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961720 | |||||||
| chr7:13961783 | G | A | 1 | a0002c0002t0009g0194 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.235+15644C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961783 | |||||||
| chr7:13961854 | A | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15573T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961854 | |||||||
| chr7:13961859 | T | C | 2 | a0001c0001t0004g0137 a0001c0001t0014g0080 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+15568A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961859 | |||||||
| chr7:13961944 | A | G | 16 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+15483T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961944 | |||||||
| chr7:13962038 | G | A | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+15389C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962038 | |||||||
| chr7:13962070 | A | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15357T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962070 | |||||||
| chr7:13962113 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.235+15314A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962113 | |||||||
| chr7:13962180 | T | TAC | 20 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(17): Show |
20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+15245_235+1524 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962180 | |||||||
| chr7:13962202 | C | CACGT | 9 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0006g0309 others(6): Show |
9 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+15224_235+1522 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962202 | |||||||
| chr7:13962202 | C | CGT | 13 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(10): Show |
13 | HG02055.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+15223_235+1522 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962202 | |||||||
| chr7:13962215 | A | G | 87 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.235+15212T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962215 | |||||||
| chr7:13962218 | T | C | 16 | a0001c0001t0001g0159 a0001c0001t0019g0152 a0001c0004t0001g0153 others(13): Show |
16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+15209A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962218 | |||||||
| chr7:13962248 | G | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15179C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962248 | |||||||
| chr7:13962418 | C | T | 57 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.235+15009G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962418 | |||||||
| chr7:13962432 | C | A | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+14995G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962432 | |||||||
| chr7:13962507 | C | T | 87 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.235+14920G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962507 | |||||||
| chr7:13962538 | C | A | 10 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0018g0314 others(7): Show |
10 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+14889G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962538 | |||||||
| chr7:13962604 | C | G | 1 | a0001c0003t0002g0072 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235+14823G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962604 | |||||||
| chr7:13962664 | A | G | 1 | a0001c0001t0011g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.235+14763T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962664 | |||||||
| chr7:13962923 | T | C | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+14504A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962923 | |||||||
| chr7:13963115 | C | G | 1 | a0002c0002t0018g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+14312G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963115 | |||||||
| chr7:13963181 | G | A | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+14246C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963181 | |||||||
| chr7:13963310 | G | A | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+14117C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963310 | |||||||
| chr7:13963480 | C | T | 83 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.235+13947G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963480 | |||||||
| chr7:13963522 | C | T | 10 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0018g0314 others(7): Show |
10 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+13905G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963522 | |||||||
| chr7:13963531 | CA | C | 85 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.235+13895delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963531 | |||||||
| chr7:13963578 | G | T | 17 | a0001c0001t0001g0159 a0001c0001t0002g0091 a0001c0001t0019g0152 others(14): Show |
17 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+13849C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963578 | |||||||
| chr7:13963593 | T | C | 2 | a0001c0001t0018g0314 a0002c0002t0007g0311 |
2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+13834A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963593 | |||||||
| chr7:13963634 | G | A | 15 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(12): Show |
15 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+13793C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963634 | |||||||
| chr7:13963692 | A | G | 1 | a0001c0001t0005g0245 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.235+13735T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963692 | |||||||
| chr7:13963702 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0002g0049 a0002c0002t0002g0109 others(1): Show |
4 | HG00735.hp1 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13725G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963702 | |||||||
| chr7:13963725 | A | T | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235+13702T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963725 | |||||||
| chr7:13963750 | G | C | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13677C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963750 | |||||||
| chr7:13963818 | G | A | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+13609C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963818 | |||||||
| chr7:13963874 | C | T | 1 | a0001c0001t0010g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.235+13553G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963874 | |||||||
| chr7:13963899 | C | T | 16 | a0001c0001t0001g0159 a0001c0001t0019g0152 a0001c0004t0001g0153 others(13): Show |
16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+13528G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963899 | |||||||
| chr7:13964104 | T | A | 1 | a0001c0001t0005g0233 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.235+13323A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964104 | |||||||
| chr7:13964167 | A | T | 16 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+13260T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964167 | |||||||
| chr7:13964181 | A | C | 1 | a0001c0001t0007g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.235+13246T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964181 | |||||||
| chr7:13964273 | T | C | 16 | a0001c0001t0004g0236 a0001c0001t0006g0300 a0001c0001t0006g0305 others(13): Show |
16 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+13154A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964273 | |||||||
| chr7:13964287 | T | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13140A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964287 | |||||||
| chr7:13964316 | C | T | 1 | a0002c0002t0012g0047 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.235+13111G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964316 | |||||||
| chr7:13964341 | C | G | 70 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(67): Show |
70 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.235+13086G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964341 | |||||||
| chr7:13964361 | G | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13066C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964361 | |||||||
| chr7:13964389 | T | C | 1 | a0001c0001t0003g0277 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.235+13038A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964389 | |||||||
| chr7:13964454 | C | T | 87 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.235+12973G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964454 | |||||||
| chr7:13964485 | G | T | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12942C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964485 | |||||||
| chr7:13964528 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0006g0089 |
2 | HG00735.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.235+12899C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964528 | |||||||
| chr7:13964537 | C | A | 16 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+12890G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964537 | |||||||
| chr7:13964613 | G | T | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12814C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964613 | |||||||
| chr7:13964678 | C | T | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12749G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964678 | |||||||
| chr7:13964705 | A | G | 10 | a0001c0001t0002g0038 a0001c0001t0009g0143 a0001c0001t0010g0044 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+12722T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964705 | |||||||
| chr7:13964716 | C | T | 1 | a0002c0002t0007g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+12711G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964716 | |||||||
| chr7:13964720 | A | T | 1 | a0001c0001t0021g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.235+12707T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964720 | |||||||
| chr7:13964722 | CTGGAATA others(17): Show |
C | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12681_235+1270 others(28): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964722 | |||||||
| chr7:13964747 | T | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12680A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964747 | |||||||
| chr7:13964749 | T | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12678A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964749 | |||||||
| chr7:13964750 | T | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12677A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964750 | |||||||
| chr7:13964768 | G | T | 1 | a0001c0001t0027g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.235+12659C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964768 | |||||||
| chr7:13964833 | C | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12594G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964833 | |||||||
| chr7:13964847 | T | C | 78 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.235+12580A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964847 | |||||||
| chr7:13965014 | G | A | 2 | a0002c0002t0001g0164 a0002c0002t0005g0272 |
2 | NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.235+12413C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965014 | |||||||
| chr7:13965019 | A | G | 2 | a0001c0001t0017g0023 a0002c0002t0033g0022 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+12408T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965019 | |||||||
| chr7:13965045 | C | T | 160 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.235+12382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965045 | |||||||
| chr7:13965085 | C | T | 159 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.235+12342G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965085 | |||||||
| chr7:13965183 | A | G | 2 | a0001c0001t0004g0137 a0001c0001t0014g0080 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+12244T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965183 | |||||||
| chr7:13965238 | A | C | 1 | a0001c0001t0030g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235+12189T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965238 | |||||||
| chr7:13965264 | A | G | 1 | a0002c0002t0010g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235+12163T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965264 | |||||||
| chr7:13965312 | C | T | 1 | a0001c0001t0008g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.235+12115G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965312 | |||||||
| chr7:13965459 | T | A | 1 | a0001c0001t0042g0301 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235+11968A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965459 | |||||||
| chr7:13965497 | T | C | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+11930A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965497 | |||||||
| chr7:13965597 | C | T | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+11830G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965597 | |||||||
| chr7:13965662 | A | G | 14 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0006g0309 others(11): Show |
14 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.235+11765T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965662 | |||||||
| chr7:13965701 | G | C | 18 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(15): Show |
18 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+11726C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965701 | |||||||
| chr7:13965980 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235+11447G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965980 | |||||||
| chr7:13966002 | A | C | 1 | a0001c0001t0002g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235+11425T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966002 | |||||||
| chr7:13966069 | T | A | 1 | a0001c0001t0003g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.235+11358A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966069 | |||||||
| chr7:13966163 | T | C | 4 | a0001c0001t0010g0037 a0001c0001t0010g0121 a0001c0001t0010g0122 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+11264A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966163 | |||||||
| chr7:13966285 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.235+11142G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966285 | |||||||
| chr7:13966392 | G | C | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+11035C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966392 | |||||||
| chr7:13966504 | C | T | 1 | a0001c0001t0004g0186 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.235+10923G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966504 | |||||||
| chr7:13966548 | A | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+10879T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966548 | |||||||
| chr7:13966604 | G | T | 158 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.235+10823C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966604 | |||||||
| chr7:13966630 | G | C | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+10797C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966630 | |||||||
| chr7:13966685 | T | C | 2 | a0001c0001t0018g0314 a0002c0002t0007g0311 |
2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+10742A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966685 | |||||||
| chr7:13966689 | A | C | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+10738T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966689 | |||||||
| chr7:13967008 | A | G | 3 | a0001c0001t0020g0250 a0001c0001t0028g0239 a0002c0002t0027g0240 |
3 | HG02258.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235+10419T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967008 | |||||||
| chr7:13967012 | G | A | 5 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0005g0260 others(2): Show |
5 | HG01099.hp1 HG01168.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+10415C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967012 | |||||||
| chr7:13967119 | T | C | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+10308A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967119 | |||||||
| chr7:13967235 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.235+10192A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967235 | |||||||
| chr7:13967270 | T | C | 69 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(66): Show |
69 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.235+10157A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967270 | |||||||
| chr7:13967636 | A | G | 1 | a0001c0001t0016g0266 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.235+9791T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967636 | |||||||
| chr7:13967677 | C | G | 234 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+9750G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967677 | |||||||
| chr7:13967694 | A | T | 2 | a0002c0002t0004g0168 a0002c0002t0007g0311 |
2 | HG03209.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.235+9733T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967694 | |||||||
| chr7:13967758 | T | TG | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+9668dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967758 | |||||||
| chr7:13968004 | T | C | 1 | a0001c0001t0019g0221 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.235+9423A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968004 | |||||||
| chr7:13968040 | T | C | 166 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.235+9387A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968040 | |||||||
| chr7:13968045 | C | T | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+9382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968045 | |||||||
| chr7:13968494 | T | G | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+8933A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968494 | |||||||
| chr7:13968621 | T | A | 1 | a0002c0002t0013g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+8806A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968621 | |||||||
| chr7:13968799 | A | C | 4 | a0001c0001t0010g0037 a0001c0001t0010g0121 a0001c0001t0010g0122 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8628T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968799 | |||||||
| chr7:13968841 | T | C | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8586A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968841 | |||||||
| chr7:13968954 | T | C | 161 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.235+8473A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968954 | |||||||
| chr7:13969001 | C | T | 160 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.235+8426G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969001 | |||||||
| chr7:13969031 | G | T | 2 | a0001c0001t0004g0137 a0001c0001t0014g0080 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+8396C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969031 | |||||||
| chr7:13969034 | C | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8393G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969034 | |||||||
| chr7:13969206 | A | C | 234 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+8221T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969206 | |||||||
| chr7:13969214 | T | C | 1 | a0001c0001t0030g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235+8213A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969214 | |||||||
| chr7:13969231 | T | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235+8196A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969231 | |||||||
| chr7:13969303 | A | G | 3 | a0001c0001t0020g0250 a0001c0001t0028g0239 a0002c0002t0027g0240 |
3 | HG02258.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235+8124T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969303 | |||||||
| chr7:13969305 | GAATA | G | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8118_235+8121d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969305 | |||||||
| chr7:13969377 | A | T | 41 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(38): Show |
41 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.235+8050T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969377 | |||||||
| chr7:13969391 | A | T | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+8036T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969391 | |||||||
| chr7:13969447 | A | G | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+7980T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969447 | |||||||
| chr7:13969512 | A | G | 12 | a0001c0001t0006g0298 a0001c0001t0006g0306 a0001c0001t0015g0134 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+7915T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969512 | |||||||
| chr7:13969557 | C | A | 2 | a0001c0001t0004g0137 a0001c0001t0014g0080 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+7870G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969557 | |||||||
| chr7:13969801 | A | C | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+7626T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969801 | |||||||
| chr7:13969825 | G | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235+7602C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969825 | |||||||
| chr7:13969956 | T | C | 18 | a0001c0001t0004g0236 a0001c0001t0006g0300 a0001c0001t0006g0305 others(15): Show |
18 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+7471A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969956 | |||||||
| chr7:13969968 | T | C | 2 | a0001c0001t0015g0136 a0001c0001t0020g0133 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.235+7459A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969968 | |||||||
| chr7:13970023 | G | A | 17 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(14): Show |
17 | HG00544.hp1 HG01978.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+7404C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970023 | |||||||
| chr7:13970100 | C | CA | 17 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(14): Show |
17 | HG00544.hp1 HG01978.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+7326dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970100 | |||||||
| chr7:13970116 | C | T | 1 | a0002c0002t0005g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.235+7311G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970116 | |||||||
| chr7:13970122 | G | A | 1 | a0001c0001t0013g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+7305C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970122 | |||||||
| chr7:13970153 | C | T | 16 | a0001c0001t0001g0159 a0001c0001t0019g0152 a0001c0004t0001g0153 others(13): Show |
16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+7274G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970153 | |||||||
| chr7:13970244 | G | A | 215 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.235+7183C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970244 | |||||||
| chr7:13970244 | G | C | 16 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+7183C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970244 | |||||||
| chr7:13970257 | T | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+7170A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970257 | |||||||
| chr7:13970262 | AAACACAC others(6): Show |
A | 1 | a0002c0002t0027g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.235+7152_235+7164d others(15): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970262 | |||||||
| chr7:13970262 | AAACACAC others(14): Show |
A | 1 | a0001c0001t0008g0193 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235+7144_235+7164d others(23): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970262 | |||||||
| chr7:13970263 | A | AAC | 19 | a0001c0001t0001g0200 a0001c0001t0001g0242 a0001c0001t0001g0255 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+7162_235+7163d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | A | AACAC | 3 | a0001c0001t0002g0281 a0001c0001t0012g0115 a0002c0002t0004g0141 |
3 | HG02165.hp1 HG02165.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.235+7160_235+7163d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | A | AACACAC | 6 | a0001c0001t0005g0173 a0001c0001t0040g0011 a0002c0002t0001g0203 others(3): Show |
6 | HG00544.hp2 HG01123.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+7158_235+7163d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | A | AACACACA others(1): Show |
3 | a0001c0001t0003g0276 a0001c0001t0012g0295 a0002c0002t0005g0150 |
3 | HG03834.hp2 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.235+7156_235+7163d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | A | AACACACA others(5): Show |
1 | a0002c0002t0008g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.235+7152_235+7163d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | A | C | 2 | a0002c0002t0001g0204 a0002c0002t0022g0001 |
2 | HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.235+7164T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AAC | A | 20 | a0001c0001t0001g0159 a0001c0001t0001g0251 a0001c0001t0003g0287 others(17): Show |
20 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.235+7162_235+7163d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACAC | A | 25 | a0001c0001t0001g0220 a0001c0001t0002g0024 a0001c0001t0003g0280 others(22): Show |
25 | HG00597.hp1 HG01993.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.235+7160_235+7163d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACAC | A | 16 | a0001c0001t0002g0026 a0001c0001t0003g0286 a0001c0001t0004g0261 others(13): Show |
16 | HG00544.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+7158_235+7163d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(1): Show |
A | 10 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0006g0300 others(7): Show |
10 | HG01070.hp1 HG02080.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+7156_235+7163d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(3): Show |
A | 3 | a0001c0001t0004g0236 a0001c0001t0017g0023 a0002c0002t0034g0312 |
3 | HG02886.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.235+7154_235+7163d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(5): Show |
A | 5 | a0001c0001t0006g0306 a0001c0001t0015g0134 a0001c0001t0015g0136 others(2): Show |
5 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+7152_235+7163d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(7): Show |
A | 2 | a0001c0001t0006g0298 a0001c0001t0007g0067 |
2 | HG00642.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.235+7150_235+7163d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(9): Show |
A | 6 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0010g0068 others(3): Show |
6 | HG00140.hp2 HG01071.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+7148_235+7163d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(11): Show |
A | 6 | a0001c0001t0002g0038 a0001c0001t0003g0056 a0001c0001t0004g0003 others(3): Show |
7 | HG02109.hp1 HG02976.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+7146_235+7163d others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(13): Show |
A | 40 | a0001c0001t0001g0222 a0001c0001t0002g0049 a0001c0001t0003g0051 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+7144_235+7163d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(15): Show |
A | 85 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(82): Show |
85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.235+7142_235+7163d others(24): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(17): Show |
A | 23 | a0001c0001t0004g0166 a0001c0001t0004g0181 a0001c0001t0004g0186 others(20): Show |
23 | HG00423.hp2 HG00621.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.235+7140_235+7163d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(19): Show |
A | 5 | a0001c0001t0011g0101 a0001c0001t0013g0098 a0001c0001t0054g0188 others(2): Show |
5 | HG00438.hp2 HG01346.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+7138_235+7163d others(28): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970263 | AACACACA others(23): Show |
A | 1 | a0001c0001t0046g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.235+7134_235+7163d others(32): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | |||||||
| chr7:13970265 | C | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235+7162G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970265 | |||||||
| chr7:13970267 | C | A | 2 | a0001c0001t0050g0142 a0002c0002t0013g0313 |
2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7160G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970267 | |||||||
| chr7:13970269 | C | A | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+7158G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970269 | |||||||
| chr7:13970271 | C | A | 3 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0002c0002t0013g0313 |
3 | HG02717.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235+7156G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970271 | |||||||
| chr7:13970273 | C | A | 3 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 |
3 | HG02717.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7154G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970273 | |||||||
| chr7:13970275 | C | A | 1 | a0002c0002t0013g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+7152G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970275 | |||||||
| chr7:13970277 | C | A | 2 | a0001c0001t0004g0137 a0001c0001t0014g0080 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+7150G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970277 | |||||||
| chr7:13970305 | C | G | 3 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 |
3 | HG02717.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7122G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970305 | |||||||
| chr7:13970305 | CACACACA others(14): Show |
C | 1 | a0001c0001t0003g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.235+7101_235+7121d others(23): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970305 | |||||||
| chr7:13970307 | C | G | 1 | a0002c0002t0013g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+7120G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970307 | |||||||
| chr7:13970311 | CACACACA others(8): Show |
C | 1 | a0001c0001t0006g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.235+7101_235+7115d others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970311 | |||||||
| chr7:13970315 | CACACACA others(4): Show |
C | 1 | a0002c0002t0007g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+7101_235+7111d others(13): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970315 | |||||||
| chr7:13970327 | A | C | 4 | a0001c0001t0004g0137 a0001c0001t0014g0080 a0001c0001t0050g0142 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+7100T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970327 | |||||||
| chr7:13970366 | A | G | 8 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(5): Show |
8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+7061T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970366 | |||||||
| chr7:13970812 | C | T | 1 | a0002c0002t0009g0194 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.235+6615G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970812 | |||||||
| chr7:13970821 | G | A | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.235+6606C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970821 | |||||||
| chr7:13970879 | G | A | 158 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.235+6548C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970879 | |||||||
| chr7:13971026 | C | T | 2 | a0001c0001t0017g0023 a0002c0002t0033g0022 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+6401G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971026 | |||||||
| chr7:13971045 | C | T | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.235+6382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971045 | |||||||
| chr7:13971048 | G | A | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+6379C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971048 | |||||||
| chr7:13971057 | T | C | 2 | a0001c0001t0010g0083 a0001c0001t0045g0111 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.235+6370A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971057 | |||||||
| chr7:13971076 | A | G | 2 | a0001c0001t0017g0023 a0002c0002t0033g0022 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+6351T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971076 | |||||||
| chr7:13971120 | C | T | 211 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.235+6307G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971120 | |||||||
| chr7:13971160 | G | A | 40 | a0001c0001t0001g0222 a0001c0001t0002g0012 a0001c0001t0002g0013 others(37): Show |
41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.235+6267C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971160 | |||||||
| chr7:13971167 | C | T | 4 | a0001c0001t0038g0304 a0002c0002t0013g0302 a0002c0002t0013g0303 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+6260G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971167 | |||||||
| chr7:13971183 | C | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+6244G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971183 | |||||||
| chr7:13971251 | G | A | 1 | a0002c0002t0001g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235+6176C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971251 | |||||||
| chr7:13971264 | C | A | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.235+6163G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971264 | |||||||
| chr7:13971413 | T | G | 16 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0280 others(13): Show |
16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+6014A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971413 | |||||||
| chr7:13971423 | T | G | 235 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(232): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.235+6004A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971423 | |||||||
| chr7:13971503 | T | C | 15 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(12): Show |
15 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+5924A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971503 | |||||||
| chr7:13971642 | C | T | 1 | a0001c0001t0007g0315 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+5785G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971642 | |||||||
| chr7:13971780 | C | T | 1 | a0001c0001t0006g0089 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.235+5647G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971780 | |||||||
| chr7:13971825 | T | C | 17 | a0001c0001t0004g0236 a0001c0001t0006g0300 a0001c0001t0006g0305 others(14): Show |
17 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+5602A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971825 | |||||||
| chr7:13971870 | G | A | 13 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0006g0309 others(10): Show |
13 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+5557C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971870 | |||||||
| chr7:13972046 | G | T | 234 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+5381C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972046 | |||||||
| chr7:13972064 | C | T | 17 | a0001c0001t0004g0236 a0001c0001t0006g0300 a0001c0001t0006g0305 others(14): Show |
17 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+5363G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972064 | |||||||
| chr7:13972085 | G | A | 234 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+5342C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972085 | |||||||
| chr7:13972186 | T | A | 1 | a0002c0002t0004g0223 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.235+5241A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972186 | |||||||
| chr7:13972189 | T | C | 1 | a0001c0001t0010g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.235+5238A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972189 | |||||||
| chr7:13972208 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+5219G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972208 | |||||||
| chr7:13972288 | C | T | 1 | a0001c0001t0018g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.235+5139G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972288 | |||||||
| chr7:13972469 | T | C | 6 | a0001c0001t0015g0132 a0001c0001t0015g0139 a0001c0001t0021g0140 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+4958A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972469 | |||||||
| chr7:13972534 | A | T | 11 | a0001c0001t0002g0034 a0001c0001t0006g0298 a0001c0001t0006g0306 others(8): Show |
11 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+4893T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972534 | |||||||
| chr7:13972551 | C | A | 223 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235+4876G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972551 | |||||||
| chr7:13972635 | A | G | 2 | a0001c0001t0012g0295 a0001c0001t0012g0296 |
2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.235+4792T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972635 | |||||||
| chr7:13972738 | T | C | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.235+4689A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972738 | |||||||
| chr7:13972867 | C | T | 1 | a0002c0002t0004g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.235+4560G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972867 | |||||||
| chr7:13973015 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.235+4412T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973015 | |||||||
| chr7:13973129 | A | C | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+4298T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973129 | |||||||
| chr7:13973261 | T | C | 8 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0065 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+4166A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973261 | |||||||
| chr7:13973300 | T | A | 2 | a0001c0001t0015g0136 a0001c0001t0020g0133 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.235+4127A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973300 | |||||||
| chr7:13973374 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+4053A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973374 | |||||||
| chr7:13973404 | G | A | 32 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(29): Show |
32 | HG00544.hp1 HG01070.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.235+4023C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973404 | |||||||
| chr7:13973436 | T | C | 10 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3991A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973436 | |||||||
| chr7:13973560 | G | C | 21 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(18): Show |
21 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.235+3867C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973560 | |||||||
| chr7:13973594 | A | G | 233 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.235+3833T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973594 | |||||||
| chr7:13973644 | C | CT | 28 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(25): Show |
28 | HG00544.hp1 HG01070.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.235+3782dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973644 | |||||||
| chr7:13973703 | A | T | 223 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235+3724T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973703 | |||||||
| chr7:13973827 | G | A | 234 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+3600C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973827 | |||||||
| chr7:13973855 | G | A | 3 | a0002c0002t0009g0225 a0002c0002t0009g0226 a0002c0002t0012g0033 |
3 | HG01070.hp2 HG01071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.235+3572C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973855 | |||||||
| chr7:13973873 | T | A | 2 | a0001c0001t0003g0019 a0001c0001t0009g0227 |
2 | HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.235+3554A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973873 | |||||||
| chr7:13973895 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.235+3532C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973895 | |||||||
| chr7:13973979 | C | T | 232 | a0001c0001t0001g0167 a0001c0001t0001g0182 a0001c0001t0001g0183 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.235+3448G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973979 | |||||||
| chr7:13974009 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.235+3418G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974009 | |||||||
| chr7:13974074 | T | C | 1 | a0001c0001t0023g0008 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.235+3353A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974074 | |||||||
| chr7:13974186 | C | T | 2 | a0001c0001t0004g0261 a0002c0002t0018g0297 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+3241G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974186 | |||||||
| chr7:13974366 | G | A | 1 | a0001c0001t0006g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+3061C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974366 | |||||||
| chr7:13974381 | G | C | 26 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(23): Show |
26 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+3046C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974381 | |||||||
| chr7:13974428 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+2999A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974428 | |||||||
| chr7:13974474 | G | C | 2 | a0001c0001t0028g0239 a0002c0002t0027g0240 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.235+2953C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974474 | |||||||
| chr7:13974729 | G | C | 7 | a0001c0001t0004g0236 a0001c0001t0009g0143 a0001c0001t0015g0136 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+2698C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974729 | |||||||
| chr7:13974735 | G | A | 4 | a0001c0001t0003g0277 a0001c0001t0003g0279 a0001c0001t0006g0278 others(1): Show |
4 | NA18944.hp1 NA18949.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+2692C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974735 | |||||||
| chr7:13974738 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0006g0035 a0001c0001t0020g0237 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+2689C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974738 | |||||||
| chr7:13974809 | G | A | 1 | a0002c0002t0034g0312 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.235+2618C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974809 | |||||||
| chr7:13974843 | C | T | 1 | a0001c0001t0028g0239 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+2584G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974843 | |||||||
| chr7:13974964 | G | C | 2 | a0001c0001t0004g0137 a0001c0001t0015g0138 |
2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.235+2463C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974964 | |||||||
| chr7:13975135 | C | T | 4 | a0001c0001t0015g0136 a0001c0001t0017g0023 a0001c0001t0020g0133 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+2292G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975135 | |||||||
| chr7:13975145 | A | G | 2 | a0001c0001t0028g0239 a0002c0002t0027g0240 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.235+2282T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975145 | |||||||
| chr7:13975155 | C | T | 7 | a0001c0001t0006g0306 a0001c0001t0007g0315 a0001c0001t0018g0314 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2272G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975155 | |||||||
| chr7:13975197 | G | T | 1 | a0001c0001t0020g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.235+2230C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975197 | |||||||
| chr7:13975223 | A | C | 1 | a0001c0001t0007g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.235+2204T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975223 | |||||||
| chr7:13975240 | A | T | 1 | a0001c0001t0013g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+2187T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975240 | |||||||
| chr7:13975252 | T | C | 3 | a0001c0001t0004g0261 a0001c0001t0046g0071 a0002c0002t0018g0297 |
3 | HG03195.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+2175A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975252 | |||||||
| chr7:13975291 | G | A | 17 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(14): Show |
17 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+2136C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975291 | |||||||
| chr7:13975328 | C | T | 1 | a0001c0001t0006g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+2099G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975328 | |||||||
| chr7:13975343 | G | A | 1 | a0002c0002t0001g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.235+2084C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975343 | |||||||
| chr7:13975357 | C | T | 1 | a0001c0001t0020g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.235+2070G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975357 | |||||||
| chr7:13975386 | A | G | 1 | a0002c0002t0018g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+2041T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975386 | |||||||
| chr7:13975442 | A | AGGCTGAG others(10): Show |
16 | a0001c0001t0001g0159 a0001c0001t0004g0181 a0001c0001t0019g0152 others(13): Show |
16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+1968_235+1984d others(19): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975442 | |||||||
| chr7:13975442 | AGGCTGAG others(10): Show |
A | 1 | a0001c0001t0025g0307 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235+1968_235+1984d others(19): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975442 | |||||||
| chr7:13975521 | C | G | 1 | a0002c0002t0004g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.235+1906G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975521 | |||||||
| chr7:13975562 | C | CA | 8 | a0001c0001t0004g0236 a0001c0001t0006g0298 a0001c0001t0009g0227 others(5): Show |
8 | HG01884.hp2 HG02080.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+1864dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975562 | |||||||
| chr7:13975562 | C | CAAAA | 12 | a0001c0001t0002g0024 a0001c0001t0003g0280 a0001c0001t0003g0288 others(9): Show |
12 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+1861_235+1864d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975562 | |||||||
| chr7:13975580 | G | A | 3 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0287 |
3 | NA18965.hp2 NA18967.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.235+1847C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975580 | |||||||
| chr7:13975590 | G | GA | 146 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(143): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.235+1836dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975590 | |||||||
| chr7:13975601 | A | G | 4 | a0001c0001t0038g0304 a0002c0002t0013g0302 a0002c0002t0013g0303 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+1826T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975601 | |||||||
| chr7:13975613 | G | C | 1 | a0001c0005t0010g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.235+1814C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975613 | |||||||
| chr7:13975634 | A | G | 21 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(18): Show |
21 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.235+1793T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975634 | |||||||
| chr7:13975688 | A | G | 3 | a0001c0001t0015g0132 a0001c0001t0021g0263 a0001c0001t0021g0264 |
3 | HG01891.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.235+1739T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975688 | |||||||
| chr7:13975693 | T | A | 205 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(202): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.235+1734A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975693 | |||||||
| chr7:13975910 | T | A | 1 | a0001c0001t0028g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235+1517A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975910 | |||||||
| chr7:13975968 | A | G | 2 | a0001c0001t0009g0143 a0001c0001t0020g0237 |
2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.235+1459T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975968 | |||||||
| chr7:13975982 | C | A | 20 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(17): Show |
20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+1445G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975982 | |||||||
| chr7:13976150 | A | G | 2 | a0001c0001t0004g0179 a0001c0001t0009g0002 |
3 | HG02602.hp2 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.235+1277T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976150 | |||||||
| chr7:13976419 | A | G | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235+1008T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976419 | |||||||
| chr7:13976468 | C | T | 1 | a0001c0001t0013g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+959G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976468 | |||||||
| chr7:13976485 | A | G | 1 | a0001c0001t0004g0177 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.235+942T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976485 | |||||||
| chr7:13976548 | C | T | 24 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.235+879G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976548 | |||||||
| chr7:13976554 | T | C | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+873A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976554 | |||||||
| chr7:13977039 | A | G | 35 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(32): Show |
35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+388T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977039 | |||||||
| chr7:13977045 | C | T | 35 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(32): Show |
35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977045 | |||||||
| chr7:13977124 | T | A | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+303A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977124 | |||||||
| chr7:13977223 | T | C | 1 | a0002c0002t0010g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235+204A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977223 | |||||||
| chr7:13977314 | T | C | 167 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(164): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.235+113A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977314 | |||||||
| chr7:13977382 | C | T | 166 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(163): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.235+45G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977382 | |||||||
| chr7:13977383 | C | G | 166 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(163): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.235+44G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977383 | |||||||
| chr7:13977501 | T | TA | 166 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(163): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.182-22dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977501 | |||||||
| chr7:13977612 | C | A | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182-132G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977612 | |||||||
| chr7:13977671 | T | C | 1 | a0001c0001t0005g0230 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.182-191A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977671 | |||||||
| chr7:13977728 | C | T | 16 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0279 others(13): Show |
16 | HG00544.hp2 HG02015.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.182-248G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977728 | |||||||
| chr7:13977780 | T | C | 15 | a0001c0001t0001g0159 a0001c0001t0019g0152 a0001c0004t0001g0153 others(12): Show |
15 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-300A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977780 | |||||||
| chr7:13978047 | T | G | 9 | a0001c0001t0004g0236 a0001c0001t0004g0261 a0001c0001t0009g0143 others(6): Show |
9 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-567A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978047 | |||||||
| chr7:13978177 | A | C | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182-697T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978177 | |||||||
| chr7:13978202 | T | G | 1 | a0001c0001t0007g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.182-722A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978202 | |||||||
| chr7:13978331 | A | G | 1 | a0001c0001t0011g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.182-851T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978331 | |||||||
| chr7:13978334 | G | A | 5 | a0001c0001t0004g0236 a0001c0001t0004g0261 a0001c0001t0009g0143 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-854C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978334 | |||||||
| chr7:13978385 | A | G | 1 | a0001c0001t0020g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.182-905T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978385 | |||||||
| chr7:13978398 | AAC | A | 222 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(219): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.182-920_182-919del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978398 | |||||||
| chr7:13978418 | C | T | 1 | a0001c0001t0012g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.182-938G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978418 | |||||||
| chr7:13978519 | C | T | 175 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(172): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.182-1039G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978519 | |||||||
| chr7:13978531 | G | A | 131 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(128): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.182-1051C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978531 | |||||||
| chr7:13978576 | C | T | 199 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(196): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.182-1096G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978576 | |||||||
| chr7:13978625 | T | A | 15 | a0001c0001t0001g0159 a0001c0001t0019g0152 a0001c0004t0001g0153 others(12): Show |
15 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-1145A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978625 | |||||||
| chr7:13978735 | G | T | 171 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(168): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.182-1255C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978735 | |||||||
| chr7:13978807 | A | G | 2 | a0001c0001t0028g0239 a0002c0002t0027g0240 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.182-1327T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978807 | |||||||
| chr7:13978840 | G | T | 1 | a0001c0001t0006g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.182-1360C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978840 | |||||||
| chr7:13978869 | C | T | 199 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(196): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.182-1389G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978869 | |||||||
| chr7:13978918 | C | T | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.182-1438G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978918 | |||||||
| chr7:13978951 | C | A | 3 | a0001c0001t0004g0236 a0001c0001t0051g0235 a0002c0002t0018g0297 |
3 | HG02723.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.182-1471G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978951 | |||||||
| chr7:13978974 | C | G | 1 | a0001c0001t0002g0085 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.182-1494G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978974 | |||||||
| chr7:13979014 | G | T | 7 | a0001c0001t0006g0306 a0001c0001t0007g0315 a0001c0001t0018g0314 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-1534C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979014 | |||||||
| chr7:13979018 | A | T | 20 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(17): Show |
20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-1538T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979018 | |||||||
| chr7:13979032 | G | A | 5 | a0001c0001t0004g0236 a0001c0001t0004g0261 a0001c0001t0009g0143 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-1552C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979032 | |||||||
| chr7:13979051 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.182-1571T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979051 | |||||||
| chr7:13979098 | A | C | 4 | a0001c0001t0015g0132 a0001c0001t0021g0263 a0001c0001t0021g0264 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1618T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979098 | |||||||
| chr7:13979120 | G | A | 2 | a0001c0001t0004g0261 a0001c0001t0009g0143 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.182-1640C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979120 | |||||||
| chr7:13979237 | C | T | 7 | a0001c0001t0006g0306 a0001c0001t0007g0315 a0001c0001t0018g0314 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-1757G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979237 | |||||||
| chr7:13979276 | C | A | 24 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(21): Show |
24 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.182-1796G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979276 | |||||||
| chr7:13979317 | T | C | 3 | a0002c0002t0001g0231 a0002c0002t0001g0232 a0002c0002t0029g0163 |
3 | HG01109.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.182-1837A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979317 | |||||||
| chr7:13979498 | G | A | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.182-2018C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979498 | |||||||
| chr7:13979500 | AG | A | 20 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(17): Show |
20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-2021delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979500 | |||||||
| chr7:13979617 | A | G | 211 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(208): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.182-2137T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979617 | |||||||
| chr7:13979649 | A | T | 3 | a0001c0001t0004g0236 a0001c0001t0051g0235 a0002c0002t0018g0297 |
3 | HG02723.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.182-2169T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979649 | |||||||
| chr7:13979785 | A | C | 2 | a0002c0002t0003g0119 a0002c0002t0003g0120 |
2 | NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.182-2305T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979785 | |||||||
| chr7:13979823 | T | C | 165 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(162): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.182-2343A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979823 | |||||||
| chr7:13979915 | G | T | 158 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.182-2435C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979915 | |||||||
| chr7:13980052 | T | G | 2 | a0001c0001t0015g0139 a0001c0001t0021g0140 |
2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.182-2572A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980052 | |||||||
| chr7:13980110 | A | T | 1 | a0001c0001t0020g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.182-2630T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980110 | |||||||
| chr7:13980190 | C | G | 8 | a0001c0001t0004g0137 a0001c0001t0015g0134 a0001c0001t0015g0136 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.182-2710G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980190 | |||||||
| chr7:13980415 | A | C | 2 | a0001c0001t0004g0166 a0001c0001t0016g0165 |
2 | NA18948.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.182-2935T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980415 | |||||||
| chr7:13980557 | G | A | 1 | a0001c0001t0007g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.182-3077C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980557 | |||||||
| chr7:13980658 | C | T | 1 | a0001c0001t0039g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.182-3178G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980658 | |||||||
| chr7:13980679 | C | T | 23 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-3199G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980679 | |||||||
| chr7:13980695 | G | T | 1 | a0001c0001t0020g0237 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.182-3215C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980695 | |||||||
| chr7:13980804 | C | T | 10 | a0001c0001t0006g0306 a0001c0001t0006g0309 a0001c0001t0007g0315 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-3324G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980804 | |||||||
| chr7:13980907 | T | G | 1 | a0001c0001t0051g0235 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-3427A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980907 | |||||||
| chr7:13980951 | GC | G | 23 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-3472delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980951 | |||||||
| chr7:13981018 | G | A | 3 | a0001c0001t0002g0117 a0001c0001t0006g0130 a0002c0002t0007g0118 |
3 | HG02074.hp1 NA18964.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.182-3538C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981018 | |||||||
| chr7:13981061 | T | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(157): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.182-3581A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981061 | |||||||
| chr7:13981137 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.182-3657G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981137 | |||||||
| chr7:13981138 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.182-3658T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981138 | |||||||
| chr7:13981182 | C | T | 1 | a0001c0001t0016g0266 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.182-3702G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981182 | |||||||
| chr7:13981225 | T | C | 3 | a0002c0002t0003g0079 a0002c0002t0003g0119 a0002c0002t0003g0120 |
3 | NA18983.hp2 NA19078.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.182-3745A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981225 | |||||||
| chr7:13981470 | G | A | 130 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(127): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.182-3990C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981470 | |||||||
| chr7:13981496 | C | G | 169 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4016G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981496 | |||||||
| chr7:13981501 | TTACA | T | 29 | a0001c0001t0001g0242 a0001c0001t0004g0137 a0001c0001t0004g0236 others(26): Show |
29 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.182-4025_182-4022d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981501 | |||||||
| chr7:13981501 | TTACATAC others(5): Show |
T | 4 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0279 others(1): Show |
4 | NA18944.hp1 NA18949.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4033_182-4022d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981501 | |||||||
| chr7:13981532 | C | CATACAT | 16 | a0001c0001t0003g0280 a0001c0001t0003g0285 a0001c0001t0003g0286 others(13): Show |
16 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-4053_182-4052i others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981532 | |||||||
| chr7:13981532 | C | T | 16 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0279 others(13): Show |
16 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-4052G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981532 | |||||||
| chr7:13981536 | T | C | 1 | a0001c0001t0006g0298 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.182-4056A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981536 | |||||||
| chr7:13981544 | T | C | 25 | a0001c0001t0002g0024 a0001c0001t0003g0276 a0001c0001t0003g0277 others(22): Show |
25 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.182-4064A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | |||||||
| chr7:13981544 | T | TAC | 5 | a0001c0001t0038g0304 a0001c0003t0002g0072 a0002c0002t0013g0302 others(2): Show |
5 | HG00280.hp2 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-4066_182-4065d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | |||||||
| chr7:13981544 | T | TATAC | 128 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.182-4065_182-4064i others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | |||||||
| chr7:13981708 | T | G | 169 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4228A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981708 | |||||||
| chr7:13981709 | T | C | 169 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4229A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981709 | |||||||
| chr7:13981732 | A | G | 6 | a0001c0001t0006g0306 a0001c0001t0007g0315 a0001c0001t0018g0314 others(3): Show |
6 | HG02280.hp2 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-4252T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981732 | |||||||
| chr7:13981926 | G | A | 4 | a0001c0001t0006g0309 a0001c0001t0025g0307 a0002c0002t0006g0078 others(1): Show |
4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4446C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981926 | |||||||
| chr7:13982061 | C | A | 1 | a0001c0001t0035g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.181+4577G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982061 | |||||||
| chr7:13982061 | C | T | 158 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(155): Show |
158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.181+4577G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982061 | |||||||
| chr7:13982236 | CTCTAATG others(9): Show |
C | 1 | a0001c0001t0011g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.181+4386_181+4401d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982236 | |||||||
| chr7:13982318 | C | T | 2 | a0001c0001t0020g0237 a0001c0001t0050g0142 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+4320G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982318 | |||||||
| chr7:13982438 | T | A | 1 | a0001c0001t0004g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.181+4200A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982438 | |||||||
| chr7:13982439 | A | T | 7 | a0001c0001t0010g0083 a0001c0001t0015g0132 a0001c0001t0021g0263 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+4199T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982439 | |||||||
| chr7:13982590 | C | A | 8 | a0001c0001t0004g0137 a0001c0001t0015g0134 a0001c0001t0015g0136 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+4048G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982590 | |||||||
| chr7:13982667 | G | C | 2 | a0001c0001t0020g0237 a0001c0001t0050g0142 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+3971C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982667 | |||||||
| chr7:13982736 | T | C | 1 | a0001c0001t0043g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.181+3902A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982736 | |||||||
| chr7:13982740 | G | A | 151 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(148): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.181+3898C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982740 | |||||||
| chr7:13982749 | G | A | 2 | a0001c0001t0020g0237 a0001c0001t0050g0142 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+3889C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982749 | |||||||
| chr7:13982819 | A | G | 169 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+3819T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982819 | |||||||
| chr7:13982886 | T | C | 1 | a0001c0001t0056g0259 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181+3752A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982886 | |||||||
| chr7:13982893 | T | C | 1 | a0001c0001t0007g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.181+3745A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982893 | |||||||
| chr7:13982897 | A | G | 169 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+3741T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982897 | |||||||
| chr7:13983081 | GGTTGTT | G | 4 | a0001c0001t0004g0236 a0001c0001t0004g0261 a0001c0001t0009g0143 others(1): Show |
4 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+3551_181+3556d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983081 | |||||||
| chr7:13983231 | A | G | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.181+3407T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983231 | |||||||
| chr7:13983267 | A | C | 1 | a0001c0001t0004g0265 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.181+3371T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983267 | |||||||
| chr7:13983297 | A | C | 8 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(5): Show |
8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+3341T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983297 | |||||||
| chr7:13983305 | T | G | 1 | a0001c0001t0003g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.181+3333A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983305 | |||||||
| chr7:13983398 | T | G | 1 | a0001c0001t0004g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.181+3240A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983398 | |||||||
| chr7:13983435 | G | A | 1 | a0001c0001t0024g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.181+3203C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983435 | |||||||
| chr7:13983617 | C | T | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.181+3021G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983617 | |||||||
| chr7:13983618 | T | C | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+3020A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983618 | |||||||
| chr7:13983621 | C | CT | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+3016dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983621 | |||||||
| chr7:13983666 | G | T | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2972C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983666 | |||||||
| chr7:13983681 | A | G | 3 | a0001c0001t0002g0082 a0001c0001t0011g0081 a0001c0001t0030g0004 |
3 | HG01167.hp2 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181+2957T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983681 | |||||||
| chr7:13983714 | T | TA | 169 | a0001c0001t0002g0012 a0001c0001t0002g0014 a0001c0001t0002g0015 others(166): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+2923dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983714 | |||||||
| chr7:13983823 | G | T | 1 | a0002c0002t0004g0241 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.181+2815C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983823 | |||||||
| chr7:13983833 | A | C | 3 | a0001c0001t0028g0238 a0001c0001t0028g0239 a0002c0002t0027g0240 |
3 | HG02258.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.181+2805T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983833 | |||||||
| chr7:13983837 | A | G | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2801T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983837 | |||||||
| chr7:13983863 | C | G | 8 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(5): Show |
8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2775G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983863 | |||||||
| chr7:13983881 | T | C | 1 | a0002c0002t0002g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.181+2757A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983881 | |||||||
| chr7:13983899 | C | T | 10 | a0001c0001t0006g0306 a0001c0001t0006g0309 a0001c0001t0007g0315 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+2739G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983899 | |||||||
| chr7:13983924 | C | G | 8 | a0001c0001t0006g0300 a0001c0001t0006g0305 a0001c0001t0010g0299 others(5): Show |
8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2714G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983924 | |||||||
| chr7:13983987 | T | C | 10 | a0001c0001t0006g0306 a0001c0001t0006g0309 a0001c0001t0007g0315 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+2651A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983987 | |||||||
| chr7:13984024 | A | C | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2614T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984024 | |||||||
| chr7:13984182 | C | G | 228 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0243 others(225): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.181+2456G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984182 | |||||||
| chr7:13984197 | A | G | 1 | a0002c0002t0003g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.181+2441T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984197 | |||||||
| chr7:13984290 | C | T | 1 | a0001c0001t0008g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.181+2348G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984290 | |||||||
| chr7:13984378 | G | C | 2 | a0001c0001t0015g0134 a0001c0001t0058g0135 |
2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.181+2260C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984378 | |||||||
| chr7:13984487 | G | A | 23 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.181+2151C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984487 | |||||||
| chr7:13984523 | C | G | 2 | a0001c0001t0020g0237 a0001c0001t0050g0142 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+2115G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984523 | |||||||
| chr7:13984548 | G | A | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2090C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984548 | |||||||
| chr7:13984606 | C | T | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2032G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984606 | |||||||
| chr7:13984755 | C | T | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1883G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984755 | |||||||
| chr7:13984771 | A | T | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1867T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984771 | |||||||
| chr7:13984917 | T | TCAA | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1720_181+1721i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984917 | |||||||
| chr7:13984921 | T | TTA | 3 | a0001c0001t0006g0309 a0002c0002t0006g0078 a0002c0002t0014g0308 |
3 | HG02723.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.181+1716_181+1717i others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984921 | |||||||
| chr7:13984922 | C | A | 4 | a0001c0001t0006g0309 a0001c0001t0025g0307 a0002c0002t0006g0078 others(1): Show |
4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1716G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984922 | |||||||
| chr7:13984922 | C | T | 164 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.181+1716G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984922 | |||||||
| chr7:13984926 | AGT | A | 157 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(154): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.181+1710_181+1711d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984926 | |||||||
| chr7:13984926 | AGTT | A | 7 | a0001c0001t0006g0306 a0001c0001t0007g0315 a0001c0001t0010g0126 others(4): Show |
7 | HG02280.hp2 HG03209.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+1709_181+1711d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984926 | |||||||
| chr7:13984927 | G | A | 4 | a0001c0001t0006g0309 a0001c0001t0025g0307 a0002c0002t0006g0078 others(1): Show |
4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1711C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984927 | |||||||
| chr7:13984928 | T | A | 4 | a0001c0001t0006g0309 a0001c0001t0025g0307 a0002c0002t0006g0078 others(1): Show |
4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1710A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984928 | |||||||
| chr7:13984929 | T | A | 161 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(158): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.181+1709A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984929 | |||||||
| chr7:13984964 | AAG | A | 5 | a0001c0001t0004g0137 a0001c0001t0015g0136 a0001c0001t0015g0138 others(2): Show |
5 | HG01081.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+1672_181+1673d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984964 | |||||||
| chr7:13984999 | A | G | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.181+1639T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984999 | |||||||
| chr7:13985242 | G | A | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1396C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985242 | |||||||
| chr7:13985252 | A | G | 1 | a0002c0002t0018g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.181+1386T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985252 | |||||||
| chr7:13985260 | T | A | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.181+1378A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985260 | |||||||
| chr7:13985455 | A | G | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.181+1183T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985455 | |||||||
| chr7:13985528 | A | AT | 4 | a0001c0001t0002g0012 a0001c0001t0002g0027 a0001c0001t0024g0028 others(1): Show |
4 | HG01175.hp2 HG01192.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+1109dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985528 | |||||||
| chr7:13985536 | C | T | 10 | a0001c0001t0006g0306 a0001c0001t0006g0309 a0001c0001t0007g0315 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+1102G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985536 | |||||||
| chr7:13985597 | C | T | 2 | a0001c0001t0012g0295 a0001c0001t0012g0296 |
2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.181+1041G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985597 | |||||||
| chr7:13985599 | C | A | 2 | a0001c0001t0012g0295 a0001c0001t0012g0296 |
2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.181+1039G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985599 | |||||||
| chr7:13985692 | A | G | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+946T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985692 | |||||||
| chr7:13985721 | C | G | 2 | a0001c0001t0017g0023 a0002c0002t0033g0022 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.181+917G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985721 | |||||||
| chr7:13985744 | T | C | 139 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(136): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.181+894A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985744 | |||||||
| chr7:13985786 | T | G | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+852A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985786 | |||||||
| chr7:13985819 | G | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0027 a0001c0001t0003g0030 others(4): Show |
7 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+819C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985819 | |||||||
| chr7:13985849 | A | G | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+789T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985849 | |||||||
| chr7:13985857 | C | T | 6 | a0001c0001t0015g0132 a0001c0001t0021g0263 a0001c0001t0021g0264 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+781G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985857 | |||||||
| chr7:13985892 | A | G | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.181+746T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985892 | |||||||
| chr7:13985903 | C | A | 22 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(19): Show |
22 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+735G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985903 | |||||||
| chr7:13986015 | G | A | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.181+623C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986015 | |||||||
| chr7:13986054 | T | A | 3 | a0001c0001t0015g0132 a0001c0001t0021g0263 a0001c0001t0021g0264 |
3 | HG01891.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.181+584A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986054 | |||||||
| chr7:13986065 | T | C | 1 | a0002c0002t0008g0262 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.181+573A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986065 | |||||||
| chr7:13986094 | T | A | 8 | a0001c0001t0004g0137 a0001c0001t0015g0134 a0001c0001t0015g0136 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+544A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986094 | |||||||
| chr7:13986102 | C | T | 167 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(164): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.181+536G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986102 | |||||||
| chr7:13986141 | T | A | 168 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(165): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+497A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986141 | |||||||
| chr7:13986282 | C | T | 2 | a0002c0002t0004g0144 a0002c0002t0005g0145 |
2 | NA18978.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.181+356G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986282 | |||||||
| chr7:13986583 | T | C | 1 | a0002c0002t0005g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.181+55A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986583 | |||||||
| chr7:13986732 | A | G | 213 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(210): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.134-47T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986732 | |||||||
| chr7:13986738 | A | G | 1 | a0001c0001t0028g0238 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.134-53T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986738 | |||||||
| chr7:13986775 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-90A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986775 | |||||||
| chr7:13986813 | TA | T | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-129delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986813 | |||||||
| chr7:13987059 | G | C | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.134-374C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987059 | |||||||
| chr7:13987112 | A | G | 163 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(160): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.134-427T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987112 | |||||||
| chr7:13987148 | GTAT | G | 9 | a0001c0001t0006g0306 a0001c0001t0006g0309 a0001c0001t0007g0315 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-466_134-464del others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987148 | |||||||
| chr7:13987177 | A | C | 55 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0026 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-492T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987177 | |||||||
| chr7:13987190 | C | T | 1 | a0001c0001t0014g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.134-505G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987190 | |||||||
| chr7:13987204 | G | C | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-519C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987204 | |||||||
| chr7:13987248 | G | A | 4 | a0001c0001t0010g0126 a0001c0001t0011g0128 a0001c0001t0011g0129 others(1): Show |
4 | HG01123.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-563C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987248 | |||||||
| chr7:13987302 | G | A | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-617C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987302 | |||||||
| chr7:13987315 | A | G | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-630T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987315 | |||||||
| chr7:13987333 | G | A | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-648C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987333 | |||||||
| chr7:13987413 | T | C | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.133+673A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987413 | |||||||
| chr7:13987418 | T | G | 170 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(167): Show |
170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.133+668A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987418 | |||||||
| chr7:13987458 | G | A | 131 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(128): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.133+628C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987458 | |||||||
| chr7:13987494 | G | T | 1 | a0001c0001t0006g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133+592C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987494 | |||||||
| chr7:13987553 | T | C | 131 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(128): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.133+533A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987553 | |||||||
| chr7:13987734 | A | G | 2 | a0001c0001t0017g0023 a0002c0002t0033g0022 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.133+352T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987734 | |||||||
| chr7:13987852 | G | A | 171 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(168): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.133+234C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987852 | |||||||
| chr7:13987932 | G | A | 213 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(210): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.133+154C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987932 | |||||||
| chr7:13988242 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.46-69C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988242 | |||||||
| chr7:13988242 | G | GCA | 159 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(156): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.46-71_46-70dupTG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988242 | |||||||
| chr7:13988366 | T | C | 172 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(169): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.46-193A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988366 | |||||||
| chr7:13988422 | C | T | 1 | a0001c0001t0003g0280 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.46-249G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988422 | |||||||
| chr7:13988431 | A | G | 2 | a0001c0001t0004g0236 a0001c0001t0051g0235 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.46-258T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988431 | |||||||
| chr7:13988564 | CA | C | 171 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(168): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.46-392delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988564 | |||||||
| chr7:13988595 | G | GA | 145 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0026 others(142): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.45+412dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | |||||||
| chr7:13988595 | G | GAA | 22 | a0001c0001t0002g0281 a0001c0001t0003g0280 a0001c0001t0003g0285 others(19): Show |
22 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+411_45+412dupTT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | |||||||
| chr7:13988595 | GA | G | 39 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(36): Show |
39 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.45+412delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | |||||||
| chr7:13988620 | G | GA | 186 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0251 others(183): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+387dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988620 | |||||||
| chr7:13988729 | A | G | 1 | a0001c0001t0013g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.45+279T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988729 | |||||||
| chr7:13988745 | C | T | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.45+263G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988745 | |||||||
| chr7:13988919 | C | T | 1 | a0001c0001t0020g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+89G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988919 | |||||||
| chr7:13989169 | T | TA | 41 | a0001c0001t0002g0281 a0001c0001t0003g0276 a0001c0001t0003g0277 others(38): Show |
41 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(38): Show |
intron_variant | MODIFIER | c.-87-31dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989169 | |||||||
| chr7:13989169 | T | TAA | 125 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-87-32_-87-31dupTT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989169 | |||||||
| chr7:13989235 | CA | C | 125 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-88+32delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989235 |