| geneid | 345930 |
|---|---|
| ensemblid | ENSG00000203734.13 |
| hgncid | 21118 |
| symbol | ECT2L |
| name | epithelial cell transforming 2 like |
| refseq_nuc | NM_001077706.3 |
| refseq_prot | NP_001071174.1 |
| ensembl_nuc | ENST00000541398.7 |
| ensembl_prot | ENSP00000442307.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 138796087 |
| end | 138904070 |
| strand | + |
| ver | v1.2 |
| region | chr6:138796087-138904070 |
| region5000 | chr6:138791087-138909070 |
| regionname0 | ECT2L_chr6_138796087_138904070 |
| regionname5000 | ECT2L_chr6_138791087_138909070 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 904 | 196 | 32 | 41 | 93 | 10 | 18 | 79 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002 | 0/0 | 904 | 71 | 9 | 10 | 39 | 2 | 11 | 29 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003 | 0/0 | 904 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004 | 0/0 | 904 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0005 | 0/0 | 904 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006 | 0/0 | 904 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0007 | 0/0 | 904 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008 | 0/0 | 904 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009 | 0/0 | 904 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0010 | 0/0 | 904 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0011 | 0/0 | 904 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0012 | 0/0 | 904 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0013 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0014 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0015 | 0/0 | 904 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0016 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0017 | 0/0 | 560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0018 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0019 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0020 | 0/0 | 904 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0021 | 0/0 | 904 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0022 | 0/0 | 754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0023 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0024 | 0/0 | 904 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2715 | 144 | 22 | 38 | 57 | 9 | 16 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0002 | 0/0 | 2715 | 65 | 6 | 10 | 36 | 2 | 11 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0003 | 0/0 | 2715 | 43 | 7 | 1 | 33 | 0 | 2 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0004 | 0/0 | 2715 | 9 | 8 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0005 | 0/0 | 2715 | 6 | 3 | 0 | 3 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0006 | 0/0 | 2715 | 5 | 5 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0007 | 0/0 | 2715 | 5 | 5 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0008 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0009 | 0/0 | 2715 | 3 | 0 | 1 | 1 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0010 | 0/0 | 2715 | 3 | 2 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0011 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0012 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0013 | 0/0 | 2715 | 3 | 2 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0014 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0015 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0016 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0017 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0018 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0019 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0020 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0021 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0022 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0023 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0024 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0025 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0026 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0027 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0028 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0029 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0030 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0031 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0032 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0033 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0034 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0035 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0036 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0037 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| c0038 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1793 | 85 | 12 | 12 | 46 | 2 | 13 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0002 | 0/0 | 1793 | 63 | 14 | 14 | 27 | 3 | 5 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0003 | 0/1 | 1793 | 45 | 8 | 8 | 22 | 3 | 3 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0004 | 0/0 | 1793 | 30 | 5 | 2 | 21 | 2 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0005 | 0/0 | 1793 | 21 | 6 | 8 | 5 | 0 | 2 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0006 | 1/0 | 1793 | 19 | 0 | 4 | 8 | 1 | 5 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0007 | 0/0 | 1793 | 9 | 6 | 1 | 1 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0008 | 0/0 | 1793 | 9 | 5 | 0 | 4 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0009 | 0/0 | 1793 | 9 | 8 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0010 | 0/0 | 1793 | 4 | 3 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0011 | 0/0 | 1792 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0012 | 0/0 | 1793 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0013 | 0/0 | 1793 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0014 | 0/0 | 1793 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0015 | 0/0 | 1793 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0016 | 0/0 | 1793 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0017 | 0/0 | 1793 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0018 | 0/0 | 1793 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0019 | 0/0 | 1793 | 2 | 0 | 1 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0020 | 0/0 | 1792 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0021 | 0/0 | 1793 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0022 | 0/0 | 1793 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0023 | 0/0 | 1793 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0024 | 0/0 | 1793 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0025 | 0/0 | 1792 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0026 | 0/0 | 1793 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0027 | 0/0 | 1793 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0028 | 0/0 | 1793 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| t0029 | 0/0 | 1793 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2715 | 144 | 22 | 38 | 57 | 9 | 16 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0003 | 0/0 | 2715 | 43 | 7 | 1 | 33 | 0 | 2 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0009 | 0/0 | 2715 | 3 | 0 | 1 | 1 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0018 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0021 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0022 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0033 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0034 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002 | 0/0 | 2715 | 65 | 6 | 10 | 36 | 2 | 11 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0005 | 0/0 | 2715 | 6 | 3 | 0 | 3 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003c0004 | 0/0 | 2715 | 9 | 8 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0006 | 0/0 | 2715 | 5 | 5 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0008 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0005c0007 | 0/0 | 2715 | 5 | 5 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0005c0024 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006c0011 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006c0015 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0007c0010 | 0/0 | 2715 | 3 | 2 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0007c0014 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008c0013 | 0/0 | 2715 | 3 | 2 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008c0031 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009c0012 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009c0025 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0010c0017 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0011c0016 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0012c0019 | 0/0 | 2715 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0013c0038 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0014c0037 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0015c0023 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0016c0027 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0017c0035 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0018c0030 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0019c0032 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0020c0029 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0021c0028 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0022c0026 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0023c0036 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0024c0020 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4507 | 43 | 4 | 7 | 26 | 0 | 6 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0002 | 0/0 | 4507 | 23 | 1 | 12 | 4 | 3 | 3 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0003 | 0/1 | 4507 | 21 | 2 | 7 | 7 | 3 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0004 | 0/0 | 4507 | 17 | 2 | 1 | 13 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0005 | 0/0 | 4507 | 9 | 0 | 7 | 0 | 0 | 2 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0006 | 1/0 | 4507 | 15 | 0 | 2 | 7 | 1 | 4 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0007 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0008 | 0/0 | 4507 | 4 | 4 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0009 | 0/0 | 4507 | 5 | 4 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0010 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0016 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0022 | 0/0 | 4507 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0024 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0001t0029 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0003t0002 | 0/0 | 4507 | 21 | 3 | 0 | 17 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0003t0003 | 0/0 | 4507 | 16 | 3 | 1 | 11 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0003t0005 | 0/0 | 4507 | 5 | 0 | 0 | 5 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0003t0013 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0009t0001 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0009t0004 | 0/0 | 4507 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0009t0028 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0018t0002 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0018t0020 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0021t0004 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0022t0003 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0033t0002 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0001c0034t0023 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0001 | 0/0 | 4507 | 31 | 0 | 5 | 17 | 2 | 7 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0002 | 0/0 | 4507 | 4 | 2 | 0 | 2 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0003 | 0/0 | 4507 | 3 | 0 | 0 | 2 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0004 | 0/0 | 4507 | 8 | 0 | 1 | 7 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0005 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0006 | 0/0 | 4507 | 4 | 0 | 2 | 1 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0007 | 0/0 | 4507 | 4 | 2 | 0 | 1 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0008 | 0/0 | 4507 | 5 | 1 | 0 | 4 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0017 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0019 | 0/0 | 4507 | 2 | 0 | 1 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0026 | 0/0 | 4507 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0002t0027 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0005t0002 | 0/0 | 4507 | 4 | 1 | 0 | 3 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0002c0005t0013 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003c0004t0004 | 0/0 | 4507 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003c0004t0007 | 0/0 | 4507 | 4 | 3 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003c0004t0011 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0003c0004t0025 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0006t0001 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0006t0009 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0006t0015 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0004c0008t0009 | 0/0 | 4507 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0005c0007t0001 | 0/0 | 4507 | 5 | 5 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0005c0024t0005 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006c0011t0014 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006c0011t0021 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0006c0015t0003 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0007c0010t0010 | 0/0 | 4507 | 3 | 2 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0007c0014t0005 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008c0013t0002 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008c0013t0005 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0008c0031t0017 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009c0012t0003 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009c0012t0018 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0009c0025t0020 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0010c0017t0012 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0011c0016t0002 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0012c0019t0011 | 0/0 | 4506 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0013c0038t0002 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0014c0037t0002 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0015c0023t0002 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0016c0027t0001 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0017c0035t0003 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0018c0030t0001 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0019c0032t0005 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0020c0029t0001 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0021c0028t0002 | 0/0 | 4507 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0022c0026t0012 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0023c0036t0002 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| a0024c0020t0002 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | copy fasta | chr6 | 138791087 | 138909070 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0280 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0016g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0022g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0024g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0001t0029g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0003t0013g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0009t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0009t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0009t0028g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0018t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0018t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0021t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0022t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0033t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0001c0034t0023g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0019g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0026g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0002t0027g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0002c0005t0013g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0007g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0011g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0003c0004t0025g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0006t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0006t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0006t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0006t0015g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0008t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0008t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0004c0008t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0007t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0007t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0007t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0007t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0007t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0005c0024t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0006c0011t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0006c0011t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0006c0011t0021g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0006c0015t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0006c0015t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0007c0010t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0007c0010t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0007c0010t0010g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0007c0014t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0007c0014t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0008c0013t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0008c0013t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0008c0013t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0008c0031t0017g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0009c0012t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0009c0012t0018g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0009c0012t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0009c0025t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0010c0017t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0010c0017t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0011c0016t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0011c0016t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0012c0019t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0012c0019t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0013c0038t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0014c0037t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0015c0023t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0016c0027t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0017c0035t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0018c0030t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0019c0032t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0020c0029t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0021c0028t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0022c0026t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0023c0036t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| a0024c0020t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0230 | EUR | GBR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00099 | hp2 | a0001 | c0001 | t0022 | g0287 | EUR | GBR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | FIN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0029 | EUR | FIN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | FIN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0225 | EUR | FIN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0164 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0150 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0234 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00733 | hp2 | a0002 | c0002 | t0006 | g0284 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00738 | hp1 | a0008 | c0013 | t0002 | g0043 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0289 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0020 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01081 | hp1 | a0009 | c0025 | t0020 | g0004 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01106 | hp1 | a0007 | c0010 | t0010 | g0210 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01168 | hp2 | a0002 | c0002 | t0005 | g0290 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01169 | hp1 | a0002 | c0002 | t0006 | g0033 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01175 | hp1 | a0001 | c0009 | t0028 | g0107 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0283 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01192 | hp2 | a0002 | c0002 | t0019 | g0091 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0152 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01257 | hp1 | a0002 | c0002 | t0004 | g0096 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0092 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0291 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01358 | hp2 | a0015 | c0023 | t0002 | g0180 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01361 | hp1 | a0001 | c0034 | t0023 | g0016 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0282 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01433 | hp1 | a0003 | c0004 | t0007 | g0321 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01496 | hp2 | a0001 | c0001 | t0024 | g0031 | AMR | CLM | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0175 | EUR | IBS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | IBS | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0158 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01884 | hp2 | a0005 | c0007 | t0001 | g0301 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0294 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02015 | hp2 | a0002 | c0002 | t0007 | g0233 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0326 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02132 | hp2 | a0013 | c0038 | t0002 | g0173 | EAS | KHV | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02145 | hp1 | a0024 | c0020 | t0002 | g0315 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02145 | hp2 | a0002 | c0005 | t0002 | g0323 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | CDX | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | CDX | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02257 | hp1 | a0002 | c0002 | t0007 | g0288 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02257 | hp2 | a0005 | c0007 | t0001 | g0300 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02280 | hp2 | a0005 | c0007 | t0001 | g0317 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02451 | hp1 | a0023 | c0036 | t0002 | g0305 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02451 | hp2 | a0002 | c0002 | t0008 | g0153 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02572 | hp1 | a0008 | c0013 | t0005 | g0267 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0319 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0058 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02622 | hp1 | a0010 | c0017 | t0012 | g0221 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02622 | hp2 | a0003 | c0004 | t0007 | g0320 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02630 | hp1 | a0006 | c0011 | t0014 | g0013 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02630 | hp2 | a0010 | c0017 | t0012 | g0219 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02647 | hp1 | a0008 | c0013 | t0005 | g0269 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0318 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02683 | hp2 | a0002 | c0002 | t0006 | g0224 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02717 | hp1 | a0004 | c0006 | t0015 | g0312 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0211 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0212 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02723 | hp2 | a0004 | c0008 | t0009 | g0309 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0254 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02809 | hp1 | a0001 | c0018 | t0002 | g0059 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02809 | hp2 | a0002 | c0002 | t0017 | g0010 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02886 | hp1 | a0004 | c0006 | t0001 | g0313 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02886 | hp2 | a0019 | c0032 | t0005 | g0268 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02895 | hp1 | a0006 | c0015 | t0003 | g0238 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02895 | hp2 | a0002 | c0005 | t0013 | g0217 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02896 | hp1 | a0006 | c0015 | t0003 | g0239 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02896 | hp2 | a0003 | c0004 | t0004 | g0242 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02897 | hp1 | a0002 | c0005 | t0013 | g0220 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02897 | hp2 | a0003 | c0004 | t0004 | g0241 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02922 | hp1 | a0003 | c0004 | t0025 | g0244 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0248 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02965 | hp1 | a0007 | c0014 | t0005 | g0207 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0124 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02970 | hp1 | a0001 | c0018 | t0020 | g0007 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0037 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02976 | hp2 | a0009 | c0012 | t0018 | g0009 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0274 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03041 | hp2 | a0004 | c0008 | t0009 | g0298 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03098 | hp1 | a0004 | c0008 | t0009 | g0314 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03098 | hp2 | a0016 | c0027 | t0001 | g0005 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03130 | hp1 | a0007 | c0014 | t0005 | g0208 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03130 | hp2 | a0009 | c0012 | t0018 | g0008 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03139 | hp1 | a0005 | c0007 | t0001 | g0303 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03139 | hp2 | a0006 | c0011 | t0021 | g0236 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0108 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03209 | hp2 | a0004 | c0006 | t0001 | g0311 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03225 | hp2 | a0011 | c0016 | t0002 | g0308 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03453 | hp1 | a0004 | c0006 | t0015 | g0213 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03453 | hp2 | a0003 | c0004 | t0004 | g0243 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03486 | hp1 | a0006 | c0011 | t0014 | g0237 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03486 | hp2 | a0011 | c0016 | t0002 | g0307 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03490 | hp1 | a0002 | c0002 | t0026 | g0039 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0278 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03516 | hp2 | a0003 | c0004 | t0007 | g0324 | AFR | ESN | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03579 | hp1 | a0001 | c0003 | t0013 | g0222 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03579 | hp2 | a0004 | c0006 | t0009 | g0310 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0075 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03831 | hp2 | a0002 | c0002 | t0007 | g0166 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0055 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0235 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03942 | hp1 | a0021 | c0028 | t0002 | g0089 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0286 | SAS | STU | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | STU | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | STU | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18522 | hp1 | a0005 | c0024 | t0005 | g0276 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18522 | hp2 | a0007 | c0010 | t0010 | g0206 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18612 | hp1 | a0001 | c0003 | t0005 | g0257 | EAS | CHB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0163 | EAS | CHB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18747 | hp1 | a0020 | c0029 | t0001 | g0054 | EAS | CHB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0135 | EAS | CHB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0304 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0148 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18944 | hp1 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18947 | hp2 | a0001 | c0021 | t0004 | g0143 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0191 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0147 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18957 | hp1 | a0002 | c0002 | t0008 | g0064 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18959 | hp1 | a0001 | c0003 | t0003 | g0231 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18962 | hp2 | a0002 | c0002 | t0006 | g0261 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18964 | hp2 | a0002 | c0002 | t0027 | g0062 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18966 | hp2 | a0002 | c0002 | t0008 | g0118 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18968 | hp1 | a0002 | c0002 | t0019 | g0167 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18969 | hp2 | a0001 | c0003 | t0005 | g0260 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0122 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18974 | hp2 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18981 | hp1 | a0002 | c0005 | t0002 | g0070 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0139 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18985 | hp2 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18989 | hp2 | a0002 | c0005 | t0002 | g0223 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18990 | hp1 | a0001 | c0003 | t0002 | g0192 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18990 | hp2 | a0018 | c0030 | t0001 | g0061 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0132 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA18998 | hp2 | a0017 | c0035 | t0003 | g0159 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19004 | hp1 | a0001 | c0003 | t0003 | g0245 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19005 | hp2 | a0002 | c0002 | t0008 | g0119 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19006 | hp2 | a0001 | c0022 | t0003 | g0142 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19009 | hp1 | a0001 | c0003 | t0005 | g0275 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19010 | hp1 | a0002 | c0002 | t0004 | g0216 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19010 | hp2 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19011 | hp2 | a0002 | c0005 | t0002 | g0069 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19030 | hp1 | a0003 | c0004 | t0007 | g0322 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19030 | hp2 | a0009 | c0012 | t0003 | g0021 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19043 | hp1 | a0001 | c0001 | t0029 | g0262 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19056 | hp2 | a0002 | c0002 | t0008 | g0120 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19060 | hp2 | a0001 | c0009 | t0001 | g0170 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19065 | hp2 | a0001 | c0003 | t0005 | g0259 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19072 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0228 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19079 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19087 | hp2 | a0001 | c0003 | t0005 | g0292 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19088 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19240 | hp1 | a0001 | c0033 | t0002 | g0299 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA19240 | hp2 | a0014 | c0037 | t0002 | g0036 | AFR | YRI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20129 | hp1 | a0007 | c0010 | t0010 | g0209 | AFR | ASW | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20752 | hp1 | a0001 | c0009 | t0004 | g0121 | EUR | TSI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | TSI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0189 | EUR | TSI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | TSI | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | GIH | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02109 | hp1 | a0005 | c0007 | t0001 | g0302 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02559 | hp1 | a0008 | c0031 | t0017 | g0316 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG02559 | hp2 | a0012 | c0019 | t0011 | g0168 | AFR | ACB | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03471 | hp1 | a0022 | c0026 | t0012 | g0218 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | MSL | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG06807 | hp1 | a0012 | c0019 | t0011 | g0151 | AFR | USA | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| HG06807 | hp2 | a0002 | c0002 | t0007 | g0247 | AFR | USA | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | USA | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA20300 | hp2 | a0003 | c0004 | t0011 | g0325 | AFR | USA | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0271 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | LWK | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0018 | REF | REF | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0280 | REF | REF | ECT2L_chr6_138791087_138909070 | ECT2L | chr6 | 138791087 | 138909070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138812975
|
C | T | 9 | a0001a0002a0003others(6): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
splice_region_variant | LOW | c.-106C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/22 | chr6 | 138812975 | ||||||
| chr6:138813286
|
C | A | 2 | a0004a0024 | 9 | HG02145.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
missense_variant | MODERATE | c.12C>A | p.Phe4Leu | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/22 | 361/4507 | 12/2715 | 4/904 | chr6 | 138813286 | ||
| chr6:138814569
|
G | A | 1 | a0003 | 9 | HG01433.hp1 HG02622.hp2 HG02896.hp2 others(6): Show |
missense_variant | MODERATE | c.145G>A | p.Ala49Thr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/22 | 494/4507 | 145/2715 | 49/904 | chr6 | 138814569 | ||
| chr6:138838380
|
A | T | 1 | a0013 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.208A>T | p.Met70Leu | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/22 | 557/4507 | 208/2715 | 70/904 | chr6 | 138838380 | ||
| chr6:138843073
|
T | C | 1 | a0007 | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
missense_variant | MODERATE | c.437T>C | p.Ile146Thr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/22 | 786/4507 | 437/2715 | 146/904 | chr6 | 138843073 | ||
| chr6:138844465
|
G | A | 1 | a0006 | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.649G>A | p.Val217Met | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/22 | 998/4507 | 649/2715 | 217/904 | chr6 | 138844465 | ||
| chr6:138846650
|
A | C | 1 | a0014 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.876A>C | p.Leu292Phe | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/22 | 1225/4507 | 876/2715 | 292/904 | chr6 | 138846650 | ||
| chr6:138849275
|
A | G | 2 | a0012a0023 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.910A>G | p.Met304Val | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1259/4507 | 910/2715 | 304/904 | chr6 | 138849275 | ||
| chr6:138849276
|
T | A | 1 | a0015 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.911T>A | p.Met304Lys | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1260/4507 | 911/2715 | 304/904 | chr6 | 138849276 | ||
| chr6:138849323
|
G | A | 1 | a0023 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.958G>A | p.Val320Ile | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1307/4507 | 958/2715 | 320/904 | chr6 | 138849323 | ||
| chr6:138849324
|
T | C | 1 | a0023 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.959T>C | p.Val320Ala | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1308/4507 | 959/2715 | 320/904 | chr6 | 138849324 | ||
| chr6:138849389
|
G | A | 2 | a0011a0024 | 3 | HG02145.hp1 HG03225.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1024G>A | p.Gly342Arg | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1373/4507 | 1024/2715 | 342/904 | chr6 | 138849389 | ||
| chr6:138849416
|
G | A | 5 | a0005a0009a0010others(2): Show | 14 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.1051G>A | p.Glu351Lys | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/22 | 1400/4507 | 1051/2715 | 351/904 | chr6 | 138849416 | ||
| chr6:138854091
|
A | T | 1 | a0023 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1135A>T | p.Ser379Cys | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/22 | 1484/4507 | 1135/2715 | 379/904 | chr6 | 138854091 | ||
| chr6:138854101
|
C | A | 1 | a0023 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1145C>A | p.Ala382Asp | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/22 | 1494/4507 | 1145/2715 | 382/904 | chr6 | 138854101 | ||
| chr6:138865022
|
T | G | 2 | a0005a0016 | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
missense_variant | MODERATE | c.1318T>G | p.Trp440Gly | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/22 | 1667/4507 | 1318/2715 | 440/904 | chr6 | 138865022 | ||
| chr6:138875859
|
GCCTGTAA others(8510): Show |
G | 1 | a0022 | 1 | HG03471.hp1 | exon_loss_variant | HIGH | c.1579-592_2029-1110 others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr6 | 138875859 | |||||
| chr6:138876472
|
G | A | 4 | a0002a0010a0020others(1): Show | 75 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
missense_variant&splice_region_variant | MODERATE | c.1579G>A | p.Glu527Lys | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/22 | 1928/4507 | 1579/2715 | 527/904 | chr6 | 138876472 | ||
| chr6:138880972
|
A | T | 1 | a0017 | 1 | NA18998.hp2 | stop_gained | HIGH | c.1681A>T | p.Lys561* | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/22 | 2030/4507 | 1681/2715 | 561/904 | chr6 | 138880972 | ||
| chr6:138881035
|
G | A | 1 | a0018 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.1744G>A | p.Val582Met | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/22 | 2093/4507 | 1744/2715 | 582/904 | chr6 | 138881035 | ||
| chr6:138881071
|
G | A | 2 | a0008a0019 | 5 | HG00738.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
missense_variant | MODERATE | c.1780G>A | p.Ala594Thr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/22 | 2129/4507 | 1780/2715 | 594/904 | chr6 | 138881071 | ||
| chr6:138882744
|
G | C | 1 | a0021 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1901G>C | p.Arg634Thr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/22 | 2250/4507 | 1901/2715 | 634/904 | chr6 | 138882744 | ||
| chr6:138885762
|
C | T | 1 | a0019 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2191C>T | p.His731Tyr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/22 | 2540/4507 | 2191/2715 | 731/904 | chr6 | 138885762 | ||
| chr6:138902596
|
G | A | 1 | a0020 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2684G>A | p.Arg895Gln | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 3033/4507 | 2684/2715 | 895/904 | chr6 | 138902596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138843044
|
T | C | 1 | a0001c0009 | 3 | HG01175.hp1 NA19060.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.408T>C | p.Asn136Asn | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/22 | 757/4507 | 408/2715 | 136/904 | chr6 | 138843044 | ||
| chr6:138844536
|
G | A | 2 | a0001c0021a0001c0022 | 2 | NA18947.hp2 NA19006.hp2 |
synonymous_variant | LOW | c.720G>A | p.Leu240Leu | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/22 | 1069/4507 | 720/2715 | 240/904 | chr6 | 138844536 | ||
| chr6:138881148
|
T | C | 5 | a0001c0018a0001c0033a0004c0008others(2): Show | 9 | HG01081.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.1857T>C | p.Ile619Ile | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/22 | 2206/4507 | 1857/2715 | 619/904 | chr6 | 138881148 | ||
| chr6:138882781
|
G | A | 1 | a0009c0025 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.1938G>A | p.Val646Val | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/22 | 2287/4507 | 1938/2715 | 646/904 | chr6 | 138882781 | ||
| chr6:138885734
|
C | T | 1 | a0001c0034 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.2163C>T | p.Tyr721Tyr | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/22 | 2512/4507 | 2163/2715 | 721/904 | chr6 | 138885734 | ||
| chr6:138885800
|
A | G | 16 | a0001c0003a0001c0022a0001c0033others(13): Show | 70 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(67): Show |
synonymous_variant | LOW | c.2229A>G | p.Gln743Gln | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/22 | 2578/4507 | 2229/2715 | 743/904 | chr6 | 138885800 | ||
| chr6:138900975
|
C | T | 2 | a0001c0033a0006c0015 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.2442C>T | p.Ser814Ser | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/22 | 2791/4507 | 2442/2715 | 814/904 | chr6 | 138900975 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138812897
|
C | T | 4 | a0001c0003t0013a0002c0005t0013a0010c0017t0012others(1): Show | 6 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-184C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/22 | chr6 | 138812897 | ||||||
| chr6:138812900
|
G | A | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
5_prime_UTR_variant | MODIFIER | c.-181G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/22 | 375 | chr6 | 138812900 | |||||
| chr6:138812904
|
G | C | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(24): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-177G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/22 | 371 | chr6 | 138812904 | |||||
| chr6:138812966
|
G | A | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(24): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-115G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/22 | 309 | chr6 | 138812966 | |||||
| chr6:138902813
|
A | G | 2 | a0002c0002t0017a0008c0031t0017 | 2 | HG02559.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*186A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 186 | chr6 | 138902813 | |||||
| chr6:138903186
|
C | T | 1 | a0006c0011t0014 | 2 | HG02630.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*559C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 559 | chr6 | 138903186 | |||||
| chr6:138903229
|
C | G | 5 | a0001c0001t0009a0001c0001t0010a0004c0006t0009others(2): Show | 13 | HG01106.hp1 HG01243.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*602C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 602 | chr6 | 138903229 | |||||
| chr6:138903247
|
C | T | 1 | a0001c0001t0029 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 620 | chr6 | 138903247 | |||||
| chr6:138903254
|
C | G | 53 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(50): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*627C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 627 | chr6 | 138903254 | |||||
| chr6:138903334
|
T | C | 1 | a0002c0002t0026 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 707 | chr6 | 138903334 | |||||
| chr6:138903371
|
G | A | 2 | a0004c0006t0015a0006c0011t0021 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*744G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 744 | chr6 | 138903371 | |||||
| chr6:138903371
|
GA | G | 5 | a0001c0018t0020a0003c0004t0011a0003c0004t0025others(2): Show | 6 | HG01081.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*754delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 754 | INFO_REALIGN_3_PRIME | chr6 | 138903371 | ||||
| chr6:138903372
|
A | G | 2 | a0004c0006t0015a0006c0011t0021 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*745A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 745 | chr6 | 138903372 | |||||
| chr6:138903443
|
G | A | 1 | a0001c0009t0028 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 816 | chr6 | 138903443 | |||||
| chr6:138903510
|
G | A | 1 | a0009c0012t0018 | 2 | HG02976.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*883G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 883 | chr6 | 138903510 | |||||
| chr6:138903549
|
C | A | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(33): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 922 | chr6 | 138903549 | |||||
| chr6:138903608
|
C | T | 1 | a0003c0004t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*981C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 981 | chr6 | 138903608 | |||||
| chr6:138903766
|
A | G | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0029others(6): Show | 23 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1139A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 1139 | chr6 | 138903766 | |||||
| chr6:138903807
|
T | A | 1 | a0001c0001t0022 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1180T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 1180 | chr6 | 138903807 | |||||
| chr6:138903895
|
C | G | 1 | a0001c0034t0023 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 1268 | chr6 | 138903895 | |||||
| chr6:138903925
|
T | C | 1 | a0001c0001t0016 | 2 | HG02717.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1298T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 1298 | chr6 | 138903925 | |||||
| chr6:138904036
|
T | C | 1 | a0002c0002t0027 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1409T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 22/22 | 1409 | chr6 | 138904036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:138796526
|
A | G | 32 | a0001c0001t0001g0306a0001c0001t0002g0296a0001c0001t0008g0318others(29): Show | 32 | HG01433.hp1 HG01884.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.-244+334A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138796526 | ||||||
| chr6:138796599
|
G | A | 2 | a0001c0003t0003g0001a0002c0002t0004g0002 | 2 | NA19005.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-244+407G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138796599 | ||||||
| chr6:138796654
|
A | C | 1 | a0001c0003t0002g0326 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-244+462A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138796654 | ||||||
| chr6:138796876
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-244+684G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138796876 | ||||||
| chr6:138796988
|
CTTGT | C | 6 | a0001c0001t0007g0006a0001c0018t0020g0007a0009c0012t0018g0008others(3): Show | 6 | HG01081.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+802_-244+805d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138796988 | |||||
| chr6:138797007
|
G | A | 275 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(272): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-244+815G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797007 | ||||||
| chr6:138797174
|
T | C | 3 | a0001c0001t0009g0011a0001c0001t0009g0012a0002c0002t0017g0010 | 3 | HG02109.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-244+982T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797174 | ||||||
| chr6:138797223
|
A | C | 5 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+1031A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797223 | ||||||
| chr6:138797400
|
C | T | 5 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+1208C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797400 | ||||||
| chr6:138797409
|
G | A | 1 | a0006c0011t0014g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+1217G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797409 | ||||||
| chr6:138797432
|
G | A | 150 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(147): Show | 150 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-244+1240G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797432 | ||||||
| chr6:138797644
|
G | GA | 22 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-244+1462dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138797644 | |||||
| chr6:138797655
|
C | A | 1 | a0002c0002t0017g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-244+1463C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797655 | ||||||
| chr6:138797704
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-244+1512C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797704 | ||||||
| chr6:138797740
|
C | T | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+1548C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797740 | ||||||
| chr6:138797774
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-244+1582G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797774 | ||||||
| chr6:138797962
|
G | A | 2 | a0001c0003t0002g0037a0014c0037t0002g0036 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-244+1770G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797962 | ||||||
| chr6:138797991
|
G | A | 5 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0004g0157others(2): Show | 5 | HG01081.hp1 HG01255.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+1799G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138797991 | ||||||
| chr6:138798119
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-244+1927G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798119 | ||||||
| chr6:138798140
|
G | A | 2 | a0001c0001t0004g0157a0001c0001t0008g0158 | 2 | HG01255.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-244+1948G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798140 | ||||||
| chr6:138798251
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-244+2059C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798251 | ||||||
| chr6:138798261
|
T | C | 276 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(273): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-244+2069T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798261 | ||||||
| chr6:138798419
|
G | A | 1 | a0004c0008t0009g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-244+2227G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798419 | ||||||
| chr6:138798545
|
A | G | 2 | a0006c0015t0003g0238a0006c0015t0003g0239 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-244+2353A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798545 | ||||||
| chr6:138798722
|
G | A | 2 | a0001c0001t0004g0157a0001c0001t0008g0158 | 2 | HG01255.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-244+2530G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798722 | ||||||
| chr6:138798740
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-244+2548T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798740 | ||||||
| chr6:138798776
|
G | C | 280 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(277): Show | 280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.-244+2584G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798776 | ||||||
| chr6:138798919
|
CTG | C | 4 | a0001c0018t0020g0007a0009c0012t0018g0008a0009c0012t0018g0009others(1): Show | 4 | HG01081.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+2731_-244+273 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138798919 | |||||
| chr6:138798974
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-244+2782T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138798974 | ||||||
| chr6:138799069
|
C | T | 1 | a0001c0003t0003g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-244+2877C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799069 | ||||||
| chr6:138799090
|
A | C | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+2898A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799090 | ||||||
| chr6:138799117
|
G | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0004g0157others(10): Show | 13 | HG01255.hp2 HG01433.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-244+2925G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799117 | ||||||
| chr6:138799258
|
A | AT | 26 | a0001c0001t0001g0149a0001c0001t0003g0230a0001c0001t0004g0225others(23): Show | 26 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.-244+3079dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138799258 | |||||
| chr6:138799258
|
A | ATT | 7 | a0002c0002t0008g0153a0004c0006t0001g0311a0004c0006t0001g0313others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-244+3078_-244+307 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138799258 | |||||
| chr6:138799258
|
AT | A | 60 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(57): Show | 60 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-244+3079delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138799258 | |||||
| chr6:138799354
|
T | C | 15 | a0001c0001t0001g0161a0001c0001t0002g0160a0001c0001t0007g0006others(12): Show | 15 | HG00423.hp1 HG00558.hp2 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-244+3162T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799354 | ||||||
| chr6:138799378
|
G | T | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+3186G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799378 | ||||||
| chr6:138799419
|
T | A | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+3227T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799419 | ||||||
| chr6:138799431
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-244+3239A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799431 | ||||||
| chr6:138799449
|
G | A | 1 | a0001c0001t0006g0251 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-244+3257G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799449 | ||||||
| chr6:138799490
|
C | T | 51 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(48): Show | 51 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-244+3298C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799490 | ||||||
| chr6:138799502
|
G | A | 3 | a0001c0001t0004g0040a0001c0001t0007g0006a0016c0027t0001g0005 | 3 | HG03098.hp2 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-244+3310G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799502 | ||||||
| chr6:138799547
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-244+3355G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799547 | ||||||
| chr6:138799650
|
C | T | 50 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-244+3458C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138799650 | ||||||
| chr6:138800089
|
T | C | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+3897T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800089 | ||||||
| chr6:138800293
|
T | C | 1 | a0006c0011t0021g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-244+4101T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800293 | ||||||
| chr6:138800306
|
A | G | 3 | a0009c0012t0018g0008a0009c0012t0018g0009a0009c0025t0020g0004 | 3 | HG01081.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-244+4114A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800306 | ||||||
| chr6:138800417
|
G | T | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+4225G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800417 | ||||||
| chr6:138800518
|
C | T | 1 | a0001c0001t0005g0294 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-244+4326C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800518 | ||||||
| chr6:138800729
|
T | C | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-244+4537T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800729 | ||||||
| chr6:138800796
|
A | G | 1 | a0002c0002t0008g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-244+4604A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800796 | ||||||
| chr6:138800924
|
C | T | 1 | a0001c0009t0004g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-244+4732C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800924 | ||||||
| chr6:138800930
|
CTTG | C | 8 | a0004c0006t0001g0311a0004c0006t0001g0313a0004c0006t0009g0310others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-244+4745_-244+474 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138800930 | |||||
| chr6:138800993
|
T | C | 18 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0008g0318others(15): Show | 18 | HG01433.hp1 HG01952.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.-244+4801T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800993 | ||||||
| chr6:138800996
|
A | G | 18 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0008g0318others(15): Show | 18 | HG01433.hp1 HG01952.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.-244+4804A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138800996 | ||||||
| chr6:138801103
|
A | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-244+4911A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801103 | ||||||
| chr6:138801181
|
A | G | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-244+4989A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801181 | ||||||
| chr6:138801204
|
A | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-244+5012A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801204 | ||||||
| chr6:138801480
|
G | A | 1 | a0004c0006t0015g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-244+5288G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801480 | ||||||
| chr6:138801648
|
A | G | 221 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(218): Show | 221 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.-244+5456A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801648 | ||||||
| chr6:138801741
|
C | T | 1 | a0001c0003t0003g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-244+5549C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801741 | ||||||
| chr6:138801779
|
C | A | 88 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(85): Show | 88 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-244+5587C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801779 | ||||||
| chr6:138801860
|
A | G | 3 | a0001c0001t0009g0152a0002c0002t0008g0153a0012c0019t0011g0151 | 3 | HG01243.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-244+5668A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801860 | ||||||
| chr6:138801915
|
T | C | 1 | a0008c0031t0017g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-244+5723T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138801915 | ||||||
| chr6:138802074
|
C | A | 2 | a0001c0001t0007g0006a0016c0027t0001g0005 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-244+5882C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802074 | ||||||
| chr6:138802161
|
C | A | 1 | a0002c0002t0004g0216 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-244+5969C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802161 | ||||||
| chr6:138802218
|
A | C | 1 | a0006c0011t0014g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+6026A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802218 | ||||||
| chr6:138802512
|
C | A | 2 | a0001c0003t0003g0122a0001c0003t0003g0123 | 2 | NA18944.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-244+6320C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802512 | ||||||
| chr6:138802537
|
T | C | 4 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0016g0211others(1): Show | 4 | HG01952.hp2 HG01978.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+6345T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802537 | ||||||
| chr6:138802704
|
A | G | 5 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+6512A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802704 | ||||||
| chr6:138802748
|
T | A | 3 | a0001c0001t0003g0018a0001c0001t0004g0157a0001c0001t0008g0158 | 3 | HG01255.hp2 HG01884.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-244+6556T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802748 | ||||||
| chr6:138802755
|
C | T | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+6563C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802755 | ||||||
| chr6:138802871
|
G | A | 1 | a0002c0002t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-244+6679G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802871 | ||||||
| chr6:138802885
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-244+6693G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802885 | ||||||
| chr6:138802945
|
G | A | 1 | a0008c0013t0002g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-244+6753G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138802945 | ||||||
| chr6:138803076
|
C | CA | 37 | a0001c0001t0001g0252a0001c0001t0001g0266a0001c0001t0001g0272others(34): Show | 37 | HG00609.hp2 HG00621.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-244+6897dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138803076 | |||||
| chr6:138803084
|
A | AT | 63 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(60): Show | 63 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-244+6892_-244+689 others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803084 | ||||||
| chr6:138803087
|
A | AT | 156 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(153): Show | 156 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-244+6895_-244+689 others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803087 | ||||||
| chr6:138803087
|
A | T | 112 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-244+6895A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803087 | ||||||
| chr6:138803119
|
C | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-244+6927C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803119 | ||||||
| chr6:138803255
|
T | TA | 20 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0003g0018others(17): Show | 20 | HG01255.hp2 HG01433.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-244+7074dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138803255 | |||||
| chr6:138803317
|
T | TAC | 4 | a0001c0001t0001g0293a0001c0001t0002g0035a0001c0001t0003g0291others(1): Show | 4 | HG01346.hp1 NA19087.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+7151_-244+715 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138803317 | |||||
| chr6:138803317
|
TAC | T | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0203others(8): Show | 11 | HG01106.hp1 HG01952.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.-244+7151_-244+715 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138803317 | |||||
| chr6:138803317
|
TACAC | T | 206 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(203): Show | 206 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.-244+7149_-244+715 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138803317 | |||||
| chr6:138803325
|
C | T | 1 | a0002c0002t0001g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-244+7133C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803325 | ||||||
| chr6:138803467
|
C | A | 116 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0001g0165others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-244+7275C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138803467 | ||||||
| chr6:138804003
|
A | G | 223 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(220): Show | 223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-244+7811A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804003 | ||||||
| chr6:138804030
|
A | G | 1 | a0001c0001t0016g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-244+7838A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804030 | ||||||
| chr6:138804487
|
A | G | 1 | a0005c0024t0005g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-244+8295A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804487 | ||||||
| chr6:138804541
|
T | C | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-8297T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804541 | ||||||
| chr6:138804582
|
A | AAC | 22 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0201others(19): Show | 22 | HG01081.hp1 HG01952.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-243-8228_-243-822 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138804582 | |||||
| chr6:138804582
|
A | AACAC | 7 | a0001c0001t0003g0018a0001c0001t0004g0157a0001c0001t0008g0158others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-243-8230_-243-822 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138804582 | |||||
| chr6:138804582
|
A | AACACAC | 12 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0002t0008g0118others(9): Show | 12 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-243-8232_-243-822 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138804582 | |||||
| chr6:138804582
|
A | AACACACA others(5): Show |
5 | a0001c0001t0004g0040a0007c0010t0010g0206a0007c0010t0010g0209others(2): Show | 5 | HG02965.hp1 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-8238_-243-822 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138804582 | |||||
| chr6:138804582
|
A | AACACACA others(7): Show |
1 | a0007c0010t0010g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-243-8240_-243-822 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138804582 | |||||
| chr6:138804758
|
A | C | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-8080A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804758 | ||||||
| chr6:138804814
|
G | A | 223 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(220): Show | 223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-243-8024G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804814 | ||||||
| chr6:138804888
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-243-7950T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804888 | ||||||
| chr6:138804948
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0016g0211a0001c0001t0016g0212 | 3 | HG02717.hp2 HG02723.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-243-7890G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138804948 | ||||||
| chr6:138805072
|
C | T | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-243-7766C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805072 | ||||||
| chr6:138805097
|
C | T | 1 | a0001c0001t0008g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-243-7741C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805097 | ||||||
| chr6:138805172
|
C | T | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-7666C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805172 | ||||||
| chr6:138805349
|
A | G | 9 | a0001c0001t0001g0044a0001c0001t0016g0211a0001c0001t0016g0212others(6): Show | 9 | HG01106.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-7489A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805349 | ||||||
| chr6:138805429
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-243-7409A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805429 | ||||||
| chr6:138805479
|
G | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-243-7359G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805479 | ||||||
| chr6:138805562
|
A | G | 16 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0008g0318others(13): Show | 16 | HG01433.hp1 HG01952.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-243-7276A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805562 | ||||||
| chr6:138805654
|
C | T | 1 | a0002c0002t0008g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-243-7184C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805654 | ||||||
| chr6:138805835
|
T | C | 18 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0008g0318others(15): Show | 18 | HG01243.hp1 HG01433.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-7003T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805835 | ||||||
| chr6:138805974
|
G | T | 91 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(88): Show | 91 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-243-6864G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138805974 | ||||||
| chr6:138806169
|
A | C | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-6669A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806169 | ||||||
| chr6:138806242
|
G | T | 1 | a0001c0001t0009g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-243-6596G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806242 | ||||||
| chr6:138806395
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-243-6443T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806395 | ||||||
| chr6:138806421
|
C | T | 113 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0001g0165others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-243-6417C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806421 | ||||||
| chr6:138806511
|
C | CT | 8 | a0001c0001t0004g0040a0001c0001t0005g0289a0001c0003t0005g0292others(5): Show | 8 | HG00741.hp1 HG01168.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-243-6308dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTCTT | 59 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-243-6325_-243-632 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTT | 8 | a0001c0001t0002g0155a0001c0001t0008g0318a0001c0001t0010g0319others(5): Show | 8 | HG01433.hp1 HG01978.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-243-6311_-243-630 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTT | 20 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0156others(17): Show | 20 | HG00558.hp1 HG00738.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-243-6312_-243-630 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTTT | 91 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(88): Show | 91 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-243-6313_-243-630 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTTTT | 22 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(19): Show | 22 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-243-6314_-243-630 others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTTTT others(1): Show |
60 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(57): Show | 60 | HG00438.hp1 HG00609.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.-243-6315_-243-630 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTTTT others(2): Show |
30 | a0001c0001t0001g0032a0001c0001t0001g0266a0001c0001t0003g0030others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-243-6316_-243-630 others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806511
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0007g0006a0016c0027t0001g0005 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-243-6317_-243-630 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806511 | |||||
| chr6:138806757
|
C | T | 6 | a0004c0006t0015g0213a0007c0010t0010g0206a0007c0010t0010g0209others(3): Show | 6 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-6081C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806757 | ||||||
| chr6:138806765
|
G | A | 91 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(88): Show | 91 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-243-6073G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806765 | ||||||
| chr6:138806961
|
ATGT | A | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-5875_-243-587 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138806961 | |||||
| chr6:138806978
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | NA18973.hp1 NA18981.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-243-5860A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806978 | ||||||
| chr6:138806986
|
G | A | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-243-5852G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138806986 | ||||||
| chr6:138807115
|
A | AT | 90 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-243-5710dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138807115 | |||||
| chr6:138807149
|
T | A | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-243-5689T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807149 | ||||||
| chr6:138807165
|
G | C | 3 | a0001c0001t0001g0051a0001c0003t0002g0052a0002c0002t0001g0053 | 3 | NA18944.hp2 NA18964.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-243-5673G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807165 | ||||||
| chr6:138807446
|
G | C | 105 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(102): Show | 105 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.-243-5392G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807446 | ||||||
| chr6:138807508
|
C | G | 1 | a0004c0006t0015g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-243-5330C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807508 | ||||||
| chr6:138807618
|
A | G | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-5220A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807618 | ||||||
| chr6:138807698
|
A | C | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-5140A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807698 | ||||||
| chr6:138807700
|
T | A | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-5138T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138807700 | ||||||
| chr6:138808142
|
T | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-243-4696T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138808142 | ||||||
| chr6:138808302
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-243-4536G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138808302 | ||||||
| chr6:138808464
|
G | A | 63 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(60): Show | 63 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-243-4374G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138808464 | ||||||
| chr6:138808722
|
CTCTTT | C | 89 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(86): Show | 89 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-243-4109_-243-410 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138808722 | |||||
| chr6:138808726
|
TTTC | T | 9 | a0001c0001t0008g0318a0001c0001t0010g0319a0002c0005t0002g0323others(6): Show | 9 | HG01433.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-243-4109_-243-410 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138808726 | |||||
| chr6:138808751
|
G | T | 2 | a0001c0001t0007g0006a0016c0027t0001g0005 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-243-4087G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138808751 | ||||||
| chr6:138808753
|
G | T | 2 | a0001c0001t0007g0006a0016c0027t0001g0005 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-243-4085G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138808753 | ||||||
| chr6:138809000
|
T | C | 1 | a0002c0002t0008g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-243-3838T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809000 | ||||||
| chr6:138809001
|
A | G | 100 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(97): Show | 100 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-243-3837A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809001 | ||||||
| chr6:138809076
|
G | A | 276 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(273): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-243-3762G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809076 | ||||||
| chr6:138809156
|
T | C | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-243-3682T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809156 | ||||||
| chr6:138809250
|
G | A | 1 | a0002c0002t0007g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-243-3588G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809250 | ||||||
| chr6:138809419
|
T | G | 4 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-243-3419T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809419 | ||||||
| chr6:138809479
|
G | A | 101 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(98): Show | 101 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-243-3359G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809479 | ||||||
| chr6:138809533
|
A | C | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-3305A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809533 | ||||||
| chr6:138809925
|
A | C | 93 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(90): Show | 93 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-243-2913A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809925 | ||||||
| chr6:138809981
|
G | A | 122 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0001g0165others(119): Show | 122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.-243-2857G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809981 | ||||||
| chr6:138809985
|
G | A | 1 | a0001c0001t0006g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-243-2853G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138809985 | ||||||
| chr6:138810035
|
G | A | 1 | a0002c0002t0019g0167 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-243-2803G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810035 | ||||||
| chr6:138810103
|
C | T | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-2735C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810103 | ||||||
| chr6:138810191
|
G | A | 2 | a0001c0001t0009g0152a0012c0019t0011g0151 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-243-2647G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810191 | ||||||
| chr6:138810448
|
C | G | 11 | a0001c0001t0001g0051a0001c0001t0001g0103a0001c0001t0002g0098others(8): Show | 11 | HG00639.hp2 HG01258.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-243-2390C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810448 | ||||||
| chr6:138810569
|
T | C | 1 | a0012c0019t0011g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-243-2269T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810569 | ||||||
| chr6:138810640
|
C | T | 1 | a0001c0001t0009g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-243-2198C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810640 | ||||||
| chr6:138810657
|
A | G | 124 | a0001c0001t0001g0044a0001c0001t0001g0161a0001c0001t0001g0165others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-243-2181A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810657 | ||||||
| chr6:138810823
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-243-2015G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810823 | ||||||
| chr6:138810845
|
G | C | 4 | a0001c0001t0003g0018a0001c0001t0004g0157a0001c0001t0008g0158others(1): Show | 4 | HG01175.hp1 HG01255.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-243-1993G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810845 | ||||||
| chr6:138810859
|
G | A | 97 | a0001c0001t0001g0161a0001c0001t0001g0165a0001c0001t0001g0169others(94): Show | 97 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-243-1979G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810859 | ||||||
| chr6:138810905
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-1933C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138810905 | ||||||
| chr6:138811432
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-243-1406C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811432 | ||||||
| chr6:138811434
|
C | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0009g0271 | 3 | HG01952.hp2 HG01978.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-243-1404C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811434 | ||||||
| chr6:138811514
|
T | C | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-243-1324T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811514 | ||||||
| chr6:138811590
|
A | G | 1 | a0002c0002t0001g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-243-1248A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811590 | ||||||
| chr6:138811632
|
G | A | 209 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(206): Show | 209 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-243-1206G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811632 | ||||||
| chr6:138811703
|
G | A | 109 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(106): Show | 109 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-243-1135G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811703 | ||||||
| chr6:138811802
|
C | T | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-243-1036C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811802 | ||||||
| chr6:138811849
|
C | T | 167 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(164): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.-243-989C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811849 | ||||||
| chr6:138811904
|
G | T | 47 | a0001c0001t0001g0044a0001c0001t0003g0095a0001c0001t0003g0137others(44): Show | 47 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-243-934G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811904 | ||||||
| chr6:138811949
|
A | T | 1 | a0002c0002t0019g0167 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-243-889A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138811949 | ||||||
| chr6:138812045
|
G | A | 8 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(5): Show | 8 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-243-793G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812045 | ||||||
| chr6:138812202
|
T | C | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-243-636T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812202 | ||||||
| chr6:138812245
|
G | A | 173 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(170): Show | 173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-243-593G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812245 | ||||||
| chr6:138812575
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-263G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812575 | ||||||
| chr6:138812606
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0002g0155a0001c0001t0002g0156 | 3 | HG01952.hp2 HG01978.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-243-232A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812606 | ||||||
| chr6:138812659
|
G | T | 64 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-243-179G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812659 | ||||||
| chr6:138812714
|
AGAATG | A | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-121_-243-117d others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr6 | 138812714 | |||||
| chr6:138812773
|
C | A | 6 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-65C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812773 | ||||||
| chr6:138812791
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-243-47C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 1/21 | chr6 | 138812791 | ||||||
| chr6:138813121
|
T | C | 10 | a0004c0006t0001g0311a0004c0006t0001g0313a0004c0006t0009g0310others(7): Show | 10 | HG02145.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103-51T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 2/21 | chr6 | 138813121 | ||||||
| chr6:138813421
|
C | T | 173 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(170): Show | 173 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.66+81C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138813421 | ||||||
| chr6:138813617
|
T | C | 167 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(164): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.66+277T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138813617 | ||||||
| chr6:138813841
|
C | T | 167 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(164): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.66+501C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138813841 | ||||||
| chr6:138813922
|
A | G | 1 | a0004c0008t0009g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-569A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138813922 | ||||||
| chr6:138813940
|
C | T | 97 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.67-551C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138813940 | ||||||
| chr6:138814015
|
G | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.67-476G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814015 | ||||||
| chr6:138814114
|
G | A | 2 | a0001c0001t0009g0011a0001c0003t0002g0304 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67-377G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814114 | ||||||
| chr6:138814178
|
T | C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-313T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814178 | ||||||
| chr6:138814255
|
A | C | 167 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(164): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.67-236A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814255 | ||||||
| chr6:138814281
|
C | T | 68 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0071others(65): Show | 68 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.67-210C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814281 | ||||||
| chr6:138814362
|
G | A | 3 | a0001c0001t0003g0095a0001c0001t0004g0225a0002c0002t0004g0096 | 3 | HG00323.hp2 HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.67-129G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 3/21 | chr6 | 138814362 | ||||||
| chr6:138814652
|
G | A | 1 | a0001c0001t0008g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179+49G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138814652 | ||||||
| chr6:138814692
|
C | G | 1 | a0001c0001t0006g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.179+89C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138814692 | ||||||
| chr6:138814802
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.179+199G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138814802 | ||||||
| chr6:138814853
|
C | A | 167 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(164): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.179+250C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138814853 | ||||||
| chr6:138814939
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179+336G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138814939 | ||||||
| chr6:138815026
|
G | C | 3 | a0001c0001t0001g0044a0001c0001t0002g0155a0001c0001t0002g0156 | 3 | HG01952.hp2 HG01978.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.179+423G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138815026 | ||||||
| chr6:138815104
|
C | T | 9 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(6): Show | 9 | HG01433.hp1 HG02622.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.179+501C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138815104 | ||||||
| chr6:138815155
|
G | A | 1 | a0001c0001t0008g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179+552G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138815155 | ||||||
| chr6:138815335
|
T | C | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+732T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138815335 | ||||||
| chr6:138816177
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179+1574C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816177 | ||||||
| chr6:138816205
|
A | G | 1 | a0001c0003t0003g0245 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.179+1602A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816205 | ||||||
| chr6:138816354
|
G | A | 265 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.179+1751G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816354 | ||||||
| chr6:138816363
|
A | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.179+1760A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816363 | ||||||
| chr6:138816389
|
T | G | 276 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.179+1786T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816389 | ||||||
| chr6:138816393
|
T | G | 2 | a0001c0001t0006g0029a0002c0002t0019g0091 | 2 | HG00280.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.179+1790T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816393 | ||||||
| chr6:138816397
|
G | T | 1 | a0001c0001t0005g0285 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.179+1794G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816397 | ||||||
| chr6:138816630
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.179+2027G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816630 | ||||||
| chr6:138816634
|
A | G | 2 | a0001c0001t0006g0263a0001c0003t0005g0292 | 2 | HG02015.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.179+2031A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816634 | ||||||
| chr6:138816641
|
C | T | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.179+2038C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816641 | ||||||
| chr6:138816726
|
C | G | 6 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+2123C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816726 | ||||||
| chr6:138816727
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179+2124T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816727 | ||||||
| chr6:138816728
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179+2125G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816728 | ||||||
| chr6:138816731
|
T | C | 160 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(157): Show | 160 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.179+2128T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816731 | ||||||
| chr6:138816876
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.179+2273G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816876 | ||||||
| chr6:138816928
|
C | G | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.179+2325C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816928 | ||||||
| chr6:138816928
|
C | T | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+2325C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138816928 | ||||||
| chr6:138817258
|
T | C | 6 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+2655T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817258 | ||||||
| chr6:138817430
|
A | C | 4 | a0001c0001t0001g0306a0011c0016t0002g0307a0011c0016t0002g0308others(1): Show | 4 | HG02976.hp1 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+2827A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817430 | ||||||
| chr6:138817779
|
C | T | 1 | a0003c0004t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.179+3176C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817779 | ||||||
| chr6:138817781
|
A | C | 3 | a0001c0001t0003g0137a0001c0003t0003g0245a0002c0002t0007g0166 | 3 | HG02165.hp1 HG03831.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.179+3178A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817781 | ||||||
| chr6:138817847
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179+3244T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817847 | ||||||
| chr6:138817858
|
C | T | 2 | a0001c0001t0003g0023a0001c0001t0024g0031 | 2 | HG01496.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.179+3255C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138817858 | ||||||
| chr6:138818137
|
A | G | 271 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.179+3534A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818137 | ||||||
| chr6:138818206
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.179+3603C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818206 | ||||||
| chr6:138818313
|
G | C | 7 | a0001c0001t0007g0006a0001c0033t0002g0299a0005c0007t0001g0300others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179+3710G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818313 | ||||||
| chr6:138818320
|
TAAGA | T | 6 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+3718_179+3721d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818320 | ||||||
| chr6:138818356
|
C | G | 1 | a0001c0003t0002g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.179+3753C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818356 | ||||||
| chr6:138818374
|
C | T | 1 | a0001c0003t0002g0304 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.179+3771C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818374 | ||||||
| chr6:138818452
|
G | A | 153 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(150): Show | 153 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.179+3849G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818452 | ||||||
| chr6:138818608
|
G | A | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+4005G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818608 | ||||||
| chr6:138818629
|
A | T | 3 | a0001c0001t0004g0197a0001c0003t0002g0192a0001c0003t0003g0198 | 3 | NA18978.hp1 NA18986.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.179+4026A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818629 | ||||||
| chr6:138818745
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.179+4142G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818745 | ||||||
| chr6:138818761
|
G | A | 13 | a0001c0001t0004g0249a0001c0001t0007g0006a0001c0003t0003g0124others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.179+4158G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818761 | ||||||
| chr6:138818772
|
A | C | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+4169A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818772 | ||||||
| chr6:138818893
|
T | G | 6 | a0001c0003t0013g0222a0002c0005t0013g0217a0002c0005t0013g0220others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+4290T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138818893 | ||||||
| chr6:138819036
|
T | C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.179+4433T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819036 | ||||||
| chr6:138819045
|
G | C | 9 | a0001c0001t0007g0006a0001c0003t0003g0124a0001c0033t0002g0299others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.179+4442G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819045 | ||||||
| chr6:138819246
|
A | AAG | 86 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.179+4644_179+4645i others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138819246 | |||||
| chr6:138819246
|
A | AG | 54 | a0001c0001t0001g0125a0001c0001t0003g0019a0001c0001t0005g0115others(51): Show | 54 | HG00280.hp2 HG00609.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.179+4643_179+4644i others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819246 | ||||||
| chr6:138819246
|
A | G | 18 | a0001c0001t0004g0249a0001c0001t0007g0006a0001c0003t0002g0191others(15): Show | 18 | HG01169.hp1 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.179+4643A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819246 | ||||||
| chr6:138819247
|
A | G | 150 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(147): Show | 150 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.179+4644A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819247 | ||||||
| chr6:138819248
|
A | G | 3 | a0001c0001t0009g0012a0002c0002t0027g0062a0018c0030t0001g0061 | 3 | HG02109.hp2 NA18964.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.179+4645A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819248 | ||||||
| chr6:138819250
|
AAGG | A | 150 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(147): Show | 150 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.179+4649_179+4651d others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138819250 | |||||
| chr6:138819251
|
AGG | A | 3 | a0001c0001t0009g0012a0002c0002t0027g0062a0018c0030t0001g0061 | 3 | HG02109.hp2 NA18964.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.179+4649_179+4650d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819251 | ||||||
| chr6:138819253
|
G | A | 157 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.179+4650G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819253 | ||||||
| chr6:138819301
|
C | CT | 13 | a0001c0001t0004g0249a0001c0001t0007g0006a0001c0003t0003g0124others(10): Show | 13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.179+4707dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138819301 | |||||
| chr6:138819309
|
T | G | 191 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(188): Show | 191 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.179+4706T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819309 | ||||||
| chr6:138819519
|
T | A | 2 | a0002c0002t0001g0063a0002c0002t0008g0064 | 2 | NA18947.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.179+4916T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819519 | ||||||
| chr6:138819531
|
C | T | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.179+4928C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819531 | ||||||
| chr6:138819542
|
CT | C | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.179+4943delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138819542 | |||||
| chr6:138819544
|
T | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.179+4941T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819544 | ||||||
| chr6:138819744
|
G | A | 64 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.179+5141G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819744 | ||||||
| chr6:138819754
|
G | A | 108 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.179+5151G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819754 | ||||||
| chr6:138819779
|
C | T | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+5176C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819779 | ||||||
| chr6:138819813
|
G | A | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+5210G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819813 | ||||||
| chr6:138819820
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0001g0272a0001c0001t0002g0047others(5): Show | 8 | HG00738.hp2 HG01109.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.179+5217G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819820 | ||||||
| chr6:138819884
|
G | A | 3 | a0001c0001t0001g0071a0002c0005t0002g0069a0002c0005t0002g0070 | 3 | NA18981.hp1 NA18986.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+5281G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819884 | ||||||
| chr6:138819888
|
C | CA | 10 | a0001c0001t0002g0240a0001c0001t0006g0251a0001c0003t0013g0222others(7): Show | 10 | HG00733.hp1 HG01175.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.179+5295dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138819888 | |||||
| chr6:138819952
|
A | C | 199 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.179+5349A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138819952 | ||||||
| chr6:138820000
|
C | A | 199 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.179+5397C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820000 | ||||||
| chr6:138820057
|
C | A | 3 | a0011c0016t0002g0307a0011c0016t0002g0308a0012c0019t0011g0151 | 3 | HG03225.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.179+5454C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820057 | ||||||
| chr6:138820169
|
G | A | 1 | a0002c0002t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.179+5566G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820169 | ||||||
| chr6:138820178
|
G | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.179+5575G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820178 | ||||||
| chr6:138820236
|
A | G | 1 | a0001c0001t0008g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.179+5633A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820236 | ||||||
| chr6:138820377
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.179+5774A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820377 | ||||||
| chr6:138820396
|
A | C | 1 | a0002c0002t0006g0284 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.179+5793A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820396 | ||||||
| chr6:138820557
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.179+5954T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820557 | ||||||
| chr6:138820579
|
A | G | 84 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(81): Show | 84 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.179+5976A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820579 | ||||||
| chr6:138820664
|
A | T | 224 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(221): Show | 224 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.179+6061A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820664 | ||||||
| chr6:138820819
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.179+6216G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820819 | ||||||
| chr6:138820823
|
T | C | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+6220T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820823 | ||||||
| chr6:138820968
|
G | A | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+6365G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138820968 | ||||||
| chr6:138821124
|
A | G | 1 | a0004c0006t0015g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.179+6521A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821124 | ||||||
| chr6:138821263
|
T | C | 133 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(130): Show | 133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.179+6660T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821263 | ||||||
| chr6:138821383
|
C | T | 1 | a0001c0003t0002g0192 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.179+6780C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821383 | ||||||
| chr6:138821422
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.179+6819C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821422 | ||||||
| chr6:138821446
|
A | G | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+6843A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821446 | ||||||
| chr6:138821555
|
G | A | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.179+6952G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821555 | ||||||
| chr6:138821718
|
C | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.179+7115C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821718 | ||||||
| chr6:138821772
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.179+7169C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821772 | ||||||
| chr6:138821804
|
A | G | 132 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.179+7201A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821804 | ||||||
| chr6:138821870
|
C | T | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.179+7267C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821870 | ||||||
| chr6:138821951
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.179+7348A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821951 | ||||||
| chr6:138821966
|
A | C | 78 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(75): Show | 78 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.179+7363A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138821966 | ||||||
| chr6:138822002
|
C | G | 1 | a0001c0034t0023g0016 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.179+7399C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822002 | ||||||
| chr6:138822055
|
G | T | 78 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(75): Show | 78 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.179+7452G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822055 | ||||||
| chr6:138822137
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.179+7534A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822137 | ||||||
| chr6:138822329
|
G | A | 78 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(75): Show | 78 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.179+7726G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822329 | ||||||
| chr6:138822443
|
T | C | 77 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(74): Show | 77 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.179+7840T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822443 | ||||||
| chr6:138822464
|
G | A | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+7861G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822464 | ||||||
| chr6:138822509
|
T | G | 2 | a0002c0002t0004g0234a0002c0002t0007g0233 | 2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.179+7906T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822509 | ||||||
| chr6:138822554
|
C | CATAAATA others(1): Show |
79 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(76): Show | 79 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.179+7961_179+7968d others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138822554 | |||||
| chr6:138822572
|
C | T | 1 | a0014c0037t0002g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.179+7969C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822572 | ||||||
| chr6:138822700
|
G | A | 7 | a0001c0033t0002g0299a0002c0002t0007g0247a0005c0007t0001g0300others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.179+8097G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822700 | ||||||
| chr6:138822731
|
A | G | 8 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(5): Show | 8 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.179+8128A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822731 | ||||||
| chr6:138822806
|
C | T | 3 | a0001c0001t0001g0071a0002c0005t0002g0069a0002c0005t0002g0070 | 3 | NA18981.hp1 NA18986.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.179+8203C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138822806 | ||||||
| chr6:138823142
|
C | T | 132 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.179+8539C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823142 | ||||||
| chr6:138823175
|
T | A | 132 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.179+8572T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823175 | ||||||
| chr6:138823309
|
T | C | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.179+8706T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823309 | ||||||
| chr6:138823366
|
T | C | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179+8763T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823366 | ||||||
| chr6:138823547
|
C | T | 2 | a0001c0003t0002g0190a0001c0003t0002g0193 | 2 | NA18980.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.179+8944C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823547 | ||||||
| chr6:138823556
|
C | T | 85 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0067others(82): Show | 85 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.179+8953C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823556 | ||||||
| chr6:138823619
|
T | C | 132 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.179+9016T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823619 | ||||||
| chr6:138823656
|
GT | G | 3 | a0001c0001t0003g0095a0001c0001t0004g0225a0002c0002t0004g0096 | 3 | HG00323.hp2 HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.179+9058delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138823656 | |||||
| chr6:138823894
|
C | T | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.179+9291C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823894 | ||||||
| chr6:138823963
|
A | T | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+9360A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138823963 | ||||||
| chr6:138824039
|
A | G | 52 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.179+9436A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824039 | ||||||
| chr6:138824185
|
A | T | 1 | a0014c0037t0002g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.179+9582A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824185 | ||||||
| chr6:138824307
|
T | TA | 5 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(2): Show | 5 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+9713dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824307 | |||||
| chr6:138824376
|
G | T | 1 | a0002c0005t0002g0323 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.179+9773G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824376 | ||||||
| chr6:138824523
|
C | A | 1 | a0001c0001t0004g0195 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.179+9920C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824523 | ||||||
| chr6:138824538
|
C | CA | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+9937dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824538 | |||||
| chr6:138824541
|
T | A | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+9938T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824541 | ||||||
| chr6:138824541
|
T | TA | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00280.hp1 HG01081.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.179+9951dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824541 | |||||
| chr6:138824541
|
TA | T | 169 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(166): Show | 169 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.179+9951delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824541 | |||||
| chr6:138824541
|
TAA | T | 7 | a0001c0001t0008g0318a0002c0002t0008g0153a0002c0002t0027g0062others(4): Show | 7 | HG00738.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.179+9950_179+9951d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824541 | |||||
| chr6:138824543
|
A | T | 20 | a0001c0001t0029g0262a0001c0018t0020g0007a0003c0004t0004g0241others(17): Show | 20 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.179+9940A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824543 | ||||||
| chr6:138824558
|
T | TA | 145 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(142): Show | 145 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.179+9964dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824558 | |||||
| chr6:138824558
|
T | TAA | 128 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(125): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.179+9963_179+9964d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824558 | |||||
| chr6:138824568
|
C | A | 2 | a0001c0001t0001g0114a0002c0002t0001g0024 | 2 | HG01109.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.179+9965C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824568 | ||||||
| chr6:138824575
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179+9972C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824575 | ||||||
| chr6:138824576
|
A | AAAAAAC | 8 | a0001c0001t0002g0240a0001c0003t0013g0222a0001c0009t0028g0107others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.179+9977_179+9978i others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824576 | |||||
| chr6:138824577
|
A | AAAAAC | 65 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.179+9977_179+9978i others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138824577 | |||||
| chr6:138824580
|
AC | A | 55 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.179+9978delC | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824580 | ||||||
| chr6:138824581
|
C | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.179+9978C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824581 | ||||||
| chr6:138824678
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179+10075G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824678 | ||||||
| chr6:138824701
|
C | T | 1 | a0001c0003t0002g0326 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.179+10098C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824701 | ||||||
| chr6:138824760
|
C | T | 8 | a0001c0001t0007g0006a0001c0033t0002g0299a0002c0002t0007g0247others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+10157C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824760 | ||||||
| chr6:138824810
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.179+10207T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824810 | ||||||
| chr6:138824962
|
G | A | 1 | a0001c0001t0007g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179+10359G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138824962 | ||||||
| chr6:138825212
|
G | A | 76 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.179+10609G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825212 | ||||||
| chr6:138825273
|
T | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0013c0038t0002g0173 | 3 | HG02132.hp2 NA18973.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.179+10670T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825273 | ||||||
| chr6:138825301
|
C | T | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.179+10698C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825301 | ||||||
| chr6:138825351
|
G | A | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+10748G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825351 | ||||||
| chr6:138825377
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.179+10774C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825377 | ||||||
| chr6:138825496
|
T | A | 1 | a0001c0001t0007g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179+10893T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825496 | ||||||
| chr6:138825534
|
G | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.179+10931G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825534 | ||||||
| chr6:138825538
|
G | A | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+10935G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825538 | ||||||
| chr6:138825654
|
C | T | 1 | a0001c0018t0002g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179+11051C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825654 | ||||||
| chr6:138825693
|
G | A | 1 | a0001c0003t0005g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.179+11090G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825693 | ||||||
| chr6:138825695
|
A | G | 1 | a0002c0002t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.179+11092A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825695 | ||||||
| chr6:138825712
|
C | T | 1 | a0001c0003t0003g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.179+11109C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825712 | ||||||
| chr6:138825913
|
C | G | 1 | a0001c0001t0004g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.179+11310C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138825913 | ||||||
| chr6:138826046
|
G | T | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.179+11443G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826046 | ||||||
| chr6:138826048
|
T | A | 1 | a0013c0038t0002g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.179+11445T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826048 | ||||||
| chr6:138826055
|
G | A | 8 | a0001c0001t0007g0006a0001c0033t0002g0299a0002c0002t0007g0247others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+11452G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826055 | ||||||
| chr6:138826063
|
C | G | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.179+11460C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826063 | ||||||
| chr6:138826082
|
C | T | 1 | a0002c0002t0008g0120 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.179+11479C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826082 | ||||||
| chr6:138826209
|
C | T | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.179+11606C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826209 | ||||||
| chr6:138826232
|
A | G | 1 | a0001c0001t0006g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.179+11629A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826232 | ||||||
| chr6:138826284
|
A | T | 130 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(127): Show | 130 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.179+11681A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826284 | ||||||
| chr6:138826446
|
G | T | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.179+11843G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826446 | ||||||
| chr6:138826491
|
C | T | 8 | a0001c0001t0007g0006a0001c0033t0002g0299a0002c0002t0007g0247others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.180-11861C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826491 | ||||||
| chr6:138826545
|
A | G | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-11807A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826545 | ||||||
| chr6:138826740
|
C | T | 2 | a0001c0001t0003g0018a0001c0009t0004g0121 | 2 | NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.180-11612C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826740 | ||||||
| chr6:138826761
|
G | C | 1 | a0003c0004t0025g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.180-11591G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826761 | ||||||
| chr6:138826764
|
G | A | 3 | a0002c0002t0001g0042a0002c0002t0001g0110a0002c0002t0005g0290 | 3 | HG00639.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.180-11588G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826764 | ||||||
| chr6:138826817
|
G | T | 91 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(88): Show | 91 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.180-11535G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826817 | ||||||
| chr6:138826842
|
G | C | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.180-11510G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826842 | ||||||
| chr6:138826998
|
A | G | 124 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.180-11354A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138826998 | ||||||
| chr6:138827013
|
C | T | 6 | a0001c0003t0013g0222a0002c0005t0013g0217a0002c0005t0013g0220others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-11339C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827013 | ||||||
| chr6:138827219
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.180-11133A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827219 | ||||||
| chr6:138827263
|
T | C | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-11089T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827263 | ||||||
| chr6:138827282
|
A | AGGTT | 6 | a0001c0001t0004g0249a0001c0003t0003g0124a0001c0003t0003g0246others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-11068_180-1106 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138827282 | |||||
| chr6:138827351
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-11001C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827351 | ||||||
| chr6:138827558
|
T | G | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.180-10794T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827558 | ||||||
| chr6:138827694
|
G | A | 2 | a0001c0001t0003g0291a0002c0002t0007g0288 | 2 | HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.180-10658G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827694 | ||||||
| chr6:138827711
|
A | G | 2 | a0001c0003t0002g0187a0001c0003t0002g0188 | 2 | NA18942.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.180-10641A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827711 | ||||||
| chr6:138827747
|
C | T | 1 | a0001c0003t0005g0260 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.180-10605C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827747 | ||||||
| chr6:138827838
|
A | G | 1 | a0002c0002t0008g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.180-10514A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827838 | ||||||
| chr6:138827861
|
T | C | 1 | a0002c0002t0001g0072 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.180-10491T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827861 | ||||||
| chr6:138827942
|
A | AT | 264 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.180-10400dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138827942 | |||||
| chr6:138827965
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.180-10387C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138827965 | ||||||
| chr6:138828085
|
C | T | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-10267C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138828085 | ||||||
| chr6:138828086
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.180-10266G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138828086 | ||||||
| chr6:138828086
|
G | C | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-10266G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138828086 | ||||||
| chr6:138828331
|
A | G | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-10021A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138828331 | ||||||
| chr6:138828475
|
AT | A | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-9870delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138828475 | |||||
| chr6:138828794
|
T | C | 8 | a0001c0001t0007g0006a0001c0033t0002g0299a0002c0002t0007g0247others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.180-9558T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138828794 | ||||||
| chr6:138829021
|
AAT | A | 74 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(71): Show | 74 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.180-9330_180-9329d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829021 | ||||||
| chr6:138829022
|
A | AT | 35 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(32): Show | 35 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.180-9315dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138829022 | |||||
| chr6:138829022
|
AT | A | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.180-9315delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138829022 | |||||
| chr6:138829237
|
G | A | 4 | a0006c0011t0014g0237a0006c0011t0021g0236a0006c0015t0003g0238others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-9115G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829237 | ||||||
| chr6:138829267
|
T | C | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-9085T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829267 | ||||||
| chr6:138829285
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0169a0001c0001t0001g0171 | 3 | NA18943.hp2 NA18959.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.180-9067G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829285 | ||||||
| chr6:138829314
|
C | T | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-9038C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829314 | ||||||
| chr6:138829354
|
T | C | 1 | a0021c0028t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.180-8998T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829354 | ||||||
| chr6:138829691
|
G | A | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-8661G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829691 | ||||||
| chr6:138829720
|
G | GT | 11 | a0001c0001t0001g0088a0001c0001t0003g0146a0001c0001t0005g0115others(8): Show | 11 | HG00438.hp2 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.180-8623dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138829720 | |||||
| chr6:138829721
|
T | G | 13 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(10): Show | 13 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.180-8631T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829721 | ||||||
| chr6:138829730
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0114 | 2 | HG01109.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.180-8622C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829730 | ||||||
| chr6:138829731
|
C | CT | 41 | a0001c0001t0002g0240a0001c0001t0003g0095a0001c0001t0003g0137others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.180-8612dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138829731 | |||||
| chr6:138829731
|
C | CTT | 60 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(57): Show | 60 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.180-8613_180-8612d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138829731 | |||||
| chr6:138829731
|
C | T | 3 | a0001c0001t0004g0229a0001c0003t0002g0192a0002c0002t0004g0234 | 3 | HG00609.hp1 NA18978.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.180-8621C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829731 | ||||||
| chr6:138829867
|
C | T | 1 | a0001c0001t0009g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.180-8485C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829867 | ||||||
| chr6:138829868
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.180-8484G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829868 | ||||||
| chr6:138829872
|
G | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.180-8480G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829872 | ||||||
| chr6:138829880
|
G | T | 4 | a0001c0001t0004g0136a0001c0003t0003g0122a0001c0003t0003g0123others(1): Show | 4 | HG00438.hp1 NA18944.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-8472G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829880 | ||||||
| chr6:138829884
|
G | T | 64 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.180-8468G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829884 | ||||||
| chr6:138829962
|
G | A | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-8390G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138829962 | ||||||
| chr6:138830476
|
G | A | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-7876G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830476 | ||||||
| chr6:138830647
|
G | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.180-7705G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830647 | ||||||
| chr6:138830701
|
C | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.180-7651C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830701 | ||||||
| chr6:138830729
|
T | C | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-7623T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830729 | ||||||
| chr6:138830770
|
C | A | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-7582C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830770 | ||||||
| chr6:138830859
|
C | T | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.180-7493C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138830859 | ||||||
| chr6:138831204
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.180-7148T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831204 | ||||||
| chr6:138831433
|
C | T | 1 | a0001c0003t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.180-6919C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831433 | ||||||
| chr6:138831568
|
C | T | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-6784C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831568 | ||||||
| chr6:138831601
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.180-6751A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831601 | ||||||
| chr6:138831665
|
A | T | 1 | a0002c0002t0004g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.180-6687A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831665 | ||||||
| chr6:138831707
|
G | T | 1 | a0002c0002t0027g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.180-6645G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831707 | ||||||
| chr6:138831753
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-6599G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831753 | ||||||
| chr6:138831761
|
G | A | 1 | a0001c0003t0002g0304 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.180-6591G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831761 | ||||||
| chr6:138831774
|
T | C | 1 | a0003c0004t0011g0325 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.180-6578T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138831774 | ||||||
| chr6:138832026
|
CA | C | 62 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.180-6324delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832026 | |||||
| chr6:138832028
|
A | AT | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-6316dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832028 | |||||
| chr6:138832028
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.180-6324A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832028 | ||||||
| chr6:138832157
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.180-6195A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832157 | ||||||
| chr6:138832184
|
G | GT | 15 | a0002c0002t0001g0295a0003c0004t0004g0241a0003c0004t0004g0242others(12): Show | 15 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.180-6156dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832184 | |||||
| chr6:138832184
|
G | GTT | 53 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.180-6157_180-6156d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832184 | |||||
| chr6:138832184
|
GT | G | 11 | a0001c0001t0004g0249a0001c0001t0006g0029a0001c0001t0016g0211others(8): Show | 11 | HG00280.hp2 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.180-6156delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832184 | |||||
| chr6:138832184
|
GTT | G | 39 | a0001c0001t0002g0240a0001c0001t0003g0095a0001c0001t0003g0137others(36): Show | 39 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.180-6157_180-6156d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832184 | |||||
| chr6:138832196
|
T | C | 8 | a0001c0001t0007g0006a0001c0033t0002g0299a0002c0002t0007g0247others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.180-6156T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832196 | ||||||
| chr6:138832207
|
A | G | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-6145A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832207 | ||||||
| chr6:138832297
|
C | T | 56 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.180-6055C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832297 | ||||||
| chr6:138832362
|
A | T | 1 | a0001c0001t0003g0014 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.180-5990A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832362 | ||||||
| chr6:138832519
|
C | T | 1 | a0006c0011t0021g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.180-5833C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832519 | ||||||
| chr6:138832651
|
G | A | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-5701G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832651 | ||||||
| chr6:138832745
|
T | G | 128 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(125): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.180-5607T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832745 | ||||||
| chr6:138832751
|
G | GT | 32 | a0001c0001t0001g0125a0001c0001t0001g0186a0001c0001t0002g0240others(29): Show | 32 | HG00280.hp2 HG00609.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.180-5591dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138832751 | |||||
| chr6:138832751
|
G | T | 37 | a0001c0001t0003g0095a0001c0001t0003g0137a0001c0001t0003g0230others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.180-5601G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832751 | ||||||
| chr6:138832754
|
T | G | 62 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.180-5598T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832754 | ||||||
| chr6:138832766
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.180-5586T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832766 | ||||||
| chr6:138832863
|
T | C | 3 | a0008c0013t0005g0267a0008c0013t0005g0269a0019c0032t0005g0268 | 3 | HG02572.hp1 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.180-5489T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832863 | ||||||
| chr6:138832879
|
A | T | 1 | a0001c0003t0002g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.180-5473A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832879 | ||||||
| chr6:138832919
|
T | G | 165 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.180-5433T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138832919 | ||||||
| chr6:138833013
|
T | C | 103 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(100): Show | 103 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.180-5339T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833013 | ||||||
| chr6:138833017
|
G | A | 55 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.180-5335G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833017 | ||||||
| chr6:138833032
|
G | A | 4 | a0004c0006t0009g0310a0009c0012t0018g0008a0009c0012t0018g0009others(1): Show | 4 | HG01081.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-5320G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833032 | ||||||
| chr6:138833110
|
G | A | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.180-5242G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833110 | ||||||
| chr6:138833186
|
G | C | 277 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.180-5166G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833186 | ||||||
| chr6:138833313
|
C | T | 1 | a0002c0002t0001g0042 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.180-5039C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833313 | ||||||
| chr6:138833369
|
T | C | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-4983T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833369 | ||||||
| chr6:138833575
|
A | G | 1 | a0001c0009t0004g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.180-4777A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833575 | ||||||
| chr6:138833619
|
G | C | 1 | a0002c0002t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.180-4733G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833619 | ||||||
| chr6:138833636
|
T | C | 278 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.180-4716T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833636 | ||||||
| chr6:138833670
|
C | A | 1 | a0001c0001t0001g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.180-4682C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833670 | ||||||
| chr6:138833699
|
G | A | 64 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(61): Show | 64 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.180-4653G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833699 | ||||||
| chr6:138833716
|
C | T | 3 | a0009c0012t0018g0008a0009c0012t0018g0009a0009c0025t0020g0004 | 3 | HG01081.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.180-4636C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833716 | ||||||
| chr6:138833818
|
A | T | 1 | a0001c0009t0004g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.180-4534A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833818 | ||||||
| chr6:138833823
|
T | TA | 10 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0033t0002g0299others(7): Show | 10 | HG01884.hp2 HG01952.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.180-4520dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138833823 | |||||
| chr6:138833823
|
T | TAA | 132 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(129): Show | 132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.180-4521_180-4520d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138833823 | |||||
| chr6:138833823
|
T | TTA | 73 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0071others(70): Show | 73 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.180-4529_180-4528i others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833823 | ||||||
| chr6:138833888
|
A | G | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-4464A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138833888 | ||||||
| chr6:138834063
|
C | A | 1 | a0014c0037t0002g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.180-4289C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834063 | ||||||
| chr6:138834244
|
A | T | 1 | a0001c0001t0004g0229 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.180-4108A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834244 | ||||||
| chr6:138834311
|
CCCTA | C | 3 | a0002c0002t0001g0042a0002c0002t0001g0110a0002c0002t0005g0290 | 3 | HG00639.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.180-4037_180-4034d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834311 | |||||
| chr6:138834316
|
C | G | 1 | a0001c0003t0002g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.180-4036C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834316 | ||||||
| chr6:138834407
|
A | G | 1 | a0001c0003t0002g0188 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.180-3945A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834407 | ||||||
| chr6:138834540
|
G | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.180-3812G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834540 | ||||||
| chr6:138834553
|
T | C | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.180-3799T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834553 | ||||||
| chr6:138834576
|
G | A | 16 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0130others(13): Show | 16 | HG01928.hp1 HG01952.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.180-3776G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834576 | ||||||
| chr6:138834705
|
G | C | 1 | a0021c0028t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.180-3647G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834705 | ||||||
| chr6:138834718
|
A | G | 229 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(226): Show | 229 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.180-3634A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834718 | ||||||
| chr6:138834894
|
T | TAC | 38 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0002g0101others(35): Show | 38 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.180-3417_180-3416d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
T | TACAC | 29 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0090others(26): Show | 29 | HG00597.hp1 HG01106.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.180-3419_180-3416d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
T | TACACAC | 22 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0165others(19): Show | 22 | HG00639.hp2 HG01109.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.180-3421_180-3416d others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
T | TACACACA others(1): Show |
6 | a0001c0001t0001g0199a0001c0001t0002g0201a0001c0003t0002g0185others(3): Show | 6 | HG02132.hp2 HG02683.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-3423_180-3416d others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
T | TACACACA others(3): Show |
1 | a0002c0002t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.180-3425_180-3416d others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
T | TACACACA others(5): Show |
2 | a0001c0003t0002g0187a0001c0003t0002g0188 | 2 | NA18942.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.180-3427_180-3416d others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
TAC | T | 11 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0002g0184others(8): Show | 11 | HG00323.hp1 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.180-3417_180-3416d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
TACAC | T | 5 | a0001c0001t0001g0032a0001c0001t0006g0270a0001c0003t0002g0304others(2): Show | 5 | HG01169.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-3419_180-3416d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
TACACAC | T | 3 | a0001c0001t0001g0086a0001c0018t0020g0007a0016c0027t0001g0005 | 3 | HG02970.hp1 HG03098.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.180-3421_180-3416d others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
TACACACA others(1): Show |
T | 5 | a0001c0001t0029g0262a0004c0006t0015g0213a0004c0008t0009g0298others(2): Show | 5 | HG02559.hp1 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-3423_180-3416d others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834894
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0004g0144a0002c0002t0004g0131 | 2 | NA18985.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.180-3425_180-3416d others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834894 | |||||
| chr6:138834931
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.180-3421A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834931 | ||||||
| chr6:138834933
|
A | ACT | 4 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0015t0003g0238others(1): Show | 4 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-3418_180-3417i others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834933 | |||||
| chr6:138834933
|
A | ACTCT | 3 | a0001c0003t0002g0326a0002c0002t0001g0113a0008c0013t0002g0043 | 3 | HG00738.hp1 HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.180-3418_180-3417i others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834933 | |||||
| chr6:138834933
|
A | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG00438.hp2 HG02129.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.180-3419A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834933 | ||||||
| chr6:138834935
|
A | ACACACAC others(11): Show |
2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-3416_180-3415i others(20): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACAC others(5): Show |
1 | a0001c0003t0003g0214 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.180-3416_180-3415i others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACAC others(3): Show |
5 | a0001c0001t0003g0095a0001c0001t0004g0249a0001c0003t0003g0235others(2): Show | 5 | HG02922.hp2 HG03540.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACAC others(5): Show |
4 | a0001c0001t0009g0108a0001c0003t0002g0058a0001c0018t0002g0059others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACT | 3 | a0011c0016t0002g0307a0011c0016t0002g0308a0012c0019t0011g0151 | 3 | HG03225.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.180-3416_180-3415i others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACTC others(1): Show |
22 | a0001c0001t0003g0137a0001c0001t0003g0291a0001c0001t0004g0136others(19): Show | 22 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACACTC others(3): Show |
13 | a0001c0001t0001g0045a0001c0001t0001g0272a0001c0001t0009g0012others(10): Show | 13 | HG00558.hp1 HG00597.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACTCT | 13 | a0001c0001t0004g0094a0001c0001t0004g0229a0001c0001t0004g0264others(10): Show | 13 | HG02015.hp2 NA18943.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACTCTC others(1): Show |
17 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0306others(14): Show | 17 | HG00738.hp2 HG01261.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.180-3416_180-3415i others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACACTCTC others(3): Show |
1 | a0005c0007t0001g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.180-3416_180-3415i others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACTCT | 3 | a0001c0001t0003g0230a0001c0003t0003g0196a0002c0002t0004g0234 | 3 | HG00099.hp1 HG00609.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.180-3415_180-3412d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | ACTCTCT | 48 | a0001c0001t0001g0060a0001c0001t0001g0071a0001c0001t0001g0079others(45): Show | 48 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.180-3412_180-3411i others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138834935 | |||||
| chr6:138834935
|
A | T | 22 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0086others(19): Show | 22 | HG00438.hp2 HG00738.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.180-3417A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834935 | ||||||
| chr6:138834937
|
T | A | 2 | a0002c0002t0006g0261a0002c0002t0019g0167 | 2 | NA18962.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.180-3415T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834937 | ||||||
| chr6:138834941
|
A | G | 6 | a0001c0003t0013g0222a0002c0005t0013g0217a0002c0005t0013g0220others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-3411A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834941 | ||||||
| chr6:138834941
|
A | T | 1 | a0002c0002t0017g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.180-3411A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834941 | ||||||
| chr6:138834942
|
T | C | 1 | a0002c0002t0017g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.180-3410T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834942 | ||||||
| chr6:138834954
|
G | C | 1 | a0002c0002t0017g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.180-3398G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138834954 | ||||||
| chr6:138835068
|
C | T | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-3284C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835068 | ||||||
| chr6:138835130
|
A | T | 219 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(216): Show | 219 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.180-3222A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835130 | ||||||
| chr6:138835145
|
TA | T | 48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.180-3199delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138835145 | |||||
| chr6:138835166
|
C | T | 9 | a0001c0001t0001g0179a0001c0001t0002g0102a0001c0001t0002g0174others(6): Show | 9 | HG01258.hp1 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.180-3186C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835166 | ||||||
| chr6:138835260
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.180-3092T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835260 | ||||||
| chr6:138835280
|
G | A | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-3072G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835280 | ||||||
| chr6:138835422
|
A | G | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-2930A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835422 | ||||||
| chr6:138835459
|
G | A | 2 | a0001c0003t0002g0058a0001c0018t0002g0059 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.180-2893G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835459 | ||||||
| chr6:138835504
|
A | G | 1 | a0002c0002t0027g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.180-2848A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835504 | ||||||
| chr6:138835509
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-2843G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835509 | ||||||
| chr6:138835551
|
C | CA | 13 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0088others(10): Show | 13 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.180-2784dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138835551 | |||||
| chr6:138835551
|
CA | C | 108 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.180-2784delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138835551 | |||||
| chr6:138835653
|
C | T | 10 | a0001c0001t0002g0240a0001c0001t0016g0211a0001c0001t0016g0212others(7): Show | 10 | HG00733.hp1 HG01175.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.180-2699C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835653 | ||||||
| chr6:138835664
|
G | T | 1 | a0001c0001t0007g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.180-2688G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835664 | ||||||
| chr6:138835845
|
C | A | 6 | a0001c0001t0004g0249a0001c0001t0007g0006a0001c0003t0003g0124others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.180-2507C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835845 | ||||||
| chr6:138835937
|
A | T | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.180-2415A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138835937 | ||||||
| chr6:138836053
|
C | T | 4 | a0005c0024t0005g0276a0011c0016t0002g0307a0011c0016t0002g0308others(1): Show | 4 | HG03225.hp2 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-2299C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836053 | ||||||
| chr6:138836054
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-2298G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836054 | ||||||
| chr6:138836066
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.180-2286G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836066 | ||||||
| chr6:138836082
|
G | C | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.180-2270G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836082 | ||||||
| chr6:138836122
|
A | C | 215 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(212): Show | 215 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.180-2230A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836122 | ||||||
| chr6:138836177
|
T | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.180-2175T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836177 | ||||||
| chr6:138836289
|
C | CT | 9 | a0001c0001t0001g0252a0001c0001t0006g0286a0002c0002t0007g0247others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.180-2045dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138836289 | |||||
| chr6:138836289
|
CT | C | 142 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0045others(139): Show | 142 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.180-2045delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138836289 | |||||
| chr6:138836289
|
CTT | C | 8 | a0001c0001t0002g0240a0001c0001t0029g0262a0001c0009t0028g0107others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-2046_180-2045d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138836289 | |||||
| chr6:138836325
|
G | A | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-2027G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836325 | ||||||
| chr6:138836434
|
G | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.180-1918G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836434 | ||||||
| chr6:138836568
|
G | A | 2 | a0001c0001t0009g0012a0002c0002t0001g0097 | 2 | HG02109.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.180-1784G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836568 | ||||||
| chr6:138836670
|
GTGTTC | G | 205 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(202): Show | 205 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.180-1677_180-1673d others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138836670 | |||||
| chr6:138836720
|
A | G | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.180-1632A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836720 | ||||||
| chr6:138836753
|
C | T | 8 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(5): Show | 8 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-1599C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836753 | ||||||
| chr6:138836755
|
C | T | 10 | a0001c0001t0002g0240a0001c0001t0016g0211a0001c0001t0016g0212others(7): Show | 10 | HG00733.hp1 HG01175.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.180-1597C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836755 | ||||||
| chr6:138836992
|
G | A | 215 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(212): Show | 215 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.180-1360G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138836992 | ||||||
| chr6:138837055
|
G | A | 205 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(202): Show | 205 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.180-1297G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837055 | ||||||
| chr6:138837124
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.180-1228C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837124 | ||||||
| chr6:138837241
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.180-1111T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837241 | ||||||
| chr6:138837360
|
C | T | 8 | a0001c0001t0002g0240a0001c0001t0029g0262a0001c0009t0028g0107others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-992C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837360 | ||||||
| chr6:138837486
|
C | T | 8 | a0001c0001t0002g0240a0001c0001t0029g0262a0001c0009t0028g0107others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.180-866C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837486 | ||||||
| chr6:138837538
|
C | T | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-814C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837538 | ||||||
| chr6:138837539
|
G | T | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.180-813G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837539 | ||||||
| chr6:138837541
|
A | G | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-811A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837541 | ||||||
| chr6:138837639
|
C | T | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.180-713C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837639 | ||||||
| chr6:138837641
|
C | CA | 45 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.180-696dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138837641 | |||||
| chr6:138837641
|
CA | C | 214 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(211): Show | 214 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.180-696delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138837641 | |||||
| chr6:138837654
|
A | C | 214 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(211): Show | 214 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.180-698A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837654 | ||||||
| chr6:138837814
|
G | A | 1 | a0001c0001t0010g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180-538G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837814 | ||||||
| chr6:138837902
|
C | CT | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-434dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138837902 | |||||
| chr6:138837902
|
CT | C | 196 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(193): Show | 196 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.180-434delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138837902 | |||||
| chr6:138837902
|
CTT | C | 8 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0240others(5): Show | 8 | HG00733.hp1 HG01175.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.180-435_180-434del others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | 138837902 | |||||
| chr6:138837964
|
G | A | 6 | a0001c0001t0029g0262a0001c0018t0020g0007a0004c0006t0015g0213others(3): Show | 6 | HG02559.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-388G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138837964 | ||||||
| chr6:138838069
|
G | T | 215 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(212): Show | 215 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.180-283G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138838069 | ||||||
| chr6:138838096
|
T | A | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.180-256T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138838096 | ||||||
| chr6:138838186
|
G | A | 84 | a0001c0001t0001g0045a0001c0001t0001g0060a0001c0001t0001g0067others(81): Show | 84 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.180-166G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138838186 | ||||||
| chr6:138838197
|
T | C | 1 | a0002c0002t0002g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.180-155T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138838197 | ||||||
| chr6:138838245
|
T | C | 207 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(204): Show | 207 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.180-107T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 4/21 | chr6 | 138838245 | ||||||
| chr6:138838690
|
A | T | 108 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(105): Show | 108 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.342+176A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838690 | ||||||
| chr6:138838698
|
T | C | 2 | a0002c0002t0004g0234a0002c0002t0007g0233 | 2 | HG00609.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.342+184T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838698 | ||||||
| chr6:138838788
|
T | C | 1 | a0001c0001t0003g0034 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.342+274T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838788 | ||||||
| chr6:138838817
|
T | C | 314 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.342+303T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838817 | ||||||
| chr6:138838868
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.342+354G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838868 | ||||||
| chr6:138838901
|
C | G | 1 | a0001c0003t0013g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.342+387C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838901 | ||||||
| chr6:138838904
|
C | A | 6 | a0001c0003t0013g0222a0002c0005t0013g0217a0002c0005t0013g0220others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+390C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838904 | ||||||
| chr6:138838927
|
G | A | 3 | a0002c0002t0001g0042a0002c0002t0001g0110a0002c0002t0005g0290 | 3 | HG00639.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.342+413G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838927 | ||||||
| chr6:138838930
|
T | C | 317 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.342+416T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138838930 | ||||||
| chr6:138839076
|
G | A | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.342+562G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839076 | ||||||
| chr6:138839192
|
A | G | 6 | a0001c0001t0001g0067a0001c0001t0002g0047a0001c0001t0002g0048others(3): Show | 6 | HG00738.hp2 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+678A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839192 | ||||||
| chr6:138839356
|
A | T | 209 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(206): Show | 209 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.342+842A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839356 | ||||||
| chr6:138839364
|
CT | C | 197 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(194): Show | 197 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.342+865delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138839364 | |||||
| chr6:138839472
|
T | C | 1 | a0007c0014t0005g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.342+958T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839472 | ||||||
| chr6:138839511
|
G | T | 7 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+997G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839511 | ||||||
| chr6:138839561
|
G | A | 7 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(4): Show | 7 | HG02486.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+1047G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839561 | ||||||
| chr6:138839625
|
T | C | 12 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(9): Show | 12 | HG02486.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+1111T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839625 | ||||||
| chr6:138839670
|
G | A | 1 | a0002c0002t0019g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.342+1156G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839670 | ||||||
| chr6:138839760
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.342+1246T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839760 | ||||||
| chr6:138839971
|
T | A | 125 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(122): Show | 125 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.342+1457T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138839971 | ||||||
| chr6:138840102
|
T | C | 2 | a0001c0001t0002g0240a0001c0009t0028g0107 | 2 | HG00733.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.342+1588T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840102 | ||||||
| chr6:138840124
|
G | A | 142 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0060others(139): Show | 142 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.342+1610G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840124 | ||||||
| chr6:138840261
|
A | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.342+1747A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840261 | ||||||
| chr6:138840381
|
A | AT | 105 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.342+1874dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138840381 | |||||
| chr6:138840507
|
T | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0194 | 2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.342+1993T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840507 | ||||||
| chr6:138840548
|
A | G | 3 | a0001c0003t0002g0304a0011c0016t0002g0307a0011c0016t0002g0308 | 3 | HG03225.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.342+2034A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840548 | ||||||
| chr6:138840588
|
AT | A | 146 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.342+2083delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138840588 | |||||
| chr6:138840588
|
ATT | A | 17 | a0001c0033t0002g0299a0003c0004t0004g0241a0003c0004t0004g0242others(14): Show | 17 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.342+2082_342+2083d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138840588 | |||||
| chr6:138840747
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343-2232G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840747 | ||||||
| chr6:138840913
|
C | T | 255 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.343-2066C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840913 | ||||||
| chr6:138840927
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.343-2052C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138840927 | ||||||
| chr6:138841060
|
G | A | 58 | a0001c0001t0001g0045a0001c0001t0001g0083a0001c0001t0001g0085others(55): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.343-1919G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841060 | ||||||
| chr6:138841079
|
G | A | 6 | a0001c0001t0009g0152a0001c0009t0001g0170a0001c0009t0004g0121others(3): Show | 6 | HG01175.hp1 HG01243.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-1900G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841079 | ||||||
| chr6:138841082
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.343-1897T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841082 | ||||||
| chr6:138841124
|
T | C | 14 | a0001c0033t0002g0299a0003c0004t0004g0241a0003c0004t0004g0242others(11): Show | 14 | HG01433.hp1 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.343-1855T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841124 | ||||||
| chr6:138841506
|
C | A | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.343-1473C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841506 | ||||||
| chr6:138841527
|
T | C | 9 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-1452T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841527 | ||||||
| chr6:138841628
|
G | T | 3 | a0001c0009t0001g0170a0001c0009t0004g0121a0001c0009t0028g0107 | 3 | HG01175.hp1 NA19060.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.343-1351G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841628 | ||||||
| chr6:138841832
|
G | A | 11 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(8): Show | 11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.343-1147G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138841832 | ||||||
| chr6:138842002
|
T | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.343-977T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842002 | ||||||
| chr6:138842026
|
G | GATAAGTG others(2): Show |
10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-951_343-943dup others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138842026 | |||||
| chr6:138842066
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.343-913T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842066 | ||||||
| chr6:138842193
|
T | C | 18 | a0001c0033t0002g0299a0003c0004t0004g0241a0003c0004t0004g0242others(15): Show | 18 | HG01433.hp1 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.343-786T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842193 | ||||||
| chr6:138842229
|
C | T | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.343-750C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842229 | ||||||
| chr6:138842306
|
C | CA | 178 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.343-668dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr6 | 138842306 | |||||
| chr6:138842417
|
C | T | 64 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0071others(61): Show | 64 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.343-562C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842417 | ||||||
| chr6:138842500
|
G | T | 1 | a0001c0001t0006g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.343-479G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842500 | ||||||
| chr6:138842547
|
G | A | 2 | a0009c0012t0003g0021a0014c0037t0002g0036 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.343-432G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842547 | ||||||
| chr6:138842582
|
T | C | 1 | a0001c0001t0003g0133 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.343-397T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842582 | ||||||
| chr6:138842597
|
T | C | 1 | a0002c0002t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.343-382T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842597 | ||||||
| chr6:138842638
|
G | A | 16 | a0001c0001t0001g0293a0001c0001t0005g0115a0001c0001t0006g0029others(13): Show | 16 | HG00280.hp2 HG01192.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-341G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842638 | ||||||
| chr6:138842644
|
T | C | 19 | a0001c0001t0001g0293a0001c0001t0005g0115a0001c0001t0006g0029others(16): Show | 19 | HG00280.hp2 HG01192.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.343-335T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842644 | ||||||
| chr6:138842689
|
A | G | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.343-290A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842689 | ||||||
| chr6:138842697
|
G | A | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.343-282G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842697 | ||||||
| chr6:138842703
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.343-276C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842703 | ||||||
| chr6:138842841
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.343-138G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842841 | ||||||
| chr6:138842853
|
A | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.343-126A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 5/21 | chr6 | 138842853 | ||||||
| chr6:138843325
|
C | T | 1 | a0001c0001t0006g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.595+94C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843325 | ||||||
| chr6:138843629
|
G | GC | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+398_595+399ins others(1): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843629 | ||||||
| chr6:138843630
|
A | G | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.595+399A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843630 | ||||||
| chr6:138843774
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.595+543C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843774 | ||||||
| chr6:138843873
|
A | G | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-539A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843873 | ||||||
| chr6:138843997
|
G | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.596-415G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138843997 | ||||||
| chr6:138844177
|
G | C | 15 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0004g0243others(12): Show | 15 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.596-235G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138844177 | ||||||
| chr6:138844211
|
C | G | 5 | a0007c0010t0010g0206a0007c0010t0010g0209a0007c0010t0010g0210others(2): Show | 5 | HG01106.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-201C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138844211 | ||||||
| chr6:138844321
|
T | C | 3 | a0001c0009t0001g0170a0001c0009t0004g0121a0001c0009t0028g0107 | 3 | HG01175.hp1 NA19060.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.596-91T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138844321 | ||||||
| chr6:138844376
|
A | G | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-36A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 6/21 | chr6 | 138844376 | ||||||
| chr6:138844694
|
T | C | 3 | a0001c0009t0001g0170a0001c0009t0004g0121a0001c0009t0028g0107 | 3 | HG01175.hp1 NA19060.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.764+114T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138844694 | ||||||
| chr6:138844763
|
A | G | 1 | a0001c0003t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.764+183A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138844763 | ||||||
| chr6:138844795
|
C | CT | 206 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.764+233dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138844795 | |||||
| chr6:138844795
|
C | CTT | 15 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0007g0006others(12): Show | 15 | HG00639.hp1 HG01106.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.764+232_764+233dup others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138844795 | |||||
| chr6:138844891
|
T | C | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.764+311T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138844891 | ||||||
| chr6:138845008
|
A | C | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+428A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845008 | ||||||
| chr6:138845030
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.764+450C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845030 | ||||||
| chr6:138845104
|
T | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0088others(1): Show | 4 | NA18968.hp2 NA18971.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+524T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845104 | ||||||
| chr6:138845118
|
C | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.764+538C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845118 | ||||||
| chr6:138845140
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0032others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+560C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845140 | ||||||
| chr6:138845242
|
A | AT | 13 | a0001c0001t0001g0044a0001c0001t0005g0115a0001c0001t0009g0108others(10): Show | 13 | HG00738.hp1 HG01243.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.764+680dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138845242 | |||||
| chr6:138845242
|
AT | A | 144 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.764+680delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138845242 | |||||
| chr6:138845242
|
ATT | A | 20 | a0001c0001t0001g0071a0001c0001t0001g0080a0002c0002t0001g0072others(17): Show | 20 | HG01433.hp1 HG02451.hp1 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.764+679_764+680del others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138845242 | |||||
| chr6:138845301
|
G | A | 7 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0009t0001g0170others(4): Show | 7 | HG01175.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.764+721G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845301 | ||||||
| chr6:138845313
|
G | T | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+733G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845313 | ||||||
| chr6:138845374
|
G | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.764+794G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845374 | ||||||
| chr6:138845433
|
A | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.764+853A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845433 | ||||||
| chr6:138845443
|
C | T | 1 | a0001c0003t0002g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.764+863C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845443 | ||||||
| chr6:138845532
|
G | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.764+952G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845532 | ||||||
| chr6:138845658
|
C | A | 2 | a0001c0001t0004g0136a0001c0001t0004g0265 | 2 | HG00438.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.765-881C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845658 | ||||||
| chr6:138845669
|
A | G | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.765-870A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845669 | ||||||
| chr6:138845750
|
G | T | 3 | a0001c0009t0001g0170a0001c0009t0004g0121a0001c0009t0028g0107 | 3 | HG01175.hp1 NA19060.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.765-789G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845750 | ||||||
| chr6:138845774
|
T | C | 4 | a0001c0003t0002g0190a0001c0003t0002g0191a0001c0003t0002g0193others(1): Show | 4 | NA18951.hp1 NA18980.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-765T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845774 | ||||||
| chr6:138845793
|
A | G | 1 | a0001c0001t0022g0287 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.765-746A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845793 | ||||||
| chr6:138845827
|
T | C | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.765-712T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845827 | ||||||
| chr6:138845828
|
T | C | 1 | a0001c0003t0002g0100 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.765-711T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845828 | ||||||
| chr6:138845836
|
C | T | 15 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(12): Show | 15 | HG01433.hp1 HG02451.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.765-703C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845836 | ||||||
| chr6:138845837
|
A | G | 177 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.765-702A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845837 | ||||||
| chr6:138845852
|
C | A | 4 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-687C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845852 | ||||||
| chr6:138845911
|
C | T | 2 | a0001c0033t0002g0299a0003c0004t0004g0243 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.765-628C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138845911 | ||||||
| chr6:138845985
|
TGCTTGA | T | 4 | a0003c0004t0007g0320a0003c0004t0007g0321a0003c0004t0007g0322others(1): Show | 4 | HG01433.hp1 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-551_765-546del others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr6 | 138845985 | |||||
| chr6:138846035
|
C | T | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.765-504C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138846035 | ||||||
| chr6:138846320
|
C | G | 4 | a0001c0001t0005g0115a0001c0003t0002g0187a0001c0003t0002g0188others(1): Show | 4 | HG01978.hp2 NA18942.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-219C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138846320 | ||||||
| chr6:138846442
|
T | C | 141 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.765-97T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138846442 | ||||||
| chr6:138846530
|
A | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.765-9A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 7/21 | chr6 | 138846530 | ||||||
| chr6:138846833
|
C | CA | 17 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(14): Show | 17 | HG01433.hp1 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.903+156_903+157ins others(1): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138846833 | ||||||
| chr6:138846868
|
G | A | 1 | a0001c0003t0003g0001 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.903+191G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138846868 | ||||||
| chr6:138846964
|
T | TA | 138 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.903+308dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138846964 | |||||
| chr6:138846964
|
T | TAA | 39 | a0001c0001t0001g0125a0001c0001t0001g0272a0001c0001t0002g0015others(36): Show | 39 | HG00738.hp2 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.903+307_903+308dup others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138846964 | |||||
| chr6:138846964
|
T | TAAA | 11 | a0001c0001t0001g0169a0001c0003t0002g0326a0002c0002t0017g0010others(8): Show | 11 | HG02027.hp1 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.903+306_903+308dup others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138846964 | |||||
| chr6:138846994
|
G | T | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.903+317G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138846994 | ||||||
| chr6:138847148
|
T | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.903+471T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847148 | ||||||
| chr6:138847181
|
A | T | 1 | a0002c0002t0027g0062 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.903+504A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847181 | ||||||
| chr6:138847261
|
TCAAAA | T | 15 | a0001c0001t0008g0046a0005c0007t0001g0300a0005c0007t0001g0301others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.903+604_903+608del others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847261 | |||||
| chr6:138847320
|
T | C | 1 | a0001c0003t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.903+643T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847320 | ||||||
| chr6:138847354
|
A | ATTTTTT | 7 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220others(4): Show | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+677_903+678ins others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847354 | ||||||
| chr6:138847354
|
ACTTTTTT others(6): Show |
A | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.903+678_903+690del others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847354 | ||||||
| chr6:138847355
|
C | CT | 29 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0001g0111others(26): Show | 29 | HG00558.hp2 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.903+711dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | CTT | 18 | a0001c0001t0001g0171a0001c0001t0002g0174a0001c0001t0004g0136others(15): Show | 18 | HG00280.hp2 HG00438.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.903+710_903+711dup others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | CTTT | 9 | a0001c0001t0001g0161a0001c0001t0001g0252a0001c0001t0005g0277others(6): Show | 9 | HG00438.hp2 HG01943.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+709_903+711dup others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | CTTTTTTT others(3): Show |
3 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320 | 3 | HG02622.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903+702_903+711dup others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | CTTTTTTT others(4): Show |
2 | a0004c0006t0001g0311a0004c0006t0015g0312 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.903+701_903+711dup others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | CTTTTTTT others(5): Show |
1 | a0004c0006t0001g0313 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.903+700_903+711dup others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
C | T | 9 | a0001c0003t0003g0124a0002c0002t0017g0010a0002c0005t0013g0217others(6): Show | 9 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.903+678C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847355 | ||||||
| chr6:138847355
|
CT | C | 43 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0085others(40): Show | 43 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+711delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
CTTTTT | C | 13 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0149others(10): Show | 13 | HG00609.hp1 HG02145.hp1 HG04228.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+707_903+711del others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
CTTTTTT | C | 120 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.903+706_903+711del others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.903+701_903+711del others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
CTTTTTTT others(8): Show |
C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.903+697_903+711del others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847355
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0003t0005g0292 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.903+696_903+711del others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847355 | |||||
| chr6:138847392
|
A | T | 160 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.903+715A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847392 | ||||||
| chr6:138847402
|
A | G | 172 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.903+725A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847402 | ||||||
| chr6:138847403
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.903+726C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847403 | ||||||
| chr6:138847432
|
G | A | 11 | a0001c0001t0004g0040a0001c0001t0004g0138a0001c0003t0003g0124others(8): Show | 11 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+755G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847432 | ||||||
| chr6:138847435
|
A | G | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.903+758A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847435 | ||||||
| chr6:138847497
|
A | T | 1 | a0001c0003t0002g0304 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.903+820A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847497 | ||||||
| chr6:138847511
|
C | T | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.903+834C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847511 | ||||||
| chr6:138847524
|
C | A | 1 | a0001c0001t0002g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903+847C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847524 | ||||||
| chr6:138847537
|
A | AT | 34 | a0001c0001t0001g0087a0001c0001t0001g0111a0001c0001t0001g0112others(31): Show | 34 | HG00558.hp2 HG00639.hp2 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.903+882dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr6 | 138847537 | |||||
| chr6:138847655
|
G | A | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.903+978G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847655 | ||||||
| chr6:138847661
|
G | C | 1 | a0001c0003t0003g0123 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.903+984G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847661 | ||||||
| chr6:138847942
|
G | A | 2 | a0001c0033t0002g0299a0003c0004t0004g0243 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.903+1265G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138847942 | ||||||
| chr6:138848193
|
T | G | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.904-1076T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848193 | ||||||
| chr6:138848347
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904-922T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848347 | ||||||
| chr6:138848460
|
T | G | 2 | a0001c0033t0002g0299a0003c0004t0004g0243 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.904-809T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848460 | ||||||
| chr6:138848726
|
G | A | 141 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.904-543G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848726 | ||||||
| chr6:138848898
|
G | A | 3 | a0001c0001t0004g0249a0001c0003t0003g0246a0001c0003t0003g0248 | 3 | HG02922.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.904-371G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848898 | ||||||
| chr6:138848906
|
C | T | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.904-363C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848906 | ||||||
| chr6:138848962
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.904-307C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138848962 | ||||||
| chr6:138849156
|
T | G | 11 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(8): Show | 11 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.904-113T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138849156 | ||||||
| chr6:138849169
|
T | C | 5 | a0001c0033t0002g0299a0003c0004t0004g0243a0012c0019t0011g0151others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-100T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 8/21 | chr6 | 138849169 | ||||||
| chr6:138849505
|
C | T | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+71C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849505 | ||||||
| chr6:138849573
|
C | CT | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0266others(4): Show | 7 | HG00621.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069+156dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138849573 | |||||
| chr6:138849573
|
CT | C | 24 | a0001c0001t0004g0127a0001c0001t0016g0211a0001c0001t0016g0212others(21): Show | 24 | HG01169.hp1 HG01175.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1069+156delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138849573 | |||||
| chr6:138849590
|
T | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+156T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849590 | ||||||
| chr6:138849637
|
C | T | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1069+203C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849637 | ||||||
| chr6:138849676
|
T | C | 2 | a0001c0033t0002g0299a0003c0004t0004g0243 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1069+242T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849676 | ||||||
| chr6:138849794
|
C | T | 1 | a0001c0001t0010g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1069+360C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849794 | ||||||
| chr6:138849852
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+418G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849852 | ||||||
| chr6:138849944
|
ATT | A | 139 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1069+511_1069+512d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849944 | ||||||
| chr6:138849952
|
T | G | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1069+518T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849952 | ||||||
| chr6:138849954
|
C | G | 1 | a0001c0003t0003g0196 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1069+520C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849954 | ||||||
| chr6:138849962
|
T | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+528T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138849962 | ||||||
| chr6:138850019
|
G | GA | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069+593dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850019 | |||||
| chr6:138850057
|
A | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+623A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850057 | ||||||
| chr6:138850114
|
A | G | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1069+680A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850114 | ||||||
| chr6:138850148
|
TTC | T | 14 | a0001c0001t0004g0040a0001c0001t0008g0250a0001c0001t0029g0262others(11): Show | 14 | HG02486.hp2 HG02559.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1069+716_1069+717d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850148 | |||||
| chr6:138850149
|
TC | T | 166 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1069+716delC | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850149 | ||||||
| chr6:138850150
|
C | T | 3 | a0001c0001t0001g0044a0012c0019t0011g0151a0012c0019t0011g0168 | 3 | HG02559.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+716C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850150 | ||||||
| chr6:138850158
|
G | A | 6 | a0001c0033t0002g0299a0003c0004t0004g0243a0008c0013t0002g0043others(3): Show | 6 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069+724G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850158 | ||||||
| chr6:138850160
|
G | C | 180 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1069+726G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850160 | ||||||
| chr6:138850199
|
G | A | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1069+765G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850199 | ||||||
| chr6:138850236
|
C | T | 9 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069+802C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850236 | ||||||
| chr6:138850289
|
C | T | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1069+855C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850289 | ||||||
| chr6:138850317
|
C | G | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+883C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850317 | ||||||
| chr6:138850333
|
C | T | 177 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1069+899C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850333 | ||||||
| chr6:138850378
|
C | G | 15 | a0001c0001t0008g0046a0005c0007t0001g0300a0005c0007t0001g0301others(12): Show | 15 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1069+944C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850378 | ||||||
| chr6:138850441
|
G | A | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1007G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850441 | ||||||
| chr6:138850444
|
T | C | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1010T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850444 | ||||||
| chr6:138850534
|
T | TTTTG | 311 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1069+1103_1069+110 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850534 | |||||
| chr6:138850555
|
T | G | 16 | a0001c0001t0016g0211a0001c0001t0016g0212a0003c0004t0004g0241others(13): Show | 16 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1069+1121T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850555 | ||||||
| chr6:138850685
|
T | C | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+1251T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850685 | ||||||
| chr6:138850720
|
T | A | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1286T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850720 | ||||||
| chr6:138850799
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1365C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850799 | ||||||
| chr6:138850800
|
A | G | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1366A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850800 | ||||||
| chr6:138850894
|
G | A | 1 | a0002c0002t0004g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1069+1460G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850894 | ||||||
| chr6:138850925
|
T | C | 325 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1069+1491T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850925 | ||||||
| chr6:138850933
|
G | A | 1 | a0001c0001t0029g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1069+1499G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850933 | ||||||
| chr6:138850982
|
G | A | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069+1548G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138850982 | ||||||
| chr6:138850994
|
C | CA | 37 | a0001c0001t0001g0051a0001c0001t0001g0161a0001c0001t0001g0252others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1069+1589dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
C | CAA | 6 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0029g0262others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069+1588_1069+158 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
C | CAAAAAAA others(4): Show |
1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1069+1579_1069+158 others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
C | CAAAAAAA others(5): Show |
1 | a0003c0004t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1069+1578_1069+158 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CA | C | 9 | a0001c0001t0001g0306a0001c0001t0004g0265a0001c0001t0005g0281others(6): Show | 9 | HG02615.hp1 HG02976.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069+1589delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CAA | C | 25 | a0001c0001t0001g0087a0001c0001t0001g0109a0001c0001t0001g0112others(22): Show | 25 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1069+1588_1069+158 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CAAA | C | 119 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1069+1587_1069+158 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CAAAAAAA others(1): Show |
C | 10 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0011g0325others(7): Show | 10 | HG02717.hp1 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+1582_1069+158 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CAAAAAAA others(3): Show |
C | 8 | a0002c0002t0001g0178a0002c0002t0001g0189a0002c0002t0004g0228others(5): Show | 8 | HG01081.hp1 HG02976.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1069+1580_1069+158 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138850994
|
CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0008g0046a0005c0007t0001g0300a0005c0007t0001g0301others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1069+1579_1069+158 others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138850994 | |||||
| chr6:138851022
|
A | G | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1069+1588A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851022 | ||||||
| chr6:138851101
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1069+1667C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851101 | ||||||
| chr6:138851182
|
T | C | 4 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069+1748T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851182 | ||||||
| chr6:138851249
|
T | C | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1069+1815T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851249 | ||||||
| chr6:138851390
|
T | A | 14 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(11): Show | 14 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1069+1956T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851390 | ||||||
| chr6:138851482
|
C | CT | 77 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0080others(74): Show | 77 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1069+2071dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138851482 | |||||
| chr6:138851482
|
C | CTT | 6 | a0001c0001t0001g0087a0001c0001t0001g0112a0001c0001t0008g0046others(3): Show | 6 | HG01261.hp1 HG02572.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+2070_1069+207 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138851482 | |||||
| chr6:138851482
|
CT | C | 25 | a0001c0001t0002g0015a0001c0001t0002g0068a0001c0001t0002g0201others(22): Show | 25 | HG00323.hp2 HG01106.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1069+2071delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138851482 | |||||
| chr6:138851482
|
CTT | C | 79 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(76): Show | 79 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1069+2070_1069+207 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138851482 | |||||
| chr6:138851695
|
T | C | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1069+2261T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851695 | ||||||
| chr6:138851778
|
C | T | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1070-2248C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138851778 | ||||||
| chr6:138852141
|
G | A | 1 | a0002c0002t0001g0063 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1070-1885G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852141 | ||||||
| chr6:138852195
|
G | T | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1070-1831G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852195 | ||||||
| chr6:138852329
|
CT | C | 9 | a0001c0001t0001g0179a0001c0001t0002g0102a0001c0001t0002g0174others(6): Show | 9 | HG01258.hp1 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1683delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr6 | 138852329 | |||||
| chr6:138852378
|
G | C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1070-1648G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852378 | ||||||
| chr6:138852507
|
T | C | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1070-1519T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852507 | ||||||
| chr6:138852576
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1070-1450C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852576 | ||||||
| chr6:138852639
|
A | G | 143 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1070-1387A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852639 | ||||||
| chr6:138852813
|
G | A | 4 | a0001c0001t0008g0250a0001c0001t0029g0262a0001c0018t0020g0007others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1213G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852813 | ||||||
| chr6:138852863
|
A | C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1070-1163A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852863 | ||||||
| chr6:138852908
|
G | A | 1 | a0002c0002t0006g0224 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1070-1118G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852908 | ||||||
| chr6:138852998
|
C | T | 11 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(8): Show | 11 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1070-1028C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138852998 | ||||||
| chr6:138853180
|
C | A | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1070-846C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853180 | ||||||
| chr6:138853317
|
C | A | 3 | a0012c0019t0011g0151a0012c0019t0011g0168a0023c0036t0002g0305 | 3 | HG02451.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1070-709C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853317 | ||||||
| chr6:138853338
|
T | C | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1070-688T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853338 | ||||||
| chr6:138853492
|
A | C | 1 | a0018c0030t0001g0061 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1070-534A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853492 | ||||||
| chr6:138853492
|
A | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1070-534A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853492 | ||||||
| chr6:138853498
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1070-528G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853498 | ||||||
| chr6:138853577
|
G | C | 62 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0056others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1070-449G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853577 | ||||||
| chr6:138853584
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1070-442C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853584 | ||||||
| chr6:138853733
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1070-293C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853733 | ||||||
| chr6:138853755
|
G | A | 1 | a0001c0001t0003g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1070-271G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853755 | ||||||
| chr6:138853783
|
G | A | 11 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0130others(8): Show | 11 | HG01952.hp1 HG02293.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.1070-243G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853783 | ||||||
| chr6:138853846
|
A | G | 3 | a0001c0001t0003g0095a0001c0001t0004g0225a0002c0002t0004g0096 | 3 | HG00323.hp2 HG01257.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1070-180A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853846 | ||||||
| chr6:138853902
|
A | G | 1 | a0010c0017t0012g0219 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1070-124A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853902 | ||||||
| chr6:138853909
|
T | C | 10 | a0001c0001t0004g0040a0001c0003t0003g0124a0002c0002t0017g0010others(7): Show | 10 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1070-117T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 9/21 | chr6 | 138853909 | ||||||
| chr6:138854260
|
C | T | 5 | a0003c0004t0004g0241a0003c0004t0004g0242a0004c0006t0001g0311others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198+106C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854260 | ||||||
| chr6:138854558
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1198+404C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854558 | ||||||
| chr6:138854619
|
ATG | A | 5 | a0002c0002t0006g0261a0002c0002t0008g0118a0002c0002t0008g0119others(2): Show | 5 | NA18962.hp2 NA18966.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198+466_1198+467d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854619 | ||||||
| chr6:138854808
|
T | A | 1 | a0002c0002t0003g0148 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1198+654T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854808 | ||||||
| chr6:138854842
|
TGAAGAGA others(20): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1198+689_1198+715d others(29): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854842 | ||||||
| chr6:138854981
|
T | G | 3 | a0002c0002t0001g0189a0009c0012t0018g0008a0009c0012t0018g0009 | 3 | HG02976.hp2 HG03130.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1198+827T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854981 | ||||||
| chr6:138854984
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1198+830G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854984 | ||||||
| chr6:138854985
|
T | C | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198+831T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138854985 | ||||||
| chr6:138855216
|
A | C | 1 | a0001c0001t0006g0251 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1198+1062A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855216 | ||||||
| chr6:138855245
|
C | T | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1198+1091C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855245 | ||||||
| chr6:138855369
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1198+1215C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855369 | ||||||
| chr6:138855510
|
G | GA | 67 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0051others(64): Show | 67 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1198+1364dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138855510 | |||||
| chr6:138855548
|
A | G | 2 | a0002c0005t0002g0069a0002c0005t0002g0070 | 2 | NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1198+1394A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855548 | ||||||
| chr6:138855589
|
T | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1198+1435T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855589 | ||||||
| chr6:138855618
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1198+1464A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855618 | ||||||
| chr6:138855657
|
G | A | 1 | a0002c0002t0026g0039 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1198+1503G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855657 | ||||||
| chr6:138855700
|
T | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1198+1546T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855700 | ||||||
| chr6:138855790
|
A | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1198+1636A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855790 | ||||||
| chr6:138855849
|
G | A | 23 | a0001c0001t0009g0152a0001c0001t0016g0211a0001c0001t0016g0212others(20): Show | 23 | HG01175.hp1 HG01243.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.1198+1695G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855849 | ||||||
| chr6:138855917
|
C | T | 4 | a0001c0009t0001g0170a0001c0009t0004g0121a0001c0009t0028g0107others(1): Show | 4 | HG01175.hp1 HG02451.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198+1763C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855917 | ||||||
| chr6:138855929
|
A | G | 1 | a0001c0009t0028g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1198+1775A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855929 | ||||||
| chr6:138855932
|
T | C | 9 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(6): Show | 9 | HG01175.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198+1778T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855932 | ||||||
| chr6:138855936
|
G | A | 4 | a0008c0013t0002g0043a0008c0013t0005g0267a0008c0013t0005g0269others(1): Show | 4 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198+1782G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138855936 | ||||||
| chr6:138856049
|
G | C | 1 | a0001c0001t0002g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1198+1895G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856049 | ||||||
| chr6:138856119
|
A | C | 2 | a0001c0033t0002g0299a0003c0004t0004g0243 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1198+1965A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856119 | ||||||
| chr6:138856191
|
ACCCCCAC others(20): Show |
A | 273 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1198+2046_1198+207 others(31): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138856191 | |||||
| chr6:138856200
|
ACAGCAAT others(20): Show |
A | 5 | a0001c0001t0001g0306a0001c0001t0010g0319a0002c0002t0017g0010others(2): Show | 5 | HG02615.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198+2049_1198+207 others(31): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138856200 | |||||
| chr6:138856231
|
C | T | 1 | a0001c0001t0008g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1198+2077C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856231 | ||||||
| chr6:138856232
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1198+2078G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856232 | ||||||
| chr6:138856247
|
T | C | 312 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1198+2093T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856247 | ||||||
| chr6:138856275
|
C | T | 1 | a0002c0002t0001g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1198+2121C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856275 | ||||||
| chr6:138856291
|
T | G | 2 | a0003c0004t0011g0325a0003c0004t0025g0244 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1198+2137T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856291 | ||||||
| chr6:138856458
|
C | G | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1198+2304C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856458 | ||||||
| chr6:138856544
|
C | T | 1 | a0001c0003t0003g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1198+2390C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856544 | ||||||
| chr6:138856576
|
T | C | 5 | a0001c0001t0004g0249a0001c0003t0002g0037a0001c0003t0003g0246others(2): Show | 5 | HG02922.hp2 HG02970.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198+2422T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856576 | ||||||
| chr6:138856656
|
GTCTC | G | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1198+2506_1198+250 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138856656 | |||||
| chr6:138856802
|
A | T | 1 | a0006c0011t0014g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1198+2648A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138856802 | ||||||
| chr6:138857048
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0004g0040a0001c0001t0009g0152others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1198+2894G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857048 | ||||||
| chr6:138857263
|
G | A | 69 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1198+3109G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857263 | ||||||
| chr6:138857352
|
A | C | 1 | a0002c0002t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1198+3198A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857352 | ||||||
| chr6:138857527
|
G | T | 2 | a0001c0001t0003g0023a0001c0001t0024g0031 | 2 | HG01496.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1198+3373G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857527 | ||||||
| chr6:138857672
|
CACCTCAG others(2): Show |
C | 5 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198+3519_1198+352 others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857672 | ||||||
| chr6:138857852
|
C | T | 5 | a0001c0001t0009g0152a0012c0019t0011g0151a0012c0019t0011g0168others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198+3698C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857852 | ||||||
| chr6:138857884
|
T | C | 1 | a0001c0001t0003g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1198+3730T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857884 | ||||||
| chr6:138857910
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1198+3756G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857910 | ||||||
| chr6:138857924
|
A | G | 74 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1198+3770A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857924 | ||||||
| chr6:138857995
|
A | G | 1 | a0001c0003t0003g0231 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1198+3841A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138857995 | ||||||
| chr6:138858013
|
T | C | 4 | a0001c0001t0004g0249a0001c0003t0002g0037a0001c0003t0003g0246others(1): Show | 4 | HG02922.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198+3859T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858013 | ||||||
| chr6:138858060
|
C | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1198+3906C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858060 | ||||||
| chr6:138858574
|
C | T | 325 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1199-4053C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858574 | ||||||
| chr6:138858613
|
C | G | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1199-4014C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858613 | ||||||
| chr6:138858619
|
T | C | 4 | a0001c0033t0002g0299a0009c0012t0018g0008a0009c0012t0018g0009others(1): Show | 4 | HG01081.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-4008T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858619 | ||||||
| chr6:138858697
|
CT | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0090a0001c0001t0002g0068others(6): Show | 9 | HG00323.hp2 HG00609.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1199-3903delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858697
|
CTT | C | 27 | a0001c0001t0001g0114a0001c0001t0002g0015a0001c0001t0002g0296others(24): Show | 27 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1199-3904_1199-390 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858697
|
CTTT | C | 106 | a0001c0001t0001g0026a0001c0001t0001g0060a0001c0001t0001g0067others(103): Show | 106 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1199-3905_1199-390 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858697
|
CTTTT | C | 113 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0032others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1199-3906_1199-390 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858697
|
CTTTTT | C | 12 | a0001c0001t0002g0182a0001c0001t0003g0023a0001c0001t0003g0030others(9): Show | 12 | HG01192.hp1 HG01928.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1199-3907_1199-390 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858697
|
CTTTTTTT | C | 6 | a0001c0001t0004g0040a0006c0011t0014g0013a0006c0011t0014g0237others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1199-3909_1199-390 others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138858697 | |||||
| chr6:138858729
|
C | T | 1 | a0004c0008t0009g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1199-3898C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858729 | ||||||
| chr6:138858732
|
G | A | 9 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(6): Show | 9 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1199-3895G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858732 | ||||||
| chr6:138858792
|
A | G | 5 | a0004c0006t0015g0213a0011c0016t0002g0307a0011c0016t0002g0308others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1199-3835A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858792 | ||||||
| chr6:138858909
|
T | G | 5 | a0001c0001t0009g0152a0001c0001t0016g0211a0001c0001t0016g0212others(2): Show | 5 | HG01243.hp1 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1199-3718T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858909 | ||||||
| chr6:138858985
|
C | G | 8 | a0003c0004t0004g0243a0005c0007t0001g0300a0005c0007t0001g0301others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199-3642C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138858985 | ||||||
| chr6:138859015
|
C | T | 56 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1199-3612C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859015 | ||||||
| chr6:138859063
|
T | C | 74 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1199-3564T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859063 | ||||||
| chr6:138859276
|
C | T | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1199-3351C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859276 | ||||||
| chr6:138859277
|
G | A | 1 | a0006c0011t0014g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1199-3350G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859277 | ||||||
| chr6:138859327
|
T | C | 10 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 10 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1199-3300T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859327 | ||||||
| chr6:138859371
|
T | C | 66 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1199-3256T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859371 | ||||||
| chr6:138859428
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1199-3199C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859428 | ||||||
| chr6:138859607
|
T | A | 23 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0009g0011others(20): Show | 23 | HG01106.hp1 HG01433.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1199-3020T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859607 | ||||||
| chr6:138859628
|
C | T | 8 | a0003c0004t0004g0243a0005c0007t0001g0300a0005c0007t0001g0301others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199-2999C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859628 | ||||||
| chr6:138859731
|
C | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1199-2896C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859731 | ||||||
| chr6:138859734
|
ACTGGATA others(36): Show |
A | 1 | a0012c0019t0011g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1199-2890_1199-284 others(47): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138859734 | |||||
| chr6:138859810
|
C | CT | 64 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(61): Show | 64 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1199-2806dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138859810 | |||||
| chr6:138859810
|
CTTT | C | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1199-2808_1199-280 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138859810 | |||||
| chr6:138859893
|
C | A | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1199-2734C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859893 | ||||||
| chr6:138859920
|
T | C | 2 | a0002c0002t0007g0247a0002c0005t0002g0323 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1199-2707T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859920 | ||||||
| chr6:138859950
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1199-2677G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859950 | ||||||
| chr6:138859967
|
T | C | 1 | a0002c0002t0001g0053 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1199-2660T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859967 | ||||||
| chr6:138859972
|
G | A | 40 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0293others(37): Show | 40 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1199-2655G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138859972 | ||||||
| chr6:138860185
|
C | T | 2 | a0002c0005t0002g0069a0002c0005t0002g0070 | 2 | NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1199-2442C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860185 | ||||||
| chr6:138860340
|
G | T | 8 | a0001c0001t0008g0046a0001c0001t0008g0318a0001c0001t0009g0271others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199-2287G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860340 | ||||||
| chr6:138860389
|
T | A | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1199-2238T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860389 | ||||||
| chr6:138860397
|
A | C | 2 | a0002c0005t0002g0069a0002c0005t0002g0070 | 2 | NA18981.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1199-2230A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860397 | ||||||
| chr6:138860430
|
G | C | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1199-2197G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860430 | ||||||
| chr6:138860516
|
CAGTA | C | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1199-2107_1199-210 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138860516 | |||||
| chr6:138860619
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1199-2008A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860619 | ||||||
| chr6:138860679
|
A | G | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1199-1948A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860679 | ||||||
| chr6:138860707
|
A | AT | 52 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0111others(49): Show | 52 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1199-1900dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138860707 | |||||
| chr6:138860707
|
A | ATTTT | 10 | a0003c0004t0004g0243a0004c0006t0009g0310a0005c0007t0001g0300others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1199-1903_1199-190 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138860707 | |||||
| chr6:138860707
|
A | ATTTTT | 6 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199-1904_1199-190 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138860707 | |||||
| chr6:138860707
|
ATTT | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1199-1902_1199-190 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr6 | 138860707 | |||||
| chr6:138860709
|
T | C | 18 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(15): Show | 18 | HG01106.hp1 HG01433.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1199-1918T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860709 | ||||||
| chr6:138860817
|
G | A | 14 | a0001c0001t0001g0083a0001c0001t0001g0103a0001c0001t0001g0104others(11): Show | 14 | HG00423.hp2 HG02293.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.1199-1810G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860817 | ||||||
| chr6:138860900
|
C | T | 2 | a0001c0001t0001g0060a0002c0002t0006g0033 | 2 | HG01169.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1199-1727C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138860900 | ||||||
| chr6:138861126
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1199-1501G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861126 | ||||||
| chr6:138861126
|
G | C | 92 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1199-1501G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861126 | ||||||
| chr6:138861128
|
A | T | 92 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1199-1499A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861128 | ||||||
| chr6:138861217
|
G | A | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1199-1410G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861217 | ||||||
| chr6:138861269
|
G | T | 13 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(10): Show | 13 | HG02486.hp2 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1199-1358G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861269 | ||||||
| chr6:138861364
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1199-1263A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861364 | ||||||
| chr6:138861431
|
G | A | 1 | a0001c0003t0003g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1199-1196G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861431 | ||||||
| chr6:138861480
|
G | C | 66 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1199-1147G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861480 | ||||||
| chr6:138861605
|
C | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1199-1022C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861605 | ||||||
| chr6:138861842
|
T | G | 74 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1199-785T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861842 | ||||||
| chr6:138861850
|
T | A | 2 | a0001c0003t0002g0164a0001c0003t0005g0257 | 2 | HG00423.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1199-777T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138861850 | ||||||
| chr6:138862234
|
T | G | 8 | a0003c0004t0004g0243a0005c0007t0001g0300a0005c0007t0001g0301others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199-393T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138862234 | ||||||
| chr6:138862276
|
C | G | 2 | a0001c0003t0002g0172a0001c0003t0003g0232 | 2 | NA19079.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1199-351C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138862276 | ||||||
| chr6:138862330
|
A | G | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1199-297A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138862330 | ||||||
| chr6:138862461
|
G | T | 17 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(14): Show | 17 | HG01106.hp1 HG01433.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1199-166G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138862461 | ||||||
| chr6:138862604
|
C | T | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1199-23C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 10/21 | chr6 | 138862604 | ||||||
| chr6:138862742
|
G | A | 66 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1291+23G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138862742 | ||||||
| chr6:138862855
|
C | T | 40 | a0001c0001t0006g0278a0001c0003t0003g0020a0001c0022t0003g0142others(37): Show | 40 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1291+136C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138862855 | ||||||
| chr6:138862907
|
C | G | 275 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1291+188C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138862907 | ||||||
| chr6:138863004
|
A | C | 2 | a0002c0002t0002g0273a0002c0002t0002g0274 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1291+285A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863004 | ||||||
| chr6:138863080
|
G | A | 1 | a0001c0001t0003g0128 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1291+361G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863080 | ||||||
| chr6:138863137
|
T | C | 44 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0293others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1291+418T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863137 | ||||||
| chr6:138863225
|
G | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1291+506G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863225 | ||||||
| chr6:138863245
|
C | G | 66 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1291+526C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863245 | ||||||
| chr6:138863341
|
A | C | 60 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1291+622A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863341 | ||||||
| chr6:138863424
|
T | G | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1291+705T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863424 | ||||||
| chr6:138863456
|
C | T | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1291+737C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863456 | ||||||
| chr6:138863503
|
T | A | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1291+784T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863503 | ||||||
| chr6:138863622
|
T | G | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1291+903T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863622 | ||||||
| chr6:138863637
|
G | A | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1291+918G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863637 | ||||||
| chr6:138863722
|
T | A | 1 | a0002c0002t0019g0167 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1291+1003T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863722 | ||||||
| chr6:138863773
|
G | A | 1 | a0001c0003t0002g0304 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1291+1054G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863773 | ||||||
| chr6:138863860
|
C | T | 56 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(53): Show | 56 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1292-1136C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138863860 | ||||||
| chr6:138864002
|
T | TA | 96 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1292-967dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAA | 78 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0087others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1292-968_1292-967d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAA | 46 | a0001c0001t0001g0079a0001c0001t0001g0125a0001c0001t0001g0165others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1292-969_1292-967d others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAA | 18 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0114others(15): Show | 18 | HG00280.hp2 HG01106.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-970_1292-967d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(2): Show |
9 | a0001c0001t0007g0006a0001c0001t0009g0012a0001c0001t0009g0108others(6): Show | 9 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-975_1292-967d others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0009g0011a0007c0010t0010g0209a0007c0010t0010g0210others(1): Show | 4 | HG01106.hp1 HG02559.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-976_1292-967d others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0008g0250 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1292-977_1292-967d others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(9): Show |
2 | a0005c0007t0001g0303a0005c0007t0001g0317 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1292-982_1292-967d others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(10): Show |
3 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302 | 3 | HG01884.hp2 HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1292-983_1292-967d others(19): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(13): Show |
1 | a0005c0024t0005g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1292-986_1292-967d others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
T | TAAAAAAA others(16): Show |
1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1292-989_1292-967d others(25): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864002
|
TAAAAA | T | 8 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(5): Show | 8 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1292-971_1292-967d others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr6 | 138864002 | |||||
| chr6:138864322
|
A | G | 3 | a0003c0004t0004g0241a0003c0004t0004g0242a0004c0006t0001g0311 | 3 | HG02896.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1292-674A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864322 | ||||||
| chr6:138864412
|
C | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0068a0001c0001t0004g0157others(10): Show | 13 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-584C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864412 | ||||||
| chr6:138864425
|
T | C | 1 | a0004c0008t0009g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1292-571T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864425 | ||||||
| chr6:138864518
|
G | A | 13 | a0001c0001t0002g0015a0001c0001t0002g0068a0001c0001t0004g0157others(10): Show | 13 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1292-478G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864518 | ||||||
| chr6:138864560
|
T | C | 211 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1292-436T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864560 | ||||||
| chr6:138864711
|
A | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(6): Show | 9 | HG00438.hp1 HG01109.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1292-285A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864711 | ||||||
| chr6:138864747
|
A | G | 75 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1292-249A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864747 | ||||||
| chr6:138864846
|
A | G | 10 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 10 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1292-150A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864846 | ||||||
| chr6:138864937
|
T | C | 157 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1292-59T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864937 | ||||||
| chr6:138864944
|
T | C | 64 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0087others(61): Show | 64 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1292-52T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864944 | ||||||
| chr6:138864991
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1292-5G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 11/21 | chr6 | 138864991 | ||||||
| chr6:138865191
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1474+13G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865191 | ||||||
| chr6:138865320
|
C | T | 60 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1474+142C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865320 | ||||||
| chr6:138865351
|
C | G | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1474+173C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865351 | ||||||
| chr6:138865471
|
G | A | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474+293G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865471 | ||||||
| chr6:138865614
|
C | T | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1474+436C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865614 | ||||||
| chr6:138865824
|
C | G | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1474+646C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865824 | ||||||
| chr6:138865863
|
A | G | 5 | a0006c0011t0014g0013a0006c0011t0014g0237a0006c0011t0021g0236others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474+685A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138865863 | ||||||
| chr6:138866094
|
A | G | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1474+916A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866094 | ||||||
| chr6:138866149
|
G | GT | 70 | a0001c0001t0001g0079a0001c0001t0001g0125a0001c0001t0001g0154others(67): Show | 70 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1474+988dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138866149 | |||||
| chr6:138866149
|
G | GTT | 63 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1474+987_1474+988d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138866149 | |||||
| chr6:138866149
|
G | GTTTT | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1474+985_1474+988d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138866149 | |||||
| chr6:138866149
|
GT | G | 11 | a0001c0001t0004g0138a0001c0001t0006g0055a0003c0004t0004g0241others(8): Show | 11 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474+988delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138866149 | |||||
| chr6:138866299
|
C | T | 9 | a0001c0001t0008g0046a0001c0001t0008g0318a0001c0001t0009g0271others(6): Show | 9 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474+1121C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866299 | ||||||
| chr6:138866355
|
G | T | 2 | a0003c0004t0011g0325a0003c0004t0025g0244 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1474+1177G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866355 | ||||||
| chr6:138866519
|
A | G | 75 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1474+1341A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866519 | ||||||
| chr6:138866660
|
T | C | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-1443T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866660 | ||||||
| chr6:138866729
|
A | G | 60 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1475-1374A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866729 | ||||||
| chr6:138866734
|
C | T | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-1369C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866734 | ||||||
| chr6:138866744
|
T | A | 1 | a0001c0003t0005g0292 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1475-1359T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866744 | ||||||
| chr6:138866995
|
G | A | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1475-1108G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138866995 | ||||||
| chr6:138867029
|
G | A | 1 | a0002c0002t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1475-1074G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867029 | ||||||
| chr6:138867074
|
A | AAAAAAAA others(1): Show |
10 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 10 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1475-1001_1475-994 others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867074 | |||||
| chr6:138867074
|
AAAAAAAA others(1): Show |
A | 18 | a0001c0001t0004g0040a0001c0001t0009g0011a0001c0001t0009g0012others(15): Show | 18 | HG01106.hp1 HG02109.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1475-1001_1475-994 others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867074 | |||||
| chr6:138867177
|
T | C | 1 | a0001c0003t0003g0123 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1475-926T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867177 | ||||||
| chr6:138867363
|
G | C | 2 | a0023c0036t0002g0305a0024c0020t0002g0315 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1475-740G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867363 | ||||||
| chr6:138867397
|
C | A | 39 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0293others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1475-706C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867397 | ||||||
| chr6:138867426
|
A | G | 2 | a0009c0012t0018g0008a0009c0012t0018g0009 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1475-677A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867426 | ||||||
| chr6:138867558
|
C | T | 49 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1475-545C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867558 | ||||||
| chr6:138867590
|
A | G | 49 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1475-513A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867590 | ||||||
| chr6:138867655
|
C | CA | 19 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0116others(16): Show | 19 | HG01081.hp1 HG02027.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1475-425dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867655
|
CA | C | 17 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0101others(14): Show | 17 | HG00639.hp2 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1475-425delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867655
|
CAAAA | C | 11 | a0001c0001t0002g0202a0001c0001t0004g0040a0001c0003t0002g0172others(8): Show | 11 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1475-428_1475-425d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867655
|
CAAAAA | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0032others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1475-429_1475-425d others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867655
|
CAAAAAAA | C | 47 | a0001c0001t0001g0079a0001c0001t0001g0111a0001c0001t0001g0114others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.1475-431_1475-425d others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867655
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0002g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1475-435_1475-425d others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867655 | |||||
| chr6:138867689
|
C | A | 39 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0293others(36): Show | 39 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1475-414C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867689 | ||||||
| chr6:138867693
|
G | C | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1475-410G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867693 | ||||||
| chr6:138867769
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1475-334C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867769 | ||||||
| chr6:138867817
|
G | A | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-286G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867817 | ||||||
| chr6:138867830
|
A | AAAAT | 67 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1475-257_1475-254d others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867830 | |||||
| chr6:138867927
|
T | TGAGCTCA others(2): Show |
7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-175_1475-174i others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867927 | |||||
| chr6:138867929
|
G | A | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-174G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138867929 | ||||||
| chr6:138867999
|
C | CA | 32 | a0001c0001t0008g0046a0001c0001t0008g0318a0001c0001t0009g0011others(29): Show | 32 | HG01106.hp1 HG01109.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.1475-84dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867999 | |||||
| chr6:138867999
|
C | CAAAAAA | 55 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 55 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1475-89_1475-84dup others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867999 | |||||
| chr6:138867999
|
C | CAAAAAAA others(3): Show |
1 | a0006c0011t0014g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1475-93_1475-84dup others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867999 | |||||
| chr6:138867999
|
CAAA | C | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1475-86_1475-84del others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138867999 | |||||
| chr6:138868016
|
A | AAG | 15 | a0001c0001t0001g0079a0001c0001t0001g0111a0001c0001t0002g0068others(12): Show | 15 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1475-86_1475-85ins others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr6 | 138868016 | |||||
| chr6:138868016
|
A | AG | 26 | a0001c0001t0001g0085a0001c0001t0001g0114a0001c0001t0001g0149others(23): Show | 26 | HG00438.hp1 HG00738.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1475-87_1475-86ins others(1): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138868016 | ||||||
| chr6:138868016
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1475-87A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 12/21 | chr6 | 138868016 | ||||||
| chr6:138868255
|
A | G | 1 | a0001c0001t0006g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1578+49A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868255 | ||||||
| chr6:138868322
|
A | G | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+116A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868322 | ||||||
| chr6:138868481
|
CT | C | 42 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0056others(39): Show | 42 | HG00323.hp1 HG00597.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1578+289delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138868481 | |||||
| chr6:138868575
|
T | C | 10 | a0001c0001t0002g0296a0002c0002t0006g0261a0002c0002t0007g0166others(7): Show | 10 | HG02015.hp2 HG02257.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.1578+369T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868575 | ||||||
| chr6:138868679
|
C | T | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1578+473C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868679 | ||||||
| chr6:138868811
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1578+605G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868811 | ||||||
| chr6:138868936
|
G | A | 1 | a0001c0001t0009g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1578+730G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868936 | ||||||
| chr6:138868941
|
C | T | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1578+735C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138868941 | ||||||
| chr6:138869036
|
G | A | 2 | a0001c0001t0007g0006a0001c0001t0029g0262 | 2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1578+830G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869036 | ||||||
| chr6:138869039
|
C | T | 8 | a0001c0001t0004g0040a0001c0003t0003g0124a0004c0006t0009g0310others(5): Show | 8 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+833C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869039 | ||||||
| chr6:138869116
|
G | A | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+910G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869116 | ||||||
| chr6:138869338
|
T | C | 1 | a0002c0002t0003g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+1132T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869338 | ||||||
| chr6:138869638
|
A | T | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+1432A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869638 | ||||||
| chr6:138869700
|
T | C | 1 | a0002c0002t0001g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1578+1494T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869700 | ||||||
| chr6:138869746
|
A | G | 1 | a0002c0002t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1578+1540A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869746 | ||||||
| chr6:138869751
|
A | G | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1578+1545A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869751 | ||||||
| chr6:138869822
|
C | A | 63 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1578+1616C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869822 | ||||||
| chr6:138869992
|
G | A | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1578+1786G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138869992 | ||||||
| chr6:138870012
|
A | G | 1 | a0001c0009t0028g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1578+1806A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870012 | ||||||
| chr6:138870023
|
T | C | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+1817T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870023 | ||||||
| chr6:138870024
|
G | A | 14 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(11): Show | 14 | HG01433.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1578+1818G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870024 | ||||||
| chr6:138870110
|
T | C | 1 | a0002c0002t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1578+1904T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870110 | ||||||
| chr6:138870263
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2057G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870263 | ||||||
| chr6:138870566
|
G | A | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+2360G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870566 | ||||||
| chr6:138870602
|
T | G | 1 | a0001c0001t0003g0129 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1578+2396T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870602 | ||||||
| chr6:138870604
|
A | ATGCAAT | 323 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1578+2400_1578+240 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138870604 | |||||
| chr6:138870630
|
A | AT | 8 | a0001c0001t0008g0046a0001c0001t0008g0318a0001c0001t0009g0271others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1578+2433dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138870630 | |||||
| chr6:138870665
|
C | CT | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1578+2467dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138870665 | |||||
| chr6:138870686
|
T | C | 2 | a0006c0015t0003g0238a0006c0015t0003g0239 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1578+2480T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870686 | ||||||
| chr6:138870872
|
C | T | 5 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+2666C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870872 | ||||||
| chr6:138870992
|
C | G | 1 | a0002c0002t0019g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1578+2786C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138870992 | ||||||
| chr6:138871237
|
G | A | 210 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1578+3031G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871237 | ||||||
| chr6:138871288
|
T | C | 75 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1578+3082T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871288 | ||||||
| chr6:138871300
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1578+3094G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871300 | ||||||
| chr6:138871525
|
G | C | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3319G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871525 | ||||||
| chr6:138871557
|
G | A | 8 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(5): Show | 8 | HG01106.hp1 HG02109.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1578+3351G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871557 | ||||||
| chr6:138871558
|
C | T | 40 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0071others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1578+3352C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871558 | ||||||
| chr6:138871584
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1578+3378T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871584 | ||||||
| chr6:138871605
|
A | G | 58 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(55): Show | 58 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1578+3399A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871605 | ||||||
| chr6:138871635
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1578+3429G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871635 | ||||||
| chr6:138871766
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1578+3560T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871766 | ||||||
| chr6:138871904
|
G | C | 103 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1578+3698G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138871904 | ||||||
| chr6:138871980
|
A | AT | 15 | a0001c0001t0001g0083a0001c0001t0007g0006a0001c0001t0008g0250others(12): Show | 15 | HG01433.hp1 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1578+3785dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138871980 | |||||
| chr6:138871980
|
A | ATT | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+3784_1578+378 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138871980 | |||||
| chr6:138872004
|
C | T | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578+3798C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872004 | ||||||
| chr6:138872146
|
A | G | 1 | a0001c0003t0003g0231 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1578+3940A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872146 | ||||||
| chr6:138872163
|
T | C | 2 | a0002c0005t0013g0217a0002c0005t0013g0220 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1578+3957T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872163 | ||||||
| chr6:138872303
|
A | G | 14 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(11): Show | 14 | HG01433.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1578+4097A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872303 | ||||||
| chr6:138872428
|
A | G | 77 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1579-4044A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872428 | ||||||
| chr6:138872429
|
C | T | 25 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(22): Show | 25 | HG00438.hp1 HG00738.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1579-4043C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872429 | ||||||
| chr6:138872466
|
A | G | 77 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1579-4006A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872466 | ||||||
| chr6:138872536
|
T | C | 77 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1579-3936T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872536 | ||||||
| chr6:138872550
|
C | T | 1 | a0002c0002t0006g0261 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1579-3922C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138872550 | ||||||
| chr6:138873033
|
T | G | 1 | a0002c0002t0004g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1579-3439T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873033 | ||||||
| chr6:138873053
|
G | A | 7 | a0001c0001t0004g0040a0001c0003t0003g0124a0006c0011t0014g0013others(4): Show | 7 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-3419G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873053 | ||||||
| chr6:138873083
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1579-3389C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873083 | ||||||
| chr6:138873184
|
T | C | 6 | a0001c0001t0009g0271a0003c0004t0011g0325a0003c0004t0025g0244others(3): Show | 6 | HG02723.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-3288T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873184 | ||||||
| chr6:138873221
|
A | G | 1 | a0001c0001t0003g0291 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1579-3251A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873221 | ||||||
| chr6:138873227
|
A | AT | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-3243dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873227 | |||||
| chr6:138873229
|
T | TA | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1579-3235dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873229 | |||||
| chr6:138873230
|
A | T | 1 | a0001c0001t0006g0270 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1579-3242A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873230 | ||||||
| chr6:138873240
|
G | A | 37 | a0001c0001t0006g0278a0001c0003t0003g0020a0001c0022t0003g0142others(34): Show | 37 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1579-3232G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873240 | ||||||
| chr6:138873283
|
C | G | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-3189C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873283 | ||||||
| chr6:138873350
|
A | C | 1 | a0002c0002t0004g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1579-3122A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873350 | ||||||
| chr6:138873351
|
C | T | 1 | a0002c0002t0004g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1579-3121C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873351 | ||||||
| chr6:138873380
|
A | AT | 6 | a0001c0001t0009g0271a0003c0004t0011g0325a0003c0004t0025g0244others(3): Show | 6 | HG02723.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-3091dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873380 | |||||
| chr6:138873416
|
T | C | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-3056T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873416 | ||||||
| chr6:138873489
|
A | G | 14 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(11): Show | 14 | HG01433.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1579-2983A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873489 | ||||||
| chr6:138873504
|
A | G | 10 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 10 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1579-2968A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873504 | ||||||
| chr6:138873515
|
C | T | 1 | a0015c0023t0002g0180 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1579-2957C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873515 | ||||||
| chr6:138873529
|
C | G | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-2943C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873529 | ||||||
| chr6:138873544
|
G | A | 1 | a0001c0033t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1579-2928G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873544 | ||||||
| chr6:138873655
|
C | G | 89 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1579-2817C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873655 | ||||||
| chr6:138873702
|
G | A | 7 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-2770G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873702 | ||||||
| chr6:138873705
|
A | G | 1 | a0002c0002t0002g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1579-2767A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873705 | ||||||
| chr6:138873832
|
G | C | 3 | a0002c0002t0001g0049a0002c0002t0001g0073a0002c0002t0001g0076 | 3 | HG00558.hp1 HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1579-2640G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873832 | ||||||
| chr6:138873872
|
C | CTCTGTGT others(13): Show |
3 | a0001c0001t0007g0006a0001c0001t0008g0250a0008c0031t0017g0316 | 3 | HG02486.hp2 HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1579-2599_1579-259 others(24): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTCTGTGT others(17): Show |
1 | a0001c0001t0029g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1579-2599_1579-259 others(28): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTCTGTGT others(23): Show |
1 | a0001c0018t0020g0007 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1579-2599_1579-259 others(34): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTG | 17 | a0001c0001t0001g0087a0001c0001t0001g0104a0001c0001t0001g0105others(14): Show | 17 | HG01109.hp1 HG01358.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1579-2558_1579-255 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTG | 5 | a0001c0001t0001g0083a0002c0002t0001g0066a0002c0002t0001g0178others(2): Show | 5 | HG01261.hp1 HG03942.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-2560_1579-255 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTG | 12 | a0001c0001t0001g0060a0001c0001t0001g0272a0001c0001t0006g0254others(9): Show | 12 | HG00733.hp2 HG01169.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1579-2562_1579-255 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTGT others(1): Show |
3 | a0002c0002t0001g0050a0002c0002t0001g0175a0002c0002t0005g0290 | 3 | HG01168.hp2 HG01515.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1579-2564_1579-255 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTGT others(3): Show |
1 | a0002c0002t0004g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1579-2566_1579-255 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTGT others(5): Show |
3 | a0002c0002t0001g0078a0002c0002t0001g0162a0002c0005t0002g0223 | 3 | HG00558.hp2 HG02165.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1579-2568_1579-255 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTGT others(7): Show |
1 | a0002c0002t0004g0147 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1579-2570_1579-255 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
C | CTGTGTGT others(9): Show |
1 | a0002c0002t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1579-2572_1579-255 others(20): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873872
|
CTGTGTGT others(15): Show |
C | 11 | a0001c0022t0003g0142a0002c0002t0001g0049a0002c0002t0001g0053others(8): Show | 11 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579-2578_1579-255 others(26): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873872 | |||||
| chr6:138873890
|
G | GTGTGTGT others(7): Show |
2 | a0001c0003t0002g0304a0001c0003t0003g0245 | 2 | NA18906.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1579-2569_1579-256 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873890 | |||||
| chr6:138873890
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1579-2567_1579-256 others(20): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873890 | |||||
| chr6:138873890
|
G | GTGTGTGT others(11): Show |
34 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0003g0137others(31): Show | 34 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1579-2565_1579-256 others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873890 | |||||
| chr6:138873890
|
G | GTGTGTGT others(13): Show |
2 | a0001c0001t0003g0291a0001c0003t0002g0100 | 2 | HG01346.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1579-2563_1579-256 others(24): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873890 | |||||
| chr6:138873892
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1579-2569_1579-256 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873892
|
G | GTGTGTGT others(7): Show |
4 | a0001c0001t0010g0319a0009c0012t0018g0008a0009c0012t0018g0009others(1): Show | 4 | HG01081.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-2567_1579-256 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873892
|
G | GTGTGTGT others(9): Show |
3 | a0001c0001t0009g0152a0012c0019t0011g0151a0012c0019t0011g0168 | 3 | HG01243.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1579-2565_1579-256 others(20): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873892
|
G | GTGTGTGT others(11): Show |
2 | a0001c0033t0002g0299a0004c0008t0009g0314 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1579-2563_1579-256 others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873892
|
G | GTGTGTGT others(25): Show |
1 | a0001c0001t0009g0271 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1579-2563_1579-256 others(36): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873892
|
G | GTGTGTGT others(15): Show |
4 | a0003c0004t0011g0325a0003c0004t0025g0244a0004c0008t0009g0298others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-2559_1579-255 others(26): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873892 | |||||
| chr6:138873894
|
G | GTGTGTGT others(3): Show |
30 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(27): Show | 30 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1579-2569_1579-256 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(5): Show |
68 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0032others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.1579-2567_1579-256 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(7): Show |
7 | a0001c0003t0002g0187a0001c0003t0002g0188a0001c0003t0005g0275others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-2565_1579-256 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(9): Show |
16 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1579-2563_1579-256 others(20): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(11): Show |
3 | a0001c0001t0009g0108a0011c0016t0002g0307a0011c0016t0002g0308 | 3 | HG03209.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1579-2561_1579-256 others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(13): Show |
2 | a0004c0006t0015g0213a0016c0027t0001g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1579-2559_1579-255 others(24): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873894
|
G | GTGTGTGT others(15): Show |
7 | a0001c0001t0001g0026a0005c0007t0001g0300a0005c0007t0001g0301others(4): Show | 7 | HG01884.hp2 HG01943.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-2557_1579-255 others(26): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873894 | |||||
| chr6:138873896
|
G | GTGTGTGT others(15): Show |
1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-2557_1579-255 others(26): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873896 | |||||
| chr6:138873898
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-2574G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138873898 | ||||||
| chr6:138873898
|
G | GTGTGTGT others(5): Show |
9 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(6): Show | 9 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-2563_1579-256 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873898 | |||||
| chr6:138873900
|
G | GTGTGTGT others(5): Show |
1 | a0001c0003t0003g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1579-2561_1579-256 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873900 | |||||
| chr6:138873900
|
G | GTGTGTGT others(11): Show |
6 | a0001c0001t0004g0040a0006c0011t0014g0013a0006c0011t0014g0237others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579-2557_1579-255 others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr6 | 138873900 | |||||
| chr6:138874048
|
C | T | 3 | a0002c0002t0001g0042a0002c0002t0001g0110a0002c0002t0005g0290 | 3 | HG00639.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1579-2424C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874048 | ||||||
| chr6:138874049
|
G | A | 1 | a0016c0027t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1579-2423G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874049 | ||||||
| chr6:138874075
|
C | A | 1 | a0002c0002t0006g0224 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1579-2397C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874075 | ||||||
| chr6:138874146
|
A | G | 81 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(78): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1579-2326A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874146 | ||||||
| chr6:138874258
|
G | A | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1579-2214G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874258 | ||||||
| chr6:138874408
|
A | G | 9 | a0003c0004t0004g0241a0003c0004t0004g0242a0003c0004t0007g0320others(6): Show | 9 | HG01433.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-2064A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874408 | ||||||
| chr6:138874454
|
C | G | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-2018C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874454 | ||||||
| chr6:138874534
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1579-1938G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874534 | ||||||
| chr6:138874911
|
C | A | 25 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0111others(22): Show | 25 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1579-1561C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874911 | ||||||
| chr6:138874977
|
A | C | 21 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(18): Show | 21 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1579-1495A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138874977 | ||||||
| chr6:138875004
|
T | C | 1 | a0001c0003t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1579-1468T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875004 | ||||||
| chr6:138875019
|
C | T | 18 | a0002c0002t0003g0022a0002c0002t0006g0224a0002c0002t0006g0261others(15): Show | 18 | HG01192.hp2 HG02015.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579-1453C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875019 | ||||||
| chr6:138875034
|
C | G | 27 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(24): Show | 27 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1579-1438C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875034 | ||||||
| chr6:138875119
|
T | C | 61 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(58): Show | 61 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1579-1353T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875119 | ||||||
| chr6:138875123
|
T | C | 49 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(46): Show | 49 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1579-1349T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875123 | ||||||
| chr6:138875352
|
C | G | 1 | a0002c0002t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1579-1120C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875352 | ||||||
| chr6:138875387
|
G | A | 319 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0051others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1579-1085G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875387 | ||||||
| chr6:138875480
|
C | T | 22 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(19): Show | 22 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1579-992C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875480 | ||||||
| chr6:138875481
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1579-991G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875481 | ||||||
| chr6:138875553
|
A | G | 319 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0051others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1579-919A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875553 | ||||||
| chr6:138875670
|
G | A | 22 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(19): Show | 22 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1579-802G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875670 | ||||||
| chr6:138875724
|
T | C | 143 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(140): Show | 143 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579-748T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875724 | ||||||
| chr6:138875731
|
A | G | 1 | a0008c0013t0005g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1579-741A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875731 | ||||||
| chr6:138875764
|
C | T | 1 | a0002c0002t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1579-708C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875764 | ||||||
| chr6:138875779
|
A | G | 21 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(18): Show | 21 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1579-693A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875779 | ||||||
| chr6:138875788
|
G | T | 21 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(18): Show | 21 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1579-684G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875788 | ||||||
| chr6:138875982
|
G | A | 38 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0293others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.1579-490G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138875982 | ||||||
| chr6:138876068
|
G | A | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579-404G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138876068 | ||||||
| chr6:138876097
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1579-375C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138876097 | ||||||
| chr6:138876471
|
G | C | 7 | a0004c0006t0015g0213a0005c0007t0001g0300a0005c0007t0001g0301others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1579-1G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 13/21 | chr6 | 138876471 | ||||||
| chr6:138876604
|
T | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0306a0001c0001t0002g0015others(4): Show | 7 | HG00741.hp1 HG01106.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1665+46T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138876604 | ||||||
| chr6:138876669
|
T | C | 75 | a0002c0002t0001g0024a0002c0002t0001g0038a0002c0002t0001g0041others(72): Show | 75 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1665+111T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138876669 | ||||||
| chr6:138876670
|
T | TA | 23 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(20): Show | 23 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1665+124dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138876670 | |||||
| chr6:138876670
|
TA | T | 87 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0083others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1665+124delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138876670 | |||||
| chr6:138876748
|
AGAAGTTG others(228): Show |
A | 1 | a0002c0002t0003g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1665+192_1665+426d others(2): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138876748 | |||||
| chr6:138876855
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1665+297C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138876855 | ||||||
| chr6:138877024
|
G | A | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1665+466G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877024 | ||||||
| chr6:138877041
|
T | C | 1 | a0002c0002t0001g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1665+483T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877041 | ||||||
| chr6:138877141
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1665+583G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877141 | ||||||
| chr6:138877157
|
TG | T | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1665+604delG | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138877157 | |||||
| chr6:138877400
|
A | G | 46 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(43): Show | 46 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1665+842A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877400 | ||||||
| chr6:138877415
|
T | C | 22 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(19): Show | 22 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1665+857T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877415 | ||||||
| chr6:138877456
|
C | T | 24 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(21): Show | 24 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1665+898C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877456 | ||||||
| chr6:138877650
|
C | T | 2 | a0012c0019t0011g0151a0012c0019t0011g0168 | 2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1665+1092C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877650 | ||||||
| chr6:138877671
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1665+1113T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877671 | ||||||
| chr6:138877778
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1665+1220T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877778 | ||||||
| chr6:138877841
|
C | T | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1665+1283C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877841 | ||||||
| chr6:138877842
|
G | T | 1 | a0002c0002t0001g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1665+1284G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877842 | ||||||
| chr6:138877967
|
A | T | 3 | a0002c0002t0007g0166a0002c0002t0007g0233a0002c0002t0008g0064 | 3 | HG02015.hp2 HG03831.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1665+1409A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138877967 | ||||||
| chr6:138878278
|
T | A | 3 | a0001c0001t0009g0152a0001c0001t0016g0211a0001c0001t0016g0212 | 3 | HG01243.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1665+1720T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878278 | ||||||
| chr6:138878296
|
C | CAT | 43 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0085others(40): Show | 43 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1665+1748_1665+174 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878296 | |||||
| chr6:138878306
|
T | TAC | 3 | a0002c0002t0017g0010a0002c0005t0013g0217a0002c0005t0013g0220 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1665+1774_1665+177 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
T | TATAC | 3 | a0001c0001t0001g0149a0009c0012t0003g0021a0014c0037t0002g0036 | 3 | NA18983.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1665+1749_1665+175 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
T | TATACAC | 6 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0101others(3): Show | 6 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1665+1749_1665+175 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
T | TATACACA others(1): Show |
10 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(7): Show | 10 | HG01106.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1665+1749_1665+175 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
T | TATACACA others(3): Show |
10 | a0004c0006t0015g0213a0005c0007t0001g0301a0005c0007t0001g0302others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1665+1749_1665+175 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
T | TATACACA others(7): Show |
1 | a0005c0007t0001g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1665+1749_1665+175 others(18): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
TAC | T | 159 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0051others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1665+1774_1665+177 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878306
|
TACAC | T | 6 | a0001c0001t0001g0306a0002c0002t0001g0078a0002c0002t0004g0002others(3): Show | 6 | HG02165.hp2 HG02976.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+1772_1665+177 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878306 | |||||
| chr6:138878308
|
C | T | 73 | a0001c0001t0001g0067a0001c0001t0002g0015a0001c0001t0003g0014others(70): Show | 73 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1665+1750C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878308 | ||||||
| chr6:138878310
|
C | T | 115 | a0001c0001t0001g0027a0001c0001t0001g0125a0001c0001t0001g0161others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1665+1752C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878310 | ||||||
| chr6:138878312
|
C | T | 6 | a0001c0001t0001g0306a0001c0003t0003g0214a0002c0002t0001g0078others(3): Show | 6 | HG02165.hp2 HG02976.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1665+1754C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878312 | ||||||
| chr6:138878315
|
A | T | 1 | a0002c0002t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1665+1757A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878315 | ||||||
| chr6:138878334
|
T | C | 15 | a0002c0002t0003g0022a0002c0002t0006g0224a0002c0002t0006g0261others(12): Show | 15 | HG01192.hp2 HG02015.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1665+1776T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878334 | ||||||
| chr6:138878336
|
C | T | 15 | a0002c0002t0003g0022a0002c0002t0006g0224a0002c0002t0006g0261others(12): Show | 15 | HG01192.hp2 HG02015.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1665+1778C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878336 | ||||||
| chr6:138878339
|
A | G | 21 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(18): Show | 21 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1665+1781A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878339 | ||||||
| chr6:138878399
|
A | G | 4 | a0001c0033t0002g0299a0009c0012t0018g0008a0009c0012t0018g0009others(1): Show | 4 | HG01081.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1665+1841A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878399 | ||||||
| chr6:138878483
|
G | C | 6 | a0004c0006t0009g0310a0006c0011t0014g0013a0006c0011t0014g0237others(3): Show | 6 | HG02559.hp2 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1665+1925G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878483 | ||||||
| chr6:138878502
|
G | A | 1 | a0001c0003t0003g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1665+1944G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878502 | ||||||
| chr6:138878576
|
AGCTGGGA others(128): Show |
A | 1 | a0003c0004t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1665+2037_1665+217 others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138878576 | |||||
| chr6:138878753
|
G | A | 110 | a0001c0001t0001g0044a0001c0001t0001g0060a0001c0001t0001g0071others(107): Show | 110 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1665+2195G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878753 | ||||||
| chr6:138878856
|
T | A | 1 | a0001c0001t0009g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1666-2101T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878856 | ||||||
| chr6:138878993
|
A | G | 25 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(22): Show | 25 | HG01106.hp1 HG01433.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1666-1964A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138878993 | ||||||
| chr6:138879052
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1666-1905C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879052 | ||||||
| chr6:138879109
|
T | C | 1 | a0001c0001t0003g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1666-1848T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879109 | ||||||
| chr6:138879128
|
T | C | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.1666-1829T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879128 | ||||||
| chr6:138879134
|
G | A | 1 | a0001c0001t0003g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1666-1823G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879134 | ||||||
| chr6:138879162
|
G | A | 1 | a0002c0002t0006g0261 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1666-1795G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879162 | ||||||
| chr6:138879193
|
G | A | 22 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0002g0035others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1666-1764G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879193 | ||||||
| chr6:138879459
|
A | G | 4 | a0003c0004t0007g0320a0003c0004t0007g0321a0003c0004t0007g0322others(1): Show | 4 | HG01433.hp1 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666-1498A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879459 | ||||||
| chr6:138879725
|
T | C | 25 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(22): Show | 25 | HG01106.hp1 HG01243.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.1666-1232T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879725 | ||||||
| chr6:138879750
|
C | T | 8 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1666-1207C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879750 | ||||||
| chr6:138879757
|
A | G | 1 | a0001c0001t0002g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1666-1200A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879757 | ||||||
| chr6:138879790
|
C | T | 2 | a0006c0011t0014g0237a0006c0011t0021g0236 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1666-1167C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879790 | ||||||
| chr6:138879845
|
C | T | 113 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(110): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1666-1112C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879845 | ||||||
| chr6:138879877
|
C | A | 1 | a0002c0002t0019g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1666-1080C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879877 | ||||||
| chr6:138879905
|
A | T | 1 | a0001c0003t0005g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1666-1052A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879905 | ||||||
| chr6:138879917
|
C | T | 96 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1666-1040C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879917 | ||||||
| chr6:138879931
|
A | C | 146 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(143): Show | 146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1666-1026A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879931 | ||||||
| chr6:138879975
|
T | TA | 96 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1666-979dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr6 | 138879975 | |||||
| chr6:138879979
|
T | C | 1 | a0002c0002t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1666-978T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138879979 | ||||||
| chr6:138880127
|
C | G | 25 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(22): Show | 25 | HG01106.hp1 HG01243.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.1666-830C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880127 | ||||||
| chr6:138880168
|
G | C | 2 | a0001c0018t0002g0059a0009c0025t0020g0004 | 2 | HG01081.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1666-789G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880168 | ||||||
| chr6:138880177
|
C | T | 7 | a0001c0018t0020g0007a0001c0033t0002g0299a0004c0008t0009g0298others(4): Show | 7 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1666-780C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880177 | ||||||
| chr6:138880221
|
G | A | 25 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(22): Show | 25 | HG01106.hp1 HG01243.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.1666-736G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880221 | ||||||
| chr6:138880627
|
T | C | 115 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1666-330T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880627 | ||||||
| chr6:138880742
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1666-215C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880742 | ||||||
| chr6:138880756
|
G | A | 1 | a0001c0003t0002g0200 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1666-201G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880756 | ||||||
| chr6:138880772
|
C | A | 63 | a0001c0001t0001g0272a0001c0001t0002g0048a0001c0001t0002g0098others(60): Show | 63 | HG00639.hp2 HG00738.hp1 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.1666-185C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880772 | ||||||
| chr6:138880788
|
T | C | 4 | a0011c0016t0002g0307a0011c0016t0002g0308a0023c0036t0002g0305others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666-169T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880788 | ||||||
| chr6:138880796
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1666-161C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880796 | ||||||
| chr6:138880814
|
C | G | 3 | a0005c0024t0005g0276a0009c0012t0003g0021a0014c0037t0002g0036 | 3 | NA18522.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1666-143C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880814 | ||||||
| chr6:138880856
|
G | C | 4 | a0003c0004t0007g0320a0003c0004t0007g0321a0003c0004t0007g0322others(1): Show | 4 | HG01433.hp1 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1666-101G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880856 | ||||||
| chr6:138880877
|
G | C | 199 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(196): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1666-80G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 14/21 | chr6 | 138880877 | ||||||
| chr6:138881197
|
T | A | 1 | a0002c0002t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1880+26T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881197 | ||||||
| chr6:138881228
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1880+57G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881228 | ||||||
| chr6:138881362
|
C | T | 8 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880+191C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881362 | ||||||
| chr6:138881492
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1880+321G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881492 | ||||||
| chr6:138881495
|
G | T | 20 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(17): Show | 20 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1880+324G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881495 | ||||||
| chr6:138881664
|
A | G | 107 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0179others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1880+493A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881664 | ||||||
| chr6:138881811
|
C | T | 8 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(5): Show | 8 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1880+640C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881811 | ||||||
| chr6:138881812
|
G | A | 1 | a0013c0038t0002g0173 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1880+641G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881812 | ||||||
| chr6:138881972
|
G | A | 5 | a0003c0004t0004g0241a0003c0004t0004g0242a0004c0006t0001g0311others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1881-752G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881972 | ||||||
| chr6:138881985
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1881-739C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138881985 | ||||||
| chr6:138882170
|
G | A | 1 | a0001c0001t0022g0287 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1881-554G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138882170 | ||||||
| chr6:138882324
|
G | C | 19 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(16): Show | 19 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1881-400G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138882324 | ||||||
| chr6:138882368
|
G | T | 2 | a0008c0013t0005g0269a0019c0032t0005g0268 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1881-356G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 15/21 | chr6 | 138882368 | ||||||
| chr6:138882871
|
GGTAAATG others(7): Show |
G | 7 | a0001c0001t0001g0109a0001c0001t0001g0165a0001c0001t0001g0266others(4): Show | 7 | HG00558.hp2 HG00621.hp1 HG03710.hp1 others(4): Show |
splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.2028+1_2028+14delG others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138882871 | ||||||
| chr6:138882886
|
A | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0165a0001c0001t0001g0266others(4): Show | 7 | HG00558.hp2 HG00621.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.2028+15A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138882886 | ||||||
| chr6:138882889
|
C | A | 7 | a0001c0001t0001g0109a0001c0001t0001g0165a0001c0001t0001g0266others(4): Show | 7 | HG00558.hp2 HG00621.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.2028+18C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138882889 | ||||||
| chr6:138883129
|
T | C | 1 | a0001c0003t0002g0190 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2028+258T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883129 | ||||||
| chr6:138883167
|
T | C | 9 | a0001c0001t0002g0048a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG00639.hp2 HG01496.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.2028+296T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883167 | ||||||
| chr6:138883433
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0002g0203a0001c0001t0002g0204others(3): Show | 6 | HG00438.hp1 HG02015.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.2028+562T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883433 | ||||||
| chr6:138883601
|
G | A | 1 | a0005c0024t0005g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2028+730G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883601 | ||||||
| chr6:138883698
|
G | A | 2 | a0002c0002t0017g0010a0008c0031t0017g0316 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2028+827G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883698 | ||||||
| chr6:138883700
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0154 | 2 | HG02129.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2028+829T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883700 | ||||||
| chr6:138883714
|
C | T | 1 | a0001c0003t0002g0052 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2028+843C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883714 | ||||||
| chr6:138883750
|
T | C | 5 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2028+879T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883750 | ||||||
| chr6:138883801
|
G | A | 41 | a0001c0001t0001g0067a0001c0001t0001g0179a0001c0001t0003g0291others(38): Show | 41 | HG00423.hp1 HG00741.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.2028+930G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883801 | ||||||
| chr6:138883853
|
T | C | 5 | a0001c0001t0004g0138a0001c0001t0006g0092a0001c0001t0006g0093others(2): Show | 5 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2028+982T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138883853 | ||||||
| chr6:138884054
|
C | T | 1 | a0002c0002t0001g0178 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2028+1183C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884054 | ||||||
| chr6:138884249
|
T | C | 155 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0051others(152): Show | 155 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.2029-1257T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884249 | ||||||
| chr6:138884280
|
T | G | 8 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2029-1226T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884280 | ||||||
| chr6:138884308
|
C | T | 67 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2029-1198C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884308 | ||||||
| chr6:138884320
|
T | C | 67 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2029-1186T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884320 | ||||||
| chr6:138884353
|
T | C | 2 | a0002c0002t0002g0273a0002c0002t0002g0274 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2029-1153T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884353 | ||||||
| chr6:138884497
|
G | A | 1 | a0008c0031t0017g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2029-1009G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884497 | ||||||
| chr6:138884518
|
A | G | 2 | a0001c0001t0004g0136a0001c0001t0004g0265 | 2 | HG00438.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2029-988A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884518 | ||||||
| chr6:138884652
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2029-854C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884652 | ||||||
| chr6:138884659
|
A | T | 1 | a0001c0001t0004g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2029-847A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884659 | ||||||
| chr6:138884759
|
T | C | 1 | a0002c0002t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2029-747T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884759 | ||||||
| chr6:138884858
|
T | C | 1 | a0002c0002t0007g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2029-648T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138884858 | ||||||
| chr6:138885022
|
C | CT | 55 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0154others(52): Show | 55 | HG00423.hp1 HG00438.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.2029-460dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 138885022 | |||||
| chr6:138885022
|
CT | C | 87 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0071others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2029-460delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 138885022 | |||||
| chr6:138885022
|
CTT | C | 6 | a0001c0001t0002g0101a0001c0001t0002g0156a0001c0001t0003g0014others(3): Show | 6 | HG01081.hp2 HG01496.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2029-461_2029-460d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 138885022 | |||||
| chr6:138885022
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0044a0001c0001t0004g0040 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-470_2029-460d others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 138885022 | |||||
| chr6:138885046
|
T | G | 1 | a0001c0001t0006g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2029-460T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885046 | ||||||
| chr6:138885098
|
G | C | 1 | a0001c0001t0006g0278 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2029-408G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885098 | ||||||
| chr6:138885173
|
C | T | 70 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(67): Show | 70 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.2029-333C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885173 | ||||||
| chr6:138885174
|
G | A | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-332G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885174 | ||||||
| chr6:138885178
|
G | A | 2 | a0001c0001t0016g0211a0001c0001t0016g0212 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2029-328G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885178 | ||||||
| chr6:138885274
|
T | C | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-232T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885274 | ||||||
| chr6:138885280
|
C | T | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2029-226C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885280 | ||||||
| chr6:138885298
|
A | T | 2 | a0023c0036t0002g0305a0024c0020t0002g0315 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2029-208A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885298 | ||||||
| chr6:138885323
|
C | T | 20 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0158others(17): Show | 20 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2029-183C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885323 | ||||||
| chr6:138885382
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0004g0040 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-124T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885382 | ||||||
| chr6:138885409
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2029-97T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885409 | ||||||
| chr6:138885445
|
TG | T | 15 | a0001c0001t0008g0158a0002c0002t0007g0247a0002c0002t0007g0288others(12): Show | 15 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2029-59delG | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr6 | 138885445 | |||||
| chr6:138885455
|
G | C | 69 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(66): Show | 69 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.2029-51G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885455 | ||||||
| chr6:138885496
|
C | T | 2 | a0001c0001t0001g0306a0001c0001t0004g0249 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2029-10C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 16/21 | chr6 | 138885496 | ||||||
| chr6:138885613
|
C | T | 1 | a0003c0004t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2102+34C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 17/21 | chr6 | 138885613 | ||||||
| chr6:138885652
|
C | T | 1 | a0001c0001t0008g0318 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2103-22C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 17/21 | chr6 | 138885652 | ||||||
| chr6:138885922
|
T | C | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259+92T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138885922 | ||||||
| chr6:138886123
|
CA | C | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2259+304delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 138886123 | |||||
| chr6:138886204
|
G | GTCA | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2259+376_2259+378d others(5): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr6 | 138886204 | |||||
| chr6:138886290
|
T | C | 9 | a0001c0018t0020g0007a0003c0004t0011g0325a0003c0004t0025g0244others(6): Show | 9 | HG01081.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2259+460T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138886290 | ||||||
| chr6:138886373
|
C | A | 1 | a0002c0002t0001g0097 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2260-484C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138886373 | ||||||
| chr6:138886409
|
T | A | 3 | a0001c0018t0020g0007a0012c0019t0011g0151a0012c0019t0011g0168 | 3 | HG02559.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2260-448T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138886409 | ||||||
| chr6:138886633
|
G | C | 7 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2260-224G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138886633 | ||||||
| chr6:138886773
|
C | T | 165 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2260-84C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 18/21 | chr6 | 138886773 | ||||||
| chr6:138886981
|
T | G | 97 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0158others(94): Show | 97 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.2325+59T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138886981 | ||||||
| chr6:138887154
|
C | T | 3 | a0001c0001t0001g0252a0002c0002t0001g0082a0002c0002t0001g0297 | 3 | HG02602.hp1 HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2325+232C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887154 | ||||||
| chr6:138887168
|
C | A | 18 | a0001c0003t0002g0052a0001c0003t0002g0075a0001c0003t0002g0185others(15): Show | 18 | HG00738.hp1 HG02027.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.2325+246C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887168 | ||||||
| chr6:138887224
|
C | CTTTTT | 92 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2325+305_2325+306i others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138887224 | |||||
| chr6:138887224
|
C | T | 1 | a0002c0002t0007g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2325+302C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887224 | ||||||
| chr6:138887227
|
T | TTTTTTA | 72 | a0001c0001t0002g0174a0001c0001t0008g0318a0001c0001t0016g0211others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.2325+305_2325+306i others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887227 | ||||||
| chr6:138887229
|
A | T | 72 | a0001c0001t0002g0174a0001c0001t0008g0318a0001c0001t0016g0211others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.2325+307A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887229 | ||||||
| chr6:138887393
|
A | T | 2 | a0003c0004t0011g0325a0003c0004t0025g0244 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2325+471A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887393 | ||||||
| chr6:138887516
|
G | A | 1 | a0002c0002t0001g0178 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2325+594G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887516 | ||||||
| chr6:138887525
|
T | G | 1 | a0001c0001t0006g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2325+603T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887525 | ||||||
| chr6:138887596
|
C | A | 176 | a0001c0001t0001g0044a0001c0001t0002g0015a0001c0001t0002g0035others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2325+674C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887596 | ||||||
| chr6:138887619
|
G | A | 1 | a0001c0018t0002g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2325+697G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887619 | ||||||
| chr6:138887624
|
G | A | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2325+702G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887624 | ||||||
| chr6:138887693
|
A | G | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2325+771A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887693 | ||||||
| chr6:138887881
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2325+959G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887881 | ||||||
| chr6:138887940
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2326-1003G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887940 | ||||||
| chr6:138887972
|
T | A | 2 | a0006c0011t0014g0013a0006c0011t0014g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2326-971T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138887972 | ||||||
| chr6:138888012
|
C | A | 1 | a0004c0006t0001g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2326-931C>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888012 | ||||||
| chr6:138888092
|
T | C | 4 | a0003c0004t0007g0320a0003c0004t0007g0321a0003c0004t0007g0322others(1): Show | 4 | HG01433.hp1 HG02622.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2326-851T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888092 | ||||||
| chr6:138888197
|
T | TCA | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2326-745_2326-744d others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138888197 | |||||
| chr6:138888249
|
C | T | 2 | a0001c0001t0009g0271a0004c0006t0009g0310 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2326-694C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888249 | ||||||
| chr6:138888317
|
C | CT | 74 | a0001c0001t0001g0027a0001c0001t0001g0060a0001c0001t0001g0067others(71): Show | 74 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2326-609dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138888317 | |||||
| chr6:138888317
|
C | CTTTCT | 16 | a0001c0001t0008g0158a0002c0002t0007g0233a0002c0002t0007g0247others(13): Show | 16 | HG01192.hp2 HG01884.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2326-623_2326-622i others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138888317 | |||||
| chr6:138888319
|
T | TTC | 69 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(66): Show | 69 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.2326-623_2326-622i others(4): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138888319 | |||||
| chr6:138888388
|
C | T | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2326-555C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888388 | ||||||
| chr6:138888452
|
C | T | 2 | a0001c0001t0005g0282a0001c0001t0005g0294 | 2 | HG01361.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2326-491C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888452 | ||||||
| chr6:138888477
|
AT | A | 164 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2326-458delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr6 | 138888477 | |||||
| chr6:138888541
|
T | C | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2326-402T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888541 | ||||||
| chr6:138888565
|
C | T | 2 | a0002c0002t0002g0057a0002c0002t0003g0148 | 2 | NA18943.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2326-378C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888565 | ||||||
| chr6:138888566
|
G | A | 6 | a0001c0001t0004g0094a0001c0001t0004g0138a0001c0001t0006g0092others(3): Show | 6 | HG00609.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2326-377G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888566 | ||||||
| chr6:138888622
|
T | C | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2326-321T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888622 | ||||||
| chr6:138888655
|
C | T | 1 | a0008c0031t0017g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2326-288C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888655 | ||||||
| chr6:138888698
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0004g0136a0001c0001t0004g0265others(1): Show | 4 | HG00438.hp1 HG02015.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.2326-245T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 19/21 | chr6 | 138888698 | ||||||
| chr6:138889317
|
T | C | 21 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0158others(18): Show | 21 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2414+286T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889317 | ||||||
| chr6:138889366
|
G | A | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+335G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889366 | ||||||
| chr6:138889470
|
T | C | 272 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0060others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.2414+439T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889470 | ||||||
| chr6:138889583
|
G | A | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2414+552G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889583 | ||||||
| chr6:138889806
|
C | T | 3 | a0004c0006t0015g0213a0004c0006t0015g0312a0006c0011t0021g0236 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2414+775C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889806 | ||||||
| chr6:138889930
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2414+899C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889930 | ||||||
| chr6:138889961
|
T | C | 1 | a0002c0002t0007g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2414+930T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889961 | ||||||
| chr6:138889994
|
T | G | 1 | a0001c0003t0013g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2414+963T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138889994 | ||||||
| chr6:138890077
|
T | C | 1 | a0002c0002t0004g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2414+1046T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890077 | ||||||
| chr6:138890130
|
G | T | 3 | a0004c0006t0015g0213a0004c0006t0015g0312a0006c0011t0021g0236 | 3 | HG02717.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2414+1099G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890130 | ||||||
| chr6:138890204
|
A | G | 4 | a0001c0018t0020g0007a0009c0025t0020g0004a0012c0019t0011g0151others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414+1173A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890204 | ||||||
| chr6:138890311
|
A | G | 1 | a0001c0003t0013g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2414+1280A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890311 | ||||||
| chr6:138890313
|
T | C | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2414+1282T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890313 | ||||||
| chr6:138890338
|
T | A | 2 | a0001c0001t0001g0044a0001c0001t0004g0040 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2414+1307T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890338 | ||||||
| chr6:138890492
|
C | CT | 13 | a0001c0001t0001g0032a0001c0001t0007g0006a0001c0001t0008g0046others(10): Show | 13 | HG01169.hp2 HG02015.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2414+1489dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTT | 9 | a0001c0001t0009g0012a0001c0001t0009g0108a0001c0001t0009g0152others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2414+1488_2414+148 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTT | 13 | a0001c0001t0009g0011a0001c0001t0009g0271a0004c0006t0015g0213others(10): Show | 13 | HG01106.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2414+1487_2414+148 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTT | 15 | a0001c0001t0001g0044a0001c0001t0001g0171a0001c0001t0004g0195others(12): Show | 15 | HG00609.hp1 HG00621.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.2414+1484_2414+148 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT | 23 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0169others(20): Show | 23 | HG01257.hp1 HG01261.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.2414+1483_2414+148 others(11): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(1): Show |
22 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0106others(19): Show | 22 | HG00639.hp1 HG01255.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.2414+1482_2414+148 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0004g0127others(6): Show | 9 | HG00558.hp1 HG00597.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2414+1481_2414+148 others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0080a0001c0001t0001g0083others(11): Show | 14 | HG01109.hp2 HG02015.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.2414+1480_2414+148 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0116others(14): Show | 17 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.2414+1479_2414+148 others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(5): Show |
10 | a0001c0001t0001g0056a0001c0001t0001g0109a0001c0001t0001g0112others(7): Show | 10 | HG00597.hp1 HG03098.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2414+1478_2414+148 others(16): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0266others(3): Show | 6 | HG00621.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2414+1477_2414+148 others(17): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0004g0138 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2414+1475_2414+148 others(19): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0004g0265 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2414+1473_2414+148 others(21): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0136 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2414+1472_2414+148 others(22): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(1): Show |
C | 67 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2414+1482_2414+148 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0002g0174a0001c0001t0002g0203a0001c0001t0003g0134others(7): Show | 10 | HG00741.hp1 HG01261.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.2414+1481_2414+148 others(13): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(3): Show |
C | 63 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2414+1480_2414+148 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0129 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2414+1479_2414+148 others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0009t0004g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2414+1477_2414+148 others(17): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890492
|
CTTTTTTT others(8): Show |
C | 1 | a0004c0008t0009g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2414+1475_2414+148 others(19): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890492 | |||||
| chr6:138890589
|
A | G | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+1558A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890589 | ||||||
| chr6:138890656
|
T | C | 1 | a0019c0032t0005g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2414+1625T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890656 | ||||||
| chr6:138890849
|
G | GT | 68 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2414+1824dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138890849 | |||||
| chr6:138890947
|
A | G | 3 | a0001c0018t0020g0007a0012c0019t0011g0151a0012c0019t0011g0168 | 3 | HG02559.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2414+1916A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138890947 | ||||||
| chr6:138891060
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0004g0249 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2414+2029T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891060 | ||||||
| chr6:138891083
|
C | T | 1 | a0001c0001t0003g0140 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2414+2052C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891083 | ||||||
| chr6:138891093
|
TCTC | T | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2414+2067_2414+206 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138891093 | |||||
| chr6:138891259
|
C | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+2228C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891259 | ||||||
| chr6:138891360
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2414+2329T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891360 | ||||||
| chr6:138891495
|
CT | C | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2414+2466delT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138891495 | |||||
| chr6:138891588
|
TC | T | 253 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0067others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.2414+2564delC | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138891588 | |||||
| chr6:138891595
|
CA | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0155a0001c0001t0002g0156 | 3 | HG01952.hp2 HG01978.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2414+2565delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891595 | ||||||
| chr6:138891695
|
C | T | 5 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2414+2664C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891695 | ||||||
| chr6:138891696
|
C | T | 1 | a0001c0018t0020g0007 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2414+2665C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891696 | ||||||
| chr6:138891807
|
C | CTCTT | 165 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2414+2777_2414+277 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138891807 | |||||
| chr6:138891937
|
A | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+2906A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891937 | ||||||
| chr6:138891942
|
C | T | 47 | a0001c0003t0002g0037a0001c0003t0002g0058a0001c0003t0002g0100others(44): Show | 47 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2414+2911C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138891942 | ||||||
| chr6:138892050
|
G | A | 47 | a0001c0003t0002g0037a0001c0003t0002g0058a0001c0003t0002g0100others(44): Show | 47 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2414+3019G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892050 | ||||||
| chr6:138892083
|
A | C | 1 | a0001c0001t0002g0240 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2414+3052A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892083 | ||||||
| chr6:138892130
|
T | C | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2414+3099T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892130 | ||||||
| chr6:138892135
|
G | A | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414+3104G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892135 | ||||||
| chr6:138892139
|
C | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+3108C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892139 | ||||||
| chr6:138892196
|
A | G | 1 | a0004c0006t0009g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2414+3165A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892196 | ||||||
| chr6:138892358
|
C | G | 1 | a0005c0007t0001g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2414+3327C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892358 | ||||||
| chr6:138892828
|
C | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+3797C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138892828 | ||||||
| chr6:138893085
|
A | AGAG | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+4058_2414+406 others(7): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893085 | |||||
| chr6:138893174
|
G | GT | 76 | a0001c0001t0002g0174a0001c0001t0003g0134a0001c0003t0002g0037others(73): Show | 76 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.2414+4153dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893174 | |||||
| chr6:138893175
|
TTTTTTTT others(3): Show |
T | 2 | a0001c0001t0001g0306a0001c0001t0004g0249 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2414+4164_2414+417 others(14): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893175 | |||||
| chr6:138893185
|
G | GT | 9 | a0001c0001t0001g0060a0001c0001t0001g0112a0001c0001t0001g0114others(6): Show | 9 | HG00733.hp2 HG01109.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.2414+4163dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893185 | |||||
| chr6:138893185
|
G | T | 1 | a0001c0022t0003g0142 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2414+4154G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893185 | ||||||
| chr6:138893186
|
T | G | 1 | a0001c0022t0003g0142 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2414+4155T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893186 | ||||||
| chr6:138893194
|
T | G | 73 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.2414+4163T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893194 | ||||||
| chr6:138893195
|
G | T | 73 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.2414+4164G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893195 | ||||||
| chr6:138893225
|
G | A | 41 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0158others(38): Show | 41 | HG00738.hp1 HG01192.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.2414+4194G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893225 | ||||||
| chr6:138893397
|
G | T | 4 | a0001c0018t0020g0007a0009c0025t0020g0004a0012c0019t0011g0151others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414+4366G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893397 | ||||||
| chr6:138893408
|
T | C | 1 | a0001c0018t0002g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2414+4377T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893408 | ||||||
| chr6:138893411
|
A | AT | 18 | a0001c0001t0008g0158a0002c0002t0007g0166a0002c0002t0007g0233others(15): Show | 18 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2414+4381dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893411 | |||||
| chr6:138893411
|
A | T | 1 | a0001c0001t0002g0156 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2414+4380A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893411 | ||||||
| chr6:138893412
|
TA | T | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2414+4382delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893412 | ||||||
| chr6:138893413
|
A | AT | 5 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2414+4389dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138893413 | |||||
| chr6:138893413
|
A | T | 78 | a0001c0001t0002g0048a0001c0001t0002g0068a0001c0001t0002g0098others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2414+4382A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893413 | ||||||
| chr6:138893415
|
T | A | 21 | a0001c0001t0004g0144a0001c0001t0006g0256a0001c0003t0002g0052others(18): Show | 21 | HG00738.hp1 HG01081.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.2414+4384T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893415 | ||||||
| chr6:138893608
|
G | T | 2 | a0001c0001t0001g0179a0001c0001t0004g0157 | 2 | HG01255.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2414+4577G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893608 | ||||||
| chr6:138893641
|
C | T | 1 | a0003c0004t0004g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2414+4610C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893641 | ||||||
| chr6:138893682
|
G | A | 164 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2414+4651G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893682 | ||||||
| chr6:138893720
|
C | T | 1 | a0002c0002t0001g0178 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2414+4689C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893720 | ||||||
| chr6:138893755
|
A | C | 31 | a0001c0003t0002g0100a0001c0003t0002g0150a0001c0003t0002g0163others(28): Show | 31 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2414+4724A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893755 | ||||||
| chr6:138893798
|
T | C | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+4767T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893798 | ||||||
| chr6:138893846
|
G | C | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+4815G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893846 | ||||||
| chr6:138893868
|
A | T | 29 | a0001c0001t0001g0090a0001c0001t0001g0105a0001c0001t0001g0106others(26): Show | 29 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.2414+4837A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893868 | ||||||
| chr6:138893901
|
C | G | 5 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2414+4870C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893901 | ||||||
| chr6:138893976
|
G | A | 2 | a0006c0011t0014g0013a0006c0011t0014g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2414+4945G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138893976 | ||||||
| chr6:138894081
|
G | A | 2 | a0006c0011t0014g0013a0006c0011t0014g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2414+5050G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894081 | ||||||
| chr6:138894126
|
A | G | 1 | a0002c0002t0001g0113 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2414+5095A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894126 | ||||||
| chr6:138894159
|
C | T | 3 | a0005c0024t0005g0276a0009c0012t0003g0021a0014c0037t0002g0036 | 3 | NA18522.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2414+5128C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894159 | ||||||
| chr6:138894183
|
A | G | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+5152A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894183 | ||||||
| chr6:138894230
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2414+5199T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894230 | ||||||
| chr6:138894241
|
G | A | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2414+5210G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894241 | ||||||
| chr6:138894367
|
G | A | 5 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2414+5336G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894367 | ||||||
| chr6:138894453
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2414+5422T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894453 | ||||||
| chr6:138894492
|
T | C | 65 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(62): Show | 65 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.2414+5461T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894492 | ||||||
| chr6:138894850
|
A | G | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2414+5819A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894850 | ||||||
| chr6:138894856
|
C | T | 2 | a0023c0036t0002g0305a0024c0020t0002g0315 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2414+5825C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894856 | ||||||
| chr6:138894866
|
A | G | 3 | a0001c0018t0020g0007a0012c0019t0011g0151a0012c0019t0011g0168 | 3 | HG02559.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2414+5835A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894866 | ||||||
| chr6:138894891
|
T | C | 1 | a0009c0025t0020g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2414+5860T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894891 | ||||||
| chr6:138894909
|
T | A | 1 | a0002c0002t0007g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2414+5878T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894909 | ||||||
| chr6:138894991
|
G | A | 1 | a0002c0002t0004g0131 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2415-5957G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138894991 | ||||||
| chr6:138895100
|
G | GA | 8 | a0001c0001t0003g0023a0001c0001t0003g0030a0001c0001t0003g0133others(5): Show | 8 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2415-5839dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138895100 | |||||
| chr6:138895111
|
G | T | 65 | a0001c0003t0002g0037a0001c0003t0002g0052a0001c0003t0002g0058others(62): Show | 65 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.2415-5837G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895111 | ||||||
| chr6:138895115
|
T | C | 5 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415-5833T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895115 | ||||||
| chr6:138895173
|
T | C | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2415-5775T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895173 | ||||||
| chr6:138895273
|
A | G | 2 | a0023c0036t0002g0305a0024c0020t0002g0315 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2415-5675A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895273 | ||||||
| chr6:138895289
|
T | C | 47 | a0001c0003t0002g0037a0001c0003t0002g0058a0001c0003t0002g0100others(44): Show | 47 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2415-5659T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895289 | ||||||
| chr6:138895489
|
T | C | 2 | a0003c0004t0011g0325a0003c0004t0025g0244 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2415-5459T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895489 | ||||||
| chr6:138895562
|
CATAT | C | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-5375_2415-537 others(8): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138895562 | |||||
| chr6:138895575
|
A | T | 65 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0087others(62): Show | 65 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2415-5373A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895575 | ||||||
| chr6:138895682
|
T | A | 47 | a0001c0003t0002g0037a0001c0003t0002g0058a0001c0003t0002g0100others(44): Show | 47 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2415-5266T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895682 | ||||||
| chr6:138895813
|
T | G | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-5135T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895813 | ||||||
| chr6:138895825
|
G | A | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-5123G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895825 | ||||||
| chr6:138895874
|
T | C | 1 | a0001c0003t0005g0292 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2415-5074T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895874 | ||||||
| chr6:138895889
|
G | A | 2 | a0001c0001t0003g0095a0001c0018t0020g0007 | 2 | HG02970.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2415-5059G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895889 | ||||||
| chr6:138895949
|
A | C | 4 | a0001c0018t0020g0007a0009c0025t0020g0004a0012c0019t0011g0151others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-4999A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138895949 | ||||||
| chr6:138896016
|
A | G | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0002c0002t0001g0053others(3): Show | 6 | NA18960.hp1 NA18962.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.2415-4932A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896016 | ||||||
| chr6:138896084
|
A | ATGTCTGT others(10): Show |
73 | a0001c0001t0016g0212a0001c0003t0002g0037a0001c0003t0002g0052others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.2415-4863_2415-486 others(21): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138896084 | |||||
| chr6:138896086
|
T | G | 1 | a0001c0001t0016g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415-4862T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896086 | ||||||
| chr6:138896087
|
G | T | 1 | a0001c0001t0016g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415-4861G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896087 | ||||||
| chr6:138896090
|
G | GTGATTTT others(22): Show |
1 | a0001c0001t0016g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415-4858_2415-485 others(33): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896090 | ||||||
| chr6:138896091
|
A | AGTTTT | 21 | a0001c0003t0002g0052a0001c0003t0002g0075a0001c0003t0002g0176others(18): Show | 21 | HG00738.hp1 HG02027.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2415-4857_2415-485 others(9): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896091 | ||||||
| chr6:138896091
|
A | AGTTTTT | 47 | a0001c0003t0002g0037a0001c0003t0002g0058a0001c0003t0002g0100others(44): Show | 47 | HG00423.hp1 HG00438.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.2415-4857_2415-485 others(10): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896091 | ||||||
| chr6:138896091
|
A | AGTTTTTT others(4): Show |
1 | a0001c0001t0016g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2415-4857_2415-485 others(15): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896091 | ||||||
| chr6:138896091
|
A | T | 1 | a0001c0001t0016g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2415-4857A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896091 | ||||||
| chr6:138896092
|
A | AT | 27 | a0001c0001t0004g0229a0001c0001t0007g0006a0001c0001t0008g0046others(24): Show | 27 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2415-4841dupT | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138896092 | |||||
| chr6:138896092
|
A | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-4856A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896092 | ||||||
| chr6:138896126
|
C | T | 165 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2415-4822C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896126 | ||||||
| chr6:138896160
|
G | A | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2415-4788G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896160 | ||||||
| chr6:138896162
|
C | T | 2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | NA18954.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2415-4786C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896162 | ||||||
| chr6:138896211
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0006g0256 | 2 | NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2415-4737G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896211 | ||||||
| chr6:138896238
|
A | G | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-4710A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896238 | ||||||
| chr6:138896260
|
T | C | 1 | a0001c0001t0024g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2415-4688T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896260 | ||||||
| chr6:138896300
|
G | A | 4 | a0001c0018t0020g0007a0009c0025t0020g0004a0012c0019t0011g0151others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-4648G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896300 | ||||||
| chr6:138896375
|
GA | G | 3 | a0008c0013t0002g0043a0008c0013t0005g0267a0008c0013t0005g0269 | 3 | HG00738.hp1 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2415-4570delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138896375 | |||||
| chr6:138896506
|
A | T | 1 | a0002c0002t0004g0002 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2415-4442A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896506 | ||||||
| chr6:138896723
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2415-4225C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896723 | ||||||
| chr6:138896750
|
C | T | 1 | a0004c0008t0009g0309 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2415-4198C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896750 | ||||||
| chr6:138896760
|
G | C | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2415-4188G>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896760 | ||||||
| chr6:138896963
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0250others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415-3985G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138896963 | ||||||
| chr6:138897123
|
T | A | 23 | a0001c0001t0007g0006a0001c0001t0008g0046a0001c0001t0008g0158others(20): Show | 23 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2415-3825T>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897123 | ||||||
| chr6:138897255
|
A | C | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2415-3693A>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897255 | ||||||
| chr6:138897259
|
T | C | 3 | a0004c0008t0009g0298a0004c0008t0009g0309a0004c0008t0009g0314 | 3 | HG02723.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2415-3689T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897259 | ||||||
| chr6:138897366
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2415-3582C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897366 | ||||||
| chr6:138897568
|
T | C | 5 | a0005c0007t0001g0300a0005c0007t0001g0301a0005c0007t0001g0302others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415-3380T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897568 | ||||||
| chr6:138897790
|
C | T | 6 | a0001c0001t0009g0011a0001c0001t0009g0012a0001c0001t0009g0108others(3): Show | 6 | HG01106.hp1 HG02109.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2415-3158C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897790 | ||||||
| chr6:138897899
|
A | G | 1 | a0001c0003t0005g0259 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2415-3049A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897899 | ||||||
| chr6:138897977
|
C | T | 74 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.2415-2971C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138897977 | ||||||
| chr6:138898060
|
T | TA | 64 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.2415-2876dupA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138898060 | |||||
| chr6:138898060
|
TA | T | 24 | a0001c0001t0001g0044a0001c0001t0004g0040a0001c0001t0007g0006others(21): Show | 24 | HG01192.hp2 HG01433.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.2415-2876delA | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138898060 | |||||
| chr6:138898060
|
TAA | T | 75 | a0001c0001t0016g0211a0001c0001t0016g0212a0001c0003t0002g0037others(72): Show | 75 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.2415-2877_2415-287 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138898060 | |||||
| chr6:138898087
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0008g0250a0001c0001t0029g0262 | 3 | HG02486.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2415-2861C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898087 | ||||||
| chr6:138898253
|
C | T | 173 | a0001c0001t0001g0044a0001c0001t0002g0015a0001c0001t0002g0035others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.2415-2695C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898253 | ||||||
| chr6:138898430
|
G | A | 2 | a0023c0036t0002g0305a0024c0020t0002g0315 | 2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2415-2518G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898430 | ||||||
| chr6:138898457
|
T | C | 2 | a0002c0002t0002g0273a0002c0002t0002g0274 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2415-2491T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898457 | ||||||
| chr6:138898781
|
GC | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0088others(1): Show | 4 | NA18968.hp2 NA18971.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-2166delC | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898781 | ||||||
| chr6:138898817
|
C | T | 1 | a0005c0007t0001g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2415-2131C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898817 | ||||||
| chr6:138898851
|
T | G | 166 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2415-2097T>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138898851 | ||||||
| chr6:138899170
|
AAG | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0032 | 3 | HG01168.hp1 HG01169.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.2415-1769_2415-176 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138899170 | |||||
| chr6:138899307
|
A | T | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-1641A>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899307 | ||||||
| chr6:138899439
|
T | TTG | 91 | a0001c0001t0003g0291a0001c0001t0007g0006a0001c0001t0008g0046others(88): Show | 91 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.2415-1489_2415-148 others(6): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138899439 | |||||
| chr6:138899439
|
T | TTGTGTGT others(1): Show |
6 | a0001c0003t0002g0058a0001c0003t0002g0304a0007c0014t0005g0207others(3): Show | 6 | HG02615.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2415-1495_2415-148 others(12): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr6 | 138899439 | |||||
| chr6:138899548
|
T | C | 1 | a0005c0024t0005g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2415-1400T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899548 | ||||||
| chr6:138899575
|
C | T | 98 | a0001c0001t0003g0291a0001c0001t0007g0006a0001c0001t0008g0046others(95): Show | 98 | HG00423.hp1 HG00438.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.2415-1373C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899575 | ||||||
| chr6:138899584
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2415-1364A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899584 | ||||||
| chr6:138899617
|
G | A | 2 | a0001c0001t0009g0271a0004c0006t0009g0310 | 2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2415-1331G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899617 | ||||||
| chr6:138899654
|
A | G | 67 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2415-1294A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899654 | ||||||
| chr6:138899947
|
A | G | 1 | a0002c0002t0001g0178 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2415-1001A>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138899947 | ||||||
| chr6:138900030
|
T | C | 63 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0087others(60): Show | 63 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2415-918T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900030 | ||||||
| chr6:138900296
|
G | A | 3 | a0001c0033t0002g0299a0006c0015t0003g0238a0006c0015t0003g0239 | 3 | HG02895.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2415-652G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900296 | ||||||
| chr6:138900378
|
G | A | 2 | a0006c0011t0014g0013a0006c0011t0014g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2415-570G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900378 | ||||||
| chr6:138900534
|
C | T | 1 | a0001c0003t0003g0132 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2415-414C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900534 | ||||||
| chr6:138900537
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0004g0249 | 2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2415-411G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900537 | ||||||
| chr6:138900629
|
C | T | 1 | a0002c0002t0019g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2415-319C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900629 | ||||||
| chr6:138900704
|
T | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0114a0001c0001t0001g0306others(7): Show | 10 | HG00733.hp2 HG01109.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.2415-244T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900704 | ||||||
| chr6:138900713
|
G | T | 256 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0067others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2415-235G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900713 | ||||||
| chr6:138900801
|
T | C | 4 | a0001c0001t0016g0211a0001c0001t0016g0212a0006c0011t0014g0013others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2415-147T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900801 | ||||||
| chr6:138900870
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0149a0001c0001t0004g0136others(3): Show | 6 | HG00438.hp1 HG02015.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415-78T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 20/21 | chr6 | 138900870 | ||||||
| chr6:138901269
|
T | C | 1 | a0002c0002t0001g0117 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2587+149T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138901269 | ||||||
| chr6:138901546
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0088others(1): Show | 4 | NA18968.hp2 NA18971.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2587+426C>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138901546 | ||||||
| chr6:138901621
|
T | C | 1 | a0023c0036t0002g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2587+501T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138901621 | ||||||
| chr6:138901672
|
C | G | 68 | a0001c0001t0002g0015a0001c0001t0002g0035a0001c0001t0002g0047others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2587+552C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138901672 | ||||||
| chr6:138901972
|
G | T | 62 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0090others(59): Show | 62 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2588-528G>T | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138901972 | ||||||
| chr6:138902055
|
T | C | 2 | a0001c0003t0002g0163a0001c0022t0003g0142 | 2 | NA18612.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.2588-445T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138902055 | ||||||
| chr6:138902151
|
G | A | 1 | a0001c0003t0013g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2588-349G>A | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138902151 | ||||||
| chr6:138902173
|
C | G | 2 | a0006c0011t0014g0013a0006c0011t0014g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2588-327C>G | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138902173 | ||||||
| chr6:138902432
|
T | C | 1 | a0001c0001t0006g0263 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2588-68T>C | ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | chr6 | 138902432 | ||||||
| chr6:138902453
|
ATTG | A | 4 | a0001c0018t0020g0007a0009c0025t0020g0004a0012c0019t0011g0151others(1): Show | 4 | HG01081.hp1 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2588-44_2588-42del others(3): Show |
ECT2L | ENSG00000203734.13 | transcript | ENST00000541398.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr6 | 138902453 |