Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2004 |
|---|---|
| ensemblid | ENSG00000111145.8 |
| hgncid | 3325 |
| symbol | ELK3 |
| name | ETS transcription factor ELK3 |
| refseq_nuc | NM_005230.4 |
| refseq_prot | NP_005221.2 |
| ensembl_nuc | ENST00000228741.8 |
| ensembl_prot | ENSP00000228741.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 96194375 |
| end | 96269824 |
| strand | + |
| ver | v1.2 |
| region | chr12:96194375-96269824 |
| region5000 | chr12:96189375-96274824 |
| regionname0 | ELK3_chr12_96194375_96269824 |
| regionname5000 | ELK3_chr12_96189375_96274824 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 407 | 319 | 79 | 73 | 115 | 14 | 36 | 86 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002 | 0/0 | 407 | 31 | 11 | 1 | 13 | 2 | 4 | 7 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0003 | 0/0 | 407 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0004 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0005 | 0/0 | 407 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1224 | 314 | 77 | 73 | 112 | 14 | 36 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0002 | 0/0 | 1224 | 30 | 11 | 1 | 13 | 2 | 3 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0003 | 0/0 | 1224 | 2 | 0 | 0 | 2 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0004 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0005 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0006 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0007 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0008 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0009 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0010 | 0/0 | 1224 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| c0011 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2973 | 122 | 33 | 20 | 58 | 1 | 10 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0002 | 1/0 | 2978 | 91 | 17 | 10 | 40 | 7 | 16 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0003 | 0/1 | 2973 | 29 | 8 | 10 | 0 | 3 | 7 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0004 | 0/0 | 2978 | 22 | 4 | 2 | 16 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0005 | 0/0 | 2973 | 21 | 1 | 11 | 9 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0006 | 0/0 | 2973 | 19 | 14 | 1 | 0 | 0 | 4 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0007 | 0/0 | 2978 | 10 | 4 | 3 | 0 | 3 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0008 | 0/0 | 2973 | 8 | 8 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0009 | 0/0 | 2978 | 7 | 0 | 6 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0010 | 0/0 | 2974 | 5 | 0 | 1 | 4 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0011 | 0/0 | 2978 | 4 | 0 | 3 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0012 | 0/0 | 2978 | 2 | 0 | 1 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0013 | 0/0 | 2973 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0014 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0015 | 0/0 | 2992 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0016 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0017 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0018 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0019 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0020 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0021 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0022 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0023 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0024 | 0/0 | 2978 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| t0025 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0337 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1224 | 314 | 77 | 73 | 112 | 14 | 36 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0004 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0005 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0007 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0008 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0011 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0002 | 0/0 | 1224 | 30 | 11 | 1 | 13 | 2 | 3 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0010 | 0/0 | 1224 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0003c0003 | 0/0 | 1224 | 2 | 0 | 0 | 2 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0004c0006 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0005c0009 | 0/0 | 1224 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4196 | 114 | 29 | 20 | 54 | 1 | 10 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0002 | 1/0 | 4201 | 66 | 10 | 10 | 26 | 6 | 13 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0003 | 0/1 | 4196 | 29 | 8 | 10 | 0 | 3 | 7 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0004 | 0/0 | 4201 | 22 | 4 | 2 | 16 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0005 | 0/0 | 4196 | 21 | 1 | 11 | 9 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0006 | 0/0 | 4196 | 18 | 13 | 1 | 0 | 0 | 4 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0007 | 0/0 | 4201 | 10 | 4 | 3 | 0 | 3 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0008 | 0/0 | 4196 | 7 | 7 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0009 | 0/0 | 4201 | 7 | 0 | 6 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0010 | 0/0 | 4197 | 5 | 0 | 1 | 4 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0011 | 0/0 | 4201 | 4 | 0 | 3 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0013 | 0/0 | 4196 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0014 | 0/0 | 4196 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0016 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0017 | 0/0 | 4201 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0018 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0019 | 0/0 | 4196 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0020 | 0/0 | 4196 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0021 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0023 | 0/0 | 4196 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0001t0025 | 0/0 | 4196 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0004t0001 | 0/0 | 4196 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0005t0002 | 0/0 | 4201 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0007t0022 | 0/0 | 4201 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0008t0001 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0001c0011t0001 | 0/0 | 4196 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0002t0001 | 0/0 | 4196 | 3 | 3 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0002t0002 | 0/0 | 4201 | 24 | 7 | 0 | 13 | 1 | 3 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0002t0012 | 0/0 | 4201 | 2 | 0 | 1 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0002t0024 | 0/0 | 4201 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0002c0010t0015 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0003c0003t0001 | 0/0 | 4196 | 2 | 0 | 0 | 2 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0004c0006t0008 | 0/0 | 4196 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| a0005c0009t0006 | 0/0 | 4196 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | copy fasta | chr12 | 96189375 | 96274824 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0003g0337 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0009g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0010g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0011g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0011g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0013g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0014g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0016g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0017g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0018g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0020g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0021g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0023g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0001t0025g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0005t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0007t0022g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0008t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0001c0011t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0012g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0002t0024g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0002c0010t0015g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0004c0006t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| a0005c0009t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | GBR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0051 | EUR | GBR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0156 | EUR | GBR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0031 | EUR | GBR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0126 | EUR | FIN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | FIN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | FIN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0177 | EUR | FIN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00408 | hp2 | a0001 | c0005 | t0002 | g0335 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00558 | hp1 | a0001 | c0001 | t0018 | g0250 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0246 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0014 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00735 | hp2 | a0001 | c0001 | t0014 | g0231 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0081 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00738 | hp2 | a0001 | c0001 | t0013 | g0011 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0012 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01070 | hp1 | a0001 | c0001 | t0009 | g0015 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0082 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0239 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0320 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0181 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | PUR | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01255 | hp2 | a0002 | c0002 | t0012 | g0146 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0291 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0144 | EUR | IBS | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0259 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01928 | hp1 | a0001 | c0001 | t0011 | g0080 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0194 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0019 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01975 | hp2 | a0001 | c0001 | t0025 | g0309 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0234 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0016 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0341 | EAS | KHV | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | CDX | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CDX | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02293 | hp2 | a0001 | c0001 | t0009 | g0017 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PEL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0086 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0221 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03041 | hp2 | a0004 | c0006 | t0008 | g0100 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0333 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03209 | hp1 | a0002 | c0002 | t0024 | g0084 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0274 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0139 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03579 | hp1 | a0001 | c0007 | t0022 | g0103 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03688 | hp1 | a0002 | c0010 | t0015 | g0153 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0190 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0345 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0155 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | STU | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | CHB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | CHB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | CHB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0342 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0301 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0338 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18969 | hp2 | a0001 | c0008 | t0001 | g0281 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18982 | hp2 | a0001 | c0001 | t0010 | g0258 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19002 | hp1 | a0001 | c0001 | t0010 | g0254 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19007 | hp2 | a0001 | c0001 | t0021 | g0325 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0119 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | LWK | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19056 | hp1 | a0001 | c0011 | t0001 | g0222 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0214 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0247 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ASW | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ASW | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20752 | hp2 | a0002 | c0002 | t0012 | g0178 | EUR | TSI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0292 | EUR | TSI | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0013 | SAS | GIH | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20905 | hp2 | a0001 | c0001 | t0017 | g0127 | SAS | GIH | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | CLM | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | MSL | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | USA | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | USA | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | USA | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA21309 | hp1 | a0005 | c0009 | t0006 | g0069 | AFR | LWK | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | LWK | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0337 | REF | REF | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0039 | REF | REF | ELK3_chr12_96189375_96274824 | ELK3 | chr12 | 96189375 | 96274824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96247225
|
A | G | 1 | a0003 | 2 | HG00609.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.493A>G | p.Lys165Glu | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 826/4201 | 493/1224 | 165/407 | chr12 | 96247225 | ||
| chr12:96247238
|
C | T | 1 | a0002 | 31 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(28): Show |
missense_variant | MODERATE | c.506C>T | p.Pro169Leu | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 839/4201 | 506/1224 | 169/407 | chr12 | 96247238 | ||
| chr12:96247355
|
C | T | 1 | a0005 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.623C>T | p.Ala208Val | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 956/4201 | 623/1224 | 208/407 | chr12 | 96247355 | ||
| chr12:96247541
|
C | A | 1 | a0004 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.809C>A | p.Ser270Tyr | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 1142/4201 | 809/1224 | 270/407 | chr12 | 96247541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96223584
|
G | A | 1 | a0001c0004 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.18G>A | p.Thr6Thr | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/5 | 351/4201 | 18/1224 | 6/407 | chr12 | 96223584 | ||
| chr12:96247137
|
C | T | 1 | a0001c0011 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.405C>T | p.Asn135Asn | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 738/4201 | 405/1224 | 135/407 | chr12 | 96247137 | ||
| chr12:96247242
|
C | T | 1 | a0002c0010 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.510C>T | p.Pro170Pro | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 843/4201 | 510/1224 | 170/407 | chr12 | 96247242 | ||
| chr12:96247320
|
G | A | 1 | a0001c0005 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.588G>A | p.Arg196Arg | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 921/4201 | 588/1224 | 196/407 | chr12 | 96247320 | ||
| chr12:96247566
|
G | A | 1 | a0001c0007 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.834G>A | p.Ser278Ser | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 1167/4201 | 834/1224 | 278/407 | chr12 | 96247566 | ||
| chr12:96247665
|
C | T | 1 | a0001c0008 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.933C>T | p.Ile311Ile | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/5 | 1266/4201 | 933/1224 | 311/407 | chr12 | 96247665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96194387
|
G | C | 1 | a0001c0001t0014 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 29180 | chr12 | 96194387 | |||||
| chr12:96194412
|
C | CCGGGGCG others(7): Show |
1 | a0002c0010t0015 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-288_-275dupCGCGGC others(8): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 29133 | INFO_REALIGN_3_PRIME | chr12 | 96194412 | ||||
| chr12:96194494
|
C | T | 1 | a0001c0001t0025 | 1 | HG01975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-214C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 29073 | chr12 | 96194494 | |||||
| chr12:96194530
|
C | A | 1 | a0001c0001t0016 | 1 | NA19081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-178C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 29037 | chr12 | 96194530 | |||||
| chr12:96194551
|
A | G | 1 | a0002c0002t0024 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 29016 | chr12 | 96194551 | |||||
| chr12:96194627
|
C | G | 1 | a0001c0001t0009 | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-81C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 28940 | chr12 | 96194627 | |||||
| chr12:96194650
|
G | T | 1 | a0001c0001t0023 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 28917 | chr12 | 96194650 | |||||
| chr12:96194690
|
A | G | 3 | a0001c0001t0008a0001c0007t0022a0004c0006t0008 | 9 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-18A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/5 | 28877 | chr12 | 96194690 | |||||
| chr12:96267206
|
C | T | 1 | a0001c0001t0021 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 26 | chr12 | 96267206 | |||||
| chr12:96267207
|
A | G | 1 | a0001c0001t0013 | 2 | HG00738.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 27 | chr12 | 96267207 | |||||
| chr12:96267236
|
G | A | 4 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(1): Show | 32 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 56 | chr12 | 96267236 | |||||
| chr12:96267468
|
A | C | 1 | a0002c0002t0012 | 2 | HG01255.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*288A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 288 | chr12 | 96267468 | |||||
| chr12:96267572
|
C | T | 1 | a0001c0001t0007 | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*392C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 392 | chr12 | 96267572 | |||||
| chr12:96267832
|
TAAAAG | T | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 209 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*661delGAAAA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 657 | INFO_REALIGN_3_PRIME | chr12 | 96267832 | ||||
| chr12:96267923
|
C | T | 1 | a0001c0001t0003 | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*743C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 743 | chr12 | 96267923 | |||||
| chr12:96267986
|
A | C | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG01243.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*806A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 806 | chr12 | 96267986 | |||||
| chr12:96268260
|
T | C | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG01243.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1080T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 1080 | chr12 | 96268260 | |||||
| chr12:96268289
|
AAGGC | A | 1 | a0001c0001t0010 | 5 | HG01978.hp2 NA18964.hp2 NA18982.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1110_*1113delAGGC | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 1110 | chr12 | 96268289 | |||||
| chr12:96268542
|
T | C | 1 | a0001c0001t0019 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1362T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 1362 | chr12 | 96268542 | |||||
| chr12:96268796
|
T | C | 1 | a0001c0001t0005 | 21 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1616T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 1616 | chr12 | 96268796 | |||||
| chr12:96269137
|
A | G | 1 | a0001c0001t0017 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1957A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 1957 | chr12 | 96269137 | |||||
| chr12:96269321
|
A | G | 1 | a0001c0001t0007 | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2141A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 2141 | chr12 | 96269321 | |||||
| chr12:96269343
|
A | C | 1 | a0001c0001t0011 | 4 | HG00140.hp2 HG00738.hp1 HG01074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2163A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 2163 | chr12 | 96269343 | |||||
| chr12:96269369
|
T | C | 2 | a0001c0001t0006a0005c0009t0006 | 19 | HG01978.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2189T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 2189 | chr12 | 96269369 | |||||
| chr12:96269579
|
G | C | 1 | a0001c0001t0018 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2399G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 5/5 | 2399 | chr12 | 96269579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96194909
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-3+204C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96194909 | ||||||
| chr12:96195281
|
TG | T | 4 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0013g0011others(1): Show | 4 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+581delG | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96195281 | |||||
| chr12:96195319
|
G | A | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+614G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195319 | ||||||
| chr12:96195324
|
G | C | 1 | a0001c0001t0003g0020 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-3+619G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195324 | ||||||
| chr12:96195392
|
G | A | 1 | a0001c0001t0007g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-3+687G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195392 | ||||||
| chr12:96195450
|
C | T | 1 | a0002c0002t0002g0345 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-3+745C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195450 | ||||||
| chr12:96195506
|
A | T | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+801A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195506 | ||||||
| chr12:96195576
|
C | G | 5 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(2): Show | 5 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+871C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195576 | ||||||
| chr12:96195610
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-3+905G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96195610 | ||||||
| chr12:96195795
|
CTG | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG02027.hp1 HG02080.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-3+1093_-3+1094del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96195795 | |||||
| chr12:96196077
|
A | T | 1 | a0001c0001t0002g0343 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-3+1372A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196077 | ||||||
| chr12:96196412
|
C | T | 5 | a0001c0001t0002g0339a0001c0001t0005g0338a0001c0001t0005g0340others(2): Show | 5 | HG02040.hp1 HG02132.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+1707C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196412 | ||||||
| chr12:96196413
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-3+1708T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196413 | ||||||
| chr12:96196421
|
TG | T | 330 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(327): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-3+1724delG | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196421 | |||||
| chr12:96196501
|
C | G | 1 | a0001c0001t0003g0337 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-3+1796C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196501 | ||||||
| chr12:96196519
|
C | T | 1 | a0001c0001t0002g0336 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3+1814C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196519 | ||||||
| chr12:96196637
|
A | G | 2 | a0001c0001t0002g0334a0001c0005t0002g0335 | 2 | HG00408.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-3+1932A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196637 | ||||||
| chr12:96196681
|
CCT | C | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+1977_-3+1978del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196681 | ||||||
| chr12:96196747
|
GT | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0329others(9): Show | 13 | HG01975.hp1 HG02145.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3+2063delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196747 | |||||
| chr12:96196747
|
GTT | G | 150 | a0001c0001t0001g0188a0001c0001t0001g0192a0001c0001t0001g0199others(147): Show | 152 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-3+2062_-3+2063del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196747 | |||||
| chr12:96196747
|
GTTT | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0088others(124): Show | 129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-3+2061_-3+2063del others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196747 | |||||
| chr12:96196747
|
GTTTT | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0061others(36): Show | 42 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3+2060_-3+2063del others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196747 | |||||
| chr12:96196747
|
GTTTTT | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0003g0337others(3): Show | 6 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+2059_-3+2063del others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96196747 | |||||
| chr12:96196796
|
G | A | 4 | a0001c0001t0003g0079a0001c0001t0011g0080a0001c0001t0011g0081others(1): Show | 4 | HG00738.hp1 HG01074.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+2091G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196796 | ||||||
| chr12:96196810
|
G | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0075others(6): Show | 9 | HG00639.hp1 HG01192.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+2105G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196810 | ||||||
| chr12:96196840
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-3+2135G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196840 | ||||||
| chr12:96196860
|
A | G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+2155A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196860 | ||||||
| chr12:96196890
|
T | C | 12 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0075others(9): Show | 12 | HG00639.hp1 HG01192.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+2185T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96196890 | ||||||
| chr12:96197218
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-3+2513G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197218 | ||||||
| chr12:96197221
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-3+2516T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197221 | ||||||
| chr12:96197274
|
T | C | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-3+2569T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197274 | ||||||
| chr12:96197298
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+2593G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197298 | ||||||
| chr12:96197352
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+2647A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197352 | ||||||
| chr12:96197373
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0087others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+2668T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197373 | ||||||
| chr12:96197410
|
ATTTAC | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+2710_-3+2714del others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96197410 | |||||
| chr12:96197511
|
G | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-3+2806G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197511 | ||||||
| chr12:96197648
|
A | T | 2 | a0001c0001t0013g0011a0001c0001t0013g0012 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-3+2943A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197648 | ||||||
| chr12:96197658
|
C | T | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+2953C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197658 | ||||||
| chr12:96197871
|
A | G | 1 | a0001c0001t0005g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-3+3166A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197871 | ||||||
| chr12:96197874
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0061others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-3+3169A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197874 | ||||||
| chr12:96197970
|
T | C | 2 | a0001c0001t0002g0107a0001c0004t0001g0189 | 2 | HG03834.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+3265T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96197970 | ||||||
| chr12:96198015
|
A | G | 9 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+3310A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198015 | ||||||
| chr12:96198164
|
G | A | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+3459G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198164 | ||||||
| chr12:96198310
|
C | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(116): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-3+3605C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198310 | ||||||
| chr12:96198464
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+3759C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198464 | ||||||
| chr12:96198507
|
A | G | 2 | a0001c0001t0003g0182a0001c0001t0003g0183 | 2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-3+3802A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198507 | ||||||
| chr12:96198680
|
T | A | 1 | a0001c0001t0002g0048 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-3+3975T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198680 | ||||||
| chr12:96198691
|
A | G | 5 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0002g0323others(2): Show | 5 | NA18943.hp2 NA18966.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+3986A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198691 | ||||||
| chr12:96198895
|
C | T | 331 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(328): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-3+4190C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96198895 | ||||||
| chr12:96199028
|
G | GAACATTA others(6): Show |
1 | a0001c0001t0006g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3+4325_-3+4326ins others(13): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199028 | |||||
| chr12:96199033
|
C | T | 1 | a0001c0001t0006g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3+4328C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199033 | ||||||
| chr12:96199036
|
C | G | 1 | a0001c0001t0006g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3+4331C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199036 | ||||||
| chr12:96199037
|
C | A | 1 | a0001c0001t0006g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-3+4332C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199037 | ||||||
| chr12:96199170
|
G | C | 344 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-3+4465G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199170 | ||||||
| chr12:96199480
|
C | CTG | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(110): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.-3+4808_-3+4809dup others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
C | CTGTG | 83 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0072others(80): Show | 85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-3+4806_-3+4809dup others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
C | CTGTGTG | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0277others(10): Show | 13 | HG00423.hp2 HG01243.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3+4804_-3+4809dup others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0283a0001c0001t0005g0095 | 2 | HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-3+4800_-3+4809dup others(10): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
CTG | C | 6 | a0001c0001t0001g0192a0001c0001t0001g0322a0001c0001t0002g0009others(3): Show | 6 | HG00423.hp1 HG01109.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+4808_-3+4809del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
CTGTG | C | 54 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0186others(51): Show | 55 | HG00609.hp1 HG00639.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.-3+4806_-3+4809del others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199480
|
CTGTGTG | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+4804_-3+4809del others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96199480 | |||||
| chr12:96199715
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5010T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199715 | ||||||
| chr12:96199745
|
C | G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+5040C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199745 | ||||||
| chr12:96199976
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+5271A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96199976 | ||||||
| chr12:96200142
|
G | A | 1 | a0001c0001t0016g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-3+5437G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200142 | ||||||
| chr12:96200195
|
GA | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0087others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+5492delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96200195 | |||||
| chr12:96200335
|
A | C | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+5630A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200335 | ||||||
| chr12:96200368
|
T | C | 1 | a0001c0001t0005g0193 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-3+5663T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200368 | ||||||
| chr12:96200381
|
C | CT | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+5684dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96200381 | |||||
| chr12:96200524
|
G | A | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+5819G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200524 | ||||||
| chr12:96200626
|
CAGAT | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0075others(6): Show | 9 | HG00639.hp1 HG01192.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+5924_-3+5927del others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96200626 | |||||
| chr12:96200749
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-3+6044G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200749 | ||||||
| chr12:96200812
|
G | A | 1 | a0001c0001t0005g0194 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-3+6107G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200812 | ||||||
| chr12:96200816
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-3+6111C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96200816 | ||||||
| chr12:96201093
|
TGTG | T | 3 | a0001c0001t0001g0104a0001c0001t0004g0105a0001c0001t0004g0106 | 3 | HG02572.hp1 HG02717.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-3+6391_-3+6393del others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96201093 | |||||
| chr12:96201125
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-3+6420A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201125 | ||||||
| chr12:96201356
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(3): Show | 8 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+6651C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201356 | ||||||
| chr12:96201362
|
T | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0087others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+6657T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201362 | ||||||
| chr12:96201413
|
GAGTCTGA others(8): Show |
G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+6709_-3+6723del others(15): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201413 | ||||||
| chr12:96201429
|
T | G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+6724T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201429 | ||||||
| chr12:96201433
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-3+6728C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201433 | ||||||
| chr12:96201472
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-3+6767A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201472 | ||||||
| chr12:96201538
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+6833G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201538 | ||||||
| chr12:96201564
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-3+6859G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201564 | ||||||
| chr12:96201580
|
CA | C | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(261): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-3+6897delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96201580 | |||||
| chr12:96201580
|
CAA | C | 44 | a0001c0001t0001g0186a0001c0001t0001g0295a0001c0001t0001g0296others(41): Show | 45 | HG00609.hp1 HG01109.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.-3+6896_-3+6897del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96201580 | |||||
| chr12:96201626
|
A | C | 38 | a0001c0001t0001g0186a0001c0001t0001g0295a0001c0001t0001g0296others(35): Show | 39 | HG00609.hp1 HG01109.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.-3+6921A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201626 | ||||||
| chr12:96201650
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0087others(1): Show | 4 | HG02451.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+6945C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201650 | ||||||
| chr12:96201715
|
A | G | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-3+7010A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201715 | ||||||
| chr12:96201728
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-3+7023T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201728 | ||||||
| chr12:96201744
|
C | G | 9 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(6): Show | 9 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+7039C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201744 | ||||||
| chr12:96201770
|
T | G | 2 | a0001c0001t0001g0005a0001c0004t0001g0189 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+7065T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201770 | ||||||
| chr12:96201815
|
T | C | 2 | a0001c0001t0001g0005a0001c0004t0001g0189 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+7110T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96201815 | ||||||
| chr12:96202011
|
A | G | 8 | a0001c0001t0001g0216a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+7306A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202011 | ||||||
| chr12:96202237
|
C | G | 1 | a0001c0001t0004g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-3+7532C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202237 | ||||||
| chr12:96202243
|
A | C | 1 | a0001c0001t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-3+7538A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202243 | ||||||
| chr12:96202307
|
A | G | 1 | a0001c0001t0005g0340 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-3+7602A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202307 | ||||||
| chr12:96202350
|
A | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0010 | 2 | HG01109.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-3+7645A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202350 | ||||||
| chr12:96202355
|
A | G | 1 | a0002c0002t0002g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-3+7650A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202355 | ||||||
| chr12:96202357
|
T | G | 2 | a0001c0001t0001g0005a0001c0004t0001g0189 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+7652T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202357 | ||||||
| chr12:96202400
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-3+7695A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202400 | ||||||
| chr12:96202410
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(2): Show | 5 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+7705G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202410 | ||||||
| chr12:96202444
|
A | C | 275 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-3+7739A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202444 | ||||||
| chr12:96202505
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+7800C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202505 | ||||||
| chr12:96202523
|
C | CT | 250 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-3+7837dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96202523 | |||||
| chr12:96202523
|
C | CTT | 21 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-3+7836_-3+7837dup others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96202523 | |||||
| chr12:96202551
|
G | A | 7 | a0001c0001t0005g0006a0001c0001t0005g0024a0001c0001t0005g0194others(4): Show | 8 | HG01243.hp2 HG01928.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+7846G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202551 | ||||||
| chr12:96202554
|
T | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+7849T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202554 | ||||||
| chr12:96202567
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+7862C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202567 | ||||||
| chr12:96202909
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+8204A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202909 | ||||||
| chr12:96202951
|
C | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+8246C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96202951 | ||||||
| chr12:96203128
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-3+8423G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203128 | ||||||
| chr12:96203174
|
C | T | 1 | a0001c0001t0004g0179 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-3+8469C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203174 | ||||||
| chr12:96203334
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+8629A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203334 | ||||||
| chr12:96203432
|
G | A | 2 | a0001c0001t0006g0055a0001c0001t0006g0135 | 2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-3+8727G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203432 | ||||||
| chr12:96203465
|
T | G | 5 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0217others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+8760T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203465 | ||||||
| chr12:96203570
|
C | T | 2 | a0002c0002t0002g0175a0002c0002t0002g0176 | 2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.-3+8865C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203570 | ||||||
| chr12:96203640
|
T | A | 2 | a0001c0001t0003g0136a0001c0001t0003g0137 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-3+8935T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203640 | ||||||
| chr12:96203770
|
A | G | 34 | a0001c0001t0001g0186a0001c0001t0001g0295a0001c0001t0001g0296others(31): Show | 35 | HG00609.hp1 HG01109.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3+9065A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203770 | ||||||
| chr12:96203803
|
T | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(122): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3+9098T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203803 | ||||||
| chr12:96203812
|
A | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+9107A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203812 | ||||||
| chr12:96203869
|
C | A | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(304): Show | 312 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-3+9164C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203869 | ||||||
| chr12:96203937
|
T | A | 1 | a0001c0001t0003g0138 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3+9232T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203937 | ||||||
| chr12:96203966
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0329 | 3 | HG00438.hp1 NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-3+9261A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96203966 | ||||||
| chr12:96204101
|
C | T | 1 | a0001c0007t0022g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-3+9396C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204101 | ||||||
| chr12:96204113
|
G | A | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-3+9408G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204113 | ||||||
| chr12:96204171
|
T | G | 125 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(122): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3+9466T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204171 | ||||||
| chr12:96204207
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-3+9502A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204207 | ||||||
| chr12:96204344
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-3+9639A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204344 | ||||||
| chr12:96204585
|
A | G | 5 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(2): Show | 5 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+9880A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204585 | ||||||
| chr12:96204778
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0019g0086others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10073G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96204778 | ||||||
| chr12:96205045
|
T | A | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-3+10340T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205045 | ||||||
| chr12:96205074
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-3+10369C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205074 | ||||||
| chr12:96205305
|
T | C | 1 | a0002c0002t0002g0175 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-3+10600T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205305 | ||||||
| chr12:96205521
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+10816C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205521 | ||||||
| chr12:96205534
|
C | T | 1 | a0002c0002t0002g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-3+10829C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205534 | ||||||
| chr12:96205575
|
A | G | 337 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-3+10870A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96205575 | ||||||
| chr12:96206002
|
G | A | 147 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0042others(144): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-3+11297G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206002 | ||||||
| chr12:96206017
|
T | C | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-3+11312T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206017 | ||||||
| chr12:96206061
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+11356C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206061 | ||||||
| chr12:96206076
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(7): Show | 10 | HG01069.hp2 HG01123.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-3+11371G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206076 | ||||||
| chr12:96206096
|
A | G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+11391A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206096 | ||||||
| chr12:96206156
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+11451T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206156 | ||||||
| chr12:96206163
|
A | T | 1 | a0001c0001t0004g0065 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-3+11458A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206163 | ||||||
| chr12:96206236
|
G | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+11531G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206236 | ||||||
| chr12:96206323
|
A | AT | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+11629dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96206323 | |||||
| chr12:96206327
|
T | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0019g0086others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11622T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206327 | ||||||
| chr12:96206378
|
G | A | 124 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0058others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-3+11673G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206378 | ||||||
| chr12:96206408
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0019g0086others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+11703C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206408 | ||||||
| chr12:96206409
|
C | T | 1 | a0001c0001t0005g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-3+11704C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206409 | ||||||
| chr12:96206469
|
A | G | 2 | a0001c0001t0002g0180a0002c0002t0002g0282 | 2 | NA19003.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-3+11764A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206469 | ||||||
| chr12:96206599
|
T | C | 54 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0001g0163others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-3+11894T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206599 | ||||||
| chr12:96206667
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-3+11962C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206667 | ||||||
| chr12:96206679
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+11974A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96206679 | ||||||
| chr12:96207212
|
T | C | 2 | a0001c0001t0001g0005a0001c0004t0001g0189 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+12507T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96207212 | ||||||
| chr12:96207471
|
C | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+12766C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96207471 | ||||||
| chr12:96207662
|
A | T | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+12957A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96207662 | ||||||
| chr12:96207701
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-3+12996C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96207701 | ||||||
| chr12:96208001
|
G | A | 4 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0295others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+13296G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208001 | ||||||
| chr12:96208046
|
AGTTTTTT | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134 | 3 | NA18942.hp2 NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-3+13356_-3+13362d others(9): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96208046 | |||||
| chr12:96208089
|
G | C | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+13384G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208089 | ||||||
| chr12:96208128
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-3+13423T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208128 | ||||||
| chr12:96208331
|
C | T | 1 | a0001c0001t0017g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-3+13626C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208331 | ||||||
| chr12:96208343
|
C | T | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+13638C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208343 | ||||||
| chr12:96208350
|
C | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(6): Show | 9 | HG00609.hp1 HG01358.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+13645C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208350 | ||||||
| chr12:96208351
|
C | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-3+13646C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208351 | ||||||
| chr12:96208442
|
C | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(123): Show | 129 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-3+13737C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208442 | ||||||
| chr12:96208472
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-3+13767G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208472 | ||||||
| chr12:96208752
|
G | A | 2 | a0001c0001t0001g0005a0001c0004t0001g0189 | 3 | HG02895.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-3+14047G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208752 | ||||||
| chr12:96208860
|
G | A | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-3+14155G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208860 | ||||||
| chr12:96208950
|
C | T | 2 | a0001c0001t0005g0271a0001c0001t0005g0272 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-3+14245C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208950 | ||||||
| chr12:96208965
|
G | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(122): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-3+14260G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208965 | ||||||
| chr12:96208988
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0078others(1): Show | 4 | HG02486.hp1 HG02976.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+14283T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96208988 | ||||||
| chr12:96209333
|
C | T | 5 | a0001c0001t0002g0007a0001c0001t0002g0087a0001c0001t0002g0268others(2): Show | 6 | HG02280.hp2 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-14232C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96209333 | ||||||
| chr12:96209761
|
T | C | 6 | a0001c0001t0002g0218a0001c0001t0006g0190a0001c0001t0006g0219others(3): Show | 6 | HG01074.hp1 HG01978.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-13804T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96209761 | ||||||
| chr12:96209905
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-2-13660G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96209905 | ||||||
| chr12:96209960
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-2-13605C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96209960 | ||||||
| chr12:96209984
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-13581C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96209984 | ||||||
| chr12:96210072
|
T | A | 1 | a0001c0001t0002g0116 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-2-13493T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210072 | ||||||
| chr12:96210152
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0005c0009t0006g0069 | 3 | HG01884.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-2-13413G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210152 | ||||||
| chr12:96210191
|
A | C | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-13374A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210191 | ||||||
| chr12:96210332
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-2-13233C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210332 | ||||||
| chr12:96210333
|
T | A | 2 | a0001c0001t0008g0097a0001c0001t0008g0098 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-2-13232T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210333 | ||||||
| chr12:96210556
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-2-13009C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210556 | ||||||
| chr12:96210559
|
G | GCA | 9 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0072others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-13005_-2-13004i others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210559 | |||||
| chr12:96210559
|
G | GCACACA | 4 | a0001c0001t0001g0004a0001c0001t0001g0067a0001c0001t0001g0071others(1): Show | 5 | HG01258.hp2 HG01358.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-13005_-2-13004i others(8): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210559 | |||||
| chr12:96210561
|
G | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0067others(26): Show | 30 | HG00639.hp2 HG01070.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-2-13004G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210561 | ||||||
| chr12:96210561
|
G | GCA | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0129others(67): Show | 74 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-2-13002_-2-13001d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACA | 26 | a0001c0001t0001g0066a0001c0001t0001g0128a0001c0001t0001g0143others(23): Show | 26 | HG00438.hp2 HG01169.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-13001_-2-13000i others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACACA | 24 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0251others(21): Show | 24 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2-13001_-2-13000i others(8): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACACAC others(1): Show |
39 | a0001c0001t0001g0058a0001c0001t0001g0104a0001c0001t0001g0188others(36): Show | 39 | HG00408.hp1 HG00609.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2-13001_-2-13000i others(10): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACACAC others(3): Show |
27 | a0001c0001t0001g0199a0001c0001t0001g0213a0001c0001t0001g0215others(24): Show | 28 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-2-13001_-2-13000i others(12): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACACAC others(5): Show |
8 | a0001c0001t0001g0091a0001c0001t0001g0207a0001c0001t0001g0217others(5): Show | 8 | HG00423.hp2 HG00673.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-13001_-2-13000i others(14): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCACACAC others(19): Show |
1 | a0001c0001t0005g0194 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-2-13001_-2-13000i others(28): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(3): Show |
4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | NA18952.hp1 NA19060.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-13003_-2-13002i others(12): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(5): Show |
4 | a0001c0001t0001g0093a0001c0001t0002g0009a0001c0001t0002g0010others(1): Show | 4 | HG01109.hp1 HG02129.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-13003_-2-13002i others(14): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(7): Show |
1 | a0001c0001t0001g0264 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-2-13003_-2-13002i others(16): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(9): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0077 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2-13003_-2-13002i others(18): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(11): Show |
1 | a0001c0001t0001g0092 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-2-13003_-2-13002i others(20): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
G | GCGCACAC others(13): Show |
1 | a0001c0001t0005g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-2-13003_-2-13002i others(22): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210561
|
GCA | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-13002_-2-13001d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210561 | |||||
| chr12:96210565
|
G | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 283 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-2-13000G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210565 | ||||||
| chr12:96210565
|
G | GCA | 12 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0296others(9): Show | 13 | HG00099.hp2 HG01106.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-12968_-2-12967d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210565 | |||||
| chr12:96210565
|
G | GCGCGGGC others(7): Show |
1 | a0001c0001t0001g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-2-12999_-2-12998i others(16): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210565 | |||||
| chr12:96210595
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-2-12970A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210595 | ||||||
| chr12:96210597
|
A | ACACACCC others(2): Show |
4 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(1): Show | 4 | HG01070.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12967_-2-12966i others(11): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210597 | |||||
| chr12:96210597
|
A | ACACACCC others(7): Show |
1 | a0001c0001t0009g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-12967_-2-12966i others(16): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96210597 | |||||
| chr12:96210597
|
A | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0174a0001c0001t0019g0086 | 3 | HG02630.hp2 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-2-12968A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210597 | ||||||
| chr12:96210598
|
C | CACA | 4 | a0001c0001t0002g0148a0001c0001t0003g0136a0001c0001t0003g0147others(1): Show | 4 | HG01255.hp2 HG03942.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12967_-2-12966i others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210598 | ||||||
| chr12:96210598
|
C | CACACACA others(2): Show |
5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0330others(2): Show | 5 | HG02145.hp1 HG03492.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-12967_-2-12966i others(11): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210598 | ||||||
| chr12:96210598
|
C | CACACACA others(4): Show |
4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0006g0208others(1): Show | 4 | HG02055.hp2 HG03579.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12967_-2-12966i others(13): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210598 | ||||||
| chr12:96210669
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(264): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-2-12896A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210669 | ||||||
| chr12:96210795
|
C | G | 24 | a0001c0001t0001g0091a0001c0001t0001g0205a0001c0001t0001g0213others(21): Show | 24 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2-12770C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96210795 | ||||||
| chr12:96211087
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0329 | 3 | HG00438.hp1 NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-2-12478G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211087 | ||||||
| chr12:96211097
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-2-12468C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211097 | ||||||
| chr12:96211121
|
C | T | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2-12444C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211121 | ||||||
| chr12:96211206
|
T | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(124): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2-12359T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211206 | ||||||
| chr12:96211239
|
G | A | 3 | a0001c0001t0004g0140a0001c0001t0004g0150a0001c0001t0004g0151 | 3 | HG02132.hp1 NA18972.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-2-12326G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211239 | ||||||
| chr12:96211304
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0006g0204 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-12261G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211304 | ||||||
| chr12:96211485
|
GT | G | 25 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0163others(22): Show | 26 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2-12077delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211485 | |||||
| chr12:96211486
|
TTTG | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0128others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2-12077_-2-12075d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211486 | |||||
| chr12:96211486
|
TTTGTG | T | 14 | a0001c0001t0001g0200a0001c0001t0001g0207a0001c0001t0001g0230others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2-12077_-2-12073d others(7): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211486 | |||||
| chr12:96211486
|
TTTGTGTG | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0042others(117): Show | 123 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-2-12077_-2-12071d others(9): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211486 | |||||
| chr12:96211486
|
TTTGTGTG others(2): Show |
T | 3 | a0001c0001t0001g0237a0001c0001t0002g0332a0001c0001t0006g0204 | 3 | HG02922.hp2 NA18946.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-2-12077_-2-12069d others(11): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211486 | |||||
| chr12:96211486
|
TTTGTGTG others(8): Show |
T | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-2-12077_-2-12063d others(17): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211486 | |||||
| chr12:96211487
|
T | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0298 | 2 | NA18998.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-2-12078T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211487 | ||||||
| chr12:96211487
|
T | TG | 37 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0186others(34): Show | 37 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-2-12078_-2-12077i others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211487 | ||||||
| chr12:96211487
|
T | TGTG | 21 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG00438.hp2 HG00609.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2-12078_-2-12077i others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211487 | ||||||
| chr12:96211487
|
T | TGTGTG | 4 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0077others(1): Show | 4 | HG00738.hp2 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12078_-2-12077i others(7): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211487 | ||||||
| chr12:96211487
|
T | TTG | 10 | a0001c0001t0001g0063a0001c0001t0001g0104a0001c0001t0002g0027others(7): Show | 10 | HG00639.hp2 HG00642.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-12040_-2-12039d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211487 | |||||
| chr12:96211487
|
T | TTGTG | 4 | a0001c0001t0001g0066a0001c0001t0008g0096a0001c0001t0008g0097others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12042_-2-12039d others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211487 | |||||
| chr12:96211487
|
TTG | T | 4 | a0001c0001t0002g0034a0001c0001t0007g0291a0001c0001t0007g0292others(1): Show | 4 | HG01433.hp1 HG01515.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-12040_-2-12039d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211487 | |||||
| chr12:96211490
|
T | G | 2 | a0001c0001t0002g0109a0001c0001t0017g0127 | 2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-2-12075T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211490 | ||||||
| chr12:96211538
|
G | A | 2 | a0001c0001t0004g0299a0001c0001t0005g0304 | 2 | NA19002.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-2-12027G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211538 | ||||||
| chr12:96211582
|
TTAAC | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(6): Show | 9 | HG02486.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-11980_-2-11977d others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96211582 | |||||
| chr12:96211927
|
A | G | 48 | a0001c0001t0001g0173a0001c0001t0001g0186a0001c0001t0001g0295others(45): Show | 49 | HG00438.hp2 HG00609.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-2-11638A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211927 | ||||||
| chr12:96211987
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-2-11578T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96211987 | ||||||
| chr12:96212020
|
A | T | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2-11545A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212020 | ||||||
| chr12:96212044
|
C | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-11521C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212044 | ||||||
| chr12:96212109
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-2-11456G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212109 | ||||||
| chr12:96212255
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-2-11310T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212255 | ||||||
| chr12:96212797
|
C | T | 1 | a0001c0001t0004g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-2-10768C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212797 | ||||||
| chr12:96212822
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-10743A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212822 | ||||||
| chr12:96212860
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-2-10705C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212860 | ||||||
| chr12:96212861
|
G | A | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-10704G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212861 | ||||||
| chr12:96212865
|
G | A | 1 | a0001c0001t0002g0317 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-2-10700G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212865 | ||||||
| chr12:96212866
|
A | G | 1 | a0001c0001t0002g0317 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-2-10699A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212866 | ||||||
| chr12:96212925
|
G | A | 6 | a0001c0001t0002g0218a0001c0001t0006g0190a0001c0001t0006g0219others(3): Show | 6 | HG01074.hp1 HG01978.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-10640G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212925 | ||||||
| chr12:96212986
|
A | T | 4 | a0001c0001t0001g0289a0001c0001t0006g0288a0001c0001t0006g0333others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-10579A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96212986 | ||||||
| chr12:96213111
|
G | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(124): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2-10454G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213111 | ||||||
| chr12:96213176
|
G | A | 35 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0058others(32): Show | 35 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2-10389G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213176 | ||||||
| chr12:96213181
|
A | G | 7 | a0001c0001t0009g0013a0001c0001t0009g0014a0001c0001t0009g0015others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-10384A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213181 | ||||||
| chr12:96213329
|
C | A | 327 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-2-10236C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213329 | ||||||
| chr12:96213489
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-2-10076C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213489 | ||||||
| chr12:96213524
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-2-10041A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213524 | ||||||
| chr12:96213650
|
G | GT | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-9914dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96213650 | |||||
| chr12:96213723
|
C | CT | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-9833dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96213723 | |||||
| chr12:96213869
|
G | A | 1 | a0001c0001t0007g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2-9696G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213869 | ||||||
| chr12:96213921
|
C | CTCA | 341 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-2-9642_-2-9641ins others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96213921 | |||||
| chr12:96213924
|
G | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(179): Show | 186 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.-2-9641G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96213924 | ||||||
| chr12:96213968
|
CCCT | C | 29 | a0001c0001t0001g0058a0001c0001t0001g0067a0001c0001t0001g0068others(26): Show | 29 | HG00099.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-9592_-2-9590del others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96213968 | |||||
| chr12:96214052
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-9513A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96214052 | ||||||
| chr12:96214272
|
A | G | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0007g0126others(1): Show | 4 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-9293A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96214272 | ||||||
| chr12:96214362
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-2-9203C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96214362 | ||||||
| chr12:96214455
|
C | CA | 10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(7): Show | 10 | HG02055.hp2 HG02273.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-9099dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96214455 | |||||
| chr12:96214459
|
A | C | 11 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-9106A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96214459 | ||||||
| chr12:96214904
|
T | A | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2-8661T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96214904 | ||||||
| chr12:96215106
|
C | CT | 14 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0003g0049others(11): Show | 14 | HG01175.hp2 HG01891.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-8445dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96215106 | |||||
| chr12:96215120
|
T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0063 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-8445T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215120 | ||||||
| chr12:96215130
|
C | T | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2-8435C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215130 | ||||||
| chr12:96215330
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-2-8235G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215330 | ||||||
| chr12:96215392
|
G | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-8173G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215392 | ||||||
| chr12:96215393
|
C | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-8172C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215393 | ||||||
| chr12:96215398
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0245 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-2-8167A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215398 | ||||||
| chr12:96215566
|
C | T | 72 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-2-7999C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215566 | ||||||
| chr12:96215567
|
G | A | 3 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0002g0319 | 3 | NA19011.hp1 NA19062.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-2-7998G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215567 | ||||||
| chr12:96215629
|
C | CT | 9 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-7915dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96215629 | |||||
| chr12:96215629
|
CT | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0075a0001c0001t0001g0104others(8): Show | 13 | HG01069.hp1 HG01192.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2-7915delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96215629 | |||||
| chr12:96215629
|
CTT | C | 19 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0061others(16): Show | 19 | HG00639.hp1 HG00673.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2-7916_-2-7915del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96215629 | |||||
| chr12:96215629
|
CTTT | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0092others(124): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2-7917_-2-7915del others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96215629 | |||||
| chr12:96215751
|
C | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 329 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-2-7814C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215751 | ||||||
| chr12:96215801
|
A | G | 8 | a0001c0001t0002g0109a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-7764A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215801 | ||||||
| chr12:96215879
|
C | A | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-2-7686C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96215879 | ||||||
| chr12:96216087
|
G | T | 1 | a0001c0001t0002g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-2-7478G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216087 | ||||||
| chr12:96216089
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-2-7476C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216089 | ||||||
| chr12:96216101
|
G | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-7464G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216101 | ||||||
| chr12:96216216
|
C | G | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-7349C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216216 | ||||||
| chr12:96216240
|
G | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-7325G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216240 | ||||||
| chr12:96216297
|
C | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(6): Show | 9 | HG02486.hp1 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-7268C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216297 | ||||||
| chr12:96216394
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-2-7171G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216394 | ||||||
| chr12:96216460
|
C | T | 11 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0008g0096others(8): Show | 11 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-7105C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216460 | ||||||
| chr12:96216613
|
C | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-6952C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216613 | ||||||
| chr12:96216858
|
G | C | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-6707G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216858 | ||||||
| chr12:96216880
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-2-6685C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216880 | ||||||
| chr12:96216884
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-6681A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216884 | ||||||
| chr12:96216906
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-6659G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216906 | ||||||
| chr12:96216982
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG00323.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-2-6583C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96216982 | ||||||
| chr12:96217255
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0245 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-2-6310A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217255 | ||||||
| chr12:96217818
|
G | A | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-5747G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217818 | ||||||
| chr12:96217853
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2-5712G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217853 | ||||||
| chr12:96217870
|
A | G | 151 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(148): Show | 154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2-5695A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217870 | ||||||
| chr12:96217882
|
G | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-5683G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217882 | ||||||
| chr12:96217893
|
G | A | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-2-5672G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96217893 | ||||||
| chr12:96217937
|
C | CA | 53 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0058others(50): Show | 56 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-2-5608dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96217937 | |||||
| chr12:96217937
|
C | CAA | 45 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0001g0066others(42): Show | 45 | HG01070.hp2 HG01192.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.-2-5609_-2-5608dup others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96217937 | |||||
| chr12:96217937
|
C | CAAA | 100 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(97): Show | 103 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-2-5610_-2-5608dup others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96217937 | |||||
| chr12:96217937
|
C | CAAAA | 26 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0213others(23): Show | 26 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2-5611_-2-5608dup others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96217937 | |||||
| chr12:96218028
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-5537A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218028 | ||||||
| chr12:96218211
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-2-5354C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218211 | ||||||
| chr12:96218223
|
G | A | 3 | a0001c0001t0002g0336a0001c0001t0003g0059a0001c0001t0003g0060 | 3 | HG00099.hp1 HG02004.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-2-5342G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218223 | ||||||
| chr12:96218316
|
A | G | 151 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(148): Show | 154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2-5249A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218316 | ||||||
| chr12:96218365
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-5200C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218365 | ||||||
| chr12:96218437
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-5128C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218437 | ||||||
| chr12:96218502
|
C | A | 1 | a0002c0002t0001g0057 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-2-5063C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218502 | ||||||
| chr12:96218621
|
G | C | 7 | a0001c0001t0002g0053a0001c0001t0003g0052a0001c0001t0003g0054others(4): Show | 8 | HG00099.hp2 HG01106.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-4944G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218621 | ||||||
| chr12:96218648
|
A | AT | 12 | a0001c0001t0001g0205a0001c0001t0001g0224a0001c0001t0001g0251others(9): Show | 12 | HG00642.hp1 HG00741.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-4899dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96218648 | |||||
| chr12:96218648
|
A | ATTTT | 6 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-4902_-2-4899dup others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96218648 | |||||
| chr12:96218648
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-2-4917A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218648 | ||||||
| chr12:96218648
|
AT | A | 80 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-2-4899delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96218648 | |||||
| chr12:96218680
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-4885G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218680 | ||||||
| chr12:96218790
|
A | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-4775A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218790 | ||||||
| chr12:96218858
|
C | T | 2 | a0001c0001t0005g0271a0001c0001t0005g0272 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-2-4707C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218858 | ||||||
| chr12:96218859
|
G | A | 7 | a0001c0001t0002g0053a0001c0001t0003g0052a0001c0001t0003g0054others(4): Show | 8 | HG00099.hp2 HG01106.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-4706G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218859 | ||||||
| chr12:96218875
|
C | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-4690C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218875 | ||||||
| chr12:96218894
|
C | T | 1 | a0001c0001t0006g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-4671C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218894 | ||||||
| chr12:96218928
|
G | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0008g0096others(8): Show | 11 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-4637G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218928 | ||||||
| chr12:96218983
|
T | A | 1 | a0001c0001t0002g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-2-4582T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218983 | ||||||
| chr12:96218984
|
A | T | 151 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(148): Show | 154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-2-4581A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218984 | ||||||
| chr12:96218990
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-2-4575A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96218990 | ||||||
| chr12:96219082
|
T | G | 1 | a0001c0001t0004g0145 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2-4483T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219082 | ||||||
| chr12:96219206
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-2-4359A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219206 | ||||||
| chr12:96219296
|
G | GA | 150 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(147): Show | 153 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-2-4260dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96219296 | |||||
| chr12:96219314
|
A | AT | 10 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG02486.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-4243dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96219314 | |||||
| chr12:96219331
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-4234A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219331 | ||||||
| chr12:96219332
|
G | A | 11 | a0001c0001t0001g0066a0001c0001t0001g0104a0001c0001t0008g0096others(8): Show | 11 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-4233G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219332 | ||||||
| chr12:96219340
|
C | T | 25 | a0001c0001t0001g0091a0001c0001t0001g0205a0001c0001t0001g0213others(22): Show | 25 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-2-4225C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219340 | ||||||
| chr12:96219529
|
ATAGT | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-4033_-2-4030del others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96219529 | |||||
| chr12:96219610
|
T | C | 1 | a0001c0001t0004g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-2-3955T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219610 | ||||||
| chr12:96219637
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-2-3928C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219637 | ||||||
| chr12:96219847
|
G | A | 1 | a0001c0001t0009g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-3718G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219847 | ||||||
| chr12:96219894
|
A | G | 5 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(2): Show | 5 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-3671A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219894 | ||||||
| chr12:96219905
|
A | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0004g0041others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-3660A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219905 | ||||||
| chr12:96219918
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-3647G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219918 | ||||||
| chr12:96219986
|
C | T | 40 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0002g0053others(37): Show | 41 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-2-3579C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219986 | ||||||
| chr12:96219990
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-2-3575G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96219990 | ||||||
| chr12:96220200
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-2-3365T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220200 | ||||||
| chr12:96220347
|
C | T | 148 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(145): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-2-3218C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220347 | ||||||
| chr12:96220382
|
A | AT | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(99): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-2-3161dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96220382 | |||||
| chr12:96220382
|
A | ATT | 55 | a0001c0001t0001g0072a0001c0001t0001g0173a0001c0001t0001g0186others(52): Show | 55 | HG00438.hp2 HG00609.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2-3162_-2-3161dup others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96220382 | |||||
| chr12:96220382
|
AT | A | 16 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0061others(13): Show | 16 | HG00639.hp1 HG01074.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-2-3161delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96220382 | |||||
| chr12:96220382
|
ATT | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0075others(124): Show | 130 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-2-3162_-2-3161del others(2): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96220382 | |||||
| chr12:96220417
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0005g0194 | 2 | HG01928.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-2-3148C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220417 | ||||||
| chr12:96220427
|
G | T | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-3138G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220427 | ||||||
| chr12:96220447
|
G | A | 148 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0040others(145): Show | 151 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-2-3118G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220447 | ||||||
| chr12:96220450
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0244 | 2 | HG01257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-2-3115C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220450 | ||||||
| chr12:96220455
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-3110T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220455 | ||||||
| chr12:96220471
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-2-3094T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220471 | ||||||
| chr12:96220493
|
T | G | 2 | a0003c0003t0001g0246a0003c0003t0001g0247 | 2 | HG00609.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-2-3072T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220493 | ||||||
| chr12:96220544
|
C | T | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-2-3021C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220544 | ||||||
| chr12:96220850
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-2715G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220850 | ||||||
| chr12:96220929
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0245 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-2-2636T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96220929 | ||||||
| chr12:96221035
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-2-2530A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221035 | ||||||
| chr12:96221038
|
C | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0061others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.-2-2527C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221038 | ||||||
| chr12:96221114
|
C | T | 1 | a0001c0001t0007g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-2-2451C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221114 | ||||||
| chr12:96221397
|
G | A | 2 | a0001c0001t0006g0055a0001c0001t0006g0135 | 2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-2-2168G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221397 | ||||||
| chr12:96221950
|
C | T | 1 | a0001c0001t0009g0018 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-2-1615C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221950 | ||||||
| chr12:96221984
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-1581G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96221984 | ||||||
| chr12:96222256
|
C | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(310): Show | 320 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-2-1309C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222256 | ||||||
| chr12:96222273
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0061others(129): Show | 135 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-2-1292T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222273 | ||||||
| chr12:96222370
|
CACCAGAG others(7): Show |
C | 130 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0061others(127): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.-2-1193_-2-1180del others(14): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96222370 | |||||
| chr12:96222375
|
GAGTTGAA others(3): Show |
G | 5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1188_-2-1179del others(10): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96222375 | |||||
| chr12:96222575
|
G | A | 1 | a0001c0001t0005g0194 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-2-990G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222575 | ||||||
| chr12:96222617
|
C | T | 1 | a0001c0001t0007g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-2-948C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222617 | ||||||
| chr12:96222657
|
C | G | 56 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0186others(53): Show | 57 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2-908C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222657 | ||||||
| chr12:96222689
|
T | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2-876T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222689 | ||||||
| chr12:96222808
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-2-757C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222808 | ||||||
| chr12:96222881
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-684G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222881 | ||||||
| chr12:96222991
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-2-574C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96222991 | ||||||
| chr12:96223246
|
A | G | 189 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0042others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-2-319A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96223246 | ||||||
| chr12:96223248
|
T | C | 1 | a0002c0002t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-2-317T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96223248 | ||||||
| chr12:96223497
|
CCT | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0170others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-62_-2-61delTC | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 96223497 | |||||
| chr12:96223521
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-44G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96223521 | ||||||
| chr12:96223526
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-2-39C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 1/4 | chr12 | 96223526 | ||||||
| chr12:96223800
|
G | A | 11 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0077others(8): Show | 11 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+27G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96223800 | ||||||
| chr12:96224030
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(177): Show | 185 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.207+257A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224030 | ||||||
| chr12:96224109
|
G | A | 2 | a0001c0001t0009g0013a0001c0001t0009g0014 | 2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.207+336G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224109 | ||||||
| chr12:96224128
|
C | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(115): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.207+355C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224128 | ||||||
| chr12:96224150
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.207+377G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224150 | ||||||
| chr12:96224379
|
G | A | 17 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(14): Show | 17 | HG01074.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.207+606G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224379 | ||||||
| chr12:96224451
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+678C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224451 | ||||||
| chr12:96224629
|
A | G | 1 | a0002c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.207+856A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224629 | ||||||
| chr12:96224703
|
C | G | 2 | a0001c0001t0004g0065a0001c0001t0004g0179 | 2 | NA18946.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.207+930C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224703 | ||||||
| chr12:96224803
|
G | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0170others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+1030G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224803 | ||||||
| chr12:96224985
|
A | C | 81 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0129others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.207+1212A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96224985 | ||||||
| chr12:96225022
|
C | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.207+1249C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96225022 | ||||||
| chr12:96225170
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.207+1397C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96225170 | ||||||
| chr12:96225171
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.207+1398G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96225171 | ||||||
| chr12:96225853
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0068others(83): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.207+2080G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96225853 | ||||||
| chr12:96225903
|
C | T | 1 | a0001c0001t0006g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.207+2130C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96225903 | ||||||
| chr12:96226069
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0289 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+2296C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226069 | ||||||
| chr12:96226196
|
A | G | 9 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(6): Show | 9 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+2423A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226196 | ||||||
| chr12:96226232
|
G | C | 2 | a0001c0001t0003g0059a0001c0001t0003g0060 | 2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.207+2459G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226232 | ||||||
| chr12:96226350
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.207+2577G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226350 | ||||||
| chr12:96226489
|
GAGATGTC others(45): Show |
G | 5 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(2): Show | 5 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+2748_207+2799d others(54): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96226489 | |||||
| chr12:96226516
|
C | CCACATGC others(1): Show |
311 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.207+2747_207+2748i others(10): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96226516 | |||||
| chr12:96226609
|
C | CCCACATG others(35): Show |
5 | a0001c0001t0001g0002a0001c0001t0006g0003a0001c0001t0006g0045others(2): Show | 7 | HG02257.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+2849_207+2890d others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96226609 | |||||
| chr12:96226643
|
C | T | 1 | a0002c0002t0002g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.207+2870C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226643 | ||||||
| chr12:96226697
|
C | T | 3 | a0001c0001t0004g0302a0001c0001t0004g0303a0001c0001t0004g0305 | 3 | NA18941.hp1 NA18952.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.207+2924C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226697 | ||||||
| chr12:96226757
|
T | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0170others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+2984T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226757 | ||||||
| chr12:96226812
|
GA | G | 4 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | NA18964.hp1 NA19060.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3040delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96226812 | ||||||
| chr12:96226826
|
TAAG | T | 5 | a0001c0001t0004g0307a0002c0002t0002g0083a0002c0002t0002g0085others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+3059_207+3061d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96226826 | |||||
| chr12:96227142
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.207+3369G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227142 | ||||||
| chr12:96227208
|
G | A | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.207+3435G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227208 | ||||||
| chr12:96227234
|
C | T | 48 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0001g0295others(45): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.207+3461C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227234 | ||||||
| chr12:96227402
|
C | T | 1 | a0002c0002t0002g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.207+3629C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227402 | ||||||
| chr12:96227515
|
T | A | 48 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0129others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.207+3742T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227515 | ||||||
| chr12:96227533
|
C | CCCCCGGA others(35): Show |
2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.207+3775_207+3776i others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96227533 | |||||
| chr12:96227533
|
C | CCCCCGGA others(35): Show |
1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.207+3781_207+3782i others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96227533 | |||||
| chr12:96227533
|
C | CCCCCGGA others(35): Show |
332 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(329): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.207+3792_207+3833d others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96227533 | |||||
| chr12:96227580
|
G | GGAGGAGG others(35): Show |
1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.207+3833_207+3834i others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96227580 | |||||
| chr12:96227591
|
G | GTCCCTGT others(35): Show |
1 | a0001c0001t0004g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.207+3833_207+3834i others(44): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96227591 | |||||
| chr12:96227621
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0067a0001c0001t0001g0068others(8): Show | 13 | HG01167.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+3848C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227621 | ||||||
| chr12:96227649
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.207+3876G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227649 | ||||||
| chr12:96227707
|
C | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0042others(119): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+3934C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227707 | ||||||
| chr12:96227984
|
C | G | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+4211C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96227984 | ||||||
| chr12:96228005
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0019g0086 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.207+4232C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228005 | ||||||
| chr12:96228025
|
G | A | 3 | a0001c0001t0002g0078a0001c0001t0002g0187a0001c0001t0003g0076 | 3 | HG02976.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.207+4252G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228025 | ||||||
| chr12:96228037
|
A | G | 13 | a0001c0001t0001g0163a0001c0001t0002g0053a0001c0001t0003g0020others(10): Show | 14 | HG00099.hp2 HG01106.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+4264A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228037 | ||||||
| chr12:96228076
|
G | A | 304 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.207+4303G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228076 | ||||||
| chr12:96228127
|
AAAG | A | 14 | a0001c0001t0005g0271a0001c0001t0005g0272a0001c0001t0006g0003others(11): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+4362_207+4364d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228127 | |||||
| chr12:96228141
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+4368C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228141 | ||||||
| chr12:96228255
|
TA | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(118): Show | 125 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+4487delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228255 | |||||
| chr12:96228297
|
G | A | 5 | a0001c0001t0009g0015a0001c0001t0009g0016a0001c0001t0009g0017others(2): Show | 5 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+4524G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228297 | ||||||
| chr12:96228307
|
A | G | 8 | a0001c0001t0002g0109a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+4534A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228307 | ||||||
| chr12:96228416
|
C | A | 8 | a0001c0001t0002g0109a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+4643C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228416 | ||||||
| chr12:96228416
|
C | CA | 36 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0063others(33): Show | 37 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.207+4671dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAA | 12 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0048others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+4669_207+4671d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0297others(7): Show | 10 | HG00639.hp1 HG02559.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+4663_207+4671d others(11): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(3): Show |
16 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 16 | HG01109.hp2 HG01192.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.207+4662_207+4671d others(12): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0324a0001c0001t0002g0316 | 3 | HG03453.hp2 NA18943.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.207+4661_207+4671d others(13): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0294a0001c0001t0002g0306a0001c0001t0002g0313others(3): Show | 6 | HG02129.hp1 NA18942.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4660_207+4671d others(14): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0004g0145a0001c0001t0004g0307a0002c0002t0002g0161 | 3 | HG00438.hp2 NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.207+4659_207+4671d others(15): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0004g0115a0001c0001t0004g0140a0001c0001t0004g0150others(1): Show | 4 | HG02132.hp1 NA18959.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+4658_207+4671d others(16): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0148 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.207+4657_207+4671d others(17): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CA | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(94): Show | 100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.207+4671delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAA | C | 6 | a0001c0001t0001g0091a0001c0001t0001g0329a0001c0001t0005g0238others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+4670_207+4671d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAAA | C | 7 | a0001c0001t0002g0087a0001c0001t0006g0333a0001c0001t0007g0126others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+4669_207+4671d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAAAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 7 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+4668_207+4671d others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0007g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.207+4662_207+4671d others(12): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAAAAAAA others(9): Show |
C | 48 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0129others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.207+4656_207+4671d others(18): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228416
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0319 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.207+4655_207+4671d others(19): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228416 | |||||
| chr12:96228442
|
A | AAAAAAAA others(11): Show |
3 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0019 | 3 | HG01952.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.207+4671_207+4672i others(20): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228442 | |||||
| chr12:96228442
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0009g0015a0001c0001t0009g0016 | 2 | HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.207+4671_207+4672i others(19): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228442 | |||||
| chr12:96228442
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0009g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+4671_207+4672i others(18): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228442 | |||||
| chr12:96228442
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0109 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.207+4671_207+4672i others(14): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96228442 | |||||
| chr12:96228469
|
G | A | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+4696G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228469 | ||||||
| chr12:96228656
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 141 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.207+4883T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228656 | ||||||
| chr12:96228664
|
T | A | 2 | a0001c0001t0002g0078a0001c0001t0003g0076 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.207+4891T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228664 | ||||||
| chr12:96228684
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0002c0002t0002g0090 | 3 | HG02451.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.207+4911G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228684 | ||||||
| chr12:96228791
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.207+5018G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228791 | ||||||
| chr12:96228812
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.207+5039C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228812 | ||||||
| chr12:96228824
|
C | A | 333 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.207+5051C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228824 | ||||||
| chr12:96228962
|
C | A | 333 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.207+5189C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96228962 | ||||||
| chr12:96229040
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.207+5267C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229040 | ||||||
| chr12:96229063
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.207+5290G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229063 | ||||||
| chr12:96229073
|
C | G | 1 | a0001c0001t0006g0209 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.207+5300C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229073 | ||||||
| chr12:96229076
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.207+5303G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229076 | ||||||
| chr12:96229248
|
G | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(118): Show | 125 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+5475G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229248 | ||||||
| chr12:96229410
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.207+5637C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229410 | ||||||
| chr12:96229439
|
G | A | 1 | a0002c0002t0002g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.207+5666G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229439 | ||||||
| chr12:96229492
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+5719C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229492 | ||||||
| chr12:96229523
|
C | CTT | 14 | a0001c0001t0002g0010a0001c0001t0002g0048a0001c0001t0003g0079others(11): Show | 14 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+5775_207+5776d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96229523 | |||||
| chr12:96229523
|
CT | C | 30 | a0001c0001t0001g0025a0001c0001t0001g0075a0001c0001t0001g0091others(27): Show | 30 | HG00423.hp2 HG00621.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.207+5776delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96229523 | |||||
| chr12:96229523
|
CTT | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.207+5775_207+5776d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96229523 | |||||
| chr12:96229523
|
CTTT | C | 51 | a0001c0001t0001g0026a0001c0001t0001g0128a0001c0001t0001g0129others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.207+5774_207+5776d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96229523 | |||||
| chr12:96229523
|
CTTTT | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0113a0001c0001t0002g0229others(2): Show | 6 | HG02074.hp1 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+5773_207+5776d others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96229523 | |||||
| chr12:96229565
|
T | C | 1 | a0001c0001t0008g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.207+5792T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229565 | ||||||
| chr12:96229654
|
C | G | 1 | a0001c0001t0001g0330 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+5881C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229654 | ||||||
| chr12:96229674
|
G | A | 53 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0061others(50): Show | 54 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.207+5901G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229674 | ||||||
| chr12:96229779
|
C | T | 1 | a0001c0001t0009g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.207+6006C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96229779 | ||||||
| chr12:96230087
|
A | G | 3 | a0001c0001t0005g0238a0001c0001t0005g0271a0001c0001t0005g0272 | 3 | HG01070.hp2 HG01071.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.207+6314A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230087 | ||||||
| chr12:96230299
|
A | G | 1 | a0001c0007t0022g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+6526A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230299 | ||||||
| chr12:96230340
|
T | G | 1 | a0002c0002t0002g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.207+6567T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230340 | ||||||
| chr12:96230342
|
G | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(118): Show | 125 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.207+6569G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230342 | ||||||
| chr12:96230448
|
C | T | 1 | a0001c0001t0010g0258 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.207+6675C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230448 | ||||||
| chr12:96230521
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.207+6748C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230521 | ||||||
| chr12:96230858
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0285a0001c0001t0001g0286others(12): Show | 16 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.207+7085G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230858 | ||||||
| chr12:96230977
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0174 | 2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.207+7204C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230977 | ||||||
| chr12:96230991
|
A | C | 1 | a0001c0001t0002g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.207+7218A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96230991 | ||||||
| chr12:96231002
|
G | C | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.207+7229G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231002 | ||||||
| chr12:96231214
|
GT | G | 48 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0070others(45): Show | 49 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.207+7450delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96231214 | |||||
| chr12:96231248
|
A | G | 65 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0061others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.207+7475A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231248 | ||||||
| chr12:96231285
|
C | A | 1 | a0001c0001t0002g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.207+7512C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231285 | ||||||
| chr12:96231554
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.207+7781G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231554 | ||||||
| chr12:96231640
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.207+7867G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231640 | ||||||
| chr12:96231730
|
C | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0042others(70): Show | 75 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.207+7957C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231730 | ||||||
| chr12:96231911
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.207+8138T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231911 | ||||||
| chr12:96231952
|
G | A | 1 | a0001c0007t0022g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.207+8179G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96231952 | ||||||
| chr12:96232030
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+8257G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232030 | ||||||
| chr12:96232079
|
C | T | 1 | a0001c0001t0011g0080 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.207+8306C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232079 | ||||||
| chr12:96232141
|
G | A | 39 | a0001c0001t0001g0163a0001c0001t0002g0010a0001c0001t0002g0048others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.207+8368G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232141 | ||||||
| chr12:96232239
|
T | C | 1 | a0001c0001t0009g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.207+8466T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232239 | ||||||
| chr12:96232377
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0023g0239 | 2 | HG01106.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.207+8604C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232377 | ||||||
| chr12:96232453
|
C | A | 1 | a0001c0001t0003g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.207+8680C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232453 | ||||||
| chr12:96232526
|
A | C | 2 | a0001c0001t0001g0075a0001c0001t0019g0086 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.207+8753A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232526 | ||||||
| chr12:96232578
|
A | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 194 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.207+8805A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232578 | ||||||
| chr12:96232582
|
T | A | 8 | a0001c0001t0002g0109a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+8809T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232582 | ||||||
| chr12:96232757
|
CA | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.207+8992delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96232757 | |||||
| chr12:96232919
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.207+9146T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96232919 | ||||||
| chr12:96233112
|
C | G | 1 | a0001c0001t0007g0292 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.207+9339C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233112 | ||||||
| chr12:96233162
|
T | G | 1 | a0001c0001t0006g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.207+9389T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233162 | ||||||
| chr12:96233409
|
A | C | 2 | a0001c0001t0009g0013a0001c0001t0009g0014 | 2 | HG00639.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.207+9636A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233409 | ||||||
| chr12:96233533
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.207+9760G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233533 | ||||||
| chr12:96233794
|
G | C | 15 | a0001c0001t0006g0055a0001c0001t0006g0135a0001c0001t0006g0190others(12): Show | 15 | HG01891.hp1 HG01978.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.207+10021G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233794 | ||||||
| chr12:96233824
|
G | A | 27 | a0001c0001t0001g0143a0001c0001t0001g0295a0001c0001t0001g0298others(24): Show | 27 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+10051G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233824 | ||||||
| chr12:96233841
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.207+10068G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233841 | ||||||
| chr12:96233860
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+10087G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233860 | ||||||
| chr12:96233981
|
C | T | 5 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0088others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+10208C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96233981 | ||||||
| chr12:96234143
|
C | T | 1 | a0002c0002t0001g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.207+10370C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234143 | ||||||
| chr12:96234196
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0019g0086 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.207+10423T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234196 | ||||||
| chr12:96234259
|
C | T | 2 | a0001c0001t0006g0055a0001c0001t0006g0135 | 2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.207+10486C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234259 | ||||||
| chr12:96234280
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0280 | 3 | HG01258.hp2 HG01358.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.207+10507G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234280 | ||||||
| chr12:96234400
|
G | A | 1 | a0001c0001t0005g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.207+10627G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234400 | ||||||
| chr12:96234529
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.207+10756C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234529 | ||||||
| chr12:96234563
|
C | T | 4 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0170others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+10790C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234563 | ||||||
| chr12:96234564
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+10791G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234564 | ||||||
| chr12:96234615
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.207+10842C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234615 | ||||||
| chr12:96234769
|
G | C | 7 | a0001c0001t0006g0055a0001c0001t0006g0135a0001c0001t0006g0190others(4): Show | 7 | HG01978.hp1 HG03017.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.207+10996G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234769 | ||||||
| chr12:96234792
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.207+11019C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234792 | ||||||
| chr12:96234929
|
C | A | 1 | a0001c0001t0003g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+11156C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96234929 | ||||||
| chr12:96235050
|
C | G | 1 | a0001c0001t0003g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.207+11277C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235050 | ||||||
| chr12:96235107
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.207+11334C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235107 | ||||||
| chr12:96235193
|
C | T | 3 | a0001c0001t0006g0208a0001c0001t0006g0209a0001c0001t0006g0210 | 3 | HG02055.hp2 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.207+11420C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235193 | ||||||
| chr12:96235214
|
C | A | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.207+11441C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235214 | ||||||
| chr12:96235215
|
C | G | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.207+11442C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235215 | ||||||
| chr12:96235255
|
T | C | 331 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(328): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.207+11482T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235255 | ||||||
| chr12:96235384
|
G | A | 1 | a0002c0002t0002g0282 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.208-11556G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235384 | ||||||
| chr12:96235441
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.208-11499A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235441 | ||||||
| chr12:96235564
|
C | T | 8 | a0001c0001t0008g0096a0001c0001t0008g0097a0001c0001t0008g0098others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.208-11376C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235564 | ||||||
| chr12:96235623
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.208-11317C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235623 | ||||||
| chr12:96235715
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208-11225C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235715 | ||||||
| chr12:96235766
|
C | G | 1 | a0001c0001t0013g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.208-11174C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96235766 | ||||||
| chr12:96236121
|
G | C | 1 | a0001c0001t0001g0004 | 2 | HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.208-10819G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236121 | ||||||
| chr12:96236129
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.208-10811A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236129 | ||||||
| chr12:96236161
|
G | A | 1 | a0002c0002t0002g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208-10779G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236161 | ||||||
| chr12:96236176
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.208-10764G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236176 | ||||||
| chr12:96236222
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.208-10718G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236222 | ||||||
| chr12:96236250
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.208-10690G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236250 | ||||||
| chr12:96236272
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0285a0001c0001t0001g0286others(12): Show | 16 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.208-10668C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236272 | ||||||
| chr12:96236294
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.208-10646C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236294 | ||||||
| chr12:96236456
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0173a0001c0001t0001g0188others(8): Show | 12 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-10484G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236456 | ||||||
| chr12:96236510
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.208-10430C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236510 | ||||||
| chr12:96236547
|
C | T | 2 | a0001c0001t0011g0031a0001c0001t0011g0082 | 2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.208-10393C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236547 | ||||||
| chr12:96236688
|
T | G | 1 | a0001c0001t0001g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.208-10252T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236688 | ||||||
| chr12:96236696
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0285others(13): Show | 17 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.208-10244C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236696 | ||||||
| chr12:96236730
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208-10210G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236730 | ||||||
| chr12:96236796
|
C | T | 2 | a0001c0001t0005g0340a0001c0001t0005g0342 | 2 | NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.208-10144C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236796 | ||||||
| chr12:96236812
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0019g0086 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.208-10128A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236812 | ||||||
| chr12:96236848
|
A | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(226): Show | 235 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.208-10092A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236848 | ||||||
| chr12:96236970
|
C | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 299 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.208-9970C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96236970 | ||||||
| chr12:96237097
|
C | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 294 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.208-9843C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237097 | ||||||
| chr12:96237206
|
C | T | 1 | a0001c0001t0007g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.208-9734C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237206 | ||||||
| chr12:96237301
|
C | T | 32 | a0001c0001t0001g0143a0001c0001t0001g0295a0001c0001t0001g0298others(29): Show | 32 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.208-9639C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237301 | ||||||
| chr12:96237415
|
G | GC | 39 | a0001c0001t0001g0163a0001c0001t0002g0010a0001c0001t0002g0048others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-9519dupC | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96237415 | |||||
| chr12:96237470
|
C | G | 2 | a0001c0001t0006g0288a0001c0001t0006g0333 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.208-9470C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237470 | ||||||
| chr12:96237633
|
A | G | 6 | a0001c0001t0003g0136a0001c0001t0003g0137a0001c0001t0003g0138others(3): Show | 6 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-9307A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237633 | ||||||
| chr12:96237744
|
G | T | 1 | a0001c0001t0002g0316 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.208-9196G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237744 | ||||||
| chr12:96237749
|
G | T | 1 | a0001c0001t0023g0239 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208-9191G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237749 | ||||||
| chr12:96237756
|
C | T | 5 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0009others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-9184C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237756 | ||||||
| chr12:96237789
|
T | C | 1 | a0001c0001t0010g0119 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.208-9151T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96237789 | ||||||
| chr12:96237999
|
CT | C | 33 | a0001c0001t0001g0143a0001c0001t0001g0295a0001c0001t0001g0298others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.208-8939delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96237999 | |||||
| chr12:96238064
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0027 | 3 | HG02451.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.208-8876G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96238064 | ||||||
| chr12:96238361
|
T | A | 8 | a0001c0001t0002g0109a0001c0001t0009g0013a0001c0001t0009g0014others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-8579T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96238361 | ||||||
| chr12:96238951
|
A | G | 38 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(35): Show | 39 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.208-7989A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96238951 | ||||||
| chr12:96239062
|
T | C | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-7878T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239062 | ||||||
| chr12:96239112
|
C | A | 1 | a0001c0001t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.208-7828C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239112 | ||||||
| chr12:96239123
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.208-7817T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239123 | ||||||
| chr12:96239148
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.208-7792A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239148 | ||||||
| chr12:96239422
|
A | C | 1 | a0001c0001t0007g0291 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.208-7518A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239422 | ||||||
| chr12:96239452
|
A | T | 1 | a0002c0002t0001g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.208-7488A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239452 | ||||||
| chr12:96239457
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.208-7483C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239457 | ||||||
| chr12:96239607
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-7333G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239607 | ||||||
| chr12:96239610
|
G | A | 2 | a0001c0001t0004g0065a0001c0001t0004g0179 | 2 | NA18946.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.208-7330G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239610 | ||||||
| chr12:96239765
|
C | G | 1 | a0001c0001t0010g0254 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.208-7175C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239765 | ||||||
| chr12:96239808
|
A | T | 3 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0024g0084 | 3 | HG02809.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.208-7132A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239808 | ||||||
| chr12:96239954
|
T | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0187others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-6986T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96239954 | ||||||
| chr12:96240047
|
C | T | 1 | a0001c0001t0005g0262 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.208-6893C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240047 | ||||||
| chr12:96240263
|
AATTTTG | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0187others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.208-6676_208-6671d others(8): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240263 | ||||||
| chr12:96240297
|
CAG | C | 28 | a0001c0001t0001g0143a0001c0001t0002g0148a0002c0002t0001g0056others(25): Show | 28 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.208-6642_208-6641d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240297 | ||||||
| chr12:96240427
|
A | G | 41 | a0001c0001t0001g0143a0001c0001t0002g0087a0001c0001t0002g0148others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.208-6513A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240427 | ||||||
| chr12:96240445
|
G | A | 2 | a0001c0001t0006g0288a0001c0001t0006g0333 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.208-6495G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240445 | ||||||
| chr12:96240661
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208-6279C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240661 | ||||||
| chr12:96240797
|
T | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0167 | 2 | NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.208-6143T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240797 | ||||||
| chr12:96240801
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.208-6139G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240801 | ||||||
| chr12:96240809
|
C | T | 2 | a0002c0002t0002g0094a0002c0002t0002g0177 | 2 | HG00323.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.208-6131C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240809 | ||||||
| chr12:96240847
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-6093G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240847 | ||||||
| chr12:96240859
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-6081A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96240859 | ||||||
| chr12:96241022
|
G | A | 5 | a0001c0001t0004g0008a0001c0001t0004g0212a0001c0001t0004g0302others(2): Show | 6 | NA18941.hp1 NA18944.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-5918G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241022 | ||||||
| chr12:96241211
|
G | C | 23 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0104others(20): Show | 23 | HG01243.hp1 HG01891.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.208-5729G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241211 | ||||||
| chr12:96241426
|
T | TG | 3 | a0001c0001t0001g0025a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | NA18948.hp1 NA19088.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208-5514_208-5513i others(3): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241426 | ||||||
| chr12:96241426
|
T | TTG | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(154): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.208-5482_208-5481d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96241426 | |||||
| chr12:96241426
|
T | TTGTG | 56 | a0001c0001t0001g0005a0001c0001t0001g0061a0001c0001t0001g0066others(53): Show | 58 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.208-5484_208-5481d others(6): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96241426 | |||||
| chr12:96241426
|
T | TTGTGTG | 40 | a0001c0001t0001g0071a0001c0001t0002g0009a0001c0001t0002g0032others(37): Show | 40 | HG00323.hp1 HG00609.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.208-5486_208-5481d others(8): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96241426 | |||||
| chr12:96241426
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0073others(3): Show | 7 | HG02257.hp1 HG02572.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-5488_208-5481d others(10): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96241426 | |||||
| chr12:96241426
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0009g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.208-5502_208-5481d others(24): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96241426 | |||||
| chr12:96241466
|
G | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-5474G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241466 | ||||||
| chr12:96241478
|
T | C | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208-5462T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241478 | ||||||
| chr12:96241739
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.208-5201C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241739 | ||||||
| chr12:96241765
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208-5175A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96241765 | ||||||
| chr12:96242007
|
G | A | 1 | a0001c0001t0008g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208-4933G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242007 | ||||||
| chr12:96242096
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-4844G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242096 | ||||||
| chr12:96242111
|
G | A | 49 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(46): Show | 50 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.208-4829G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242111 | ||||||
| chr12:96242673
|
CT | C | 33 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(30): Show | 33 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.208-4266delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242673 | ||||||
| chr12:96242683
|
C | T | 5 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0044others(2): Show | 5 | HG01192.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-4257C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242683 | ||||||
| chr12:96242719
|
C | G | 1 | a0001c0001t0001g0205 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.208-4221C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242719 | ||||||
| chr12:96242808
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.208-4132C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242808 | ||||||
| chr12:96242996
|
C | G | 1 | a0001c0001t0005g0340 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.208-3944C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96242996 | ||||||
| chr12:96243148
|
T | C | 1 | a0001c0001t0016g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.208-3792T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243148 | ||||||
| chr12:96243329
|
G | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0285a0001c0001t0001g0286others(5): Show | 9 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-3611G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243329 | ||||||
| chr12:96243436
|
T | C | 7 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0009others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-3504T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243436 | ||||||
| chr12:96243438
|
G | T | 7 | a0001c0001t0002g0087a0001c0001t0007g0126a0001c0001t0007g0165others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3502G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243438 | ||||||
| chr12:96243439
|
A | T | 7 | a0001c0001t0002g0087a0001c0001t0007g0126a0001c0001t0007g0165others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3501A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243439 | ||||||
| chr12:96243440
|
A | C | 7 | a0001c0001t0002g0087a0001c0001t0007g0126a0001c0001t0007g0165others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3500A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243440 | ||||||
| chr12:96243443
|
T | C | 6 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0321others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-3497T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243443 | ||||||
| chr12:96243443
|
T | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3497T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243443 | ||||||
| chr12:96243444
|
T | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3496T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243444 | ||||||
| chr12:96243445
|
C | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-3495C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243445 | ||||||
| chr12:96243479
|
T | A | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208-3461T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243479 | ||||||
| chr12:96243587
|
C | T | 1 | a0001c0001t0007g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.208-3353C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243587 | ||||||
| chr12:96243684
|
A | G | 7 | a0001c0001t0002g0087a0001c0001t0007g0126a0001c0001t0007g0165others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-3256A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243684 | ||||||
| chr12:96243757
|
G | A | 4 | a0001c0001t0003g0130a0001c0001t0003g0142a0001c0001t0003g0144others(1): Show | 4 | HG00140.hp1 HG01168.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-3183G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243757 | ||||||
| chr12:96243759
|
C | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.208-3181C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243759 | ||||||
| chr12:96243850
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0174 | 3 | HG02723.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.208-3090A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96243850 | ||||||
| chr12:96243980
|
T | TGTCCC | 9 | a0001c0001t0005g0006a0001c0001t0005g0024a0001c0001t0005g0095others(6): Show | 10 | HG01123.hp2 HG01243.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-2959_208-2958i others(7): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96243980 | |||||
| chr12:96244005
|
C | CA | 33 | a0001c0001t0001g0277a0001c0001t0002g0048a0001c0001t0002g0148others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.208-2915dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244005 | |||||
| chr12:96244005
|
CA | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(74): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.208-2915delA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244005 | |||||
| chr12:96244005
|
CAA | C | 91 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(88): Show | 92 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.208-2916_208-2915d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244005 | |||||
| chr12:96244032
|
A | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0242a0001c0001t0005g0338 | 3 | NA18965.hp1 NA18965.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.208-2908A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96244032 | ||||||
| chr12:96244447
|
A | AT | 47 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0002g0184others(44): Show | 47 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.208-2475dupT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244447 | |||||
| chr12:96244447
|
AT | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0071others(55): Show | 60 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.208-2475delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244447 | |||||
| chr12:96244447
|
ATT | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-2476_208-2475d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244447 | |||||
| chr12:96244631
|
C | T | 9 | a0001c0001t0005g0006a0001c0001t0005g0024a0001c0001t0005g0095others(6): Show | 10 | HG01123.hp2 HG01243.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-2309C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96244631 | ||||||
| chr12:96244639
|
G | GA | 7 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0009others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-2294dupA | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 96244639 | |||||
| chr12:96244719
|
C | T | 7 | a0001c0001t0002g0087a0001c0001t0007g0126a0001c0001t0007g0165others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-2221C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96244719 | ||||||
| chr12:96244965
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.208-1975G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96244965 | ||||||
| chr12:96245003
|
G | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-1937G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245003 | ||||||
| chr12:96245111
|
G | C | 1 | a0002c0002t0002g0259 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-1829G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245111 | ||||||
| chr12:96245310
|
G | A | 11 | a0001c0001t0006g0055a0001c0001t0006g0135a0001c0001t0006g0190others(8): Show | 11 | HG01243.hp1 HG01978.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-1630G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245310 | ||||||
| chr12:96245346
|
G | A | 2 | a0001c0001t0006g0288a0001c0001t0006g0333 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.208-1594G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245346 | ||||||
| chr12:96245791
|
A | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-1149A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245791 | ||||||
| chr12:96245811
|
T | C | 1 | a0001c0001t0006g0209 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208-1129T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245811 | ||||||
| chr12:96245961
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0025others(159): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.208-979A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245961 | ||||||
| chr12:96245974
|
C | T | 7 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0009others(4): Show | 7 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-966C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96245974 | ||||||
| chr12:96246063
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208-877C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246063 | ||||||
| chr12:96246127
|
T | C | 11 | a0001c0001t0006g0055a0001c0001t0006g0135a0001c0001t0006g0190others(8): Show | 11 | HG01243.hp1 HG01978.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.208-813T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246127 | ||||||
| chr12:96246325
|
T | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0240a0001c0001t0001g0249 | 3 | HG02027.hp2 NA18948.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.208-615T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246325 | ||||||
| chr12:96246373
|
A | T | 1 | a0001c0001t0005g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.208-567A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246373 | ||||||
| chr12:96246464
|
G | C | 7 | a0002c0002t0001g0056a0002c0002t0001g0057a0002c0002t0001g0064others(4): Show | 7 | HG02809.hp2 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.208-476G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246464 | ||||||
| chr12:96246639
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-301C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246639 | ||||||
| chr12:96246835
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0329 | 3 | HG00438.hp1 NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.208-105A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 2/4 | chr12 | 96246835 | ||||||
| chr12:96247813
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1002+79C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96247813 | ||||||
| chr12:96247857
|
A | G | 1 | a0001c0001t0009g0016 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1002+123A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96247857 | ||||||
| chr12:96247860
|
G | A | 1 | a0002c0002t0002g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1002+126G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96247860 | ||||||
| chr12:96248039
|
AGGGAAAG others(6): Show |
A | 3 | a0002c0002t0002g0094a0002c0002t0002g0155a0002c0002t0002g0177 | 3 | HG00323.hp2 HG04228.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1002+309_1002+321d others(15): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 96248039 | |||||
| chr12:96248070
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1002+336G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248070 | ||||||
| chr12:96248213
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+479C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248213 | ||||||
| chr12:96248303
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1002+569C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248303 | ||||||
| chr12:96248395
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1002+661A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248395 | ||||||
| chr12:96248427
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1002+693G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248427 | ||||||
| chr12:96248445
|
C | G | 3 | a0002c0002t0002g0185a0002c0002t0002g0300a0002c0002t0002g0308 | 3 | NA18747.hp1 NA18999.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1002+711C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248445 | ||||||
| chr12:96248455
|
A | G | 6 | a0001c0001t0002g0180a0001c0001t0002g0294a0001c0001t0002g0313others(3): Show | 6 | HG00609.hp1 NA18975.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+721A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248455 | ||||||
| chr12:96248516
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1002+782C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248516 | ||||||
| chr12:96248658
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1002+924A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248658 | ||||||
| chr12:96248670
|
C | T | 1 | a0001c0001t0006g0288 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1002+936C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248670 | ||||||
| chr12:96248772
|
C | T | 2 | a0001c0001t0003g0182a0001c0001t0003g0183 | 2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1002+1038C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248772 | ||||||
| chr12:96248901
|
T | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+1167T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96248901 | ||||||
| chr12:96249119
|
G | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0174 | 3 | HG02723.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1002+1385G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96249119 | ||||||
| chr12:96249140
|
G | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1406G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96249140 | ||||||
| chr12:96249235
|
C | T | 1 | a0002c0002t0002g0300 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1002+1501C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96249235 | ||||||
| chr12:96249477
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0298 | 2 | NA18998.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1002+1743C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96249477 | ||||||
| chr12:96249715
|
T | TGCCAGCC others(23): Show |
276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1002+1993_1002+202 others(34): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 96249715 | |||||
| chr12:96249723
|
C | G | 9 | a0001c0001t0002g0180a0001c0001t0002g0294a0001c0001t0002g0306others(6): Show | 9 | HG00609.hp1 HG02129.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.1002+1989C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96249723 | ||||||
| chr12:96250078
|
A | C | 29 | a0001c0001t0003g0020a0001c0001t0003g0049a0001c0001t0003g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1002+2344A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250078 | ||||||
| chr12:96250112
|
AAGG | A | 18 | a0001c0001t0006g0003a0001c0001t0006g0045a0001c0001t0006g0046others(15): Show | 19 | HG01243.hp1 HG01978.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1002+2388_1002+239 others(7): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 96250112 | |||||
| chr12:96250149
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1002+2415C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250149 | ||||||
| chr12:96250321
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1002+2587G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250321 | ||||||
| chr12:96250370
|
C | A | 8 | a0001c0001t0005g0006a0001c0001t0005g0024a0001c0001t0005g0095others(5): Show | 9 | HG01123.hp2 HG01243.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1002+2636C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250370 | ||||||
| chr12:96250378
|
C | T | 10 | a0001c0001t0006g0003a0001c0001t0006g0045a0001c0001t0006g0046others(7): Show | 11 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1002+2644C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250378 | ||||||
| chr12:96250382
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1002+2648G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250382 | ||||||
| chr12:96250472
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1002+2738C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250472 | ||||||
| chr12:96250533
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1002+2799T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250533 | ||||||
| chr12:96250575
|
A | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+2841A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250575 | ||||||
| chr12:96250754
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1002+3020G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250754 | ||||||
| chr12:96250758
|
G | A | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+3024G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250758 | ||||||
| chr12:96250865
|
A | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0278 | 2 | HG00423.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1002+3131A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250865 | ||||||
| chr12:96250871
|
G | A | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+3137G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250871 | ||||||
| chr12:96250885
|
T | C | 1 | a0001c0001t0007g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1002+3151T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250885 | ||||||
| chr12:96250927
|
G | A | 3 | a0002c0002t0001g0056a0002c0002t0001g0057a0002c0002t0001g0064 | 3 | HG02886.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1002+3193G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250927 | ||||||
| chr12:96250964
|
C | T | 1 | a0001c0001t0007g0114 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1002+3230C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96250964 | ||||||
| chr12:96251008
|
A | G | 316 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1002+3274A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251008 | ||||||
| chr12:96251027
|
T | C | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+3293T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251027 | ||||||
| chr12:96251181
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0143others(3): Show | 6 | HG00673.hp2 HG01952.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+3447T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251181 | ||||||
| chr12:96251263
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+3529C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251263 | ||||||
| chr12:96251626
|
A | C | 1 | a0001c0001t0005g0024 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1002+3892A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251626 | ||||||
| chr12:96251673
|
G | A | 96 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1002+3939G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251673 | ||||||
| chr12:96251768
|
G | A | 36 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(33): Show | 37 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1002+4034G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251768 | ||||||
| chr12:96251827
|
A | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0163a0001c0001t0001g0173others(15): Show | 19 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1002+4093A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96251827 | ||||||
| chr12:96252094
|
C | T | 1 | a0002c0002t0002g0300 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1002+4360C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252094 | ||||||
| chr12:96252151
|
G | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002+4417G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252151 | ||||||
| chr12:96252226
|
T | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0078a0001c0001t0002g0268others(2): Show | 6 | HG02280.hp2 HG02717.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+4492T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252226 | ||||||
| chr12:96252348
|
A | AAGGAGTA others(4): Show |
6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+4615_1002+462 others(15): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 96252348 | |||||
| chr12:96252368
|
A | C | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1002+4634A>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252368 | ||||||
| chr12:96252782
|
G | T | 2 | a0001c0001t0001g0037a0001c0001t0014g0231 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1002+5048G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252782 | ||||||
| chr12:96252817
|
A | G | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002+5083A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252817 | ||||||
| chr12:96252864
|
G | A | 4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(1): Show | 4 | HG01358.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002+5130G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96252864 | ||||||
| chr12:96253000
|
C | T | 9 | a0001c0001t0002g0180a0001c0001t0002g0294a0001c0001t0002g0306others(6): Show | 9 | HG00609.hp1 HG02129.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.1002+5266C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253000 | ||||||
| chr12:96253236
|
G | A | 30 | a0001c0001t0004g0008a0001c0001t0004g0041a0001c0001t0004g0043others(27): Show | 31 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1002+5502G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253236 | ||||||
| chr12:96253261
|
C | T | 5 | a0001c0001t0004g0041a0001c0001t0004g0043a0001c0001t0004g0044others(2): Show | 5 | HG01192.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002+5527C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253261 | ||||||
| chr12:96253369
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0007t0022g0103 | 3 | HG02451.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1002+5635T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253369 | ||||||
| chr12:96253506
|
A | T | 1 | a0001c0004t0001g0189 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+5772A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253506 | ||||||
| chr12:96253709
|
G | A | 136 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1002+5975G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96253709 | ||||||
| chr12:96254338
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0252a0001c0001t0014g0231 | 3 | HG00735.hp2 HG01255.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1003-5393T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96254338 | ||||||
| chr12:96254415
|
C | A | 2 | a0001c0001t0013g0011a0001c0001t0013g0012 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1003-5316C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96254415 | ||||||
| chr12:96254607
|
C | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-5124C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96254607 | ||||||
| chr12:96254660
|
T | G | 1 | a0001c0001t0001g0237 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1003-5071T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96254660 | ||||||
| chr12:96254961
|
G | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-4770G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96254961 | ||||||
| chr12:96255085
|
T | C | 31 | a0001c0001t0004g0008a0001c0001t0004g0041a0001c0001t0004g0043others(28): Show | 32 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1003-4646T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255085 | ||||||
| chr12:96255124
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1003-4607T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255124 | ||||||
| chr12:96255253
|
C | T | 29 | a0001c0001t0003g0020a0001c0001t0003g0049a0001c0001t0003g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1003-4478C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255253 | ||||||
| chr12:96255314
|
C | T | 1 | a0002c0002t0002g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1003-4417C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255314 | ||||||
| chr12:96255440
|
A | ATGGGC | 29 | a0001c0001t0003g0020a0001c0001t0003g0049a0001c0001t0003g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1003-4281_1003-427 others(9): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 96255440 | |||||
| chr12:96255580
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1003-4151C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255580 | ||||||
| chr12:96255834
|
T | C | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134others(3): Show | 6 | NA18939.hp2 NA18942.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-3897T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96255834 | ||||||
| chr12:96256008
|
TC | T | 143 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1003-3722delC | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256008 | ||||||
| chr12:96256012
|
G | T | 143 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1003-3719G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256012 | ||||||
| chr12:96256094
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1003-3637G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256094 | ||||||
| chr12:96256256
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1003-3475G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256256 | ||||||
| chr12:96256503
|
G | A | 1 | a0001c0001t0002g0328 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1003-3228G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256503 | ||||||
| chr12:96256728
|
G | C | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1003-3003G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256728 | ||||||
| chr12:96256782
|
G | T | 143 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1003-2949G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256782 | ||||||
| chr12:96256848
|
G | A | 108 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1003-2883G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96256848 | ||||||
| chr12:96257187
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1003-2544G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257187 | ||||||
| chr12:96257301
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0200a0001c0001t0001g0252others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-2430T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257301 | ||||||
| chr12:96257425
|
C | T | 1 | a0001c0001t0007g0165 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1003-2306C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257425 | ||||||
| chr12:96257444
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1003-2287A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257444 | ||||||
| chr12:96257481
|
C | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1003-2250C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257481 | ||||||
| chr12:96257614
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1003-2117C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257614 | ||||||
| chr12:96257765
|
C | T | 3 | a0002c0002t0002g0090a0002c0002t0012g0146a0002c0002t0012g0178 | 3 | HG01255.hp2 NA19043.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1003-1966C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257765 | ||||||
| chr12:96257870
|
C | G | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0013g0011others(1): Show | 4 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-1861C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257870 | ||||||
| chr12:96257870
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-1861C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96257870 | ||||||
| chr12:96258126
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1003-1605C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258126 | ||||||
| chr12:96258183
|
T | C | 36 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1003-1548T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258183 | ||||||
| chr12:96258192
|
G | A | 97 | a0001c0001t0001g0037a0001c0001t0001g0071a0001c0001t0001g0091others(94): Show | 98 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1003-1539G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258192 | ||||||
| chr12:96258277
|
A | G | 29 | a0001c0001t0003g0020a0001c0001t0003g0049a0001c0001t0003g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1003-1454A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258277 | ||||||
| chr12:96258326
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1003-1405C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258326 | ||||||
| chr12:96258580
|
C | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 136 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1003-1151C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258580 | ||||||
| chr12:96258871
|
T | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1003-860T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258871 | ||||||
| chr12:96258916
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1003-815A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96258916 | ||||||
| chr12:96259090
|
A | G | 1 | a0001c0001t0009g0014 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1003-641A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259090 | ||||||
| chr12:96259173
|
G | C | 1 | a0001c0001t0001g0248 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1003-558G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259173 | ||||||
| chr12:96259289
|
C | T | 9 | a0001c0001t0002g0180a0001c0001t0002g0294a0001c0001t0002g0306others(6): Show | 9 | HG00609.hp1 HG02129.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.1003-442C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259289 | ||||||
| chr12:96259408
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1003-323C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259408 | ||||||
| chr12:96259409
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1003-322G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259409 | ||||||
| chr12:96259501
|
G | A | 1 | a0001c0001t0009g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1003-230G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259501 | ||||||
| chr12:96259606
|
T | C | 1 | a0001c0001t0004g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1003-125T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259606 | ||||||
| chr12:96259723
|
C | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
splice_region_variant&intron_variant | LOW | c.1003-8C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 3/4 | chr12 | 96259723 | ||||||
| chr12:96259860
|
G | A | 4 | a0002c0002t0002g0083a0002c0002t0002g0085a0002c0002t0002g0170others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1125+7G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96259860 | ||||||
| chr12:96259943
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+90A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96259943 | ||||||
| chr12:96260016
|
C | CATTTTCA others(11): Show |
1 | a0001c0001t0003g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1125+167_1125+184d others(20): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 96260016 | |||||
| chr12:96260150
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(342): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1125+297G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260150 | ||||||
| chr12:96260161
|
T | C | 3 | a0001c0001t0005g0238a0001c0001t0005g0271a0001c0001t0005g0272 | 3 | HG01070.hp2 HG01071.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1125+308T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260161 | ||||||
| chr12:96260317
|
A | AAAG | 34 | a0001c0001t0001g0058a0001c0001t0004g0008a0001c0001t0004g0041others(31): Show | 35 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1125+465_1125+467d others(5): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 96260317 | |||||
| chr12:96260346
|
T | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0134 | 3 | NA18942.hp2 NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1125+493T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260346 | ||||||
| chr12:96260480
|
A | G | 14 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0070others(11): Show | 14 | HG02257.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1125+627A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260480 | ||||||
| chr12:96260544
|
A | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+691A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260544 | ||||||
| chr12:96260545
|
C | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+692C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260545 | ||||||
| chr12:96260548
|
T | TTATAGAT others(3): Show |
6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+695_1125+696i others(12): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260548 | ||||||
| chr12:96260549
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+696C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260549 | ||||||
| chr12:96260550
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+697C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260550 | ||||||
| chr12:96260554
|
C | G | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+701C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260554 | ||||||
| chr12:96260555
|
T | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+702T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260555 | ||||||
| chr12:96260702
|
G | T | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+849G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260702 | ||||||
| chr12:96260869
|
G | A | 1 | a0005c0009t0006g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1125+1016G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260869 | ||||||
| chr12:96260870
|
G | A | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+1017G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260870 | ||||||
| chr12:96260903
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0244 | 2 | HG01257.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1125+1050A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260903 | ||||||
| chr12:96260907
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 136 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1125+1054T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96260907 | ||||||
| chr12:96261052
|
A | G | 50 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0070others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1125+1199A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261052 | ||||||
| chr12:96261262
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1125+1409A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261262 | ||||||
| chr12:96261273
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1125+1420G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261273 | ||||||
| chr12:96261458
|
T | G | 29 | a0001c0001t0003g0020a0001c0001t0003g0049a0001c0001t0003g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1125+1605T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261458 | ||||||
| chr12:96261661
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+1808A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261661 | ||||||
| chr12:96261824
|
C | T | 1 | a0001c0001t0004g0065 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1125+1971C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261824 | ||||||
| chr12:96261845
|
T | C | 1 | a0001c0001t0004g0305 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1125+1992T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261845 | ||||||
| chr12:96261904
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0075a0001c0001t0001g0344 | 3 | HG01167.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1125+2051T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96261904 | ||||||
| chr12:96262017
|
CT | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(243): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1125+2183delT | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 96262017 | |||||
| chr12:96262023
|
T | C | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2170T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262023 | ||||||
| chr12:96262065
|
C | G | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2212C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262065 | ||||||
| chr12:96262099
|
A | G | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+2246A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262099 | ||||||
| chr12:96262209
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1125+2356G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262209 | ||||||
| chr12:96262255
|
G | A | 2 | a0001c0001t0002g0123a0001c0001t0002g0168 | 2 | HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1125+2402G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262255 | ||||||
| chr12:96262315
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+2462G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262315 | ||||||
| chr12:96262527
|
G | A | 1 | a0002c0002t0002g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1125+2674G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262527 | ||||||
| chr12:96262735
|
G | C | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2882G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262735 | ||||||
| chr12:96262830
|
T | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1125+2977T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262830 | ||||||
| chr12:96262831
|
A | T | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+2978A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262831 | ||||||
| chr12:96262868
|
G | A | 1 | a0005c0009t0006g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1125+3015G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262868 | ||||||
| chr12:96262934
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0174 | 3 | HG02723.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1125+3081T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262934 | ||||||
| chr12:96262945
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1125+3092T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262945 | ||||||
| chr12:96262967
|
G | A | 1 | a0001c0001t0019g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1125+3114G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96262967 | ||||||
| chr12:96263147
|
T | C | 2 | a0001c0001t0007g0291a0001c0001t0007g0292 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1125+3294T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263147 | ||||||
| chr12:96263201
|
G | T | 316 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1125+3348G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263201 | ||||||
| chr12:96263232
|
C | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+3379C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263232 | ||||||
| chr12:96263349
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1125+3496G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263349 | ||||||
| chr12:96263530
|
T | C | 1 | a0001c0001t0020g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1126-3552T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263530 | ||||||
| chr12:96263637
|
C | T | 36 | a0001c0001t0002g0113a0001c0001t0002g0148a0001c0001t0002g0229others(33): Show | 36 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1126-3445C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263637 | ||||||
| chr12:96263653
|
C | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-3429C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263653 | ||||||
| chr12:96263654
|
C | G | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-3428C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263654 | ||||||
| chr12:96263713
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1126-3369G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96263713 | ||||||
| chr12:96264059
|
C | G | 1 | a0001c0001t0018g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1126-3023C>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264059 | ||||||
| chr12:96264087
|
C | T | 143 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1126-2995C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264087 | ||||||
| chr12:96264153
|
T | G | 1 | a0001c0001t0001g0273 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1126-2929T>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264153 | ||||||
| chr12:96264257
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1126-2825G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264257 | ||||||
| chr12:96264374
|
A | G | 1 | a0001c0001t0009g0015 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1126-2708A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264374 | ||||||
| chr12:96264377
|
T | C | 1 | a0002c0002t0002g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1126-2705T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264377 | ||||||
| chr12:96264612
|
G | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 158 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1126-2470G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264612 | ||||||
| chr12:96264662
|
G | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1126-2420G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264662 | ||||||
| chr12:96264839
|
T | C | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-2243T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264839 | ||||||
| chr12:96264851
|
C | T | 2 | a0001c0001t0007g0291a0001c0001t0007g0292 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1126-2231C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96264851 | ||||||
| chr12:96265000
|
G | C | 33 | a0001c0001t0004g0008a0001c0001t0004g0041a0001c0001t0004g0043others(30): Show | 34 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1126-2082G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265000 | ||||||
| chr12:96265046
|
A | G | 1 | a0001c0001t0013g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1126-2036A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265046 | ||||||
| chr12:96265052
|
G | A | 31 | a0001c0001t0004g0008a0001c0001t0004g0041a0001c0001t0004g0043others(28): Show | 32 | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1126-2030G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265052 | ||||||
| chr12:96265160
|
C | T | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-1922C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265160 | ||||||
| chr12:96265178
|
G | C | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1126-1904G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265178 | ||||||
| chr12:96265179
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1126-1903G>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265179 | ||||||
| chr12:96265399
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1126-1683A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265399 | ||||||
| chr12:96265400
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1126-1682T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265400 | ||||||
| chr12:96265514
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1126-1568C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265514 | ||||||
| chr12:96265645
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1126-1437C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265645 | ||||||
| chr12:96265671
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1126-1411C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265671 | ||||||
| chr12:96265780
|
C | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-1302C>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265780 | ||||||
| chr12:96265782
|
A | G | 21 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0070others(18): Show | 21 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126-1300A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265782 | ||||||
| chr12:96265945
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0174 | 3 | HG02723.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1126-1137A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265945 | ||||||
| chr12:96265946
|
C | T | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-1136C>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96265946 | ||||||
| chr12:96266061
|
A | T | 4 | a0001c0001t0004g0065a0001c0001t0004g0125a0001c0001t0004g0179others(1): Show | 4 | NA18612.hp2 NA18946.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-1021A>T | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266061 | ||||||
| chr12:96266092
|
T | C | 6 | a0001c0001t0002g0109a0001c0001t0009g0015a0001c0001t0009g0016others(3): Show | 6 | HG01070.hp1 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-990T>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266092 | ||||||
| chr12:96266254
|
G | A | 5 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0172others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-828G>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266254 | ||||||
| chr12:96266321
|
G | C | 4 | a0001c0001t0004g0065a0001c0001t0004g0125a0001c0001t0004g0179others(1): Show | 4 | NA18612.hp2 NA18946.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-761G>C | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266321 | ||||||
| chr12:96266497
|
CTT | C | 7 | a0001c0001t0002g0007a0001c0001t0002g0027a0001c0001t0002g0028others(4): Show | 8 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1126-583_1126-582d others(4): Show |
ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 96266497 | |||||
| chr12:96266796
|
T | A | 9 | a0001c0001t0007g0001a0001c0001t0007g0051a0001c0001t0007g0114others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-286T>A | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266796 | ||||||
| chr12:96266933
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 178 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.1126-149A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266933 | ||||||
| chr12:96266944
|
A | G | 2 | a0001c0001t0019g0086a0001c0001t0020g0181 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1126-138A>G | ELK3 | ENSG00000111145.8 | transcript | ENST00000228741.8 | protein_coding | 4/4 | chr12 | 96266944 |