Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9440 |
|---|---|
| ensemblid | ENSG00000042429.12 |
| hgncid | 2375 |
| symbol | MED17 |
| name | mediator complex subunit 17 |
| refseq_nuc | NM_004268.5 |
| refseq_prot | NP_004259.3 |
| ensembl_nuc | ENST00000251871.9 |
| ensembl_prot | ENSP00000251871.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 93784282 |
| end | 93814963 |
| strand | + |
| ver | v1.2 |
| region | chr11:93784282-93814963 |
| region5000 | chr11:93779282-93819963 |
| regionname0 | MED17_chr11_93784282_93814963 |
| regionname5000 | MED17_chr11_93779282_93819963 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 651 | 160 | 23 | 22 | 93 | 5 | 16 | 67 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002 | 1/0 | 651 | 152 | 55 | 22 | 49 | 7 | 18 | 37 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0003 | 0/0 | 651 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0004 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0005 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0006 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1956 | 144 | 12 | 18 | 93 | 5 | 15 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0002 | 1/0 | 1956 | 82 | 42 | 13 | 6 | 5 | 15 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0003 | 0/0 | 1956 | 43 | 3 | 8 | 27 | 2 | 3 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0004 | 0/0 | 1956 | 16 | 0 | 0 | 16 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0005 | 0/0 | 1956 | 8 | 6 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0006 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0007 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0008 | 0/0 | 1956 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0009 | 0/0 | 1956 | 3 | 3 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0010 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0011 | 0/0 | 1956 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0012 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0013 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0014 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0015 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0016 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0017 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| c0018 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3132 | 215 | 56 | 27 | 94 | 9 | 27 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0002 | 0/0 | 3133 | 35 | 4 | 5 | 21 | 2 | 3 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0003 | 0/0 | 3132 | 14 | 0 | 0 | 14 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0004 | 0/0 | 3133 | 9 | 0 | 3 | 5 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0005 | 0/0 | 3132 | 6 | 0 | 3 | 0 | 1 | 2 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0006 | 0/0 | 3143 | 5 | 4 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0007 | 0/0 | 3130 | 3 | 3 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0008 | 0/0 | 3143 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0009 | 0/0 | 3130 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0010 | 0/0 | 3132 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0011 | 0/0 | 3130 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0012 | 0/0 | 3130 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0013 | 0/0 | 3132 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0014 | 0/0 | 3132 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0015 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0016 | 0/0 | 3131 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0017 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0018 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0019 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0020 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0021 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0022 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0023 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0024 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0025 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0026 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0027 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0028 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0029 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0030 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0031 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| t0032 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0002 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0005 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0006 | 0/0 | 4 | 2 | 0 | 0 | 2 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0008 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1956 | 144 | 12 | 18 | 93 | 5 | 15 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0005 | 0/0 | 1956 | 8 | 6 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0009 | 0/0 | 1956 | 3 | 3 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0011 | 0/0 | 1956 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0016 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0017 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0018 | 0/0 | 1956 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002 | 1/0 | 1956 | 82 | 42 | 13 | 6 | 5 | 15 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0003 | 0/0 | 1956 | 43 | 3 | 8 | 27 | 2 | 3 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0004 | 0/0 | 1956 | 16 | 0 | 0 | 16 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0006 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0008 | 0/0 | 1956 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0010 | 0/0 | 1956 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0012 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0003c0007 | 0/0 | 1956 | 5 | 5 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0004c0015 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0005c0014 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0006c0013 | 0/0 | 1956 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5087 | 132 | 9 | 15 | 88 | 5 | 14 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0007 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0016 | 0/0 | 5086 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0017 | 0/0 | 5114 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0018 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0020 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0021 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0023 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0024 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0026 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0028 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0030 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0001t0032 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0005t0006 | 0/0 | 5098 | 5 | 4 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0005t0008 | 0/0 | 5098 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0009t0001 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0009t0010 | 0/0 | 5087 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0011t0001 | 0/0 | 5087 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0016t0002 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0017t0009 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0001c0018t0001 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0001 | 1/0 | 5087 | 70 | 38 | 9 | 6 | 4 | 12 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0004 | 0/0 | 5088 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0005 | 0/0 | 5087 | 6 | 0 | 3 | 0 | 1 | 2 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0013 | 0/0 | 5087 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0014 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0019 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0002t0025 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0003t0002 | 0/0 | 5088 | 34 | 3 | 5 | 21 | 2 | 3 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0003t0004 | 0/0 | 5088 | 8 | 0 | 3 | 5 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0003t0027 | 0/0 | 5088 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0004t0003 | 0/0 | 5087 | 14 | 0 | 0 | 14 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0004t0015 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0004t0029 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0006t0009 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0006t0011 | 0/0 | 5085 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0006t0012 | 0/0 | 5085 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0008t0001 | 0/0 | 5087 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0010t0007 | 0/0 | 5085 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0002c0012t0031 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0003c0007t0001 | 0/0 | 5087 | 5 | 5 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0004c0015t0001 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0005c0014t0014 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| a0006c0013t0022 | 0/0 | 5087 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | copy fasta | chr11 | 93779282 | 93819963 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0002 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0016g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0017g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0018g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0020g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0023g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0024g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0026g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0028g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0030g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0001t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0005t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0009t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0009t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0009t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0011t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0011t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0016t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0017t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0001c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0014g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0019g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0002t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0003t0027g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0004t0029g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0006t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0006t0011g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0006t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0006t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0008t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0008t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0010t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0010t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0002c0012t0031g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0003c0007t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0003c0007t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0003c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0003c0007t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0004c0015t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0005c0014t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| a0006c0013t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0005 | g0194 | EUR | GBR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00140 | hp1 | a0002 | c0003 | t0002 | g0222 | EUR | GBR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | GBR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0009 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0213 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00609 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00621 | hp2 | a0002 | c0003 | t0002 | g0226 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00733 | hp1 | a0001 | c0001 | t0030 | g0035 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00741 | hp1 | a0001 | c0005 | t0008 | g0137 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01074 | hp1 | a0002 | c0002 | t0005 | g0198 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01074 | hp2 | a0002 | c0002 | t0019 | g0157 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01081 | hp2 | a0002 | c0003 | t0004 | g0238 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01099 | hp2 | a0002 | c0008 | t0001 | g0245 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01106 | hp2 | a0002 | c0002 | t0005 | g0182 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01167 | hp2 | a0002 | c0003 | t0002 | g0225 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01168 | hp1 | a0002 | c0002 | t0005 | g0181 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0014 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01169 | hp1 | a0001 | c0001 | t0026 | g0077 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01169 | hp2 | a0002 | c0003 | t0002 | g0212 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01192 | hp2 | a0002 | c0003 | t0004 | g0237 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01243 | hp1 | a0001 | c0005 | t0006 | g0128 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0224 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01256 | hp2 | a0001 | c0011 | t0001 | g0071 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01361 | hp1 | a0002 | c0003 | t0004 | g0239 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0014 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0183 | EUR | IBS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0011 | EUR | IBS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01884 | hp1 | a0002 | c0006 | t0012 | g0147 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02004 | hp2 | a0001 | c0001 | t0023 | g0082 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02015 | hp2 | a0002 | c0003 | t0002 | g0219 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02040 | hp2 | a0002 | c0004 | t0003 | g0027 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02055 | hp1 | a0001 | c0005 | t0008 | g0127 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02071 | hp1 | a0002 | c0003 | t0027 | g0220 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02145 | hp2 | a0002 | c0003 | t0002 | g0208 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02148 | hp1 | a0001 | c0011 | t0001 | g0018 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CDX | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02165 | hp2 | a0002 | c0004 | t0003 | g0026 | EAS | CDX | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02257 | hp2 | a0002 | c0002 | t0014 | g0142 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02258 | hp1 | a0002 | c0002 | t0013 | g0155 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02451 | hp2 | a0001 | c0005 | t0008 | g0129 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02572 | hp2 | a0002 | c0006 | t0011 | g0024 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02615 | hp1 | a0001 | c0017 | t0009 | g0047 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02615 | hp2 | a0002 | c0010 | t0007 | g0243 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02622 | hp1 | a0003 | c0007 | t0001 | g0017 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02622 | hp2 | a0002 | c0006 | t0011 | g0024 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02630 | hp1 | a0001 | c0005 | t0006 | g0037 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0078 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02647 | hp2 | a0001 | c0009 | t0010 | g0043 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0240 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02738 | hp1 | a0002 | c0003 | t0002 | g0210 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02809 | hp1 | a0004 | c0015 | t0001 | g0206 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02809 | hp2 | a0003 | c0007 | t0001 | g0017 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02886 | hp2 | a0002 | c0010 | t0007 | g0242 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02895 | hp1 | a0002 | c0012 | t0031 | g0144 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02922 | hp2 | a0003 | c0007 | t0001 | g0067 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02976 | hp2 | a0002 | c0008 | t0001 | g0247 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03041 | hp1 | a0001 | c0005 | t0006 | g0046 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0044 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0159 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0006 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03195 | hp1 | a0003 | c0007 | t0001 | g0065 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03195 | hp2 | a0002 | c0006 | t0012 | g0148 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03209 | hp1 | a0001 | c0005 | t0006 | g0045 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03209 | hp2 | a0002 | c0003 | t0002 | g0216 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03453 | hp1 | a0001 | c0009 | t0010 | g0042 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0215 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03491 | hp2 | a0002 | c0002 | t0005 | g0031 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03492 | hp2 | a0002 | c0002 | t0005 | g0031 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03516 | hp2 | a0002 | c0002 | t0013 | g0156 | AFR | ESN | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03579 | hp2 | a0002 | c0002 | t0025 | g0168 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03688 | hp2 | a0002 | c0003 | t0002 | g0218 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03831 | hp1 | a0002 | c0003 | t0002 | g0209 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG04228 | hp2 | a0001 | c0018 | t0001 | g0001 | SAS | STU | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18612 | hp1 | a0002 | c0003 | t0002 | g0221 | EAS | CHB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18941 | hp2 | a0002 | c0004 | t0003 | g0244 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18942 | hp2 | a0002 | c0004 | t0003 | g0173 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18943 | hp1 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18944 | hp1 | a0001 | c0001 | t0020 | g0120 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18948 | hp2 | a0002 | c0003 | t0002 | g0211 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18953 | hp2 | a0002 | c0003 | t0004 | g0016 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18959 | hp1 | a0002 | c0004 | t0003 | g0175 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18965 | hp1 | a0001 | c0001 | t0028 | g0081 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18965 | hp2 | a0002 | c0003 | t0002 | g0227 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18968 | hp1 | a0002 | c0003 | t0004 | g0235 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18969 | hp2 | a0002 | c0004 | t0003 | g0174 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18971 | hp2 | a0002 | c0004 | t0029 | g0178 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18973 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18975 | hp2 | a0002 | c0004 | t0003 | g0026 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18980 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18982 | hp2 | a0002 | c0004 | t0003 | g0027 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18986 | hp2 | a0002 | c0003 | t0004 | g0236 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18988 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0228 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18997 | hp2 | a0002 | c0004 | t0003 | g0180 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19002 | hp1 | a0002 | c0003 | t0002 | g0151 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19002 | hp2 | a0002 | c0003 | t0004 | g0016 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19009 | hp1 | a0001 | c0001 | t0032 | g0134 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19009 | hp2 | a0002 | c0004 | t0003 | g0179 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19030 | hp1 | a0001 | c0005 | t0006 | g0036 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19030 | hp2 | a0002 | c0006 | t0009 | g0146 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19054 | hp2 | a0002 | c0003 | t0004 | g0016 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19060 | hp2 | a0002 | c0004 | t0003 | g0028 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19062 | hp2 | a0002 | c0004 | t0003 | g0241 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19065 | hp2 | a0002 | c0003 | t0002 | g0214 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19066 | hp1 | a0002 | c0003 | t0002 | g0229 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19066 | hp2 | a0001 | c0001 | t0024 | g0060 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19068 | hp1 | a0002 | c0004 | t0003 | g0176 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0009 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19079 | hp1 | a0002 | c0004 | t0015 | g0028 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19085 | hp1 | a0002 | c0003 | t0002 | g0013 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19086 | hp1 | a0002 | c0004 | t0003 | g0177 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19091 | hp1 | a0001 | c0001 | t0017 | g0133 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA19240 | hp2 | a0001 | c0016 | t0002 | g0038 | AFR | YRI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20752 | hp1 | a0002 | c0003 | t0002 | g0249 | EUR | TSI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0011 | EUR | TSI | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | GIH | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20905 | hp2 | a0001 | c0001 | t0016 | g0005 | SAS | GIH | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02109 | hp1 | a0002 | c0008 | t0001 | g0246 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ACB | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | MSL | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | USA | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0163 | AFR | USA | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20300 | hp1 | a0005 | c0014 | t0014 | g0143 | AFR | USA | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | USA | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA21309 | hp1 | a0003 | c0007 | t0001 | g0066 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| NA21309 | hp2 | a0006 | c0013 | t0022 | g0167 | AFR | LWK | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0069 | REF | REF | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0158 | REF | REF | MED17_chr11_93779282_93819963 | MED17 | chr11 | 93779282 | 93819963 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:93784720
|
G | C | 2 | a0001a0003 | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
missense_variant | MODERATE | c.207G>C | p.Glu69Asp | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 439/5087 | 207/1956 | 69/651 | chr11 | 93784720 | ||
| chr11:93784737
|
C | G | 1 | a0003 | 5 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.224C>G | p.Ser75Cys | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 456/5087 | 224/1956 | 75/651 | chr11 | 93784737 | ||
| chr11:93793851
|
C | G | 1 | a0004 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.761C>G | p.Ser254Cys | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 4/12 | 993/5087 | 761/1956 | 254/651 | chr11 | 93793851 | ||
| chr11:93796468
|
T | A | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1071T>A | p.Phe357Leu | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/12 | 1303/5087 | 1071/1956 | 357/651 | chr11 | 93796468 | ||
| chr11:93797661
|
A | C | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1270A>C | p.Ser424Arg | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/12 | 1502/5087 | 1270/1956 | 424/651 | chr11 | 93797661 | ||
| chr11:93801867
|
G | A | 1 | a0005 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1361G>A | p.Arg454Gln | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/12 | 1593/5087 | 1361/1956 | 454/651 | chr11 | 93801867 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:93784708
|
C | G | 8 | a0001c0001a0001c0005a0001c0009others(5): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
synonymous_variant | LOW | c.195C>G | p.Gly65Gly | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 427/5087 | 195/1956 | 65/651 | chr11 | 93784708 | ||
| chr11:93788092
|
T | C | 3 | a0001c0005a0001c0009a0002c0012 | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
synonymous_variant | LOW | c.342T>C | p.Asp114Asp | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/12 | 574/5087 | 342/1956 | 114/651 | chr11 | 93788092 | ||
| chr11:93790672
|
C | T | 4 | a0001c0005a0001c0009a0001c0011others(1): Show | 14 | HG00741.hp1 HG01243.hp1 HG01256.hp2 others(11): Show |
synonymous_variant | LOW | c.516C>T | p.Thr172Thr | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/12 | 748/5087 | 516/1956 | 172/651 | chr11 | 93790672 | ||
| chr11:93793780
|
C | T | 1 | a0002c0010 | 2 | HG02615.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.690C>T | p.Leu230Leu | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 4/12 | 922/5087 | 690/1956 | 230/651 | chr11 | 93793780 | ||
| chr11:93795026
|
G | C | 1 | a0002c0004 | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
synonymous_variant | LOW | c.978G>C | p.Val326Val | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/12 | 1210/5087 | 978/1956 | 326/651 | chr11 | 93795026 | ||
| chr11:93796489
|
G | A | 2 | a0001c0016a0002c0003 | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
synonymous_variant | LOW | c.1092G>A | p.Pro364Pro | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/12 | 1324/5087 | 1092/1956 | 364/651 | chr11 | 93796489 | ||
| chr11:93797651
|
A | G | 3 | a0001c0009a0002c0010a0002c0012 | 6 | HG02615.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.1260A>G | p.Ser420Ser | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/12 | 1492/5087 | 1260/1956 | 420/651 | chr11 | 93797651 | ||
| chr11:93807533
|
A | G | 2 | a0001c0018a0002c0008 | 4 | HG01099.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.1482A>G | p.Gln494Gln | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/12 | 1714/5087 | 1482/1956 | 494/651 | chr11 | 93807533 | ||
| chr11:93807551
|
G | A | 2 | a0001c0017a0002c0006 | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.1500G>A | p.Glu500Glu | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/12 | 1732/5087 | 1500/1956 | 500/651 | chr11 | 93807551 | ||
| chr11:93807599
|
T | C | 4 | a0001c0009a0002c0010a0002c0012others(1): Show | 7 | HG02615.hp2 HG02647.hp2 HG02886.hp2 others(4): Show |
synonymous_variant | LOW | c.1548T>C | p.Tyr516Tyr | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/12 | 1780/5087 | 1548/1956 | 516/651 | chr11 | 93807599 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:93784282
|
A | G | 1 | a0001c0001t0032 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-232A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 232 | chr11 | 93784282 | |||||
| chr11:93784298
|
A | C | 3 | a0002c0002t0014a0002c0012t0031a0005c0014t0014 | 3 | HG02257.hp2 HG02895.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-216A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 216 | chr11 | 93784298 | |||||
| chr11:93784345
|
C | T | 1 | a0001c0001t0030 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 169 | chr11 | 93784345 | |||||
| chr11:93784435
|
C | G | 1 | a0002c0004t0029 | 1 | NA18971.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-79C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | chr11 | 93784435 | ||||||
| chr11:93784473
|
G | T | 1 | a0002c0002t0013 | 2 | HG02258.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-41G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 41 | chr11 | 93784473 | |||||
| chr11:93784486
|
C | T | 2 | a0002c0006t0011a0002c0006t0012 | 4 | HG01884.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 28 | chr11 | 93784486 | |||||
| chr11:93784511
|
A | G | 1 | a0001c0001t0028 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/12 | 3 | chr11 | 93784511 | |||||
| chr11:93812125
|
C | G | 1 | a0001c0005t0008 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*61C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 61 | chr11 | 93812125 | |||||
| chr11:93812254
|
T | C | 3 | a0002c0004t0003a0002c0004t0015a0002c0004t0029 | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*190T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 190 | chr11 | 93812254 | |||||
| chr11:93812295
|
AAT | A | 2 | a0001c0001t0007a0002c0010t0007 | 3 | HG02486.hp1 HG02615.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*234_*235delAT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 234 | INFO_REALIGN_3_PRIME | chr11 | 93812295 | ||||
| chr11:93812445
|
C | CT | 5 | a0001c0016t0002a0002c0002t0004a0002c0003t0002others(2): Show | 45 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*392dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 393 | INFO_REALIGN_3_PRIME | chr11 | 93812445 | ||||
| chr11:93812445
|
C | CTTTTTTT others(4): Show |
2 | a0001c0005t0006a0001c0005t0008 | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*382_*392dupTTTTTT others(5): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 393 | INFO_REALIGN_3_PRIME | chr11 | 93812445 | ||||
| chr11:93812445
|
CT | C | 5 | a0001c0001t0016a0001c0017t0009a0002c0006t0009others(2): Show | 7 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*392delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 392 | INFO_REALIGN_3_PRIME | chr11 | 93812445 | ||||
| chr11:93812468
|
T | G | 3 | a0001c0016t0002a0002c0003t0002a0002c0003t0027 | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 404 | chr11 | 93812468 | |||||
| chr11:93812794
|
TAACCTAC others(24): Show |
T | 1 | a0001c0001t0026 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731_*761delAACCTA others(25): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 731 | chr11 | 93812794 | |||||
| chr11:93813001
|
C | G | 1 | a0002c0004t0015 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 937 | chr11 | 93813001 | |||||
| chr11:93813133
|
A | AGGATAGA others(20): Show |
1 | a0001c0001t0017 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072_*1098dupATAG others(23): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1099 | INFO_REALIGN_3_PRIME | chr11 | 93813133 | ||||
| chr11:93813165
|
A | C | 2 | a0001c0005t0006a0001c0005t0008 | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1101 | chr11 | 93813165 | |||||
| chr11:93813181
|
C | T | 1 | a0002c0002t0025 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1117 | chr11 | 93813181 | |||||
| chr11:93813460
|
G | C | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1396 | chr11 | 93813460 | |||||
| chr11:93813587
|
T | C | 1 | a0002c0002t0019 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1523T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1523 | chr11 | 93813587 | |||||
| chr11:93813605
|
C | A | 2 | a0001c0005t0006a0001c0005t0008 | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1541C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1541 | chr11 | 93813605 | |||||
| chr11:93813804
|
G | A | 1 | a0002c0002t0025 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1740G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1740 | chr11 | 93813804 | |||||
| chr11:93813825
|
C | G | 1 | a0001c0001t0024 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1761C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1761 | chr11 | 93813825 | |||||
| chr11:93813958
|
G | A | 1 | a0002c0006t0011 | 2 | HG02572.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1894G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1894 | chr11 | 93813958 | |||||
| chr11:93813997
|
A | C | 1 | a0002c0012t0031 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1933A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1933 | chr11 | 93813997 | |||||
| chr11:93814058
|
C | T | 1 | a0001c0001t0023 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1994C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 1994 | chr11 | 93814058 | |||||
| chr11:93814083
|
TC | T | 4 | a0001c0017t0009a0002c0006t0009a0002c0006t0011others(1): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2020delC | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2020 | chr11 | 93814083 | |||||
| chr11:93814117
|
T | A | 1 | a0001c0001t0020 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2053 | chr11 | 93814117 | |||||
| chr11:93814221
|
G | GGTACGTC others(24): Show |
1 | a0001c0001t0026 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158_*2188dupGTAC others(27): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2189 | INFO_REALIGN_3_PRIME | chr11 | 93814221 | ||||
| chr11:93814243
|
C | T | 1 | a0002c0003t0027 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2179C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2179 | chr11 | 93814243 | |||||
| chr11:93814287
|
G | A | 1 | a0001c0001t0021 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2223 | chr11 | 93814287 | |||||
| chr11:93814518
|
G | C | 1 | a0002c0002t0005 | 6 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2454G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2454 | chr11 | 93814518 | |||||
| chr11:93814531
|
C | T | 1 | a0006c0013t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2467C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2467 | chr11 | 93814531 | |||||
| chr11:93814569
|
C | T | 2 | a0001c0005t0006a0001c0005t0008 | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2505C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2505 | chr11 | 93814569 | |||||
| chr11:93814717
|
T | G | 2 | a0001c0005t0006a0001c0005t0008 | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2653T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2653 | chr11 | 93814717 | |||||
| chr11:93814868
|
A | G | 1 | a0001c0009t0010 | 2 | HG02647.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2804A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 12/12 | 2804 | chr11 | 93814868 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:93784798
|
C | T | 1 | a0002c0003t0002g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.250+35C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93784798 | ||||||
| chr11:93784926
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.250+163C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93784926 | ||||||
| chr11:93785418
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.250+655G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93785418 | ||||||
| chr11:93785864
|
C | G | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.250+1101C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93785864 | ||||||
| chr11:93785983
|
A | T | 1 | a0002c0004t0003g0244 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.250+1220A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93785983 | ||||||
| chr11:93785997
|
C | G | 2 | a0002c0010t0007g0242a0002c0010t0007g0243 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.250+1234C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93785997 | ||||||
| chr11:93786004
|
CCA | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.250+1250_250+1251d others(4): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 93786004 | |||||
| chr11:93786043
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.250+1280T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786043 | ||||||
| chr11:93786046
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.250+1283A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786046 | ||||||
| chr11:93786090
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.250+1327A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786090 | ||||||
| chr11:93786158
|
T | G | 1 | a0001c0001t0030g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.250+1395T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786158 | ||||||
| chr11:93786359
|
T | G | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.250+1596T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786359 | ||||||
| chr11:93786464
|
G | T | 1 | a0002c0004t0003g0241 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.251-1537G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786464 | ||||||
| chr11:93786473
|
G | GT | 43 | a0001c0001t0001g0138a0001c0005t0008g0137a0002c0002t0001g0015others(40): Show | 54 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.251-1517dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 93786473 | |||||
| chr11:93786507
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.251-1494G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786507 | ||||||
| chr11:93786532
|
T | C | 1 | a0002c0002t0001g0141 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.251-1469T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786532 | ||||||
| chr11:93786571
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.251-1430G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786571 | ||||||
| chr11:93786735
|
C | G | 7 | a0002c0002t0004g0240a0002c0003t0004g0016a0002c0003t0004g0235others(4): Show | 9 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-1266C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786735 | ||||||
| chr11:93786974
|
T | A | 4 | a0002c0002t0001g0145a0002c0002t0014g0142a0002c0012t0031g0144others(1): Show | 4 | HG02257.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-1027T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93786974 | ||||||
| chr11:93787005
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.251-996A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787005 | ||||||
| chr11:93787050
|
CG | C | 9 | a0002c0002t0001g0207a0002c0002t0004g0240a0002c0003t0004g0016others(6): Show | 11 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-946delG | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 93787050 | |||||
| chr11:93787128
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.251-873C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787128 | ||||||
| chr11:93787135
|
C | T | 6 | a0002c0002t0001g0032a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 7 | HG02572.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-866C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787135 | ||||||
| chr11:93787136
|
G | A | 2 | a0002c0006t0009g0146a0002c0006t0011g0024 | 3 | HG02572.hp2 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.251-865G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787136 | ||||||
| chr11:93787139
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.251-862C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787139 | ||||||
| chr11:93787142
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.251-859A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787142 | ||||||
| chr11:93787149
|
C | T | 49 | a0001c0001t0001g0023a0001c0001t0001g0130a0001c0001t0001g0131others(46): Show | 60 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.251-852C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787149 | ||||||
| chr11:93787172
|
C | G | 1 | a0006c0013t0022g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.251-829C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787172 | ||||||
| chr11:93787173
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.251-828G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787173 | ||||||
| chr11:93787243
|
C | G | 1 | a0002c0002t0001g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251-758C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787243 | ||||||
| chr11:93787323
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.251-678G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787323 | ||||||
| chr11:93787368
|
G | A | 1 | a0001c0001t0030g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.251-633G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787368 | ||||||
| chr11:93787372
|
T | C | 12 | a0001c0001t0001g0033a0001c0005t0006g0036a0001c0005t0006g0037others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-629T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787372 | ||||||
| chr11:93787389
|
G | A | 2 | a0002c0002t0005g0181a0002c0002t0005g0182 | 2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.251-612G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787389 | ||||||
| chr11:93787485
|
A | G | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.251-516A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787485 | ||||||
| chr11:93787560
|
T | C | 37 | a0002c0002t0001g0008a0002c0002t0001g0011a0002c0002t0001g0012others(34): Show | 48 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.251-441T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787560 | ||||||
| chr11:93787565
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.251-436A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787565 | ||||||
| chr11:93787871
|
TAAATA | T | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.251-128_251-124del others(5): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 93787871 | |||||
| chr11:93787960
|
G | A | 3 | a0001c0017t0009g0047a0002c0006t0012g0147a0002c0006t0012g0148 | 3 | HG01884.hp1 HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.251-41G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 1/11 | chr11 | 93787960 | ||||||
| chr11:93788239
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.417+72C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788239 | ||||||
| chr11:93788259
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.417+92C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788259 | ||||||
| chr11:93788412
|
T | C | 2 | a0002c0002t0001g0149a0002c0002t0001g0150 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.417+245T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788412 | ||||||
| chr11:93788613
|
G | A | 8 | a0002c0002t0001g0008a0002c0002t0001g0011a0002c0002t0001g0025others(5): Show | 14 | HG00140.hp2 HG00733.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.417+446G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788613 | ||||||
| chr11:93788638
|
G | A | 1 | a0002c0003t0002g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.417+471G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788638 | ||||||
| chr11:93788680
|
C | CA | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.417+530dupA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 93788680 | |||||
| chr11:93788680
|
C | CAA | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0005t0006g0036others(5): Show | 8 | HG02056.hp2 HG02572.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.417+529_417+530dup others(2): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 93788680 | |||||
| chr11:93788737
|
C | A | 1 | a0002c0002t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.417+570C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788737 | ||||||
| chr11:93788849
|
G | A | 5 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154others(2): Show | 5 | HG02258.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+682G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93788849 | ||||||
| chr11:93789055
|
G | A | 1 | a0002c0006t0011g0024 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.417+888G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789055 | ||||||
| chr11:93789077
|
T | C | 2 | a0002c0002t0001g0141a0002c0002t0001g0188 | 2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.417+910T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789077 | ||||||
| chr11:93789158
|
G | A | 1 | a0002c0003t0002g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.417+991G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789158 | ||||||
| chr11:93789231
|
T | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 17 | HG00558.hp1 HG01123.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.417+1064T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789231 | ||||||
| chr11:93789305
|
T | A | 1 | a0001c0001t0024g0060 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.417+1138T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789305 | ||||||
| chr11:93789452
|
A | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 17 | HG00558.hp1 HG01123.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.418-1122A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789452 | ||||||
| chr11:93789456
|
T | A | 3 | a0002c0003t0004g0016a0002c0003t0004g0235a0002c0003t0004g0236 | 5 | NA18953.hp2 NA18968.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.418-1118T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789456 | ||||||
| chr11:93789476
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.418-1098A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93789476 | ||||||
| chr11:93789796
|
C | CA | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.418-762dupA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 93789796 | |||||
| chr11:93789796
|
C | CAA | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01175.hp2 HG02071.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-763_418-762dup others(2): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 93789796 | |||||
| chr11:93789796
|
CA | C | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-762delA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 93789796 | |||||
| chr11:93790085
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.418-489G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93790085 | ||||||
| chr11:93790340
|
A | G | 2 | a0002c0010t0007g0242a0002c0010t0007g0243 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.418-234A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93790340 | ||||||
| chr11:93790373
|
T | G | 1 | a0002c0003t0002g0211 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.418-201T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93790373 | ||||||
| chr11:93790443
|
A | G | 1 | a0002c0002t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.418-131A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 2/11 | chr11 | 93790443 | ||||||
| chr11:93790847
|
G | A | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637+54G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93790847 | ||||||
| chr11:93790880
|
T | G | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+87T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93790880 | ||||||
| chr11:93790931
|
A | G | 1 | a0002c0002t0001g0185 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.637+138A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93790931 | ||||||
| chr11:93790943
|
C | T | 1 | a0006c0013t0022g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.637+150C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93790943 | ||||||
| chr11:93790958
|
A | C | 15 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.637+165A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93790958 | ||||||
| chr11:93791079
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+286G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791079 | ||||||
| chr11:93791200
|
A | G | 1 | a0002c0002t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.637+407A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791200 | ||||||
| chr11:93791233
|
T | C | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+440T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791233 | ||||||
| chr11:93791311
|
T | C | 1 | a0002c0012t0031g0144 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.637+518T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791311 | ||||||
| chr11:93791554
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.637+761A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791554 | ||||||
| chr11:93791577
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.637+784T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791577 | ||||||
| chr11:93791597
|
T | G | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637+804T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791597 | ||||||
| chr11:93791639
|
C | G | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+846C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791639 | ||||||
| chr11:93791640
|
T | A | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+847T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791640 | ||||||
| chr11:93791660
|
T | C | 35 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(32): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.637+867T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791660 | ||||||
| chr11:93791660
|
T | G | 2 | a0001c0009t0010g0042a0001c0009t0010g0043 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.637+867T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791660 | ||||||
| chr11:93791690
|
TCAAAAAA others(5): Show |
T | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+909_637+920del others(12): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93791690 | |||||
| chr11:93791761
|
AAAAC | A | 4 | a0003c0007t0001g0017a0003c0007t0001g0065a0003c0007t0001g0066others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+980_637+983del others(4): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93791761 | |||||
| chr11:93791895
|
T | C | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+1102T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791895 | ||||||
| chr11:93791915
|
A | G | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+1122A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791915 | ||||||
| chr11:93791936
|
G | A | 2 | a0002c0008t0001g0245a0002c0008t0001g0246 | 2 | HG01099.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.637+1143G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791936 | ||||||
| chr11:93791944
|
A | G | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.637+1151A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93791944 | ||||||
| chr11:93792032
|
T | C | 3 | a0002c0002t0001g0207a0002c0002t0025g0168a0004c0015t0001g0206 | 3 | HG02809.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.637+1239T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792032 | ||||||
| chr11:93792081
|
C | CG | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.637+1291dupG | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93792081 | |||||
| chr11:93792162
|
T | A | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.637+1369T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792162 | ||||||
| chr11:93792210
|
C | T | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.637+1417C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792210 | ||||||
| chr11:93792245
|
G | A | 1 | a0001c0001t0001g0069 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.637+1452G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792245 | ||||||
| chr11:93792505
|
C | G | 29 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(26): Show | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.638-1223C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792505 | ||||||
| chr11:93792565
|
T | G | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.638-1163T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792565 | ||||||
| chr11:93792576
|
T | G | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.638-1152T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792576 | ||||||
| chr11:93792582
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG00408.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.638-1146A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792582 | ||||||
| chr11:93792592
|
A | G | 1 | a0001c0016t0002g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.638-1136A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792592 | ||||||
| chr11:93792648
|
A | C | 1 | a0002c0003t0002g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.638-1080A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792648 | ||||||
| chr11:93792650
|
C | G | 1 | a0001c0001t0020g0120 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.638-1078C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792650 | ||||||
| chr11:93792656
|
A | T | 1 | a0001c0001t0001g0059 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.638-1072A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792656 | ||||||
| chr11:93792914
|
C | G | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-814C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792914 | ||||||
| chr11:93792955
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.638-773A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93792955 | ||||||
| chr11:93793104
|
G | C | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-624G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793104 | ||||||
| chr11:93793114
|
C | CT | 9 | a0001c0001t0001g0018a0001c0011t0001g0018a0001c0011t0001g0071others(6): Show | 9 | HG01109.hp2 HG01256.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-593dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTT | 12 | a0001c0001t0001g0139a0001c0005t0006g0036a0001c0005t0006g0037others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.638-594_638-593dup others(2): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTT | 18 | a0001c0001t0001g0072a0001c0005t0008g0127a0002c0002t0001g0008others(15): Show | 27 | HG00140.hp2 HG00733.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-595_638-593dup others(3): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTT | 42 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0049others(39): Show | 59 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.638-596_638-593dup others(4): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTT | 7 | a0001c0001t0001g0050a0001c0001t0001g0064a0001c0001t0001g0080others(4): Show | 7 | HG00280.hp2 HG01361.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-597_638-593dup others(5): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.638-602_638-593dup others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(4): Show |
1 | a0002c0002t0001g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.638-603_638-593dup others(11): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(6): Show |
3 | a0002c0002t0001g0166a0002c0010t0007g0242a0002c0010t0007g0243 | 3 | HG02615.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.638-605_638-593dup others(13): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(7): Show |
3 | a0001c0017t0009g0047a0002c0002t0001g0201a0002c0006t0012g0147 | 3 | HG01884.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.638-606_638-593dup others(14): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0069others(12): Show | 18 | HG01255.hp1 HG01978.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.638-607_638-593dup others(15): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(9): Show |
29 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0033others(26): Show | 35 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.638-608_638-593dup others(16): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(10): Show |
43 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0021others(40): Show | 59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.638-609_638-593dup others(17): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(11): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(21): Show | 34 | HG00438.hp2 HG00673.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.638-610_638-593dup others(18): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(12): Show |
14 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0061others(11): Show | 14 | HG00280.hp1 HG00741.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.638-611_638-593dup others(19): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(13): Show |
5 | a0001c0001t0001g0115a0002c0002t0001g0145a0002c0002t0005g0031others(2): Show | 6 | HG02257.hp2 HG02738.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-612_638-593dup others(20): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG04199.hp2 NA18953.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.638-613_638-593dup others(21): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.638-593_638-592ins others(24): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793114
|
CT | C | 7 | a0002c0002t0001g0015a0002c0002t0001g0189a0002c0002t0001g0231others(4): Show | 9 | HG01074.hp2 HG01891.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.638-593delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793114 | |||||
| chr11:93793208
|
T | C | 1 | a0002c0002t0014g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.638-520T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793208 | ||||||
| chr11:93793223
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.638-505A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793223 | ||||||
| chr11:93793272
|
C | T | 6 | a0002c0004t0003g0028a0002c0004t0003g0173a0002c0004t0003g0174others(3): Show | 6 | NA18942.hp2 NA18959.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.638-456C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793272 | ||||||
| chr11:93793412
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.638-316T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793412 | ||||||
| chr11:93793425
|
C | T | 3 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.638-303C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793425 | ||||||
| chr11:93793489
|
T | A | 1 | a0002c0002t0001g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.638-239T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793489 | ||||||
| chr11:93793509
|
G | T | 1 | a0002c0002t0005g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.638-219G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | chr11 | 93793509 | ||||||
| chr11:93793514
|
G | GT | 20 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(17): Show | 21 | HG00741.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.638-202dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793514 | |||||
| chr11:93793514
|
GT | G | 33 | a0001c0001t0001g0100a0001c0001t0001g0101a0002c0002t0001g0008others(30): Show | 44 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.638-202delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 93793514 | |||||
| chr11:93794053
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.859+18T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794053 | ||||||
| chr11:93794116
|
GA | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.859+87delA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794116 | |||||
| chr11:93794199
|
A | AT | 76 | a0001c0001t0001g0248a0001c0001t0007g0099a0001c0016t0002g0038others(73): Show | 93 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.859+186dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794199 | |||||
| chr11:93794199
|
A | ATT | 9 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137others(6): Show | 9 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.859+185_859+186dup others(2): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794199 | |||||
| chr11:93794199
|
A | ATTT | 11 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(8): Show | 12 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.859+184_859+186dup others(3): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794199 | |||||
| chr11:93794199
|
AT | A | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0083others(5): Show | 8 | HG01256.hp2 HG01516.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+186delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794199 | |||||
| chr11:93794267
|
C | G | 35 | a0001c0001t0001g0033a0002c0002t0001g0008a0002c0002t0001g0011others(32): Show | 46 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.859+232C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794267 | ||||||
| chr11:93794308
|
G | A | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.859+273G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794308 | ||||||
| chr11:93794312
|
C | T | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.859+277C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794312 | ||||||
| chr11:93794314
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.859+279C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794314 | ||||||
| chr11:93794451
|
G | T | 1 | a0002c0002t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.859+416G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794451 | ||||||
| chr11:93794503
|
T | C | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.860-405T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794503 | ||||||
| chr11:93794518
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.860-390T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794518 | ||||||
| chr11:93794534
|
G | C | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.860-374G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794534 | ||||||
| chr11:93794624
|
A | T | 2 | a0002c0002t0014g0142a0005c0014t0014g0143 | 2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.860-284A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794624 | ||||||
| chr11:93794651
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.860-257C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794651 | ||||||
| chr11:93794735
|
C | A | 1 | a0002c0002t0001g0159 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.860-173C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794735 | ||||||
| chr11:93794743
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.860-165A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | chr11 | 93794743 | ||||||
| chr11:93794781
|
G | GA | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.860-119dupA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 93794781 | |||||
| chr11:93795262
|
T | G | 1 | a0002c0004t0003g0177 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1012+202T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795262 | ||||||
| chr11:93795343
|
T | C | 12 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1012+283T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795343 | ||||||
| chr11:93795439
|
G | A | 3 | a0002c0002t0001g0207a0002c0002t0025g0168a0004c0015t0001g0206 | 3 | HG02809.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1012+379G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795439 | ||||||
| chr11:93795472
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1012+412G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795472 | ||||||
| chr11:93795560
|
TA | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1012+514delA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 93795560 | |||||
| chr11:93795682
|
G | A | 4 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+622G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795682 | ||||||
| chr11:93795747
|
C | A | 4 | a0003c0007t0001g0017a0003c0007t0001g0065a0003c0007t0001g0066others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-663C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795747 | ||||||
| chr11:93795777
|
T | C | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-633T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795777 | ||||||
| chr11:93795854
|
A | T | 1 | a0002c0002t0001g0163 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1013-556A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795854 | ||||||
| chr11:93795866
|
C | T | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-544C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795866 | ||||||
| chr11:93795893
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1013-517G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93795893 | ||||||
| chr11:93795949
|
G | GT | 12 | a0001c0001t0001g0063a0001c0001t0001g0126a0001c0001t0018g0078others(9): Show | 14 | HG02004.hp1 HG02004.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1013-446dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 93795949 | |||||
| chr11:93796042
|
C | T | 3 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1013-368C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93796042 | ||||||
| chr11:93796089
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0119others(2): Show | 5 | HG00408.hp1 HG00673.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-321A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93796089 | ||||||
| chr11:93796268
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1013-142T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93796268 | ||||||
| chr11:93796359
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1013-51C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 6/11 | chr11 | 93796359 | ||||||
| chr11:93796614
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1143+74C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93796614 | ||||||
| chr11:93796743
|
G | T | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+203G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93796743 | ||||||
| chr11:93796782
|
C | G | 3 | a0002c0002t0001g0207a0002c0002t0025g0168a0004c0015t0001g0206 | 3 | HG02809.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1143+242C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93796782 | ||||||
| chr11:93796804
|
A | G | 1 | a0006c0013t0022g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+264A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93796804 | ||||||
| chr11:93797014
|
G | A | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+474G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797014 | ||||||
| chr11:93797018
|
A | G | 4 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+478A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797018 | ||||||
| chr11:93797081
|
C | A | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1144-454C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797081 | ||||||
| chr11:93797135
|
A | G | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1144-400A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797135 | ||||||
| chr11:93797281
|
T | G | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-254T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797281 | ||||||
| chr11:93797497
|
A | G | 1 | a0002c0002t0001g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1144-38A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 7/11 | chr11 | 93797497 | ||||||
| chr11:93797731
|
G | A | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1328+12G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93797731 | ||||||
| chr11:93797856
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1328+137G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93797856 | ||||||
| chr11:93797869
|
G | A | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1328+150G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93797869 | ||||||
| chr11:93797869
|
G | T | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1328+150G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93797869 | ||||||
| chr11:93797961
|
A | G | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1328+242A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93797961 | ||||||
| chr11:93798045
|
G | A | 1 | a0002c0003t0002g0214 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1328+326G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798045 | ||||||
| chr11:93798069
|
T | C | 1 | a0002c0002t0001g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1328+350T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798069 | ||||||
| chr11:93798254
|
C | T | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1328+535C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798254 | ||||||
| chr11:93798560
|
T | C | 2 | a0002c0002t0014g0142a0005c0014t0014g0143 | 2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1328+841T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798560 | ||||||
| chr11:93798599
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1328+880A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798599 | ||||||
| chr11:93798756
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1328+1037A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798756 | ||||||
| chr11:93798856
|
G | C | 4 | a0001c0016t0002g0038a0002c0003t0002g0208a0002c0003t0002g0215others(1): Show | 4 | HG02145.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1328+1137G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93798856 | ||||||
| chr11:93799021
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1328+1302G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799021 | ||||||
| chr11:93799055
|
T | G | 37 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(34): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1328+1336T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799055 | ||||||
| chr11:93799178
|
A | AT | 7 | a0002c0002t0001g0015a0002c0002t0001g0150a0002c0002t0001g0231others(4): Show | 9 | HG01891.hp2 HG02451.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1328+1480dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93799178 | |||||
| chr11:93799178
|
AT | A | 8 | a0001c0001t0001g0115a0001c0005t0008g0129a0001c0005t0008g0137others(5): Show | 8 | HG00741.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1328+1480delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93799178 | |||||
| chr11:93799178
|
ATT | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1328+1479_1328+148 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93799178 | |||||
| chr11:93799279
|
G | A | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1328+1560G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799279 | ||||||
| chr11:93799513
|
G | A | 37 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(34): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1328+1794G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799513 | ||||||
| chr11:93799656
|
G | C | 1 | a0002c0003t0002g0217 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1328+1937G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799656 | ||||||
| chr11:93799810
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1329-2025C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93799810 | ||||||
| chr11:93799864
|
AGT | A | 37 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(34): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1329-1958_1329-195 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93799864 | |||||
| chr11:93799946
|
AAAAC | A | 37 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(34): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1329-1881_1329-187 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93799946 | |||||
| chr11:93800006
|
A | G | 5 | a0002c0003t0002g0211a0002c0003t0002g0213a0002c0003t0002g0217others(2): Show | 5 | HG00558.hp2 HG00621.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1329-1829A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800006 | ||||||
| chr11:93800073
|
C | T | 37 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(34): Show | 44 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1329-1762C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800073 | ||||||
| chr11:93800489
|
C | T | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1329-1346C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800489 | ||||||
| chr11:93800614
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1329-1221G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800614 | ||||||
| chr11:93800628
|
CA | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1329-1187delA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93800628 | |||||
| chr11:93800628
|
CAA | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0107others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329-1188_1329-118 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 93800628 | |||||
| chr11:93800640
|
A | G | 3 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1329-1195A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800640 | ||||||
| chr11:93800684
|
T | A | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1329-1151T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800684 | ||||||
| chr11:93800687
|
A | G | 1 | a0002c0006t0009g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1329-1148A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93800687 | ||||||
| chr11:93801216
|
A | G | 1 | a0001c0001t0018g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1329-619A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801216 | ||||||
| chr11:93801305
|
C | T | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329-530C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801305 | ||||||
| chr11:93801436
|
C | T | 2 | a0002c0002t0001g0196a0002c0002t0001g0197 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1329-399C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801436 | ||||||
| chr11:93801716
|
A | G | 8 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154others(5): Show | 8 | HG01074.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329-119A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801716 | ||||||
| chr11:93801764
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1329-71T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801764 | ||||||
| chr11:93801765
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1329-70T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801765 | ||||||
| chr11:93801766
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1329-69C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801766 | ||||||
| chr11:93801767
|
G | A | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1329-68G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801767 | ||||||
| chr11:93801824
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1329-11G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 8/11 | chr11 | 93801824 | ||||||
| chr11:93802109
|
G | GT | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1466+148dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93802109 | |||||
| chr11:93802147
|
C | G | 35 | a0001c0001t0001g0033a0002c0002t0001g0008a0002c0002t0001g0011others(32): Show | 46 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1466+175C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802147 | ||||||
| chr11:93802287
|
A | G | 29 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(26): Show | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1466+315A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802287 | ||||||
| chr11:93802361
|
A | G | 4 | a0003c0007t0001g0017a0003c0007t0001g0065a0003c0007t0001g0066others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1466+389A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802361 | ||||||
| chr11:93802396
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1466+424G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802396 | ||||||
| chr11:93802495
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1466+523A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802495 | ||||||
| chr11:93802570
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1466+598G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802570 | ||||||
| chr11:93802673
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1466+701A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802673 | ||||||
| chr11:93802811
|
G | T | 1 | a0001c0001t0001g0058 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1466+839G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802811 | ||||||
| chr11:93802984
|
T | C | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466+1012T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93802984 | ||||||
| chr11:93803304
|
A | G | 6 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(3): Show | 6 | HG02615.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1466+1332A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803304 | ||||||
| chr11:93803515
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1466+1543A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803515 | ||||||
| chr11:93803625
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1466+1653G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803625 | ||||||
| chr11:93803734
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1466+1762T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803734 | ||||||
| chr11:93803804
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1466+1832C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803804 | ||||||
| chr11:93803917
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1466+1945C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803917 | ||||||
| chr11:93803967
|
GTATA | G | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1466+1997_1466+200 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803967 | |||||
| chr11:93803976
|
T | C | 2 | a0001c0005t0008g0127a0001c0005t0008g0137 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1466+2004T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803976 | ||||||
| chr11:93803980
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1466+2008T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803980 | ||||||
| chr11:93803982
|
T | C | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1466+2010T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803982 | ||||||
| chr11:93803983
|
G | A | 1 | a0001c0005t0008g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1466+2011G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803983 | ||||||
| chr11:93803985
|
G | A | 3 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1466+2013G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803985 | ||||||
| chr11:93803985
|
GTA | G | 13 | a0002c0002t0001g0149a0002c0002t0001g0161a0002c0002t0001g0231others(10): Show | 15 | HG01081.hp2 HG01192.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1466+2019_1466+202 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803985 | |||||
| chr11:93803987
|
A | G | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1466+2015A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803987 | ||||||
| chr11:93803989
|
ATATG | A | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1466+2019_1466+202 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803989 | |||||
| chr11:93803989
|
ATATGTG | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(26): Show | 35 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1466+2019_1466+202 others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803989 | |||||
| chr11:93803991
|
A | G | 60 | a0001c0009t0001g0044a0001c0016t0002g0038a0002c0002t0001g0010others(57): Show | 73 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1466+2019A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803991 | ||||||
| chr11:93803991
|
ATGTGTG | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 72 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1466+2023_1466+202 others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803991 | |||||
| chr11:93803993
|
G | A | 2 | a0001c0005t0008g0127a0001c0005t0008g0129 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1466+2021G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803993 | ||||||
| chr11:93803993
|
GTGTGTGT others(1): Show |
G | 43 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(40): Show | 60 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1466+2023_1466+203 others(12): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803993 | |||||
| chr11:93803993
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0001g0103a0005c0014t0014g0143 | 2 | NA18952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1466+2023_1466+203 others(14): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803993 | |||||
| chr11:93803993
|
GTGTGTGT others(5): Show |
G | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0106others(5): Show | 8 | HG00621.hp1 HG02165.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1466+2023_1466+203 others(16): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803993 | |||||
| chr11:93803993
|
GTGTGTGT others(7): Show |
G | 34 | a0002c0002t0001g0008a0002c0002t0001g0011a0002c0002t0001g0012others(31): Show | 45 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.1466+2023_1466+203 others(18): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803993 | |||||
| chr11:93803993
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0102 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1466+2023_1466+204 others(22): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803993 | |||||
| chr11:93803994
|
TGTGTGTA others(29): Show |
T | 2 | a0001c0009t0001g0044a0002c0012t0031g0144 | 2 | HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1466+2023_1466+205 others(40): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803994 | ||||||
| chr11:93803995
|
G | A | 14 | a0001c0005t0008g0127a0001c0005t0008g0129a0002c0004t0003g0026others(11): Show | 16 | HG02040.hp2 HG02055.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.1466+2023G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803995 | ||||||
| chr11:93803995
|
GTGTGTAT others(7): Show |
G | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1466+2025_1466+203 others(18): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803995 | |||||
| chr11:93803996
|
TGTGTATA others(27): Show |
T | 2 | a0001c0009t0010g0042a0001c0009t0010g0043 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1466+2025_1466+205 others(38): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803996 | ||||||
| chr11:93803997
|
G | A | 22 | a0001c0005t0008g0127a0001c0005t0008g0129a0002c0002t0004g0240others(19): Show | 26 | HG01081.hp2 HG01192.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1466+2025G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803997 | ||||||
| chr11:93803997
|
G | GTATATA | 5 | a0002c0002t0001g0154a0002c0002t0001g0165a0002c0002t0013g0155others(2): Show | 5 | HG01074.hp2 HG01109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1466+2026_1466+202 others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803997 | |||||
| chr11:93803999
|
G | A | 31 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137others(28): Show | 35 | HG00741.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1466+2027G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93803999 | ||||||
| chr11:93803999
|
G | GTA | 6 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0215others(3): Show | 9 | HG00544.hp2 HG00621.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1466+2054_1466+205 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803999 | |||||
| chr11:93803999
|
G | GTATA | 9 | a0002c0002t0001g0164a0002c0003t0002g0014a0002c0003t0002g0211others(6): Show | 11 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1466+2052_1466+205 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803999 | |||||
| chr11:93803999
|
G | GTATATA | 6 | a0002c0003t0002g0213a0002c0003t0002g0222a0002c0003t0002g0224others(3): Show | 6 | HG00140.hp1 HG00558.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1466+2050_1466+205 others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803999 | |||||
| chr11:93803999
|
G | GTATATAT others(3): Show |
2 | a0002c0003t0002g0210a0002c0003t0002g0216 | 2 | HG02738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1466+2046_1466+205 others(14): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803999 | |||||
| chr11:93803999
|
G | GTATATAT others(7): Show |
1 | a0002c0003t0002g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1466+2042_1466+205 others(18): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93803999 | |||||
| chr11:93804003
|
A | G | 2 | a0001c0001t0001g0075a0002c0003t0004g0239 | 2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1466+2031A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804003 | ||||||
| chr11:93804014
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1466+2044_1466+206 others(22): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804014 | |||||
| chr11:93804016
|
TATATATA others(9): Show |
T | 20 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0051others(17): Show | 25 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1466+2046_1466+206 others(20): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804016 | |||||
| chr11:93804018
|
TATATATA others(7): Show |
T | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466+2048_1466+206 others(18): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804018 | |||||
| chr11:93804020
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1466+2048T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804020 | ||||||
| chr11:93804022
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1466+2050T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804022 | ||||||
| chr11:93804022
|
TATATACA others(3): Show |
T | 1 | a0002c0008t0001g0245 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1466+2052_1466+206 others(14): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804022 | |||||
| chr11:93804023
|
A | T | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1466+2051A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804023 | ||||||
| chr11:93804024
|
TATAC | T | 2 | a0002c0003t0002g0013a0002c0003t0002g0214 | 4 | NA18966.hp1 NA18979.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466+2054_1466+205 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804024 | |||||
| chr11:93804026
|
TAC | T | 7 | a0002c0002t0004g0240a0002c0003t0004g0016a0002c0003t0004g0235others(4): Show | 9 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466+2064_1466+206 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804026 | |||||
| chr11:93804026
|
TACAC | T | 36 | a0001c0001t0001g0033a0001c0001t0001g0102a0002c0002t0001g0008others(33): Show | 47 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.1466+2062_1466+206 others(8): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804026 | |||||
| chr11:93804026
|
TACACAC | T | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0106others(7): Show | 10 | HG00621.hp1 HG02165.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1466+2060_1466+206 others(10): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804026 | |||||
| chr11:93804026
|
TACACACA others(1): Show |
T | 5 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(2): Show | 5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1466+2058_1466+206 others(12): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804026 | |||||
| chr11:93804028
|
C | T | 48 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137others(45): Show | 55 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1466+2056C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804028 | ||||||
| chr11:93804030
|
C | T | 18 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137others(15): Show | 20 | HG00741.hp1 HG02040.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1466+2058C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804030 | ||||||
| chr11:93804032
|
C | T | 9 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137others(6): Show | 9 | HG00741.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466+2060C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804032 | ||||||
| chr11:93804033
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1466+2061A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804033 | ||||||
| chr11:93804034
|
C | T | 3 | a0001c0005t0008g0127a0001c0005t0008g0129a0001c0005t0008g0137 | 3 | HG00741.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1466+2062C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804034 | ||||||
| chr11:93804035
|
ACATATAC others(5): Show |
A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1466+2066_1466+207 others(16): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804035 | |||||
| chr11:93804036
|
C | T | 18 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(15): Show | 20 | HG02040.hp2 HG02165.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.1466+2064C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804036 | ||||||
| chr11:93804047
|
G | GCA | 25 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(22): Show | 30 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1466+2088_1466+208 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93804047 | |||||
| chr11:93804132
|
A | G | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466+2160A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804132 | ||||||
| chr11:93804255
|
G | A | 1 | a0002c0008t0001g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1466+2283G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804255 | ||||||
| chr11:93804411
|
C | T | 31 | a0002c0002t0001g0008a0002c0002t0001g0011a0002c0002t0001g0012others(28): Show | 42 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1466+2439C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804411 | ||||||
| chr11:93804413
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1466+2441A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804413 | ||||||
| chr11:93804538
|
G | A | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1466+2566G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804538 | ||||||
| chr11:93804808
|
A | G | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1467-2710A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804808 | ||||||
| chr11:93804845
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1467-2673C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93804845 | ||||||
| chr11:93805028
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1467-2490T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805028 | ||||||
| chr11:93805035
|
A | T | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-2483A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805035 | ||||||
| chr11:93805089
|
T | C | 3 | a0002c0008t0001g0245a0002c0008t0001g0246a0002c0008t0001g0247 | 3 | HG01099.hp2 HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1467-2429T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805089 | ||||||
| chr11:93805191
|
G | C | 1 | a0002c0006t0009g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1467-2327G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805191 | ||||||
| chr11:93805199
|
G | C | 5 | a0001c0017t0009g0047a0002c0006t0009g0146a0002c0006t0011g0024others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467-2319G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805199 | ||||||
| chr11:93805392
|
G | C | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1467-2126G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805392 | ||||||
| chr11:93805429
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1467-2089A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805429 | ||||||
| chr11:93805471
|
C | T | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1467-2047C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805471 | ||||||
| chr11:93805479
|
A | G | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-2039A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805479 | ||||||
| chr11:93805546
|
C | G | 4 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(1): Show | 4 | HG02647.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467-1972C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805546 | ||||||
| chr11:93805562
|
T | C | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1467-1956T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805562 | ||||||
| chr11:93805616
|
T | C | 1 | a0001c0009t0010g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1467-1902T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805616 | ||||||
| chr11:93805785
|
T | G | 2 | a0002c0010t0007g0242a0002c0010t0007g0243 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1467-1733T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805785 | ||||||
| chr11:93805826
|
T | C | 70 | a0001c0001t0001g0095a0001c0001t0001g0115a0001c0016t0002g0038others(67): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1467-1692T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805826 | ||||||
| chr11:93805884
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1467-1634A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805884 | ||||||
| chr11:93805957
|
C | T | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-1561C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93805957 | ||||||
| chr11:93805975
|
C | CT | 10 | a0002c0002t0001g0161a0002c0002t0001g0191a0002c0002t0001g0207others(7): Show | 10 | HG00140.hp1 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1467-1518dupT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93805975 | |||||
| chr11:93805975
|
C | CTT | 18 | a0001c0001t0001g0095a0001c0001t0001g0115a0002c0002t0001g0012others(15): Show | 21 | HG00099.hp1 HG01074.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1467-1519_1467-151 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93805975 | |||||
| chr11:93805975
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1467-1518delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93805975 | |||||
| chr11:93805975
|
CTT | C | 14 | a0001c0001t0001g0070a0001c0001t0001g0090a0001c0001t0023g0082others(11): Show | 14 | HG00741.hp1 HG01243.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.1467-1519_1467-151 others(6): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93805975 | |||||
| chr11:93806029
|
C | T | 1 | a0002c0002t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1467-1489C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806029 | ||||||
| chr11:93806064
|
C | G | 5 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154others(2): Show | 5 | HG02258.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1467-1454C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806064 | ||||||
| chr11:93806136
|
G | A | 1 | a0001c0001t0028g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1467-1382G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806136 | ||||||
| chr11:93806174
|
A | G | 2 | a0002c0010t0007g0242a0002c0010t0007g0243 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1467-1344A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806174 | ||||||
| chr11:93806309
|
T | C | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-1209T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806309 | ||||||
| chr11:93806354
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1467-1164G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806354 | ||||||
| chr11:93806391
|
G | A | 3 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043 | 3 | HG02647.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1467-1127G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806391 | ||||||
| chr11:93806494
|
G | C | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-1024G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806494 | ||||||
| chr11:93806743
|
A | G | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1467-775A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806743 | ||||||
| chr11:93806823
|
C | T | 1 | a0002c0003t0002g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1467-695C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806823 | ||||||
| chr11:93806835
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1467-683G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93806835 | ||||||
| chr11:93807025
|
A | C | 1 | a0002c0002t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1467-493A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807025 | ||||||
| chr11:93807050
|
G | T | 1 | a0001c0001t0017g0133 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1467-468G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807050 | ||||||
| chr11:93807140
|
A | C | 6 | a0001c0009t0001g0044a0001c0009t0010g0042a0001c0009t0010g0043others(3): Show | 6 | HG02615.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1467-378A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807140 | ||||||
| chr11:93807152
|
C | T | 29 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(26): Show | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1467-366C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807152 | ||||||
| chr11:93807185
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1467-333G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807185 | ||||||
| chr11:93807342
|
A | G | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-176A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807342 | ||||||
| chr11:93807344
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0098 | 2 | NA18963.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1467-174C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807344 | ||||||
| chr11:93807390
|
G | GC | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467-127dupC | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 93807390 | |||||
| chr11:93807409
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1467-109T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 9/11 | chr11 | 93807409 | ||||||
| chr11:93807673
|
G | A | 1 | a0002c0002t0001g0193 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1584+38G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807673 | ||||||
| chr11:93807745
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0103 | 2 | NA18946.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1584+110T>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807745 | ||||||
| chr11:93807748
|
T | G | 35 | a0001c0001t0001g0033a0002c0002t0001g0008a0002c0002t0001g0011others(32): Show | 46 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1584+113T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807748 | ||||||
| chr11:93807831
|
C | G | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1584+196C>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807831 | ||||||
| chr11:93807905
|
A | G | 1 | a0002c0003t0002g0223 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1584+270A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807905 | ||||||
| chr11:93807980
|
A | G | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1584+345A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93807980 | ||||||
| chr11:93808112
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1584+477C>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808112 | ||||||
| chr11:93808118
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0068a0001c0001t0001g0096others(7): Show | 10 | HG00408.hp1 HG00673.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1584+483C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808118 | ||||||
| chr11:93808287
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1584+652T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808287 | ||||||
| chr11:93808288
|
G | A | 1 | a0001c0005t0008g0137 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1584+653G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808288 | ||||||
| chr11:93808320
|
T | C | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1584+685T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808320 | ||||||
| chr11:93808369
|
TA | T | 32 | a0001c0001t0001g0055a0001c0001t0028g0081a0001c0005t0006g0036others(29): Show | 34 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1584+757delA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 93808369 | |||||
| chr11:93808369
|
TAA | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1584+756_1584+757d others(4): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 93808369 | |||||
| chr11:93808369
|
TAAA | T | 13 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0091others(10): Show | 14 | HG00733.hp1 HG01081.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1584+755_1584+757d others(5): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 93808369 | |||||
| chr11:93808370
|
A | T | 24 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(21): Show | 33 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1584+735A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808370 | ||||||
| chr11:93808371
|
A | T | 13 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(10): Show | 13 | HG00558.hp2 HG00741.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1584+736A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808371 | ||||||
| chr11:93808372
|
A | T | 3 | a0001c0001t0001g0123a0001c0005t0006g0046a0002c0002t0001g0170 | 3 | HG03041.hp1 HG03239.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1584+737A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808372 | ||||||
| chr11:93808389
|
AAAAGGTG others(8): Show |
A | 1 | a0002c0002t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1584+755_1584+769d others(17): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808389 | ||||||
| chr11:93808424
|
A | C | 1 | a0002c0002t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1584+789A>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808424 | ||||||
| chr11:93808468
|
A | G | 1 | a0001c0001t0001g0023 | 2 | HG00438.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1584+833A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808468 | ||||||
| chr11:93808591
|
T | TA | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+964dupA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 93808591 | |||||
| chr11:93808753
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1585-964T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808753 | ||||||
| chr11:93808869
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1585-848A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93808869 | ||||||
| chr11:93809226
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1585-491C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809226 | ||||||
| chr11:93809295
|
C | T | 14 | a0002c0004t0003g0026a0002c0004t0003g0027a0002c0004t0003g0028others(11): Show | 16 | HG02040.hp2 HG02165.hp2 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.1585-422C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809295 | ||||||
| chr11:93809343
|
G | T | 1 | a0002c0002t0001g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1585-374G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809343 | ||||||
| chr11:93809358
|
C | T | 1 | a0002c0002t0001g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1585-359C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809358 | ||||||
| chr11:93809418
|
T | TA | 8 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0100others(5): Show | 11 | HG00438.hp2 HG01081.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-298dupA | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 93809418 | |||||
| chr11:93809548
|
G | A | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585-169G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809548 | ||||||
| chr11:93809627
|
C | T | 1 | a0002c0006t0012g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1585-90C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809627 | ||||||
| chr11:93809646
|
C | T | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1585-71C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 10/11 | chr11 | 93809646 | ||||||
| chr11:93809932
|
T | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0087others(3): Show | 8 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1744+56T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93809932 | ||||||
| chr11:93810023
|
G | A | 1 | a0002c0002t0025g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1744+147G>A | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810023 | ||||||
| chr11:93810054
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1744+178T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810054 | ||||||
| chr11:93810127
|
C | T | 1 | a0002c0006t0011g0024 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1744+251C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810127 | ||||||
| chr11:93810178
|
AT | A | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+303delT | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810178 | ||||||
| chr11:93810401
|
C | T | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+525C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810401 | ||||||
| chr11:93810439
|
T | G | 6 | a0001c0001t0001g0083a0001c0009t0001g0044a0002c0010t0007g0242others(3): Show | 6 | HG02615.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1744+563T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810439 | ||||||
| chr11:93810475
|
G | C | 29 | a0001c0016t0002g0038a0002c0003t0002g0009a0002c0003t0002g0013others(26): Show | 36 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1744+599G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810475 | ||||||
| chr11:93810514
|
C | T | 2 | a0002c0002t0001g0207a0004c0015t0001g0206 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1744+638C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810514 | ||||||
| chr11:93810606
|
G | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1744+730G>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810606 | ||||||
| chr11:93810699
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1744+823G>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810699 | ||||||
| chr11:93810747
|
T | C | 8 | a0001c0005t0006g0036a0001c0005t0006g0037a0001c0005t0006g0045others(5): Show | 8 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+871T>C | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810747 | ||||||
| chr11:93810971
|
C | T | 2 | a0002c0002t0001g0190a0002c0002t0001g0191 | 2 | HG01123.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1745-882C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93810971 | ||||||
| chr11:93811009
|
C | T | 35 | a0001c0001t0001g0033a0002c0002t0001g0008a0002c0002t0001g0011others(32): Show | 46 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1745-844C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811009 | ||||||
| chr11:93811076
|
C | T | 46 | a0001c0001t0001g0033a0001c0009t0001g0044a0002c0002t0001g0008others(43): Show | 58 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.1745-777C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811076 | ||||||
| chr11:93811226
|
A | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG00621.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1745-627A>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811226 | ||||||
| chr11:93811396
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1745-457C>T | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811396 | ||||||
| chr11:93811750
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1745-103A>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811750 | ||||||
| chr11:93811781
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1745-72T>G | MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 11/11 | chr11 | 93811781 |