Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80306 |
| ensemblid | ENSG00000118579.13 |
| hgncid | 24628 |
| symbol | MED28 |
| name | mediator complex subunit 28 |
| refseq_nuc | NM_025205.5 |
| refseq_prot | NP_079481.2 |
| ensembl_nuc | ENST00000237380.12 |
| ensembl_prot | ENSP00000237380.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 17614641 |
| end | 17634105 |
| strand | + |
| ver | v1.2 |
| region | chr4:17614641-17634105 |
| region5000 | chr4:17609641-17639105 |
| regionname0 | MED28_chr4_17614641_17634105 |
| regionname5000 | MED28_chr4_17609641_17639105 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 534 | 322 | 94 | 70 | 104 | 14 | 38 | MED28_chr4_17609641_17639105 | MED28 | ATGGC others(529): Show |
chr4 | 17609641 | 17639105 | ||
| a0001c0002 | 0/0 | 534 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | ATGGC others(529): Show |
chr4 | 17609641 | 17639105 | ||
| a0001c0003 | 0/0 | 534 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | ATGGC others(529): Show |
chr4 | 17609641 | 17639105 | ||
| a0001c0004 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | ATGGC others(529): Show |
chr4 | 17609641 | 17639105 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10854 | 45 | 1 | 15 | 23 | 1 | 5 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0002 | 0/0 | 10858 | 26 | 3 | 7 | 10 | 2 | 4 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0003 | 0/0 | 10860 | 16 | 5 | 7 | 1 | 1 | 2 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0004 | 0/0 | 10862 | 14 | 0 | 5 | 3 | 3 | 3 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0005 | 0/0 | 10856 | 12 | 1 | 4 | 5 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0006 | 0/0 | 10847 | 11 | 0 | 0 | 9 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10842): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0007 | 0/0 | 10860 | 10 | 0 | 5 | 3 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0008 | 0/0 | 10867 | 9 | 9 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10862): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0009 | 0/0 | 10860 | 8 | 8 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0010 | 0/0 | 10859 | 7 | 0 | 1 | 6 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0011 | 0/0 | 10854 | 6 | 3 | 1 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0012 | 0/0 | 10864 | 5 | 3 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0013 | 0/0 | 10858 | 5 | 0 | 0 | 4 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0014 | 0/0 | 10850 | 5 | 0 | 3 | 1 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10845): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0015 | 0/0 | 10860 | 4 | 4 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0016 | 0/0 | 10862 | 4 | 0 | 0 | 3 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0017 | 0/0 | 10840 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10835): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0018 | 0/0 | 10860 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0019 | 0/0 | 10849 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10844): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0020 | 0/0 | 10852 | 3 | 0 | 2 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10847): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0022 | 0/0 | 10840 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10835): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0023 | 0/0 | 10862 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0024 | 0/0 | 10862 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0025 | 0/0 | 10862 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0026 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0027 | 0/0 | 10846 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10841): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0028 | 0/0 | 10847 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10842): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0029 | 0/0 | 10848 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10843): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0030 | 0/0 | 10850 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10845): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0031 | 0/0 | 10856 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0032 | 0/0 | 10854 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0033 | 0/0 | 10856 | 2 | 0 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0034 | 0/0 | 10858 | 2 | 0 | 1 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0035 | 0/0 | 10858 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0036 | 0/0 | 10854 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0037 | 0/0 | 10856 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0038 | 0/0 | 10840 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10835): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0039 | 0/0 | 10841 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10836): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0040 | 0/0 | 10840 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10835): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0041 | 0/0 | 10906 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10901): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0042 | 0/0 | 10860 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0043 | 0/0 | 10831 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10826): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0044 | 0/0 | 10860 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0045 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0046 | 0/0 | 10859 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0047 | 0/0 | 10859 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0048 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0049 | 0/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0050 | 0/0 | 10858 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0051 | 0/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0052 | 1/0 | 10858 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0053 | 0/0 | 10858 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0054 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0055 | 0/0 | 10860 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0056 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0057 | 0/0 | 10862 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0058 | 0/0 | 10862 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0059 | 0/0 | 10862 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0060 | 0/0 | 10864 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0061 | 0/0 | 10864 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0062 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0063 | 0/0 | 10859 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0064 | 0/0 | 10861 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10856): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0065 | 0/0 | 10846 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10841): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0066 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0067 | 0/0 | 10856 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0068 | 0/0 | 10862 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0069 | 0/0 | 10846 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10841): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0070 | 0/0 | 10852 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10847): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0071 | 0/0 | 10858 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0072 | 0/0 | 10862 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0073 | 0/0 | 10857 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10852): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0074 | 0/0 | 10869 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10864): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0075 | 0/0 | 10860 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0076 | 0/0 | 10848 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10843): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0077 | 0/0 | 10849 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10844): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0078 | 0/0 | 10867 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10862): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0079 | 0/0 | 10869 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10864): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0080 | 0/0 | 10861 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10856): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0081 | 0/0 | 10854 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0082 | 0/0 | 10860 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0083 | 0/0 | 10864 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0084 | 0/0 | 10855 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10850): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0085 | 0/0 | 10859 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0086 | 0/0 | 10859 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0087 | 0/0 | 10860 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0088 | 0/0 | 10864 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0089 | 0/0 | 10882 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10877): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0090 | 0/0 | 10884 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10879): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0091 | 0/0 | 10858 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10853): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0092 | 0/0 | 10853 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10848): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0093 | 0/0 | 10856 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0094 | 0/0 | 10842 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10837): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0095 | 0/0 | 10850 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10845): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0096 | 0/0 | 10850 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10845): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0097 | 0/0 | 10852 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10847): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0098 | 0/0 | 10853 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10848): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0099 | 0/0 | 10854 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0100 | 0/0 | 10854 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0101 | 0/0 | 10854 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0102 | 0/0 | 10854 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0103 | 0/0 | 10856 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0104 | 0/0 | 10856 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0105 | 0/1 | 10829 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10824): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0106 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0107 | 0/0 | 10860 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0108 | 0/0 | 10860 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0109 | 0/0 | 10860 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0110 | 0/0 | 10862 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10857): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0111 | 0/0 | 10864 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0112 | 0/0 | 10866 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10861): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0114 | 0/0 | 10861 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10856): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0115 | 0/0 | 10854 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0116 | 0/0 | 10860 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10855): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0117 | 0/0 | 10856 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0118 | 0/0 | 10848 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10843): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0119 | 0/0 | 10848 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10843): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0120 | 0/0 | 10850 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10845): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0121 | 0/0 | 10843 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10838): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0122 | 0/0 | 10864 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10859): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0123 | 0/0 | 10859 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10854): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0124 | 0/0 | 10861 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10856): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0125 | 0/0 | 10861 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10856): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0126 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0127 | 0/0 | 10881 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10876): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0128 | 0/0 | 10885 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10880): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0129 | 0/0 | 10883 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10878): Show |
chr4 | 17609641 | 17639105 |
| a0001c0001t0130 | 0/0 | 10889 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10884): Show |
chr4 | 17609641 | 17639105 |
| a0001c0002t0021 | 0/0 | 10857 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10852): Show |
chr4 | 17609641 | 17639105 |
| a0001c0002t0113 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10858): Show |
chr4 | 17609641 | 17639105 |
| a0001c0003t0001 | 0/0 | 10854 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10849): Show |
chr4 | 17609641 | 17639105 |
| a0001c0003t0005 | 0/0 | 10856 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10851): Show |
chr4 | 17609641 | 17639105 |
| a0001c0004t0021 | 0/0 | 10857 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | GCGCC others(10852): Show |
chr4 | 17609641 | 17639105 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 1 | 8 | 11 | 1 | 4 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0001 | 0/0 | 11 | 1 | 0 | 9 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0002 | 0/0 | 7 | 2 | 2 | 1 | 1 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0002 | 0/0 | 9 | 0 | 3 | 2 | 2 | 2 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0001 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0006g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0006g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0007g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0007g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0008g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0009g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0010g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0011g0001 | 0/0 | 5 | 3 | 1 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0012g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0012g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0013g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0014g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0015g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0016g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0016g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0018g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0019g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0019g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0020g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0020g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0022g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0022g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0023g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0024g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0025g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0026g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0026g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0027g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0028g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0029g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0030g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0031g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0032g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0033g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0033g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0034g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0034g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0035g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0035g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0036g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0038g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0039g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0040g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0041g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0042g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0043g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0044g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0045g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0046g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0047g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0048g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0049g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0050g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0051g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0052g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0053g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0054g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0055g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0056g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0057g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0058g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0059g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0060g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0061g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0062g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0063g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0064g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0065g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0066g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0067g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0068g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0069g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0070g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0071g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0072g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0073g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0074g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0075g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0076g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0077g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0078g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0079g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0080g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0081g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0082g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0083g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0084g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0085g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0086g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0087g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0088g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0089g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0090g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0091g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0092g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0093g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0094g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0095g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0096g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0097g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0098g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0099g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0100g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0101g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0102g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0103g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0104g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0105g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0106g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0107g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0108g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0109g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0110g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0111g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0112g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0114g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0115g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0116g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0117g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0118g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0119g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0120g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0121g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0122g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0123g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0124g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0125g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0126g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0127g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0128g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0129g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0001t0130g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0002t0021g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0002t0113g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0003t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| a0001c0004t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0032 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0001 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0046 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | FIN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00423 | hp1 | a0001 | c0001 | t0024 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00438 | hp2 | a0001 | c0001 | t0112 | g0010 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00544 | hp1 | a0001 | c0001 | t0107 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00597 | hp2 | a0001 | c0001 | t0055 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00609 | hp2 | a0001 | c0001 | t0053 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00621 | hp1 | a0001 | c0001 | t0032 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00642 | hp1 | a0001 | c0001 | t0097 | g0005 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00673 | hp1 | a0001 | c0001 | t0047 | g0002 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0005 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01069 | hp1 | a0001 | c0001 | t0014 | g0005 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01069 | hp2 | a0001 | c0001 | t0020 | g0013 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01071 | hp2 | a0001 | c0001 | t0020 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01081 | hp1 | a0001 | c0001 | t0023 | g0002 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01109 | hp1 | a0001 | c0001 | t0029 | g0014 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0003 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01192 | hp2 | a0001 | c0001 | t0094 | g0010 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01243 | hp1 | a0001 | c0001 | t0119 | g0023 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01243 | hp2 | a0001 | c0001 | t0065 | g0096 | AMR | PUR | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01255 | hp2 | a0001 | c0001 | t0044 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01261 | hp1 | a0001 | c0001 | t0034 | g0045 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01261 | hp2 | a0001 | c0001 | t0093 | g0001 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01358 | hp2 | a0001 | c0001 | t0023 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0002 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01433 | hp2 | a0001 | c0001 | t0014 | g0018 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01496 | hp1 | a0001 | c0001 | t0096 | g0008 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0032 | EUR | IBS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01516 | hp2 | a0001 | c0001 | t0014 | g0005 | EUR | IBS | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01884 | hp1 | a0001 | c0001 | t0062 | g0085 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01884 | hp2 | a0001 | c0001 | t0029 | g0014 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01952 | hp1 | a0001 | c0001 | t0019 | g0003 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01975 | hp2 | a0001 | c0001 | t0100 | g0035 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02015 | hp1 | a0001 | c0001 | t0014 | g0047 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02015 | hp2 | a0001 | c0001 | t0084 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02027 | hp1 | a0001 | c0001 | t0032 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02027 | hp2 | a0001 | c0001 | t0060 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02074 | hp1 | a0001 | c0001 | t0082 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02129 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02132 | hp1 | a0001 | c0001 | t0059 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02135 | hp1 | a0001 | c0001 | t0061 | g0002 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02135 | hp2 | a0001 | c0001 | t0104 | g0018 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02145 | hp2 | a0001 | c0001 | t0043 | g0062 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02148 | hp1 | a0001 | c0001 | t0101 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | CDX | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02257 | hp1 | a0001 | c0001 | t0122 | g0061 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02258 | hp2 | a0001 | c0001 | t0078 | g0003 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02280 | hp1 | a0001 | c0001 | t0088 | g0011 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02280 | hp2 | a0001 | c0001 | t0028 | g0014 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02293 | hp2 | a0001 | c0001 | t0025 | g0002 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02300 | hp1 | a0001 | c0001 | t0091 | g0039 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02300 | hp2 | a0001 | c0001 | t0011 | g0001 | AMR | PEL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0067 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02451 | hp2 | a0001 | c0001 | t0129 | g0029 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02572 | hp2 | a0001 | c0001 | t0121 | g0070 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0050 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02615 | hp1 | a0001 | c0001 | t0118 | g0036 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02615 | hp2 | a0001 | c0001 | t0066 | g0022 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02622 | hp2 | a0001 | c0001 | t0046 | g0030 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02630 | hp1 | a0001 | c0001 | t0038 | g0019 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0014 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02647 | hp2 | a0001 | c0001 | t0048 | g0030 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02698 | hp1 | a0001 | c0001 | t0049 | g0082 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02698 | hp2 | a0001 | c0001 | t0109 | g0025 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02717 | hp2 | a0001 | c0001 | t0108 | g0043 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0002 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02886 | hp1 | a0001 | c0001 | t0042 | g0076 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02895 | hp2 | a0001 | c0001 | t0120 | g0023 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02896 | hp2 | a0001 | c0001 | t0090 | g0011 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02897 | hp2 | a0001 | c0001 | t0089 | g0011 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02922 | hp1 | a0001 | c0001 | t0068 | g0097 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02970 | hp1 | a0001 | c0002 | t0113 | g0012 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02970 | hp2 | a0001 | c0001 | t0041 | g0090 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0002 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02976 | hp2 | a0001 | c0002 | t0021 | g0012 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03017 | hp2 | a0001 | c0001 | t0124 | g0069 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03041 | hp1 | a0001 | c0002 | t0021 | g0012 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03041 | hp2 | a0001 | c0001 | t0086 | g0011 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03098 | hp2 | a0001 | c0001 | t0127 | g0028 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03130 | hp1 | a0001 | c0001 | t0050 | g0002 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03130 | hp2 | a0001 | c0004 | t0021 | g0012 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0078 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03139 | hp2 | a0001 | c0001 | t0063 | g0004 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0058 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03209 | hp2 | a0001 | c0001 | t0130 | g0029 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03225 | hp1 | a0001 | c0001 | t0064 | g0004 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03225 | hp2 | a0001 | c0001 | t0040 | g0019 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03239 | hp1 | a0001 | c0001 | t0033 | g0025 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03453 | hp1 | a0001 | c0001 | t0031 | g0001 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03486 | hp1 | a0001 | c0001 | t0069 | g0022 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0064 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03490 | hp2 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03491 | hp1 | a0001 | c0001 | t0035 | g0027 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03492 | hp1 | a0001 | c0001 | t0030 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03492 | hp2 | a0001 | c0001 | t0035 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03540 | hp1 | a0001 | c0001 | t0128 | g0028 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03579 | hp1 | a0001 | c0001 | t0039 | g0065 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03579 | hp2 | a0001 | c0001 | t0070 | g0015 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03654 | hp1 | a0001 | c0001 | t0125 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03654 | hp2 | a0001 | c0001 | t0117 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03710 | hp2 | a0001 | c0001 | t0126 | g0002 | SAS | PJL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03831 | hp1 | a0001 | c0001 | t0106 | g0001 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0074 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03927 | hp2 | a0001 | c0001 | t0095 | g0005 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03942 | hp1 | a0001 | c0001 | t0051 | g0002 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0001 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04184 | hp2 | a0001 | c0001 | t0054 | g0002 | SAS | BEB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0003 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04199 | hp2 | a0001 | c0001 | t0056 | g0002 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG04228 | hp2 | a0001 | c0001 | t0057 | g0002 | SAS | STU | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0063 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18612 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | CHB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | CHB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18906 | hp1 | a0001 | c0001 | t0074 | g0015 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0002 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18939 | hp1 | a0001 | c0001 | t0123 | g0068 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18945 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18946 | hp1 | a0001 | c0001 | t0115 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18947 | hp1 | a0001 | c0001 | t0036 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18950 | hp1 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0098 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18963 | hp1 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18978 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18979 | hp1 | a0001 | c0001 | t0116 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18982 | hp1 | a0001 | c0001 | t0102 | g0048 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18991 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18991 | hp2 | a0001 | c0001 | t0110 | g0044 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18993 | hp2 | a0001 | c0001 | t0036 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18998 | hp2 | a0001 | c0001 | t0077 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19000 | hp2 | a0001 | c0001 | t0027 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19004 | hp2 | a0001 | c0001 | t0081 | g0009 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19010 | hp2 | a0001 | c0001 | t0103 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19012 | hp2 | a0001 | c0001 | t0027 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19030 | hp1 | a0001 | c0001 | t0080 | g0073 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0066 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19043 | hp1 | a0001 | c0001 | t0073 | g0092 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19043 | hp2 | a0001 | c0001 | t0071 | g0095 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19056 | hp1 | a0001 | c0001 | t0076 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19056 | hp2 | a0001 | c0001 | t0098 | g0009 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19057 | hp1 | a0001 | c0001 | t0085 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19068 | hp1 | a0001 | c0001 | t0099 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19079 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19081 | hp1 | a0001 | c0001 | t0114 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19085 | hp1 | a0001 | c0001 | t0092 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19087 | hp2 | a0001 | c0001 | t0045 | g0002 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19088 | hp2 | a0001 | c0003 | t0005 | g0001 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20129 | hp1 | a0001 | c0001 | t0087 | g0011 | AFR | ASW | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ASW | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0089 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20805 | hp2 | a0001 | c0001 | t0034 | g0008 | EUR | TSI | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01123 | hp1 | a0001 | c0001 | t0033 | g0055 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0006 | AMR | CLM | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0015 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02486 | hp2 | a0001 | c0001 | t0111 | g0001 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02559 | hp1 | a0001 | c0001 | t0079 | g0003 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG02559 | hp2 | a0001 | c0001 | t0072 | g0094 | AFR | ACB | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03471 | hp1 | a0001 | c0001 | t0058 | g0031 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0019 | AFR | MSL | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| HG06807 | hp2 | a0001 | c0001 | t0026 | g0093 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA18955 | hp2 | a0001 | c0001 | t0016 | g0010 | EAS | JPT | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA20300 | hp2 | a0001 | c0001 | t0067 | g0022 | AFR | USA | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA21309 | hp1 | a0001 | c0001 | t0075 | g0015 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| NA21309 | hp2 | a0001 | c0001 | t0083 | g0052 | AFR | LWK | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0105 | g0038 | REF | REF | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0052 | g0031 | REF | REF | MED28_chr4_17609641_17639105 | MED28 | chr4 | 17609641 | 17639105 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17614663 | T | C | 1 | a0001c0003 | 2 | NA18959.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.9T>C | p.Ala3Ala | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/4 | 23/10858 | 9/537 | 3/178 | chr4 | 17614663 | |||
| chr4:17614726 | G | A | 2 | a0001c0002 a0001c0004 |
4 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.72G>A | p.Pro24Pro | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/4 | 86/10858 | 72/537 | 24/178 | chr4 | 17614726 | |||
| chr4:17619930 | C | T | 1 | a0001c0004 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.189C>T | p.Asp63Asp | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/4 | 203/10858 | 189/537 | 63/178 | chr4 | 17619930 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17623888 | C | A | 1 | a0001c0001t0037 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 90 | chr4 | 17623888 | ||||||
| chr4:17624015 | A | AT | 13 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 others(10): Show |
13 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*227dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 228 | INFO_REALIGN_3_PRIME | chr4 | 17624015 | |||||
| chr4:17624035 | A | G | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(59): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*237A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 237 | chr4 | 17624035 | ||||||
| chr4:17624125 | G | A | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*327G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 327 | chr4 | 17624125 | ||||||
| chr4:17624168 | C | T | 11 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0019 others(8): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*370C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 370 | chr4 | 17624168 | ||||||
| chr4:17624184 | T | C | 3 | a0001c0001t0012 a0001c0001t0041 a0001c0001t0042 |
7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*386T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 386 | chr4 | 17624184 | ||||||
| chr4:17624236 | A | G | 6 | a0001c0001t0008 a0001c0001t0028 a0001c0001t0029 others(3): Show |
16 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*438A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 438 | chr4 | 17624236 | ||||||
| chr4:17624272 | C | T | 12 | a0001c0001t0026 a0001c0001t0065 a0001c0001t0066 others(9): Show |
13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*474C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 474 | chr4 | 17624272 | ||||||
| chr4:17624360 | G | A | 3 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*562G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 562 | chr4 | 17624360 | ||||||
| chr4:17624374 | G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 576 | chr4 | 17624374 | ||||||
| chr4:17624471 | G | C | 1 | a0001c0001t0065 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*673G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 673 | chr4 | 17624471 | ||||||
| chr4:17624551 | T | A | 90 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(87): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*753T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 753 | chr4 | 17624551 | ||||||
| chr4:17624554 | CTG | C | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(60): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*758_*759delGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 758 | INFO_REALIGN_3_PRIME | chr4 | 17624554 | |||||
| chr4:17624633 | T | G | 1 | a0001c0001t0121 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*835T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 835 | chr4 | 17624633 | ||||||
| chr4:17624646 | C | T | 7 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(4): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 848 | chr4 | 17624646 | ||||||
| chr4:17624674 | G | T | 1 | a0001c0001t0124 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*876G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 876 | chr4 | 17624674 | ||||||
| chr4:17624740 | C | T | 1 | a0001c0001t0040 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 942 | chr4 | 17624740 | ||||||
| chr4:17624760 | G | A | 5 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0027 others(2): Show |
18 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*962G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 962 | chr4 | 17624760 | ||||||
| chr4:17624795 | G | A | 101 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(98): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 997 | chr4 | 17624795 | ||||||
| chr4:17624861 | A | T | 1 | a0001c0001t0036 | 2 | NA18947.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1063A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1063 | chr4 | 17624861 | ||||||
| chr4:17624930 | A | G | 3 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1132A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1132 | chr4 | 17624930 | ||||||
| chr4:17625097 | C | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1299C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1299 | chr4 | 17625097 | ||||||
| chr4:17625172 | G | C | 1 | a0001c0001t0081 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1374G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1374 | chr4 | 17625172 | ||||||
| chr4:17625223 | G | A | 1 | a0001c0001t0023 | 2 | HG01081.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1425G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1425 | chr4 | 17625223 | ||||||
| chr4:17625575 | C | T | 1 | a0001c0001t0117 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1777C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1777 | chr4 | 17625575 | ||||||
| chr4:17625576 | G | A | 4 | a0001c0001t0127 a0001c0001t0128 a0001c0001t0129 others(1): Show |
4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1778 | chr4 | 17625576 | ||||||
| chr4:17625671 | A | G | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(40): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1873A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1873 | chr4 | 17625671 | ||||||
| chr4:17625709 | T | C | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(84): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1911T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 1911 | chr4 | 17625709 | ||||||
| chr4:17625850 | G | A | 1 | a0001c0001t0091 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2052 | chr4 | 17625850 | ||||||
| chr4:17625962 | C | A | 1 | a0001c0001t0044 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2164 | chr4 | 17625962 | ||||||
| chr4:17626053 | C | T | 11 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0019 others(8): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2255C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2255 | chr4 | 17626053 | ||||||
| chr4:17626092 | C | G | 2 | a0001c0001t0115 a0001c0001t0116 |
2 | NA18946.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2294C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2294 | chr4 | 17626092 | ||||||
| chr4:17626131 | G | T | 6 | a0001c0001t0075 a0001c0001t0086 a0001c0001t0087 others(3): Show |
6 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2333G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2333 | chr4 | 17626131 | ||||||
| chr4:17626147 | G | T | 4 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0063 others(1): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2349G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2349 | chr4 | 17626147 | ||||||
| chr4:17626233 | G | A | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(60): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*2435G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2435 | chr4 | 17626233 | ||||||
| chr4:17626328 | G | A | 3 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2530 | chr4 | 17626328 | ||||||
| chr4:17626413 | T | C | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2615T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2615 | chr4 | 17626413 | ||||||
| chr4:17626460 | G | C | 2 | a0001c0001t0024 a0001c0001t0045 |
3 | HG00423.hp1 NA18950.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2662G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2662 | chr4 | 17626460 | ||||||
| chr4:17626524 | T | C | 1 | a0001c0001t0122 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2726 | chr4 | 17626524 | ||||||
| chr4:17626663 | C | A | 4 | a0001c0001t0127 a0001c0001t0128 a0001c0001t0129 others(1): Show |
4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2865C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2865 | chr4 | 17626663 | ||||||
| chr4:17626678 | C | CT | 11 | a0001c0001t0026 a0001c0001t0043 a0001c0001t0065 others(8): Show |
12 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2890dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2891 | INFO_REALIGN_3_PRIME | chr4 | 17626678 | |||||
| chr4:17626758 | T | C | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2960T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 2960 | chr4 | 17626758 | ||||||
| chr4:17626805 | C | T | 7 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(4): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3007C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3007 | chr4 | 17626805 | ||||||
| chr4:17626951 | A | G | 4 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0063 others(1): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3153A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3153 | chr4 | 17626951 | ||||||
| chr4:17626963 | A | AT | 15 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(12): Show |
47 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3184dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3185 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | |||||
| chr4:17626963 | AT | A | 16 | a0001c0001t0010 a0001c0001t0046 a0001c0001t0047 others(13): Show |
23 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3184delT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3184 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | |||||
| chr4:17626963 | ATT | A | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(63): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*3183_*3184delTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3183 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | |||||
| chr4:17626963 | ATTT | A | 6 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(3): Show |
9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3182_*3184delTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3182 | INFO_REALIGN_3_PRIME | chr4 | 17626963 | |||||
| chr4:17627007 | C | G | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(72): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*3209C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3209 | chr4 | 17627007 | ||||||
| chr4:17627064 | A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3266 | chr4 | 17627064 | ||||||
| chr4:17627073 | C | G | 1 | a0001c0001t0065 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3275C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3275 | chr4 | 17627073 | ||||||
| chr4:17627107 | C | T | 4 | a0001c0001t0121 a0001c0001t0122 a0001c0001t0123 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3309C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3309 | chr4 | 17627107 | ||||||
| chr4:17627115 | C | T | 1 | a0001c0001t0085 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3317C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3317 | chr4 | 17627115 | ||||||
| chr4:17627146 | T | C | 105 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(102): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*3348T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3348 | chr4 | 17627146 | ||||||
| chr4:17627164 | G | C | 7 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 others(4): Show |
7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3366G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3366 | chr4 | 17627164 | ||||||
| chr4:17627167 | A | G | 4 | a0001c0001t0121 a0001c0001t0122 a0001c0001t0123 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3369A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3369 | chr4 | 17627167 | ||||||
| chr4:17627196 | G | A | 3 | a0001c0001t0012 a0001c0001t0041 a0001c0001t0042 |
7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3398G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3398 | chr4 | 17627196 | ||||||
| chr4:17627243 | G | A | 5 | a0001c0001t0032 a0001c0001t0121 a0001c0001t0122 others(2): Show |
6 | HG00621.hp1 HG02027.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3445G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3445 | chr4 | 17627243 | ||||||
| chr4:17627334 | T | C | 2 | a0001c0001t0091 a0001c0001t0093 |
2 | HG01261.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3536T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3536 | chr4 | 17627334 | ||||||
| chr4:17627364 | A | G | 1 | a0001c0001t0035 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3566A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3566 | chr4 | 17627364 | ||||||
| chr4:17627475 | CTG | C | 11 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0019 others(8): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3679_*3680delGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3679 | INFO_REALIGN_3_PRIME | chr4 | 17627475 | |||||
| chr4:17627536 | G | A | 2 | a0001c0001t0127 a0001c0001t0128 |
2 | HG03098.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3738 | chr4 | 17627536 | ||||||
| chr4:17627626 | C | G | 1 | a0001c0001t0043 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3828C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3828 | chr4 | 17627626 | ||||||
| chr4:17627719 | C | A | 3 | a0001c0001t0012 a0001c0001t0041 a0001c0001t0042 |
7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3921C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3921 | chr4 | 17627719 | ||||||
| chr4:17627722 | A | G | 6 | a0001c0001t0012 a0001c0001t0041 a0001c0001t0042 others(3): Show |
10 | HG00099.hp2 HG01243.hp1 HG01516.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3924A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3924 | chr4 | 17627722 | ||||||
| chr4:17627739 | G | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3941G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 3941 | chr4 | 17627739 | ||||||
| chr4:17627926 | G | C | 5 | a0001c0001t0065 a0001c0001t0066 a0001c0001t0067 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4128G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4128 | chr4 | 17627926 | ||||||
| chr4:17627941 | A | G | 1 | a0001c0001t0124 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4143A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4143 | chr4 | 17627941 | ||||||
| chr4:17627943 | C | T | 1 | a0001c0001t0080 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4145C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4145 | chr4 | 17627943 | ||||||
| chr4:17628121 | A | G | 2 | a0001c0001t0123 a0001c0001t0124 |
2 | HG03017.hp2 NA18939.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4323A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4323 | chr4 | 17628121 | ||||||
| chr4:17628175 | G | A | 5 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0027 others(2): Show |
18 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4377G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4377 | chr4 | 17628175 | ||||||
| chr4:17628249 | A | G | 3 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4451A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4451 | chr4 | 17628249 | ||||||
| chr4:17628255 | C | CGT | 16 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0020 others(13): Show |
35 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4492_*4493dupGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGT | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(23): Show |
101 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4490_*4493dupGTGT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGT | 17 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0033 others(14): Show |
31 | HG00323.hp2 HG00621.hp2 HG01123.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4488_*4493dupGTGT others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(1): Show |
10 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0013 others(7): Show |
47 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4486_*4493dupGTGT others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(3): Show |
12 | a0001c0001t0007 a0001c0001t0026 a0001c0001t0072 others(9): Show |
22 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4484_*4493dupGTGT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(5): Show |
3 | a0001c0001t0016 a0001c0001t0110 a0001c0002t0113 |
6 | HG00140.hp1 HG02970.hp1 NA18945.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4482_*4493dupGTGT others(8): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(7): Show |
3 | a0001c0001t0083 a0001c0001t0088 a0001c0001t0111 |
3 | HG02280.hp1 HG02486.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4480_*4493dupGTGT others(10): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0074 a0001c0001t0112 |
2 | HG00438.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4478_*4493dupGTGT others(12): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(23): Show |
1 | a0001c0001t0127 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4464_*4493dupGTGT others(26): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(25): Show |
2 | a0001c0001t0089 a0001c0001t0129 |
2 | HG02451.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4462_*4493dupGTGT others(28): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(27): Show |
2 | a0001c0001t0090 a0001c0001t0128 |
2 | HG02896.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4460_*4493dupGTGT others(30): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | C | CGTGTGTG others(31): Show |
1 | a0001c0001t0130 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4493_*4494insGTGT others(34): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | CGTGTGTG others(1): Show |
C | 10 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0022 others(7): Show |
15 | HG01123.hp2 HG01192.hp1 HG01192.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4486_*4493delGTGT others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4486 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | CGTGTGTG others(3): Show |
C | 7 | a0001c0001t0006 a0001c0001t0027 a0001c0001t0028 others(4): Show |
20 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4484_*4493delGTGT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4484 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628255 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0121 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4476_*4493delGTGT others(14): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4476 | INFO_REALIGN_3_PRIME | chr4 | 17628255 | |||||
| chr4:17628280 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4493_*4494insGTGT others(18): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | INFO_REALIGN_3_PRIME | chr4 | 17628280 | |||||
| chr4:17628282 | G | A | 2 | a0001c0001t0012 a0001c0001t0042 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4484G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4484 | chr4 | 17628282 | ||||||
| chr4:17628290 | G | A | 1 | a0001c0001t0019 | 3 | HG01123.hp2 HG01192.hp1 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4492G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4492 | chr4 | 17628290 | ||||||
| chr4:17628292 | A | G | 2 | a0001c0001t0012 a0001c0001t0042 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4494A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4494 | chr4 | 17628292 | ||||||
| chr4:17628307 | T | C | 1 | a0001c0001t0099 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4509T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4509 | chr4 | 17628307 | ||||||
| chr4:17628316 | A | G | 74 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(71): Show |
196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*4518A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4518 | chr4 | 17628316 | ||||||
| chr4:17628326 | GTA | G | 6 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(3): Show |
9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4538_*4539delAT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4538 | INFO_REALIGN_3_PRIME | chr4 | 17628326 | |||||
| chr4:17628328 | A | G | 1 | a0001c0001t0003 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4530A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4530 | chr4 | 17628328 | ||||||
| chr4:17628332 | A | G | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4534A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4534 | chr4 | 17628332 | ||||||
| chr4:17628334 | A | G | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4536A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4536 | chr4 | 17628334 | ||||||
| chr4:17628336 | A | G | 2 | a0001c0001t0012 a0001c0001t0041 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4538A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4538 | chr4 | 17628336 | ||||||
| chr4:17628342 | G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4544G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4544 | chr4 | 17628342 | ||||||
| chr4:17628344 | G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4546G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4546 | chr4 | 17628344 | ||||||
| chr4:17628344 | G | GTATA | 1 | a0001c0001t0012 | 5 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4547_*4548insATAT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4548 | INFO_REALIGN_3_PRIME | chr4 | 17628344 | |||||
| chr4:17628346 | G | A | 2 | a0001c0001t0012 a0001c0001t0041 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4548G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4548 | chr4 | 17628346 | ||||||
| chr4:17628451 | G | A | 1 | a0001c0001t0060 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4653G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4653 | chr4 | 17628451 | ||||||
| chr4:17628461 | T | C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4663T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4663 | chr4 | 17628461 | ||||||
| chr4:17628462 | CACTTCCT others(3): Show |
C | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4666_*4675delCTTC others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4666 | INFO_REALIGN_3_PRIME | chr4 | 17628462 | |||||
| chr4:17628474 | A | G | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4676A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4676 | chr4 | 17628474 | ||||||
| chr4:17628487 | G | T | 1 | a0001c0001t0122 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4689G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4689 | chr4 | 17628487 | ||||||
| chr4:17628492 | G | A | 101 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(98): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*4694G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4694 | chr4 | 17628492 | ||||||
| chr4:17628539 | A | G | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4741A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4741 | chr4 | 17628539 | ||||||
| chr4:17628569 | G | T | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(60): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*4771G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4771 | chr4 | 17628569 | ||||||
| chr4:17628616 | C | T | 1 | a0001c0001t0056 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4818C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4818 | chr4 | 17628616 | ||||||
| chr4:17628619 | C | A | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(72): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*4821C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4821 | chr4 | 17628619 | ||||||
| chr4:17628652 | C | T | 2 | a0001c0001t0022 a0001c0001t0038 |
3 | HG02630.hp1 HG03471.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4854C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4854 | chr4 | 17628652 | ||||||
| chr4:17628686 | A | G | 4 | a0001c0001t0121 a0001c0001t0122 a0001c0001t0123 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4888A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 4888 | chr4 | 17628686 | ||||||
| chr4:17628920 | C | A | 7 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 others(4): Show |
7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5122C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5122 | chr4 | 17628920 | ||||||
| chr4:17629063 | C | T | 1 | a0001c0001t0123 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5265C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5265 | chr4 | 17629063 | ||||||
| chr4:17629071 | C | G | 2 | a0001c0001t0012 a0001c0001t0042 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5273C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5273 | chr4 | 17629071 | ||||||
| chr4:17629094 | A | T | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(72): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*5296A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5296 | chr4 | 17629094 | ||||||
| chr4:17629166 | G | A | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG02698.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5368G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5368 | chr4 | 17629166 | ||||||
| chr4:17629210 | G | T | 7 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(4): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5412G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5412 | chr4 | 17629210 | ||||||
| chr4:17629234 | AAAAC | A | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5442_*5445delAACA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5442 | INFO_REALIGN_3_PRIME | chr4 | 17629234 | |||||
| chr4:17629263 | G | T | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5465G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5465 | chr4 | 17629263 | ||||||
| chr4:17629318 | C | G | 2 | a0001c0001t0033 a0001c0001t0109 |
3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5520C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5520 | chr4 | 17629318 | ||||||
| chr4:17629326 | T | C | 1 | a0001c0001t0023 | 2 | HG01081.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5528T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5528 | chr4 | 17629326 | ||||||
| chr4:17629369 | A | G | 1 | a0001c0001t0119 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5571A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5571 | chr4 | 17629369 | ||||||
| chr4:17629439 | A | T | 2 | a0001c0001t0078 a0001c0001t0079 |
2 | HG02258.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5641A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5641 | chr4 | 17629439 | ||||||
| chr4:17629452 | C | T | 1 | a0001c0001t0096 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5654C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5654 | chr4 | 17629452 | ||||||
| chr4:17629537 | C | T | 2 | a0001c0001t0009 a0001c0001t0063 |
9 | HG02622.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5739C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5739 | chr4 | 17629537 | ||||||
| chr4:17629630 | T | C | 105 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(102): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*5832T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5832 | chr4 | 17629630 | ||||||
| chr4:17629654 | T | C | 1 | a0001c0001t0124 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5856T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 5856 | chr4 | 17629654 | ||||||
| chr4:17629834 | A | G | 1 | a0001c0001t0055 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6036A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6036 | chr4 | 17629834 | ||||||
| chr4:17629855 | A | G | 12 | a0001c0001t0026 a0001c0001t0065 a0001c0001t0066 others(9): Show |
13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6057A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6057 | chr4 | 17629855 | ||||||
| chr4:17629885 | T | G | 1 | a0001c0001t0034 | 2 | HG01261.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6087T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6087 | chr4 | 17629885 | ||||||
| chr4:17629907 | T | C | 2 | a0001c0001t0018 a0001c0001t0050 |
4 | HG02723.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6109T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6109 | chr4 | 17629907 | ||||||
| chr4:17630089 | C | T | 1 | a0001c0001t0104 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6291C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6291 | chr4 | 17630089 | ||||||
| chr4:17630151 | G | T | 3 | a0001c0001t0118 a0001c0001t0119 a0001c0001t0120 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6353G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6353 | chr4 | 17630151 | ||||||
| chr4:17630165 | G | T | 4 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0063 others(1): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6367G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6367 | chr4 | 17630165 | ||||||
| chr4:17630376 | A | G | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6578A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6578 | chr4 | 17630376 | ||||||
| chr4:17630403 | G | C | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6605G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6605 | chr4 | 17630403 | ||||||
| chr4:17630476 | C | T | 1 | a0001c0001t0108 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6678C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6678 | chr4 | 17630476 | ||||||
| chr4:17630601 | C | T | 8 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(5): Show |
9 | HG00544.hp1 HG02109.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6803C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6803 | chr4 | 17630601 | ||||||
| chr4:17630622 | G | A | 1 | a0001c0001t0030 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6824G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6824 | chr4 | 17630622 | ||||||
| chr4:17630722 | T | C | 2 | a0001c0001t0095 a0001c0001t0097 |
2 | HG00642.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6924T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6924 | chr4 | 17630722 | ||||||
| chr4:17630779 | C | CT | 5 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0029 others(2): Show |
16 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6993dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6994 | INFO_REALIGN_3_PRIME | chr4 | 17630779 | |||||
| chr4:17630779 | CT | C | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(59): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*6993delT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 6993 | INFO_REALIGN_3_PRIME | chr4 | 17630779 | |||||
| chr4:17630822 | G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7024G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7024 | chr4 | 17630822 | ||||||
| chr4:17630877 | A | G | 4 | a0001c0001t0121 a0001c0001t0122 a0001c0001t0123 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7079A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7079 | chr4 | 17630877 | ||||||
| chr4:17630980 | G | A | 2 | a0001c0001t0033 a0001c0001t0109 |
3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7182G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7182 | chr4 | 17630980 | ||||||
| chr4:17631090 | C | T | 1 | a0001c0002t0113 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7292C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7292 | chr4 | 17631090 | ||||||
| chr4:17631118 | G | A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7320G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7320 | chr4 | 17631118 | ||||||
| chr4:17631118 | G | T | 7 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(4): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7320G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7320 | chr4 | 17631118 | ||||||
| chr4:17631143 | A | G | 4 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(1): Show |
7 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7345A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7345 | chr4 | 17631143 | ||||||
| chr4:17631209 | TA | T | 4 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(1): Show |
7 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7412delA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7412 | chr4 | 17631209 | ||||||
| chr4:17631211 | T | C | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(53): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*7413T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7413 | chr4 | 17631211 | ||||||
| chr4:17631212 | A | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7414A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7414 | chr4 | 17631212 | ||||||
| chr4:17631214 | A | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7416A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7416 | chr4 | 17631214 | ||||||
| chr4:17631215 | T | C | 1 | a0001c0001t0100 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7417T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7417 | chr4 | 17631215 | ||||||
| chr4:17631216 | A | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7418A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7418 | chr4 | 17631216 | ||||||
| chr4:17631218 | A | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7420A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7420 | chr4 | 17631218 | ||||||
| chr4:17631220 | A | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(66): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*7422A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7422 | chr4 | 17631220 | ||||||
| chr4:17631222 | T | A | 2 | a0001c0001t0025 a0001c0001t0126 |
3 | HG01361.hp2 HG02293.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7424T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7424 | chr4 | 17631222 | ||||||
| chr4:17631227 | T | C | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7429T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7429 | chr4 | 17631227 | ||||||
| chr4:17631331 | CTAAT | C | 22 | a0001c0001t0026 a0001c0001t0043 a0001c0001t0065 others(19): Show |
23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7536_*7539delATTA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7536 | INFO_REALIGN_3_PRIME | chr4 | 17631331 | |||||
| chr4:17631365 | G | C | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(53): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*7567G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7567 | chr4 | 17631365 | ||||||
| chr4:17631426 | A | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(53): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*7628A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7628 | chr4 | 17631426 | ||||||
| chr4:17631454 | G | A | 3 | a0001c0001t0012 a0001c0001t0041 a0001c0001t0042 |
7 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7656G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7656 | chr4 | 17631454 | ||||||
| chr4:17631585 | C | A | 1 | a0001c0001t0051 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7787C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7787 | chr4 | 17631585 | ||||||
| chr4:17631596 | T | TAATTCC | 3 | a0001c0001t0008 a0001c0001t0078 a0001c0001t0079 |
11 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7804_*7809dupCAAT others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7810 | INFO_REALIGN_3_PRIME | chr4 | 17631596 | |||||
| chr4:17631604 | A | G | 22 | a0001c0001t0026 a0001c0001t0043 a0001c0001t0065 others(19): Show |
23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7806A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7806 | chr4 | 17631604 | ||||||
| chr4:17631690 | C | T | 1 | a0001c0001t0043 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7892C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 7892 | chr4 | 17631690 | ||||||
| chr4:17631810 | A | G | 1 | a0001c0001t0059 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8012A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8012 | chr4 | 17631810 | ||||||
| chr4:17631863 | T | TG | 4 | a0001c0001t0121 a0001c0001t0122 a0001c0001t0123 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8066dupG | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8067 | INFO_REALIGN_3_PRIME | chr4 | 17631863 | |||||
| chr4:17631907 | C | A | 1 | a0001c0001t0038 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8109C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8109 | chr4 | 17631907 | ||||||
| chr4:17632042 | AATTTTTT others(20): Show |
A | 1 | a0001c0001t0043 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8245_*8271delATTT others(23): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8245 | chr4 | 17632042 | ||||||
| chr4:17632043 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0125 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8280_*8289dupTTTT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8290 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0003 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8279_*8289dupTTTT others(7): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8290 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATT | A | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(3): Show |
9 | HG02027.hp2 HG02698.hp1 HG03098.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8288_*8289delTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8288 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTT | A | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(6): Show |
19 | HG00140.hp2 HG00544.hp2 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*8287_*8289delTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8287 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTT | A | 6 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0018 others(3): Show |
11 | HG00738.hp1 HG01074.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*8286_*8289delTTTT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8286 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0008 a0001c0001t0024 |
3 | HG00423.hp1 HG02055.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8280_*8289delTTTT others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8280 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0078 others(1): Show |
8 | HG00323.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8279_*8289delTTTT others(7): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8279 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0008 | 2 | HG02717.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8278_*8289delTTTT others(8): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8278 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0004 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8277_*8289delTTTT others(9): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8277 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0003 a0001c0001t0059 |
3 | HG02132.hp1 HG02572.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8275_*8289delTTTT others(11): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8275 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0017 a0001c0001t0022 |
3 | HG03471.hp2 HG03486.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8273_*8289delTTTT others(13): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8273 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0017 a0001c0001t0038 a0001c0001t0040 |
4 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8272_*8289delTTTT others(14): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8272 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8271_*8289delTTTT others(15): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8271 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(13): Show |
A | 6 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0027 others(3): Show |
9 | HG00099.hp2 HG01255.hp2 HG01516.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8270_*8289delTTTT others(16): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8270 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(14): Show |
A | 2 | a0001c0001t0004 a0001c0001t0006 |
3 | HG03491.hp2 HG03831.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8269_*8289delTTTT others(17): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(15): Show |
A | 5 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0027 others(2): Show |
14 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8268_*8289delTTTT others(18): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8268 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(16): Show |
A | 2 | a0001c0001t0006 a0001c0001t0057 |
2 | HG04228.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8267_*8289delTTTT others(19): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8267 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(18): Show |
A | 1 | a0001c0001t0015 | 2 | HG02818.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8265_*8289delTTTT others(21): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8265 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(19): Show |
A | 5 | a0001c0001t0065 a0001c0001t0066 a0001c0001t0067 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8264_*8289delTTTT others(22): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8264 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(20): Show |
A | 17 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0070 others(14): Show |
18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8263_*8289delTTTT others(23): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8263 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(21): Show |
A | 5 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0036 others(2): Show |
6 | HG01516.hp2 HG02257.hp1 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8262_*8289delTTTT others(24): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8262 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(22): Show |
A | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(56): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*8261_*8289delTTTT others(25): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8261 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632043 | ATTTTTTT others(23): Show |
A | 1 | a0001c0001t0001 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8260_*8289delTTTT others(26): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8260 | INFO_REALIGN_3_PRIME | chr4 | 17632043 | |||||
| chr4:17632103 | C | T | 1 | a0001c0001t0065 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8305C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8305 | chr4 | 17632103 | ||||||
| chr4:17632160 | T | TGCCTCCT others(18): Show |
1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8363_*8387dupGCCT others(21): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8388 | INFO_REALIGN_3_PRIME | chr4 | 17632160 | |||||
| chr4:17632187 | G | A | 6 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(3): Show |
9 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8389G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8389 | chr4 | 17632187 | ||||||
| chr4:17632284 | A | G | 2 | a0001c0001t0047 a0001c0001t0053 |
2 | HG00609.hp2 HG00673.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8486A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8486 | chr4 | 17632284 | ||||||
| chr4:17632330 | C | G | 1 | a0001c0001t0037 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8532C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8532 | chr4 | 17632330 | ||||||
| chr4:17632590 | A | G | 130 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(127): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*8792A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8792 | chr4 | 17632590 | ||||||
| chr4:17632632 | G | A | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(84): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*8834G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8834 | chr4 | 17632632 | ||||||
| chr4:17632633 | C | CAA | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(57): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*8841_*8842dupAA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8843 | INFO_REALIGN_3_PRIME | chr4 | 17632633 | |||||
| chr4:17632690 | A | ACC | 2 | a0001c0001t0012 a0001c0001t0042 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8893_*8894dupCC | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8895 | INFO_REALIGN_3_PRIME | chr4 | 17632690 | |||||
| chr4:17632737 | C | T | 22 | a0001c0001t0026 a0001c0001t0043 a0001c0001t0065 others(19): Show |
23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*8939C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8939 | chr4 | 17632737 | ||||||
| chr4:17632819 | G | T | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(84): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*9021G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9021 | chr4 | 17632819 | ||||||
| chr4:17632847 | T | C | 1 | a0001c0001t0074 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9049T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9049 | chr4 | 17632847 | ||||||
| chr4:17633016 | G | T | 2 | a0001c0001t0039 a0001c0001t0127 |
2 | HG03098.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9218G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9218 | chr4 | 17633016 | ||||||
| chr4:17633048 | G | A | 22 | a0001c0001t0026 a0001c0001t0043 a0001c0001t0065 others(19): Show |
23 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*9250G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9250 | chr4 | 17633048 | ||||||
| chr4:17633142 | G | A | 2 | a0001c0001t0102 a0001c0001t0103 |
2 | NA18982.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9344G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9344 | chr4 | 17633142 | ||||||
| chr4:17633218 | G | A | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9420G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9420 | chr4 | 17633218 | ||||||
| chr4:17633245 | A | G | 1 | a0001c0001t0124 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9447A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9447 | chr4 | 17633245 | ||||||
| chr4:17633321 | C | T | 1 | a0001c0001t0121 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9523C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9523 | chr4 | 17633321 | ||||||
| chr4:17633363 | G | A | 1 | a0001c0001t0123 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9565G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9565 | chr4 | 17633363 | ||||||
| chr4:17633713 | G | A | 1 | a0001c0001t0025 | 2 | HG01361.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9915G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9915 | chr4 | 17633713 | ||||||
| chr4:17633765 | G | T | 1 | a0001c0001t0043 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9967G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 9967 | chr4 | 17633765 | ||||||
| chr4:17633886 | T | C | 1 | a0001c0001t0066 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10088T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10088 | chr4 | 17633886 | ||||||
| chr4:17633933 | CAAAAT | C | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(50): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*10139_*10143delAT others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10139 | INFO_REALIGN_3_PRIME | chr4 | 17633933 | |||||
| chr4:17633987 | C | T | 5 | a0001c0001t0017 a0001c0001t0022 a0001c0001t0038 others(2): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10189C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10189 | chr4 | 17633987 | ||||||
| chr4:17633988 | G | A | 1 | a0001c0001t0106 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10190G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10190 | chr4 | 17633988 | ||||||
| chr4:17634028 | T | C | 7 | a0001c0001t0026 a0001c0001t0070 a0001c0001t0071 others(4): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10230T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10230 | chr4 | 17634028 | ||||||
| chr4:17634065 | A | G | 1 | a0001c0001t0110 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10267A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10267 | chr4 | 17634065 | ||||||
| chr4:17634080 | G | A | 2 | a0001c0001t0033 a0001c0001t0109 |
3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10282G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 10282 | chr4 | 17634080 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17614883 | G | T | 1 | a0001c0001t0010g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.159+70G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17614883 | |||||||
| chr4:17614914 | C | T | 13 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0065g0096 others(10): Show |
13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+101C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17614914 | |||||||
| chr4:17615054 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.159+241A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615054 | |||||||
| chr4:17615263 | G | C | 1 | a0001c0001t0100g0035 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.159+450G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615263 | |||||||
| chr4:17615393 | G | A | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+580G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615393 | |||||||
| chr4:17615402 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.159+589G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615402 | |||||||
| chr4:17615488 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.159+675T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615488 | |||||||
| chr4:17615563 | G | A | 1 | a0001c0001t0122g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159+750G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615563 | |||||||
| chr4:17615565 | A | G | 1 | a0001c0001t0041g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+752A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615565 | |||||||
| chr4:17615585 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.159+772G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615585 | |||||||
| chr4:17615638 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.159+825T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615638 | |||||||
| chr4:17615765 | G | A | 9 | a0001c0001t0006g0020 a0001c0001t0017g0063 a0001c0001t0017g0064 others(6): Show |
11 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+952G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615765 | |||||||
| chr4:17615850 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(195): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.159+1037C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615850 | |||||||
| chr4:17615863 | GTATT | G | 16 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0074 others(13): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+1051_159+1054d others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615863 | |||||||
| chr4:17615867 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.159+1054T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615867 | |||||||
| chr4:17615868 | G | A | 16 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0074 others(13): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.159+1055G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615868 | |||||||
| chr4:17615945 | C | T | 1 | a0001c0001t0017g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159+1132C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615945 | |||||||
| chr4:17615994 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.159+1181T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615994 | |||||||
| chr4:17615999 | C | T | 9 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+1186C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17615999 | |||||||
| chr4:17616086 | G | A | 1 | a0001c0001t0091g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.159+1273G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616086 | |||||||
| chr4:17616091 | G | T | 1 | a0001c0001t0041g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+1278G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616091 | |||||||
| chr4:17616146 | A | G | 12 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1333A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616146 | |||||||
| chr4:17616164 | C | T | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+1351C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616164 | |||||||
| chr4:17616338 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.159+1525G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616338 | |||||||
| chr4:17616386 | G | C | 1 | a0001c0001t0122g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.159+1573G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616386 | |||||||
| chr4:17616401 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.159+1588G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616401 | |||||||
| chr4:17616426 | A | G | 36 | a0001c0001t0003g0002 a0001c0001t0003g0033 a0001c0001t0003g0034 others(33): Show |
56 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+1613A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616426 | |||||||
| chr4:17616545 | C | T | 2 | a0001c0001t0119g0023 a0001c0001t0120g0023 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.159+1732C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616545 | |||||||
| chr4:17616553 | C | G | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+1740C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616553 | |||||||
| chr4:17616821 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.159+2008A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616821 | |||||||
| chr4:17616883 | T | G | 5 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+2070T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616883 | |||||||
| chr4:17616901 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.159+2088G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616901 | |||||||
| chr4:17616950 | G | A | 1 | a0001c0001t0042g0076 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.159+2137G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17616950 | |||||||
| chr4:17617034 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.159+2221G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617034 | |||||||
| chr4:17617088 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.159+2275A>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617088 | |||||||
| chr4:17617090 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.159+2277G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617090 | |||||||
| chr4:17617341 | A | G | 1 | a0001c0001t0041g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+2528A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617341 | |||||||
| chr4:17617379 | C | G | 1 | a0001c0001t0043g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.160-2522C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617379 | |||||||
| chr4:17617553 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0002g0013 a0001c0001t0020g0013 |
4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-2348A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617553 | |||||||
| chr4:17617561 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.160-2340A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617561 | |||||||
| chr4:17617632 | T | C | 1 | a0001c0001t0003g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.160-2269T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617632 | |||||||
| chr4:17617634 | C | T | 1 | a0001c0001t0031g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160-2267C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617634 | |||||||
| chr4:17617642 | C | T | 1 | a0001c0001t0003g0034 | 2 | HG01081.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.160-2259C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617642 | |||||||
| chr4:17617704 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160-2197C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617704 | |||||||
| chr4:17617759 | T | G | 7 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 others(4): Show |
7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-2142T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617759 | |||||||
| chr4:17617764 | G | C | 7 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 others(4): Show |
7 | HG01243.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-2137G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617764 | |||||||
| chr4:17617806 | C | T | 1 | a0001c0001t0121g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160-2095C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617806 | |||||||
| chr4:17617883 | G | A | 2 | a0001c0001t0046g0030 a0001c0001t0048g0030 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.160-2018G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617883 | |||||||
| chr4:17617998 | T | C | 1 | a0001c0001t0073g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.160-1903T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17617998 | |||||||
| chr4:17618013 | C | CT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.160-1872dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | ||||||
| chr4:17618013 | C | CTT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0010g0010 others(5): Show |
8 | HG00438.hp1 HG00438.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-1873_160-1872d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | ||||||
| chr4:17618013 | CTT | C | 6 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-1873_160-1872d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618013 | ||||||
| chr4:17618016 | T | TC | 9 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0065g0096 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-1885_160-1884i others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618016 | |||||||
| chr4:17618068 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.160-1833A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618068 | |||||||
| chr4:17618075 | G | A | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-1826G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618075 | |||||||
| chr4:17618101 | TC | T | 3 | a0001c0001t0012g0021 a0001c0001t0012g0032 a0001c0001t0042g0076 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-1798delC | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618101 | ||||||
| chr4:17618208 | C | A | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1693C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618208 | |||||||
| chr4:17618213 | T | C | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1688T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618213 | |||||||
| chr4:17618312 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160-1589T>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618312 | |||||||
| chr4:17618324 | G | T | 6 | a0001c0001t0009g0004 a0001c0001t0009g0077 a0001c0001t0015g0004 others(3): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-1577G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618324 | |||||||
| chr4:17618367 | A | T | 6 | a0001c0001t0009g0004 a0001c0001t0009g0077 a0001c0001t0015g0004 others(3): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.160-1534A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618367 | |||||||
| chr4:17618385 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.160-1516C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618385 | |||||||
| chr4:17618443 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.160-1458A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618443 | |||||||
| chr4:17618476 | A | G | 4 | a0001c0001t0003g0088 a0001c0002t0021g0012 a0001c0002t0113g0012 others(1): Show |
5 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-1425A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618476 | |||||||
| chr4:17618542 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.160-1359A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618542 | |||||||
| chr4:17618548 | G | A | 1 | a0001c0001t0004g0080 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.160-1353G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618548 | |||||||
| chr4:17618619 | C | T | 8 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0070g0015 others(5): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1282C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618619 | |||||||
| chr4:17618663 | C | T | 1 | a0001c0001t0124g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160-1238C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618663 | |||||||
| chr4:17618718 | G | A | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-1183G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618718 | |||||||
| chr4:17618734 | TGA | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.160-1166_160-1165d others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618734 | |||||||
| chr4:17618739 | TCGTG | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.160-1161_160-1158d others(6): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618739 | |||||||
| chr4:17618747 | CTGCCTTC others(10): Show |
C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.160-1152_160-1136d others(19): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 17618747 | ||||||
| chr4:17618775 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0005g0007 |
8 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-1126G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618775 | |||||||
| chr4:17618945 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.160-956G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17618945 | |||||||
| chr4:17619045 | T | C | 1 | a0001c0001t0065g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160-856T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619045 | |||||||
| chr4:17619067 | C | T | 7 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0070g0015 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-834C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619067 | |||||||
| chr4:17619086 | C | T | 1 | a0001c0001t0005g0053 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.160-815C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619086 | |||||||
| chr4:17619110 | C | G | 1 | a0001c0001t0083g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.160-791C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619110 | |||||||
| chr4:17619136 | A | G | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-765A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619136 | |||||||
| chr4:17619227 | A | C | 2 | a0001c0001t0028g0014 a0001c0001t0029g0014 |
4 | HG01109.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-674A>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619227 | |||||||
| chr4:17619248 | G | T | 1 | a0001c0001t0003g0087 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.160-653G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619248 | |||||||
| chr4:17619436 | G | T | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.160-465G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619436 | |||||||
| chr4:17619508 | G | C | 1 | a0001c0001t0004g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160-393G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619508 | |||||||
| chr4:17619687 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.160-214G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619687 | |||||||
| chr4:17619702 | C | T | 2 | a0001c0001t0071g0095 a0001c0001t0072g0094 |
2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.160-199C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619702 | |||||||
| chr4:17619759 | G | A | 4 | a0001c0001t0121g0070 a0001c0001t0122g0061 a0001c0001t0123g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-142G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619759 | |||||||
| chr4:17619760 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.160-141C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 1/3 | chr4 | 17619760 | |||||||
| chr4:17619986 | T | C | 3 | a0001c0001t0012g0021 a0001c0001t0012g0032 a0001c0001t0042g0076 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+19T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17619986 | |||||||
| chr4:17620038 | C | A | 1 | a0001c0001t0072g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.226+71C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620038 | |||||||
| chr4:17620141 | G | A | 1 | a0001c0001t0039g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226+174G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620141 | |||||||
| chr4:17620154 | T | TAACGAAT others(327): Show |
1 | a0001c0001t0073g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.226+201_226+202ins others(334): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620154 | ||||||
| chr4:17620190 | C | G | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+223C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620190 | |||||||
| chr4:17620337 | C | T | 1 | a0001c0001t0039g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226+370C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620337 | |||||||
| chr4:17620354 | G | GT | 29 | a0001c0001t0003g0086 a0001c0001t0006g0074 a0001c0001t0008g0072 others(26): Show |
37 | HG01123.hp1 HG01175.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.226+402dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | ||||||
| chr4:17620354 | G | GTT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.226+401_226+402dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | ||||||
| chr4:17620354 | G | GTTT | 18 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0002g0005 others(15): Show |
20 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.226+400_226+402dup others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620354 | ||||||
| chr4:17620441 | C | G | 6 | a0001c0001t0009g0004 a0001c0001t0009g0077 a0001c0001t0015g0004 others(3): Show |
14 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.226+474C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620441 | |||||||
| chr4:17620538 | G | A | 1 | a0001c0001t0049g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.226+571G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620538 | |||||||
| chr4:17620613 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0108g0043 |
3 | HG02717.hp2 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.226+646G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620613 | |||||||
| chr4:17620622 | C | T | 2 | a0001c0001t0121g0070 a0001c0001t0122g0061 |
2 | HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.226+655C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620622 | |||||||
| chr4:17620689 | TCTC | T | 5 | a0001c0001t0022g0019 a0001c0001t0022g0066 a0001c0001t0038g0019 others(2): Show |
5 | HG02630.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+723_226+725del others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620689 | |||||||
| chr4:17620690 | C | T | 3 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 |
3 | HG02451.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.226+723C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620690 | |||||||
| chr4:17620692 | C | CT | 4 | a0001c0001t0012g0021 a0001c0001t0012g0032 a0001c0001t0025g0002 others(1): Show |
7 | HG00099.hp2 HG01361.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+746dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | ||||||
| chr4:17620692 | C | CTT | 8 | a0001c0001t0008g0006 a0001c0001t0008g0071 a0001c0001t0008g0072 others(5): Show |
15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.226+745_226+746dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | ||||||
| chr4:17620692 | C | CTTTTT | 7 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0074 others(4): Show |
13 | HG01123.hp2 HG01192.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+742_226+746dup others(5): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | ||||||
| chr4:17620692 | CTT | C | 14 | a0001c0001t0001g0001 a0001c0001t0002g0001 a0001c0001t0002g0027 others(11): Show |
18 | HG01106.hp2 HG01243.hp2 HG02293.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+745_226+746del others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | ||||||
| chr4:17620692 | CTTT | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(114): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.226+744_226+746del others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17620692 | ||||||
| chr4:17620695 | T | C | 5 | a0001c0001t0022g0019 a0001c0001t0022g0066 a0001c0001t0038g0019 others(2): Show |
5 | HG02630.hp1 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+728T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620695 | |||||||
| chr4:17620713 | T | G | 1 | a0001c0001t0110g0044 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.226+746T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620713 | |||||||
| chr4:17620732 | C | G | 1 | a0001c0001t0013g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+765C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620732 | |||||||
| chr4:17620758 | A | G | 4 | a0001c0001t0121g0070 a0001c0001t0122g0061 a0001c0001t0123g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+791A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620758 | |||||||
| chr4:17620947 | G | A | 13 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0065g0096 others(10): Show |
13 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.227-640G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17620947 | |||||||
| chr4:17621018 | G | GT | 5 | a0001c0001t0008g0006 a0001c0001t0008g0072 a0001c0001t0019g0006 others(2): Show |
11 | HG01123.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.227-554dupT | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | ||||||
| chr4:17621018 | G | GTT | 21 | a0001c0001t0002g0027 a0001c0001t0008g0071 a0001c0001t0026g0015 others(18): Show |
21 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.227-555_227-554dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | ||||||
| chr4:17621018 | G | GTTT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.227-556_227-554dup others(3): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 17621018 | ||||||
| chr4:17621038 | C | T | 1 | a0001c0001t0006g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-549C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621038 | |||||||
| chr4:17621134 | C | T | 1 | a0001c0001t0015g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.227-453C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621134 | |||||||
| chr4:17621170 | C | T | 1 | a0001c0001t0012g0032 | 2 | HG00099.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.227-417C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621170 | |||||||
| chr4:17621203 | G | A | 3 | a0001c0001t0012g0021 a0001c0001t0012g0032 a0001c0001t0042g0076 |
6 | HG00099.hp2 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-384G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621203 | |||||||
| chr4:17621263 | C | T | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-324C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621263 | |||||||
| chr4:17621287 | C | T | 4 | a0001c0001t0003g0033 a0001c0001t0003g0084 a0001c0001t0003g0086 others(1): Show |
4 | HG00735.hp2 HG00738.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-300C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621287 | |||||||
| chr4:17621306 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.227-281C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621306 | |||||||
| chr4:17621369 | T | C | 1 | a0001c0001t0007g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.227-218T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621369 | |||||||
| chr4:17621391 | G | A | 4 | a0001c0001t0121g0070 a0001c0001t0122g0061 a0001c0001t0123g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-196G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621391 | |||||||
| chr4:17621401 | T | C | 10 | a0001c0001t0009g0004 a0001c0001t0009g0077 a0001c0001t0015g0004 others(7): Show |
18 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.227-186T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621401 | |||||||
| chr4:17621473 | C | T | 3 | a0001c0002t0021g0012 a0001c0002t0113g0012 a0001c0004t0021g0012 |
4 | HG02970.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-114C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621473 | |||||||
| chr4:17621557 | T | C | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.227-30T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 2/3 | chr4 | 17621557 | |||||||
| chr4:17621718 | C | G | 4 | a0001c0001t0121g0070 a0001c0001t0122g0061 a0001c0001t0123g0068 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+19C>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621718 | |||||||
| chr4:17621764 | G | T | 1 | a0001c0001t0041g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+65G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621764 | |||||||
| chr4:17621930 | G | A | 1 | a0001c0001t0041g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+231G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17621930 | |||||||
| chr4:17622046 | A | G | 8 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0070g0015 others(5): Show |
8 | HG02109.hp1 HG02559.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+347A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622046 | |||||||
| chr4:17622082 | A | G | 2 | a0001c0001t0028g0014 a0001c0001t0029g0014 |
4 | HG01109.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+383A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622082 | |||||||
| chr4:17622174 | T | C | 3 | a0001c0001t0033g0025 a0001c0001t0033g0055 a0001c0001t0109g0025 |
3 | HG01123.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.339+475T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622174 | |||||||
| chr4:17622285 | A | G | 10 | a0001c0001t0002g0008 a0001c0001t0002g0051 a0001c0001t0005g0008 others(7): Show |
15 | HG00099.hp2 HG00280.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.339+586A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622285 | |||||||
| chr4:17622377 | T | G | 4 | a0001c0001t0127g0028 a0001c0001t0128g0028 a0001c0001t0129g0029 others(1): Show |
4 | HG02451.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+678T>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622377 | |||||||
| chr4:17622411 | C | T | 8 | a0001c0001t0017g0063 a0001c0001t0017g0064 a0001c0001t0017g0067 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+712C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622411 | |||||||
| chr4:17622426 | G | C | 1 | a0001c0001t0014g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.339+727G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622426 | |||||||
| chr4:17622472 | A | T | 1 | a0001c0001t0007g0017 | 3 | HG01167.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.339+773A>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622472 | |||||||
| chr4:17622554 | TGATA | T | 16 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0074 others(13): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+859_339+862del others(4): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17622554 | ||||||
| chr4:17622623 | G | A | 5 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+924G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622623 | |||||||
| chr4:17622829 | C | T | 15 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0070g0015 others(12): Show |
15 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.340-772C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622829 | |||||||
| chr4:17622863 | G | A | 13 | a0001c0001t0026g0015 a0001c0001t0026g0093 a0001c0001t0070g0015 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-738G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622863 | |||||||
| chr4:17622869 | T | C | 4 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-732T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622869 | |||||||
| chr4:17622884 | C | A | 5 | a0001c0001t0086g0011 a0001c0001t0087g0011 a0001c0001t0088g0011 others(2): Show |
5 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-717C>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622884 | |||||||
| chr4:17622926 | T | C | 1 | a0001c0001t0124g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.340-675T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622926 | |||||||
| chr4:17622943 | C | T | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.340-658C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622943 | |||||||
| chr4:17622978 | G | A | 1 | a0001c0001t0122g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.340-623G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17622978 | |||||||
| chr4:17623039 | C | T | 1 | a0001c0001t0049g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340-562C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623039 | |||||||
| chr4:17623145 | A | G | 5 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-456A>G | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623145 | |||||||
| chr4:17623146 | ATCCTAGC others(10): Show |
A | 5 | a0001c0001t0065g0096 a0001c0001t0066g0022 a0001c0001t0067g0022 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-454_340-438del others(17): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623146 | |||||||
| chr4:17623220 | G | T | 1 | a0001c0001t0039g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.340-381G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623220 | |||||||
| chr4:17623227 | C | T | 1 | a0001c0001t0118g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340-374C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623227 | |||||||
| chr4:17623264 | G | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.340-337G>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623264 | |||||||
| chr4:17623267 | G | C | 1 | a0001c0001t0002g0054 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.340-334G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623267 | |||||||
| chr4:17623268 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.340-333G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623268 | |||||||
| chr4:17623349 | C | T | 3 | a0001c0001t0118g0036 a0001c0001t0119g0023 a0001c0001t0120g0023 |
3 | HG01243.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.340-252C>T | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623349 | |||||||
| chr4:17623398 | C | CA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(121): Show |
198 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.340-186dupA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | ||||||
| chr4:17623398 | C | CAA | 11 | a0001c0001t0001g0056 a0001c0001t0002g0016 a0001c0001t0005g0016 others(8): Show |
13 | HG00099.hp1 HG00099.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.340-187_340-186dup others(2): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | ||||||
| chr4:17623398 | CA | C | 16 | a0001c0001t0006g0003 a0001c0001t0006g0020 a0001c0001t0006g0074 others(13): Show |
34 | HG01109.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-186delA | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 17623398 | ||||||
| chr4:17623431 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.340-170T>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623431 | |||||||
| chr4:17623580 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0005g0009 a0001c0001t0081g0009 others(1): Show |
5 | HG02083.hp2 NA18982.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-21G>A | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623580 | |||||||
| chr4:17623586 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.340-15G>C | MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 3/3 | chr4 | 17623586 |