Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29079 |
| ensemblid | ENSG00000136146.15 |
| hgncid | 17903 |
| symbol | MED4 |
| name | mediator complex subunit 4 |
| refseq_nuc | NM_014166.4 |
| refseq_prot | NP_054885.1 |
| ensembl_nuc | ENST00000258648.7 |
| ensembl_prot | ENSP00000258648.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 48075724 |
| end | 48095104 |
| strand | - |
| ver | v1.2 |
| region | chr13:48075724-48095104 |
| region5000 | chr13:48070724-48100104 |
| regionname0 | MED4_chr13_48075724_48095104 |
| regionname5000 | MED4_chr13_48070724_48100104 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 270 | 407 | 86 | 69 | 188 | 18 | 44 | 152 | MED4_chr13_48070724_48100104 | MED4 | MAASS others(265): Show |
chr13 | 48070724 | 48100104 |
| a0002 | 0/0 | 270 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | MAASS others(265): Show |
chr13 | 48070724 | 48100104 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 810 | 402 | 83 | 69 | 186 | 18 | 44 | MED4_chr13_48070724_48100104 | MED4 | ATGGC others(805): Show |
chr13 | 48070724 | 48100104 | ||
| a0001c0002 | 0/0 | 810 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | ATGGC others(805): Show |
chr13 | 48070724 | 48100104 | ||
| a0001c0004 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | ATGGC others(805): Show |
chr13 | 48070724 | 48100104 | ||
| a0001c0005 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | ATGGC others(805): Show |
chr13 | 48070724 | 48100104 | ||
| a0002c0003 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | ATGGC others(805): Show |
chr13 | 48070724 | 48100104 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2254 | 310 | 59 | 50 | 162 | 15 | 22 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0002 | 0/0 | 2253 | 30 | 12 | 3 | 15 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2248): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0003 | 0/0 | 2254 | 20 | 0 | 9 | 2 | 0 | 9 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0004 | 0/0 | 2250 | 16 | 0 | 3 | 2 | 1 | 10 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2245): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0005 | 0/0 | 2255 | 4 | 3 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2250): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0006 | 0/0 | 2250 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2245): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0007 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0008 | 0/0 | 2254 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0009 | 0/0 | 2254 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0010 | 0/0 | 2254 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0011 | 0/0 | 2254 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0012 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2248): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0013 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0014 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0015 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2250): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0016 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0017 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0018 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0001t0019 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0002t0001 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0004t0001 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0001c0005t0001 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| a0002c0003t0001 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | GCGCC others(2249): Show |
chr13 | 48070724 | 48100104 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 8 | 22 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0002 | 0/0 | 26 | 0 | 7 | 18 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0003 | 0/0 | 23 | 2 | 1 | 18 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0004 | 0/0 | 20 | 0 | 3 | 12 | 1 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0005 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0006 | 0/0 | 9 | 1 | 3 | 0 | 2 | 3 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0016 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0034 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0010 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0011 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0015 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0021 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0008g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0009g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0010g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0011g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0013g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0014g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0016g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0017g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0001t0019g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0002t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0019 | g0180 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0164 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0043 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0136 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01167 | hp1 | a0001 | c0001 | t0016 | g0127 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0049 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0103 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0137 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0076 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02083 | hp2 | a0001 | c0001 | t0018 | g0119 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0113 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0117 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0043 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03654 | hp2 | a0001 | c0001 | t0010 | g0167 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03669 | hp1 | a0001 | c0001 | t0014 | g0072 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19084 | hp2 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19090 | hp2 | a0001 | c0001 | t0017 | g0125 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | GIH | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0114 | REF | REF | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0034 | REF | REF | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48077193 | A | T | 1 | a0002 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.759T>A | p.Asp253Glu | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 785/2254 | 759/813 | 253/270 | chr13 | 48077193 | |||
| chr13:48095045 | C | G | 1 | a0001 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.34G>C | p.Glu12Gln | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/7 | 60/2254 | 34/813 | 12/270 | chr13 | 48095045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48081670 | T | A | 1 | a0001c0002 | 3 | HG03130.hp1 HG03471.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.483A>T | p.Val161Val | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/7 | 509/2254 | 483/813 | 161/270 | chr13 | 48081670 | |||
| chr13:48081688 | G | A | 1 | a0001c0004 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.465C>T | p.Ile155Ile | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/7 | 491/2254 | 465/813 | 155/270 | chr13 | 48081688 | |||
| chr13:48090382 | T | C | 1 | a0001c0005 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.162A>G | p.Gln54Gln | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/7 | 188/2254 | 162/813 | 54/270 | chr13 | 48090382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48075838 | C | T | 1 | a0001c0001t0015 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1301 | chr13 | 48075838 | ||||||
| chr13:48075865 | G | T | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0013 others(1): Show |
24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1274C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1274 | chr13 | 48075865 | ||||||
| chr13:48075904 | TCTC | T | 1 | a0001c0001t0006 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1232_*1234delGAG | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1232 | chr13 | 48075904 | ||||||
| chr13:48076190 | G | T | 1 | a0001c0001t0012 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 949 | chr13 | 48076190 | ||||||
| chr13:48076304 | G | A | 1 | a0001c0001t0014 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 835 | chr13 | 48076304 | ||||||
| chr13:48076356 | A | G | 2 | a0001c0001t0003 a0001c0001t0018 |
21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*783T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 783 | chr13 | 48076356 | ||||||
| chr13:48076358 | A | C | 1 | a0001c0001t0006 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*781T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 781 | chr13 | 48076358 | ||||||
| chr13:48076565 | T | TA | 2 | a0001c0001t0005 a0001c0001t0015 |
5 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*573dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 573 | chr13 | 48076565 | ||||||
| chr13:48076565 | TA | T | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*573delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 573 | chr13 | 48076565 | ||||||
| chr13:48076585 | TACAA | T | 1 | a0001c0001t0004 | 16 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*550_*553delTTGT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 550 | chr13 | 48076585 | ||||||
| chr13:48076660 | A | G | 1 | a0001c0001t0008 | 2 | NA18978.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 479 | chr13 | 48076660 | ||||||
| chr13:48076686 | C | G | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*453G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 453 | chr13 | 48076686 | ||||||
| chr13:48076709 | C | T | 1 | a0001c0001t0007 | 3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 430 | chr13 | 48076709 | ||||||
| chr13:48076799 | T | A | 1 | a0001c0001t0010 | 2 | HG01496.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*340A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 340 | chr13 | 48076799 | ||||||
| chr13:48076842 | T | C | 1 | a0001c0001t0011 | 2 | HG00280.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*297A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 297 | chr13 | 48076842 | ||||||
| chr13:48076883 | G | A | 1 | a0001c0001t0016 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*256C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 256 | chr13 | 48076883 | ||||||
| chr13:48077037 | T | C | 1 | a0001c0001t0017 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 102 | chr13 | 48077037 | ||||||
| chr13:48077104 | A | C | 4 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(1): Show |
35 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*35T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 35 | chr13 | 48077104 | ||||||
| chr13:48077124 | G | A | 1 | a0001c0001t0018 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 15 | chr13 | 48077124 | ||||||
| chr13:48095098 | C | A | 1 | a0001c0001t0019 | 1 | HG00099.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/7 | chr13 | 48095098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48077336 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.641-25T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077336 | |||||||
| chr13:48077381 | T | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.641-70A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077381 | |||||||
| chr13:48077701 | G | A | 9 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(6): Show |
23 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.641-390C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077701 | |||||||
| chr13:48077805 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0111 |
6 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-494A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077805 | |||||||
| chr13:48077879 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(7): Show |
24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.641-568A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077879 | |||||||
| chr13:48077963 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.641-652G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077963 | |||||||
| chr13:48078069 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.641-758T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078069 | |||||||
| chr13:48078216 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-905C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078216 | |||||||
| chr13:48078223 | T | C | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-912A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078223 | |||||||
| chr13:48078251 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.641-940G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078251 | |||||||
| chr13:48078281 | AACCATTT | A | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-977_641-971del others(7): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078281 | |||||||
| chr13:48078454 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.641-1143C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078454 | |||||||
| chr13:48078460 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0151 |
3 | HG00544.hp2 NA18949.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.641-1149C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078460 | |||||||
| chr13:48078645 | T | C | 5 | a0001c0001t0002g0040 a0001c0001t0002g0092 a0001c0001t0002g0095 others(2): Show |
6 | HG02723.hp2 HG02965.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1199A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078645 | |||||||
| chr13:48078646 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0067 others(4): Show |
17 | HG00438.hp2 HG02071.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+1198T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078646 | |||||||
| chr13:48078692 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.640+1152C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078692 | |||||||
| chr13:48078779 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(7): Show |
24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+1065A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078779 | |||||||
| chr13:48078838 | A | G | 1 | a0001c0001t0001g0020 | 4 | NA18971.hp2 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1006T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078838 | |||||||
| chr13:48078860 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(7): Show |
21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+984C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078860 | |||||||
| chr13:48078912 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+932T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078912 | |||||||
| chr13:48079032 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+812G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079032 | |||||||
| chr13:48079032 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(7): Show |
21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+812G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079032 | |||||||
| chr13:48079160 | A | G | 8 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(5): Show |
21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+684T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079160 | |||||||
| chr13:48079278 | T | C | 1 | a0001c0001t0005g0163 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.640+566A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079278 | |||||||
| chr13:48079460 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0175 others(1): Show |
10 | NA18944.hp2 NA18954.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+384C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079460 | |||||||
| chr13:48079518 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640+326A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079518 | |||||||
| chr13:48079582 | A | C | 1 | a0001c0001t0005g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.640+262T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079582 | |||||||
| chr13:48079633 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.640+211C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079633 | |||||||
| chr13:48079680 | G | A | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.640+164C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079680 | |||||||
| chr13:48079728 | CA | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(55): Show |
146 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.640+115delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079728 | |||||||
| chr13:48079742 | T | A | 1 | a0001c0001t0002g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.640+102A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079742 | |||||||
| chr13:48079821 | AAC | A | 9 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(6): Show |
23 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.640+21_640+22delGT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079821 | |||||||
| chr13:48080031 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01074.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.509-56A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080031 | |||||||
| chr13:48080204 | C | CT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.509-230dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080204 | |||||||
| chr13:48080225 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509-250G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080225 | |||||||
| chr13:48080268 | G | A | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509-293C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080268 | |||||||
| chr13:48080286 | A | G | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.509-311T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080286 | |||||||
| chr13:48080319 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.509-344G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080319 | |||||||
| chr13:48080350 | T | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.509-375A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080350 | |||||||
| chr13:48080390 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.509-415G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080390 | |||||||
| chr13:48080396 | C | CA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.509-422dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | |||||||
| chr13:48080396 | C | CAA | 20 | a0001c0001t0001g0042 a0001c0001t0001g0064 a0001c0001t0001g0134 others(17): Show |
33 | HG00558.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.509-423_509-422dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | |||||||
| chr13:48080396 | C | CAAA | 8 | a0001c0001t0001g0147 a0001c0001t0001g0169 a0001c0001t0002g0040 others(5): Show |
9 | HG01515.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-424_509-422dup others(3): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | |||||||
| chr13:48080396 | CA | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0061 others(3): Show |
9 | HG01069.hp1 HG01975.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-422delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | |||||||
| chr13:48080415 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.509-440T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080415 | |||||||
| chr13:48080469 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.509-494A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080469 | |||||||
| chr13:48080486 | G | T | 1 | a0001c0001t0001g0024 | 3 | HG01515.hp2 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.509-511C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080486 | |||||||
| chr13:48080534 | C | T | 2 | a0001c0001t0007g0041 a0001c0001t0007g0112 |
3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.509-559G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080534 | |||||||
| chr13:48080613 | T | C | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509-638A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080613 | |||||||
| chr13:48080701 | G | A | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(7): Show |
24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.509-726C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080701 | |||||||
| chr13:48080741 | C | CTT | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.509-768_509-767dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080741 | |||||||
| chr13:48080741 | CT | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.509-767delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080741 | |||||||
| chr13:48080994 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.508+651G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080994 | |||||||
| chr13:48080998 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.508+647A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080998 | |||||||
| chr13:48081611 | C | T | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508+34G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48081611 | |||||||
| chr13:48081940 | A | G | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.422-209T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081940 | |||||||
| chr13:48081953 | G | A | 3 | a0001c0001t0005g0162 a0001c0001t0005g0163 a0001c0001t0005g0165 |
3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.422-222C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081953 | |||||||
| chr13:48081997 | C | T | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.422-266G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081997 | |||||||
| chr13:48082130 | C | A | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-399G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082130 | |||||||
| chr13:48082185 | G | GT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0124 others(7): Show |
41 | HG00323.hp2 HG00558.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-455dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082185 | |||||||
| chr13:48082229 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.422-498G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082229 | |||||||
| chr13:48082243 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.422-512A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082243 | |||||||
| chr13:48082296 | GA | G | 21 | a0001c0001t0001g0084 a0001c0001t0002g0009 a0001c0001t0002g0027 others(18): Show |
32 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.422-566delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082296 | |||||||
| chr13:48082404 | G | GT | 2 | a0001c0001t0001g0023 a0001c0001t0001g0066 |
4 | HG02258.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-674dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082404 | |||||||
| chr13:48082417 | G | A | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.422-686C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082417 | |||||||
| chr13:48082439 | A | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.422-708T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082439 | |||||||
| chr13:48082520 | A | T | 1 | a0001c0001t0007g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.422-789T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082520 | |||||||
| chr13:48082565 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.421+806A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082565 | |||||||
| chr13:48082605 | A | G | 1 | a0001c0001t0011g0043 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.421+766T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082605 | |||||||
| chr13:48082684 | G | A | 1 | a0001c0001t0001g0046 | 2 | NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.421+687C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082684 | |||||||
| chr13:48082718 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.421+653A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082718 | |||||||
| chr13:48082739 | G | A | 1 | a0001c0001t0001g0020 | 4 | NA18971.hp2 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+632C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082739 | |||||||
| chr13:48082741 | GGC | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0061 a0001c0001t0001g0065 |
4 | HG01975.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+628_421+629del others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082741 | |||||||
| chr13:48082757 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.421+614C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082757 | |||||||
| chr13:48082826 | C | CA | 14 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0166 others(11): Show |
22 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+544dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082826 | |||||||
| chr13:48082826 | CA | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(92): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.421+544delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082826 | |||||||
| chr13:48083447 | A | T | 1 | a0001c0001t0001g0044 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.364-19T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083447 | |||||||
| chr13:48083551 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0130 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.364-123T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083551 | |||||||
| chr13:48083625 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.364-197A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083625 | |||||||
| chr13:48083656 | T | C | 3 | a0001c0001t0005g0162 a0001c0001t0005g0163 a0001c0001t0005g0165 |
3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.364-228A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083656 | |||||||
| chr13:48083697 | G | A | 27 | a0001c0001t0001g0166 a0001c0001t0002g0009 a0001c0001t0002g0027 others(24): Show |
38 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.364-269C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083697 | |||||||
| chr13:48083786 | C | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.364-358G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083786 | |||||||
| chr13:48083843 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01192.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.364-415T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083843 | |||||||
| chr13:48083931 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0138 others(5): Show |
13 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-503A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083931 | |||||||
| chr13:48084052 | G | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.364-624C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084052 | |||||||
| chr13:48084079 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(7): Show |
21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-651C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084079 | |||||||
| chr13:48084136 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.364-708C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084136 | |||||||
| chr13:48084195 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364-767C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084195 | |||||||
| chr13:48084265 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.364-850_364-838dup others(13): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | C | CAAAAAAA others(19): Show |
1 | a0001c0001t0006g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.364-838_364-837ins others(26): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0006g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364-838_364-837ins others(27): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | CA | C | 17 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(14): Show |
28 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-838delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | CAAAA | C | 6 | a0001c0001t0004g0015 a0001c0001t0004g0021 a0001c0001t0004g0047 others(3): Show |
14 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-841_364-838del others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | CAAAAAA | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
129 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.364-843_364-838del others(6): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084265 | CAAAAAAA | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.364-844_364-838del others(7): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | |||||||
| chr13:48084371 | G | C | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-943C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084371 | |||||||
| chr13:48084389 | C | T | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.364-961G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084389 | |||||||
| chr13:48084415 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.364-987C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084415 | |||||||
| chr13:48084470 | CTCAA | C | 3 | a0001c0001t0005g0162 a0001c0001t0005g0163 a0001c0001t0005g0165 |
3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.364-1046_364-1043d others(6): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084470 | |||||||
| chr13:48084599 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.364-1171C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084599 | |||||||
| chr13:48084770 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.364-1342C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084770 | |||||||
| chr13:48084799 | G | GT | 2 | a0001c0001t0001g0032 a0001c0001t0001g0122 |
4 | NA18948.hp1 NA18948.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1372dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084799 | |||||||
| chr13:48084811 | T | C | 1 | a0001c0001t0009g0049 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1383A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084811 | |||||||
| chr13:48084858 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.363+1424A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084858 | |||||||
| chr13:48084959 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+1323G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084959 | |||||||
| chr13:48084960 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0074 others(1): Show |
8 | HG02071.hp2 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+1322C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084960 | |||||||
| chr13:48084995 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.363+1287A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084995 | |||||||
| chr13:48085011 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.363+1271G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085011 | |||||||
| chr13:48085012 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.363+1270C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085012 | |||||||
| chr13:48085060 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.363+1222C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085060 | |||||||
| chr13:48085074 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0005t0001g0076 |
7 | HG02071.hp2 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1208C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085074 | |||||||
| chr13:48085158 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.363+1124A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085158 | |||||||
| chr13:48085170 | A | AT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0054 others(16): Show |
31 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.363+1111dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | |||||||
| chr13:48085170 | AT | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0061 others(9): Show |
17 | HG01243.hp2 HG01975.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.363+1111delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | |||||||
| chr13:48085170 | ATT | A | 22 | a0001c0001t0001g0066 a0001c0001t0001g0177 a0001c0001t0002g0009 others(19): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.363+1110_363+1111d others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | |||||||
| chr13:48085170 | ATTTTTTT others(4): Show |
A | 8 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(5): Show |
21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+1101_363+1111d others(13): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | |||||||
| chr13:48085170 | ATTTTTTT others(6): Show |
A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.363+1099_363+1111d others(15): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | |||||||
| chr13:48085235 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.363+1047T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085235 | |||||||
| chr13:48085252 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0121 |
4 | HG01123.hp2 HG03710.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1030T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085252 | |||||||
| chr13:48085374 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(7): Show |
39 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.363+908A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085374 | |||||||
| chr13:48085551 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.363+731A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085551 | |||||||
| chr13:48085753 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.363+529A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085753 | |||||||
| chr13:48085943 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0039 |
5 | HG01106.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+339C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085943 | |||||||
| chr13:48085946 | C | CA | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0004g0157 others(3): Show |
7 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+335dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085946 | |||||||
| chr13:48086244 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0030 others(7): Show |
24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+38A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48086244 | |||||||
| chr13:48086267 | CCT | C | 3 | a0001c0001t0005g0162 a0001c0001t0005g0163 a0001c0001t0005g0165 |
3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.363+13_363+14delAG | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48086267 | |||||||
| chr13:48086547 | A | G | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-95T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086547 | |||||||
| chr13:48086673 | C | A | 1 | a0001c0001t0004g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-221G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086673 | |||||||
| chr13:48086717 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.193-265C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086717 | |||||||
| chr13:48086728 | G | C | 1 | a0001c0001t0001g0024 | 3 | HG01515.hp2 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.193-276C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086728 | |||||||
| chr13:48086784 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193-332A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086784 | |||||||
| chr13:48086821 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0138 others(5): Show |
13 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-369C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086821 | |||||||
| chr13:48086841 | C | G | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-389G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086841 | |||||||
| chr13:48086841 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.193-389G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086841 | |||||||
| chr13:48086904 | G | C | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-452C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086904 | |||||||
| chr13:48086918 | C | T | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-466G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086918 | |||||||
| chr13:48086983 | T | C | 10 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0097 others(7): Show |
18 | HG00558.hp1 HG01433.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.193-531A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086983 | |||||||
| chr13:48086993 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.193-541G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086993 | |||||||
| chr13:48087024 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.193-572A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087024 | |||||||
| chr13:48087104 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.193-652C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087104 | |||||||
| chr13:48087180 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-728T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087180 | |||||||
| chr13:48087226 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-774C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087226 | |||||||
| chr13:48087289 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-837G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087289 | |||||||
| chr13:48087321 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0111 |
6 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-869C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087321 | |||||||
| chr13:48087402 | C | G | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-950G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087402 | |||||||
| chr13:48087575 | G | C | 1 | a0001c0001t0002g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-1123C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087575 | |||||||
| chr13:48087594 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.193-1142C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087594 | |||||||
| chr13:48087617 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.193-1165G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087617 | |||||||
| chr13:48087678 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.193-1226G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087678 | |||||||
| chr13:48087782 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.193-1330C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087782 | |||||||
| chr13:48087858 | A | G | 1 | a0001c0001t0003g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.193-1406T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087858 | |||||||
| chr13:48087975 | C | G | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-1523G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087975 | |||||||
| chr13:48088187 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.193-1735T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088187 | |||||||
| chr13:48088374 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.193-1922A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088374 | |||||||
| chr13:48088459 | T | C | 10 | a0001c0001t0002g0009 a0001c0001t0002g0028 a0001c0001t0002g0097 others(7): Show |
18 | HG00558.hp1 HG01433.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+1893A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088459 | |||||||
| chr13:48088519 | G | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+1833C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088519 | |||||||
| chr13:48088574 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.192+1778G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088574 | |||||||
| chr13:48088738 | T | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+1614A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088738 | |||||||
| chr13:48088788 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.192+1564A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088788 | |||||||
| chr13:48088952 | A | C | 7 | a0001c0001t0004g0015 a0001c0001t0004g0021 a0001c0001t0004g0047 others(4): Show |
15 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.192+1400T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088952 | |||||||
| chr13:48088958 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.192+1394C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088958 | |||||||
| chr13:48088985 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192+1367A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088985 | |||||||
| chr13:48089030 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.192+1322T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089030 | |||||||
| chr13:48089043 | G | C | 1 | a0001c0001t0011g0043 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.192+1309C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089043 | |||||||
| chr13:48089066 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.192+1286G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089066 | |||||||
| chr13:48089107 | T | G | 2 | a0001c0001t0005g0162 a0001c0001t0005g0163 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.192+1245A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089107 | |||||||
| chr13:48089222 | A | G | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+1130T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089222 | |||||||
| chr13:48089274 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.192+1078A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089274 | |||||||
| chr13:48089352 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.192+1000C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089352 | |||||||
| chr13:48089541 | A | T | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+811T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089541 | |||||||
| chr13:48089589 | A | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(37): Show |
92 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.192+763T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089589 | |||||||
| chr13:48089638 | G | T | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+714C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089638 | |||||||
| chr13:48089700 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+652A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089700 | |||||||
| chr13:48089822 | G | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0102 a0001c0001t0002g0104 others(1): Show |
6 | HG01433.hp1 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+530C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089822 | |||||||
| chr13:48089948 | T | C | 1 | a0001c0002t0001g0161 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192+404A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089948 | |||||||
| chr13:48090313 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+39T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48090313 | |||||||
| chr13:48090332 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0064 others(2): Show |
8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+20A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48090332 | |||||||
| chr13:48090420 | T | TA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0111 others(4): Show |
7 | HG00140.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.126-3dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090420 | |||||||
| chr13:48090420 | TA | T | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.126-3delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090420 | |||||||
| chr13:48090498 | T | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-80A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090498 | |||||||
| chr13:48090630 | G | C | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-212C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090630 | |||||||
| chr13:48090822 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.126-404A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090822 | |||||||
| chr13:48090837 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.126-419C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090837 | |||||||
| chr13:48090982 | T | G | 1 | a0001c0001t0001g0037 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.126-564A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090982 | |||||||
| chr13:48091000 | T | C | 2 | a0001c0001t0004g0021 a0001c0001t0004g0164 |
5 | HG00280.hp1 HG02735.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-582A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091000 | |||||||
| chr13:48091010 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.126-592T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091010 | |||||||
| chr13:48091040 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0032 others(18): Show |
46 | HG00544.hp2 HG01346.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.126-622C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091040 | |||||||
| chr13:48091076 | T | C | 1 | a0001c0001t0005g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126-658A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091076 | |||||||
| chr13:48091222 | T | A | 19 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(16): Show |
30 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-804A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091222 | |||||||
| chr13:48091271 | T | C | 2 | a0001c0001t0007g0041 a0001c0001t0007g0112 |
3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.126-853A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091271 | |||||||
| chr13:48091280 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.126-862C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091280 | |||||||
| chr13:48091473 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.126-1055A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091473 | |||||||
| chr13:48091532 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126-1114C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091532 | |||||||
| chr13:48091578 | T | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(16): Show |
55 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.126-1160A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091578 | |||||||
| chr13:48091768 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126-1350A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091768 | |||||||
| chr13:48091869 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.126-1451C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091869 | |||||||
| chr13:48091920 | T | A | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126-1502A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091920 | |||||||
| chr13:48092002 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.126-1584G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092002 | |||||||
| chr13:48092064 | G | A | 20 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(17): Show |
31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-1646C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092064 | |||||||
| chr13:48092176 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(7): Show |
21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.126-1758G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092176 | |||||||
| chr13:48092281 | AT | A | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.126-1864delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092281 | |||||||
| chr13:48092306 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-1888A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092306 | |||||||
| chr13:48092354 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-1936G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092354 | |||||||
| chr13:48092357 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01074.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.126-1939G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092357 | |||||||
| chr13:48092554 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.126-2136C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092554 | |||||||
| chr13:48092625 | C | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.126-2207G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092625 | |||||||
| chr13:48092645 | C | A | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-2227G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092645 | |||||||
| chr13:48092646 | A | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-2228T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092646 | |||||||
| chr13:48092655 | A | T | 1 | a0001c0001t0015g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.126-2237T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092655 | |||||||
| chr13:48092692 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
96 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.125+2262C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092692 | |||||||
| chr13:48092762 | G | A | 1 | a0001c0001t0009g0049 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.125+2192C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092762 | |||||||
| chr13:48092842 | G | C | 3 | a0001c0001t0006g0105 a0001c0001t0006g0106 a0001c0001t0006g0107 |
3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.125+2112C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092842 | |||||||
| chr13:48092888 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125+2066C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092888 | |||||||
| chr13:48093137 | G | A | 1 | a0001c0001t0010g0167 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.125+1817C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093137 | |||||||
| chr13:48093261 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+1693C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093261 | |||||||
| chr13:48093561 | CAT | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+1391_125+1392d others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093561 | |||||||
| chr13:48093742 | C | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
202 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.125+1212G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093742 | |||||||
| chr13:48093788 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.125+1166C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093788 | |||||||
| chr13:48093882 | G | A | 33 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(30): Show |
55 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.125+1072C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093882 | |||||||
| chr13:48094016 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0179 |
4 | HG00738.hp1 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+938C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094016 | |||||||
| chr13:48094131 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.125+823G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094131 | |||||||
| chr13:48094253 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+701C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094253 | |||||||
| chr13:48094274 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(40): Show |
97 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.125+680T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094274 | |||||||
| chr13:48094336 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+618C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094336 | |||||||
| chr13:48094415 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.125+539G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094415 | |||||||
| chr13:48094491 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(7): Show |
39 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.125+463C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094491 | |||||||
| chr13:48094494 | G | C | 1 | a0001c0001t0003g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.125+460C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094494 | |||||||
| chr13:48094613 | G | GTC | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0050 others(7): Show |
21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.125+339_125+340dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094613 | |||||||
| chr13:48094656 | G | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(56): Show |
147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.125+298C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094656 | |||||||
| chr13:48094678 | A | G | 23 | a0001c0001t0002g0009 a0001c0001t0002g0027 a0001c0001t0002g0028 others(20): Show |
34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+276T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094678 | |||||||
| chr13:48094746 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.125+208G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094746 | |||||||
| chr13:48094851 | C | A | 1 | a0001c0001t0002g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.125+103G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094851 | |||||||
| chr13:48094928 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(50): Show |
136 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.125+26G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094928 | |||||||
| chr13:48094937 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.125+17G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094937 |