Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10001 |
| ensemblid | ENSG00000133997.12 |
| hgncid | 19970 |
| symbol | MED6 |
| name | mediator complex subunit 6 |
| refseq_nuc | NM_005466.4 |
| refseq_prot | NP_005457.2 |
| ensembl_nuc | ENST00000256379.10 |
| ensembl_prot | ENSP00000256379.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 70583221 |
| end | 70600655 |
| strand | - |
| ver | v1.2 |
| region | chr14:70583221-70600655 |
| region5000 | chr14:70578221-70605655 |
| regionname0 | MED6_chr14_70583221_70600655 |
| regionname5000 | MED6_chr14_70578221_70605655 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 246 | 403 | 86 | 64 | 193 | 12 | 46 | 150 | MED6_chr14_70578221_70605655 | MED6 | MAAVD others(241): Show |
chr14 | 70578221 | 70605655 |
| a0002 | 0/0 | 246 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | MAAVD others(241): Show |
chr14 | 70578221 | 70605655 |
| a0003 | 0/0 | 246 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | MAAVD others(241): Show |
chr14 | 70578221 | 70605655 |
| a0004 | 0/0 | 246 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | MAAVD others(241): Show |
chr14 | 70578221 | 70605655 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 738 | 397 | 80 | 64 | 193 | 12 | 46 | MED6_chr14_70578221_70605655 | MED6 | ATGGC others(733): Show |
chr14 | 70578221 | 70605655 | ||
| a0001c0002 | 0/0 | 738 | 6 | 6 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | ATGGC others(733): Show |
chr14 | 70578221 | 70605655 | ||
| a0002c0004 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | ATGGC others(733): Show |
chr14 | 70578221 | 70605655 | ||
| a0003c0005 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | ATGGC others(733): Show |
chr14 | 70578221 | 70605655 | ||
| a0004c0003 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | ATGGC others(733): Show |
chr14 | 70578221 | 70605655 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2351 | 203 | 20 | 42 | 104 | 7 | 28 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0002 | 0/0 | 2351 | 76 | 8 | 8 | 52 | 1 | 7 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0003 | 0/0 | 2351 | 29 | 15 | 3 | 11 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0004 | 0/0 | 2351 | 27 | 16 | 4 | 6 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0005 | 0/0 | 2351 | 15 | 0 | 0 | 15 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0006 | 0/0 | 2351 | 15 | 11 | 4 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0007 | 0/0 | 2351 | 10 | 1 | 3 | 3 | 1 | 2 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0009 | 0/0 | 2351 | 5 | 0 | 0 | 0 | 3 | 2 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0010 | 0/0 | 2351 | 4 | 4 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0011 | 0/0 | 2351 | 3 | 0 | 0 | 0 | 0 | 3 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0012 | 0/0 | 2351 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0013 | 0/0 | 2351 | 2 | 0 | 0 | 0 | 0 | 2 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0014 | 0/0 | 2351 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0015 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0016 | 0/0 | 2351 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0017 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0001t0018 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0001c0002t0008 | 0/0 | 2351 | 6 | 6 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0002c0004t0001 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0003c0005t0003 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| a0004c0003t0002 | 0/0 | 2351 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | GTAAA others(2346): Show |
chr14 | 70578221 | 70605655 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 41 | 2 | 12 | 17 | 3 | 6 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0002 | 0/0 | 28 | 0 | 2 | 23 | 0 | 3 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0003 | 0/0 | 28 | 1 | 8 | 19 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0004 | 0/0 | 20 | 1 | 2 | 14 | 0 | 3 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0006 | 0/0 | 15 | 1 | 7 | 2 | 1 | 4 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0026 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0005 | 0/0 | 18 | 0 | 2 | 13 | 1 | 2 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0009 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0011 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0007 | 0/0 | 14 | 6 | 1 | 7 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0014 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0008 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0005g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0005g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0006g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0006g0019 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0006g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0006g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0007g0013 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0007g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0009g0017 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0009g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0010g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0011g0031 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0012g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0013g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0015g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0001t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0002t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0002t0008g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0002t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0001c0002t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0002c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0003c0005t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| a0004c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0017 | EUR | GBR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0013 | EUR | FIN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0133 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01517 | hp2 | a0001 | c0001 | t0009 | g0017 | EUR | IBS | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02040 | hp2 | a0002 | c0004 | t0001 | g0113 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0053 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0055 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0134 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0129 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0128 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0130 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02896 | hp1 | a0001 | c0002 | t0008 | g0032 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02896 | hp2 | a0001 | c0002 | t0008 | g0034 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02897 | hp1 | a0001 | c0002 | t0008 | g0032 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03239 | hp1 | a0001 | c0001 | t0011 | g0031 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03453 | hp1 | a0001 | c0002 | t0008 | g0054 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03490 | hp2 | a0001 | c0001 | t0013 | g0044 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0017 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0017 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03492 | hp2 | a0001 | c0001 | t0013 | g0044 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0031 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03704 | hp2 | a0001 | c0001 | t0016 | g0142 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0031 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0049 | SAS | STU | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | YRI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | CHB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | CHB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18940 | hp2 | a0003 | c0005 | t0003 | g0059 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18953 | hp2 | a0001 | c0001 | t0015 | g0061 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18984 | hp2 | a0001 | c0001 | t0017 | g0118 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18993 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19012 | hp2 | a0004 | c0003 | t0002 | g0062 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0132 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | YRI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ASW | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ASW | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20805 | hp2 | a0001 | c0001 | t0009 | g0099 | EUR | TSI | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | GIH | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02109 | hp2 | a0001 | c0002 | t0008 | g0034 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | MSL | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | USA | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0103 | REF | REF | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MED6_chr14_70578221_70605655 | MED6 | chr14 | 70578221 | 70605655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70584914 | T | C | 1 | a0004 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.640A>G | p.Ile214Val | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 658/2351 | 640/741 | 214/246 | chr14 | 70584914 | |||
| chr14:70585758 | G | A | 1 | a0002 | 1 | HG02040.hp2 | missense_variant&splice_region_variant | MODERATE | c.608C>T | p.Pro203Leu | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/8 | 626/2351 | 608/741 | 203/246 | chr14 | 70585758 | |||
| chr14:70593323 | G | C | 1 | a0003 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.330C>G | p.Asp110Glu | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 4/8 | 348/2351 | 330/741 | 110/246 | chr14 | 70593323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70592974 | A | G | 1 | a0001c0002 | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.372T>C | p.His124His | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/8 | 390/2351 | 372/741 | 124/246 | chr14 | 70592974 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70583291 | A | G | 1 | a0001c0001t0015 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 1522 | chr14 | 70583291 | ||||||
| chr14:70583340 | T | C | 1 | a0001c0001t0016 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1473A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 1473 | chr14 | 70583340 | ||||||
| chr14:70583733 | A | C | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(2): Show |
25 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1080T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 1080 | chr14 | 70583733 | ||||||
| chr14:70583759 | T | C | 1 | a0001c0001t0017 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 1054 | chr14 | 70583759 | ||||||
| chr14:70583792 | A | C | 1 | a0001c0001t0013 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1021T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 1021 | chr14 | 70583792 | ||||||
| chr14:70583829 | A | G | 1 | a0001c0001t0009 | 5 | HG00140.hp2 HG01517.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 984 | chr14 | 70583829 | ||||||
| chr14:70583844 | C | G | 1 | a0001c0001t0011 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*969G>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 969 | chr14 | 70583844 | ||||||
| chr14:70583871 | C | T | 1 | a0001c0001t0005 | 15 | HG00558.hp1 HG02080.hp2 NA18612.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*942G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 942 | chr14 | 70583871 | ||||||
| chr14:70583943 | A | G | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(3): Show |
103 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*870T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 870 | chr14 | 70583943 | ||||||
| chr14:70583998 | C | T | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(1): Show |
33 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*815G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 815 | chr14 | 70583998 | ||||||
| chr14:70584075 | T | C | 1 | a0001c0001t0004 | 27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*738A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 738 | chr14 | 70584075 | ||||||
| chr14:70584175 | A | G | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
193 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*638T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 638 | chr14 | 70584175 | ||||||
| chr14:70584180 | T | G | 1 | a0001c0001t0013 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*633A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 633 | chr14 | 70584180 | ||||||
| chr14:70584212 | T | C | 1 | a0001c0001t0010 | 4 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*601A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 601 | chr14 | 70584212 | ||||||
| chr14:70584266 | A | G | 5 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0011 others(2): Show |
25 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*547T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 547 | chr14 | 70584266 | ||||||
| chr14:70584371 | A | G | 3 | a0001c0001t0002 a0001c0001t0005 a0004c0003t0002 |
92 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*442T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 442 | chr14 | 70584371 | ||||||
| chr14:70584385 | T | C | 1 | a0001c0001t0012 | 2 | HG01884.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*428A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 428 | chr14 | 70584385 | ||||||
| chr14:70584406 | G | A | 1 | a0001c0001t0014 | 2 | HG02145.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*407C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 407 | chr14 | 70584406 | ||||||
| chr14:70584516 | T | C | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
183 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 297 | chr14 | 70584516 | ||||||
| chr14:70584562 | G | T | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0015 others(1): Show |
33 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*251C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 251 | chr14 | 70584562 | ||||||
| chr14:70584577 | T | C | 1 | a0001c0002t0008 | 6 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*236A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 236 | chr14 | 70584577 | ||||||
| chr14:70584672 | G | A | 1 | a0001c0001t0010 | 4 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*141C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 8/8 | 141 | chr14 | 70584672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70585030 | A | G | 1 | a0001c0001t0001g0029 | 3 | HG01109.hp1 HG01175.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.611-87T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585030 | |||||||
| chr14:70585089 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.611-146T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585089 | |||||||
| chr14:70585196 | T | C | 1 | a0001c0002t0008g0034 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.611-253A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585196 | |||||||
| chr14:70585358 | TTCACTAC others(5): Show |
T | 1 | a0001c0001t0006g0018 | 4 | HG01081.hp1 HG02109.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+386_610+397del others(12): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585358 | |||||||
| chr14:70585391 | C | T | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.610+365G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585391 | |||||||
| chr14:70585410 | C | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(78): Show |
193 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.610+346G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585410 | |||||||
| chr14:70585445 | G | A | 1 | a0001c0001t0005g0083 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.610+311C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585445 | |||||||
| chr14:70585454 | A | C | 39 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(36): Show |
92 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.610+302T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585454 | |||||||
| chr14:70585491 | G | A | 1 | a0001c0001t0003g0056 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.610+265C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585491 | |||||||
| chr14:70585555 | C | CT | 7 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(4): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.610+200dupA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585555 | |||||||
| chr14:70585561 | T | TTTTTC | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(66): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.610+194_610+195ins others(5): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585561 | |||||||
| chr14:70585584 | T | C | 1 | a0001c0002t0008g0034 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.610+172A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 7/7 | chr14 | 70585584 | |||||||
| chr14:70585814 | G | T | 13 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0033 others(10): Show |
33 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.583-31C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70585814 | |||||||
| chr14:70586081 | C | T | 12 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(9): Show |
25 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.583-298G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586081 | |||||||
| chr14:70586307 | G | A | 4 | a0001c0001t0007g0013 a0001c0001t0007g0049 a0001c0001t0007g0133 others(1): Show |
10 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-524C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586307 | |||||||
| chr14:70586483 | C | A | 1 | a0001c0001t0002g0136 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.583-700G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586483 | |||||||
| chr14:70586589 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0009g0017 a0001c0001t0009g0099 |
7 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.583-806T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586589 | |||||||
| chr14:70586623 | T | A | 1 | a0001c0001t0002g0071 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.583-840A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586623 | |||||||
| chr14:70586804 | C | T | 4 | a0001c0001t0007g0013 a0001c0001t0007g0049 a0001c0001t0007g0133 others(1): Show |
10 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-1021G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586804 | |||||||
| chr14:70586885 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.583-1102G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586885 | |||||||
| chr14:70586890 | T | C | 7 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 others(4): Show |
10 | HG02145.hp2 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-1107A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70586890 | |||||||
| chr14:70587103 | G | C | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.583-1320C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587103 | |||||||
| chr14:70587180 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.583-1397A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587180 | |||||||
| chr14:70587330 | C | T | 1 | a0001c0001t0001g0027 | 3 | HG02293.hp1 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.583-1547G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587330 | |||||||
| chr14:70587498 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.583-1715A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587498 | |||||||
| chr14:70587609 | A | C | 2 | a0001c0001t0004g0012 a0001c0001t0004g0085 |
7 | HG00621.hp2 HG01069.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.583-1826T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587609 | |||||||
| chr14:70587667 | T | C | 77 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(74): Show |
183 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.583-1884A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587667 | |||||||
| chr14:70587761 | T | C | 43 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(40): Show |
98 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.583-1978A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587761 | |||||||
| chr14:70587910 | G | A | 1 | a0001c0001t0005g0073 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.583-2127C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70587910 | |||||||
| chr14:70588019 | G | A | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.583-2236C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588019 | |||||||
| chr14:70588026 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.583-2243A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588026 | |||||||
| chr14:70588100 | G | A | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.583-2317C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588100 | |||||||
| chr14:70588127 | A | T | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.583-2344T>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588127 | |||||||
| chr14:70588129 | T | C | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.583-2346A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588129 | |||||||
| chr14:70588275 | G | A | 39 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(36): Show |
92 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.583-2492C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588275 | |||||||
| chr14:70588369 | T | C | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.583-2586A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588369 | |||||||
| chr14:70588415 | G | C | 2 | a0001c0002t0008g0032 a0001c0002t0008g0055 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.583-2632C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588415 | |||||||
| chr14:70588480 | T | C | 4 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 others(1): Show |
5 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.583-2697A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588480 | |||||||
| chr14:70588493 | G | C | 2 | a0001c0001t0004g0008 a0001c0001t0004g0016 |
15 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.583-2710C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588493 | |||||||
| chr14:70588562 | T | C | 2 | a0001c0001t0004g0012 a0001c0001t0004g0085 |
7 | HG00621.hp2 HG01069.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.582+2704A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588562 | |||||||
| chr14:70588687 | AAAATAAT others(12): Show |
A | 1 | a0001c0001t0002g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.582+2560_582+2578d others(21): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588687 | |||||||
| chr14:70588688 | A | AAAT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0030 others(4): Show |
13 | HG00438.hp2 HG01891.hp2 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.582+2575_582+2577d others(5): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAAT | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(26): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.582+2575_582+2577d others(5): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAAT | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(20): Show |
59 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.582+2572_582+2577d others(8): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(2): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0024 others(3): Show |
6 | HG00099.hp1 HG00621.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.582+2569_582+2577d others(11): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(5): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0046 others(5): Show |
18 | HG02015.hp1 HG02145.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.582+2566_582+2577d others(14): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(8): Show |
A | 8 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(5): Show |
16 | HG01081.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.582+2563_582+2577d others(17): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(11): Show |
A | 7 | a0001c0001t0001g0002 a0001c0001t0002g0021 a0001c0001t0002g0063 others(4): Show |
13 | HG00673.hp2 HG02083.hp2 HG03239.hp1 others(10): Show |
intron_variant | MODIFIER | c.582+2560_582+2577d others(20): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(14): Show |
A | 51 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(48): Show |
118 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.582+2557_582+2577d others(23): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(17): Show |
A | 12 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0033 others(9): Show |
33 | HG00621.hp2 HG00733.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.582+2554_582+2577d others(26): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588688 | AAATAATA others(20): Show |
A | 3 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 |
4 | HG02145.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+2551_582+2577d others(29): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588688 | |||||||
| chr14:70588745 | G | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0090 others(2): Show |
34 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.582+2521C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588745 | |||||||
| chr14:70588868 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.582+2398G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588868 | |||||||
| chr14:70588932 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.582+2334A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70588932 | |||||||
| chr14:70589005 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.582+2261T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589005 | |||||||
| chr14:70589314 | T | C | 1 | a0001c0001t0001g0025 | 3 | HG00673.hp1 NA18977.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.582+1952A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589314 | |||||||
| chr14:70589414 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.582+1852G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589414 | |||||||
| chr14:70589546 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.582+1720A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589546 | |||||||
| chr14:70589592 | AT | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0058 |
3 | HG00733.hp2 HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.582+1673delA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589592 | |||||||
| chr14:70589636 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.582+1630C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589636 | |||||||
| chr14:70589846 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
4 | HG01081.hp2 HG01106.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1420A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589846 | |||||||
| chr14:70589915 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0107 |
4 | HG00280.hp1 HG00735.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+1351A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70589915 | |||||||
| chr14:70590100 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.582+1166A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590100 | |||||||
| chr14:70590190 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0110 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.582+1076G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590190 | |||||||
| chr14:70590382 | G | T | 1 | a0001c0001t0012g0050 | 2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.582+884C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590382 | |||||||
| chr14:70590392 | C | G | 1 | a0001c0002t0008g0034 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.582+874G>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590392 | |||||||
| chr14:70590595 | G | T | 1 | a0001c0001t0004g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.582+671C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590595 | |||||||
| chr14:70590706 | G | A | 2 | a0001c0001t0006g0020 a0001c0001t0006g0143 |
5 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.582+560C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590706 | |||||||
| chr14:70590719 | T | C | 7 | a0001c0001t0004g0008 a0001c0001t0004g0016 a0001c0001t0004g0084 others(4): Show |
20 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.582+547A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590719 | |||||||
| chr14:70590800 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+466A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590800 | |||||||
| chr14:70590841 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0027 others(5): Show |
52 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.582+425A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70590841 | |||||||
| chr14:70591034 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0036 a0001c0001t0002g0040 |
7 | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+232G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70591034 | |||||||
| chr14:70591065 | C | A | 6 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 others(3): Show |
9 | HG02145.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.582+201G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70591065 | |||||||
| chr14:70591116 | C | T | 1 | a0001c0001t0004g0012 | 6 | HG00621.hp2 HG02080.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+150G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70591116 | |||||||
| chr14:70591157 | G | A | 1 | a0001c0002t0008g0034 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.582+109C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70591157 | |||||||
| chr14:70591183 | T | C | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.582+83A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 6/7 | chr14 | 70591183 | |||||||
| chr14:70591418 | A | G | 1 | a0001c0002t0008g0054 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.467-37T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591418 | |||||||
| chr14:70591650 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0045 |
8 | HG01109.hp1 HG01175.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-269C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591650 | |||||||
| chr14:70591737 | T | G | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.467-356A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591737 | |||||||
| chr14:70591781 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.467-400C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591781 | |||||||
| chr14:70591902 | T | G | 1 | a0001c0001t0007g0133 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.467-521A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591902 | |||||||
| chr14:70591915 | G | A | 65 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(62): Show |
158 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.467-534C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591915 | |||||||
| chr14:70591985 | T | C | 1 | a0001c0001t0001g0024 | 3 | HG01257.hp2 HG01496.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.467-604A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591985 | |||||||
| chr14:70591994 | G | A | 2 | a0001c0001t0003g0058 a0002c0004t0001g0113 |
2 | HG01192.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.467-613C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70591994 | |||||||
| chr14:70592063 | C | A | 4 | a0001c0001t0007g0013 a0001c0001t0007g0049 a0001c0001t0007g0133 others(1): Show |
10 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.467-682G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592063 | |||||||
| chr14:70592117 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.467-736A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592117 | |||||||
| chr14:70592185 | A | C | 1 | a0001c0001t0002g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.466+695T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592185 | |||||||
| chr14:70592215 | G | C | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.466+665C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592215 | |||||||
| chr14:70592217 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.466+663T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592217 | |||||||
| chr14:70592257 | A | G | 4 | a0001c0001t0007g0013 a0001c0001t0007g0049 a0001c0001t0007g0133 others(1): Show |
10 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+623T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592257 | |||||||
| chr14:70592264 | C | T | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.466+616G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592264 | |||||||
| chr14:70592324 | A | T | 1 | a0001c0001t0018g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.466+556T>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592324 | |||||||
| chr14:70592361 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.466+519G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592361 | |||||||
| chr14:70592447 | C | T | 1 | a0001c0001t0018g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.466+433G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592447 | |||||||
| chr14:70592473 | T | C | 2 | a0001c0001t0004g0012 a0001c0001t0004g0085 |
7 | HG00621.hp2 HG01069.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+407A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592473 | |||||||
| chr14:70592478 | C | CT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(24): Show |
89 | HG00323.hp1 HG00597.hp2 HG01081.hp2 others(86): Show |
intron_variant | MODIFIER | c.466+401dupA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | C | CTT | 14 | a0001c0001t0001g0045 a0001c0001t0001g0097 a0001c0001t0002g0011 others(11): Show |
25 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.466+400_466+401dup others(2): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | C | CTTT | 4 | a0001c0001t0002g0021 a0001c0001t0002g0036 a0001c0001t0004g0086 others(1): Show |
7 | HG02615.hp2 HG02717.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+399_466+401dup others(3): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0010g0048 a0001c0001t0010g0128 |
3 | HG02818.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.466+390_466+401dup others(12): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CT | C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0110 others(14): Show |
24 | HG00738.hp1 HG01106.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.466+401delA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTT | C | 10 | a0001c0001t0003g0007 a0001c0001t0003g0033 a0001c0001t0003g0056 others(7): Show |
38 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.466+400_466+401del others(2): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTTTTTTT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(23): Show |
108 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.466+395_466+401del others(7): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0004g0085 |
3 | HG01069.hp1 HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.466+391_466+401del others(11): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0012 | 6 | HG00621.hp2 HG02080.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+390_466+401del others(12): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0010g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.466+389_466+401del others(13): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592478 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0077 a0004c0003t0002g0062 |
4 | HG00438.hp1 HG02027.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+386_466+401del others(16): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592478 | |||||||
| chr14:70592538 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(74): Show |
183 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.466+342T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592538 | |||||||
| chr14:70592595 | T | C | 76 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(73): Show |
182 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.466+285A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592595 | |||||||
| chr14:70592603 | C | T | 2 | a0001c0001t0004g0012 a0001c0001t0004g0085 |
7 | HG00621.hp2 HG01069.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+277G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | 70592603 | |||||||
| chr14:70593109 | T | C | 1 | a0001c0001t0004g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.358-121A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 4/7 | chr14 | 70593109 | |||||||
| chr14:70593412 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.275-34C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593412 | |||||||
| chr14:70593436 | G | T | 1 | a0001c0001t0002g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.275-58C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593436 | |||||||
| chr14:70593489 | C | CAATTACT others(7): Show |
1 | a0001c0001t0001g0106 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.275-125_275-112dup others(14): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593489 | |||||||
| chr14:70593546 | T | C | 3 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 |
4 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-168A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593546 | |||||||
| chr14:70593703 | G | A | 2 | a0001c0001t0006g0019 a0001c0001t0006g0053 |
3 | HG02280.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.275-325C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593703 | |||||||
| chr14:70593884 | T | C | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.275-506A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593884 | |||||||
| chr14:70593927 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(27): Show |
109 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.275-549G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593927 | |||||||
| chr14:70593929 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.275-551C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70593929 | |||||||
| chr14:70594104 | C | A | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.275-726G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594104 | |||||||
| chr14:70594120 | A | G | 56 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(53): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.275-742T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594120 | |||||||
| chr14:70594191 | C | T | 4 | a0001c0001t0007g0013 a0001c0001t0007g0049 a0001c0001t0007g0133 others(1): Show |
10 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.275-813G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594191 | |||||||
| chr14:70594201 | T | A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(4): Show |
17 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.275-823A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594201 | |||||||
| chr14:70594235 | C | G | 84 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
196 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.275-857G>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594235 | |||||||
| chr14:70594291 | T | C | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.275-913A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594291 | |||||||
| chr14:70594310 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.275-932C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594310 | |||||||
| chr14:70594368 | C | T | 4 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-990G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594368 | |||||||
| chr14:70594370 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18983.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.275-992G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594370 | |||||||
| chr14:70594418 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.275-1040T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594418 | |||||||
| chr14:70594424 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.275-1046A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594424 | |||||||
| chr14:70594556 | G | A | 4 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-1178C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594556 | |||||||
| chr14:70594575 | C | T | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.275-1197G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594575 | |||||||
| chr14:70594609 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275-1231C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594609 | |||||||
| chr14:70594689 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.275-1311G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594689 | |||||||
| chr14:70594716 | C | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0045 others(1): Show |
9 | HG01109.hp1 HG01175.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.275-1338G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594716 | |||||||
| chr14:70594734 | C | G | 39 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(36): Show |
92 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.275-1356G>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594734 | |||||||
| chr14:70594745 | G | A | 56 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(53): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.275-1367C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594745 | |||||||
| chr14:70594832 | A | G | 68 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(65): Show |
156 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.275-1454T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594832 | |||||||
| chr14:70594850 | G | C | 1 | a0001c0001t0002g0078 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.275-1472C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594850 | |||||||
| chr14:70594905 | T | A | 1 | a0001c0002t0008g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.275-1527A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70594905 | |||||||
| chr14:70595016 | A | C | 47 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(44): Show |
104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.274+1595T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595016 | |||||||
| chr14:70595119 | T | C | 47 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(44): Show |
104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.274+1492A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595119 | |||||||
| chr14:70595127 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(65): Show |
156 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.274+1484C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595127 | |||||||
| chr14:70595239 | T | C | 65 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(62): Show |
158 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.274+1372A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595239 | |||||||
| chr14:70595257 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.274+1354G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595257 | |||||||
| chr14:70595297 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.274+1314G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595297 | |||||||
| chr14:70595401 | G | A | 2 | a0001c0001t0010g0128 a0001c0001t0010g0129 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.274+1210C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595401 | |||||||
| chr14:70595422 | C | A | 1 | a0001c0001t0001g0046 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.274+1189G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595422 | |||||||
| chr14:70595524 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(120): Show |
321 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.274+1087A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595524 | |||||||
| chr14:70595541 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.274+1070C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595541 | |||||||
| chr14:70595591 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0033 others(6): Show |
27 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.274+1020G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595591 | |||||||
| chr14:70595625 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.274+986G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595625 | |||||||
| chr14:70595626 | A | G | 84 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
196 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.274+985T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595626 | |||||||
| chr14:70595661 | T | C | 1 | a0001c0001t0007g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.274+950A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595661 | |||||||
| chr14:70595662 | G | A | 1 | a0001c0001t0015g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.274+949C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595662 | |||||||
| chr14:70595715 | T | C | 56 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(53): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.274+896A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595715 | |||||||
| chr14:70595718 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(74): Show |
183 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+893G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70595718 | |||||||
| chr14:70596134 | T | G | 57 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(54): Show |
132 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.274+477A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596134 | |||||||
| chr14:70596205 | A | C | 1 | a0001c0001t0018g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274+406T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596205 | |||||||
| chr14:70596296 | G | A | 7 | a0001c0001t0004g0008 a0001c0001t0004g0016 a0001c0001t0004g0084 others(4): Show |
20 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.274+315C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596296 | |||||||
| chr14:70596354 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.274+257A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596354 | |||||||
| chr14:70596463 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+148A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596463 | |||||||
| chr14:70596511 | C | T | 4 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 others(1): Show |
7 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+100G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596511 | |||||||
| chr14:70596513 | C | A | 1 | a0001c0001t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.274+98G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596513 | |||||||
| chr14:70596563 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.274+48A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 3/7 | chr14 | 70596563 | |||||||
| chr14:70597076 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.183-374A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597076 | |||||||
| chr14:70597103 | C | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01243.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.183-401G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597103 | |||||||
| chr14:70597233 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.182+385A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597233 | |||||||
| chr14:70597273 | T | C | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.182+345A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597273 | |||||||
| chr14:70597297 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.182+321A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597297 | |||||||
| chr14:70597476 | T | A | 1 | a0001c0002t0008g0034 | 2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.182+142A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597476 | |||||||
| chr14:70597568 | A | C | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.182+50T>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597568 | |||||||
| chr14:70597597 | C | T | 81 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(78): Show |
193 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.182+21G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 2/7 | chr14 | 70597597 | |||||||
| chr14:70597860 | T | G | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-83A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70597860 | |||||||
| chr14:70597866 | G | A | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.23-89C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70597866 | |||||||
| chr14:70598050 | T | G | 1 | a0001c0001t0002g0040 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.23-273A>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598050 | |||||||
| chr14:70598209 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.23-432C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598209 | |||||||
| chr14:70598235 | T | A | 1 | a0001c0001t0011g0031 | 3 | HG03239.hp1 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.23-458A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598235 | |||||||
| chr14:70598341 | G | T | 4 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-564C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598341 | |||||||
| chr14:70598349 | C | T | 5 | a0001c0001t0006g0018 a0001c0001t0006g0019 a0001c0001t0006g0020 others(2): Show |
15 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-572G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598349 | |||||||
| chr14:70598469 | C | T | 4 | a0001c0001t0010g0048 a0001c0001t0010g0128 a0001c0001t0010g0129 others(1): Show |
7 | HG02723.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-692G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598469 | |||||||
| chr14:70598504 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.23-727G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598504 | |||||||
| chr14:70598556 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0124 |
3 | NA18952.hp2 NA18982.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.23-779C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598556 | |||||||
| chr14:70598647 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.23-870C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598647 | |||||||
| chr14:70598733 | C | CT | 6 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0064 others(3): Show |
16 | HG00609.hp2 HG01255.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.23-957dupA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598733 | |||||||
| chr14:70598733 | CT | C | 17 | a0001c0001t0004g0089 a0001c0001t0006g0018 a0001c0001t0006g0019 others(14): Show |
36 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.23-957delA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598733 | |||||||
| chr14:70598743 | T | A | 9 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0033 others(6): Show |
27 | HG00733.hp2 HG01074.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-966A>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70598743 | |||||||
| chr14:70599280 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.22+1336T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599280 | |||||||
| chr14:70599345 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.22+1271T>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599345 | |||||||
| chr14:70599491 | C | T | 1 | a0001c0001t0004g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+1125G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599491 | |||||||
| chr14:70599578 | T | C | 84 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
196 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.22+1038A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599578 | |||||||
| chr14:70599726 | AT | A | 47 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(44): Show |
104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.22+889delA | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599726 | |||||||
| chr14:70599734 | C | A | 2 | a0001c0001t0005g0041 a0001c0001t0005g0083 |
3 | NA18946.hp1 NA18948.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.22+882G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599734 | |||||||
| chr14:70599767 | A | G | 39 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(36): Show |
92 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.22+849T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599767 | |||||||
| chr14:70599776 | G | C | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+840C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599776 | |||||||
| chr14:70599811 | GAAAT | G | 42 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(39): Show |
96 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.22+801_22+804delAT others(2): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599811 | |||||||
| chr14:70599849 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.22+767G>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599849 | |||||||
| chr14:70599851 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.22+765T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599851 | |||||||
| chr14:70599851 | A | T | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.22+765T>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599851 | |||||||
| chr14:70599876 | G | C | 56 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(53): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.22+740C>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599876 | |||||||
| chr14:70599937 | G | T | 1 | a0004c0003t0002g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.22+679C>A | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599937 | |||||||
| chr14:70599994 | C | A | 4 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+622G>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70599994 | |||||||
| chr14:70600074 | T | C | 84 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(81): Show |
196 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.22+542A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600074 | |||||||
| chr14:70600078 | G | A | 56 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(53): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.22+538C>T | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600078 | |||||||
| chr14:70600317 | T | C | 3 | a0001c0002t0008g0032 a0001c0002t0008g0054 a0001c0002t0008g0055 |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+299A>G | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600317 | |||||||
| chr14:70600379 | A | G | 3 | a0001c0002t0008g0032 a0001c0002t0008g0054 a0001c0002t0008g0055 |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+237T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600379 | |||||||
| chr14:70600438 | A | AG | 9 | a0001c0001t0004g0008 a0001c0001t0004g0012 a0001c0001t0004g0016 others(6): Show |
27 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.22+177dupC | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600438 | |||||||
| chr14:70600439 | G | GA | 10 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0001t0001g0140 others(7): Show |
21 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+176dupT | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600439 | |||||||
| chr14:70600439 | GA | G | 50 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0011 others(47): Show |
123 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.22+176delT | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600439 | |||||||
| chr14:70600440 | A | G | 4 | a0001c0001t0003g0051 a0001c0001t0003g0137 a0001c0001t0003g0138 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+176T>C | MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 1/7 | chr14 | 70600440 |