Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10959 |
| ensemblid | ENSG00000086598.11 |
| hgncid | 16996 |
| symbol | TMED2 |
| name | transmembrane p24 trafficking protein 2 |
| refseq_nuc | NM_006815.4 |
| refseq_prot | NP_006806.1 |
| ensembl_nuc | ENST00000262225.8 |
| ensembl_prot | ENSP00000262225.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 123584552 |
| end | 123598582 |
| strand | + |
| ver | v1.2 |
| region | chr12:123584552-123598582 |
| region5000 | chr12:123579552-123603582 |
| regionname0 | TMED2_chr12_123584552_123598582 |
| regionname5000 | TMED2_chr12_123579552_123603582 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 603 | 265 | 88 | 64 | 62 | 18 | 32 | TMED2_chr12_123579552_123603582 | TMED2 | ATGGT others(598): Show |
chr12 | 123579552 | 123603582 | ||
| a0001c0002 | 0/0 | 603 | 13 | 0 | 0 | 13 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | ATGGT others(598): Show |
chr12 | 123579552 | 123603582 | ||
| a0001c0003 | 1/0 | 603 | 5 | 4 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | ATGGT others(598): Show |
chr12 | 123579552 | 123603582 | ||
| a0001c0004 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | ATGGT others(598): Show |
chr12 | 123579552 | 123603582 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2542 | 125 | 19 | 40 | 43 | 9 | 13 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0002 | 0/0 | 2544 | 34 | 12 | 3 | 11 | 1 | 7 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2539): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0003 | 0/0 | 2541 | 27 | 6 | 9 | 1 | 2 | 9 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0004 | 0/0 | 2543 | 19 | 15 | 3 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2538): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0005 | 0/0 | 2541 | 18 | 17 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0006 | 0/0 | 2542 | 10 | 0 | 3 | 2 | 5 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0007 | 0/0 | 2544 | 7 | 7 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2539): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0009 | 0/0 | 2532 | 5 | 4 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2527): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0010 | 0/0 | 2541 | 3 | 1 | 2 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0011 | 0/0 | 2543 | 2 | 0 | 0 | 1 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2538): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0012 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0013 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0014 | 0/0 | 2534 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2529): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0016 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2539): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0017 | 0/0 | 2542 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0018 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0019 | 0/0 | 2542 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0020 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2536): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0021 | 0/0 | 2542 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0022 | 0/0 | 2542 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0023 | 0/0 | 2543 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2538): Show |
chr12 | 123579552 | 123603582 |
| a0001c0001t0024 | 0/0 | 2542 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0002t0001 | 0/0 | 2542 | 11 | 0 | 0 | 11 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0002t0015 | 0/0 | 2542 | 2 | 0 | 0 | 2 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| a0001c0003t0008 | 1/0 | 2544 | 5 | 4 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2539): Show |
chr12 | 123579552 | 123603582 |
| a0001c0004t0001 | 0/0 | 2542 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | GAGAA others(2537): Show |
chr12 | 123579552 | 123603582 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 71 | 11 | 23 | 25 | 4 | 8 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 7 | 0 | 5 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0002 | 0/0 | 19 | 5 | 2 | 8 | 1 | 3 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0003 | 0/0 | 16 | 4 | 5 | 1 | 1 | 5 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0015 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0007g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0009g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0010g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0017g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0019g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0020g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0021g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0022g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0023g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0002t0015g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0003t0008g0011 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0029 | EUR | GBR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0037 | EUR | GBR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00280 | hp1 | a0001 | c0001 | t0022 | g0004 | EUR | FIN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0015 | EUR | FIN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01167 | hp1 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0058 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0039 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0008 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0028 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0038 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0008 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01978 | hp1 | a0001 | c0001 | t0017 | g0008 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0055 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02572 | hp2 | a0001 | c0003 | t0008 | g0011 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02809 | hp2 | a0001 | c0003 | t0008 | g0011 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02818 | hp2 | a0001 | c0003 | t0008 | g0011 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0056 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0049 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | BEB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0033 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0003 | AFR | YRI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18939 | hp2 | a0001 | c0002 | t0015 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18987 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18995 | hp2 | a0001 | c0002 | t0015 | g0072 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18999 | hp1 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19005 | hp1 | a0001 | c0001 | t0021 | g0003 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19057 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19062 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA19240 | hp2 | a0001 | c0003 | t0008 | g0011 | AFR | YRI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | TSI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | GIH | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | USA | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | USA | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | LWK | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0061 | REF | REF | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0008 | g0011 | REF | REF | TMED2_chr12_123579552_123603582 | TMED2 | chr12 | 123579552 | 123603582 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123584666 | T | C | 3 | a0001c0001 a0001c0002 a0001c0004 |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
synonymous_variant | LOW | c.30T>C | p.Leu10Leu | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 115/2544 | 30/606 | 10/201 | chr12 | 123584666 | |||
| chr12:123584667 | C | T | 1 | a0001c0002 | 13 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(10): Show |
synonymous_variant | LOW | c.31C>T | p.Leu11Leu | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 116/2544 | 31/606 | 11/201 | chr12 | 123584667 | |||
| chr12:123584780 | G | A | 1 | a0001c0004 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.144G>A | p.Glu48Glu | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 229/2544 | 144/606 | 48/201 | chr12 | 123584780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123584559 | C | T | 1 | a0001c0002t0015 | 2 | NA18939.hp2 NA18995.hp2 |
5_prime_UTR_variant | MODIFIER | c.-78C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 78 | chr12 | 123584559 | ||||||
| chr12:123584564 | GGGC | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
5_prime_UTR_variant | MODIFIER | c.-48_-46delGGC | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 46 | INFO_REALIGN_3_PRIME | chr12 | 123584564 | |||||
| chr12:123584564 | GGGCGGCG others(5): Show |
G | 2 | a0001c0001t0009 a0001c0001t0014 |
7 | HG01243.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-57_-46delGGCGGCGG others(4): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/4 | 46 | INFO_REALIGN_3_PRIME | chr12 | 123584564 | |||||
| chr12:123596837 | C | T | 1 | a0001c0001t0024 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 108 | chr12 | 123596837 | ||||||
| chr12:123597026 | C | A | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0017 |
9 | HG01243.hp1 HG01346.hp2 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*297C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 297 | chr12 | 123597026 | ||||||
| chr12:123597232 | G | T | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(1): Show |
29 | HG01109.hp2 HG01243.hp2 HG01256.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*503G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 503 | chr12 | 123597232 | ||||||
| chr12:123597351 | C | T | 1 | a0001c0001t0022 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 622 | chr12 | 123597351 | ||||||
| chr12:123597693 | C | A | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0018 others(6): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 964 | chr12 | 123597693 | ||||||
| chr12:123597786 | C | T | 1 | a0001c0001t0013 | 2 | HG02145.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1057C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1057 | chr12 | 123597786 | ||||||
| chr12:123597847 | C | CT | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0017 others(7): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*1134dupT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1135 | INFO_REALIGN_3_PRIME | chr12 | 123597847 | |||||
| chr12:123597847 | C | CTT | 4 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0014 others(1): Show |
24 | HG01109.hp2 HG01243.hp2 HG01256.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1133_*1134dupTT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1135 | INFO_REALIGN_3_PRIME | chr12 | 123597847 | |||||
| chr12:123597847 | C | CTTT | 1 | a0001c0001t0007 | 7 | HG02109.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1132_*1134dupTTT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1135 | INFO_REALIGN_3_PRIME | chr12 | 123597847 | |||||
| chr12:123597972 | C | G | 1 | a0001c0001t0019 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1243 | chr12 | 123597972 | ||||||
| chr12:123598038 | G | T | 1 | a0001c0001t0023 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1309 | chr12 | 123598038 | ||||||
| chr12:123598295 | G | A | 1 | a0001c0001t0012 | 2 | HG02976.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1566 | chr12 | 123598295 | ||||||
| chr12:123598316 | G | A | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1587 | chr12 | 123598316 | ||||||
| chr12:123598375 | A | C | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0020 others(1): Show |
31 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1646A>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1646 | chr12 | 123598375 | ||||||
| chr12:123598436 | A | G | 1 | a0001c0001t0016 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1707A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1707 | chr12 | 123598436 | ||||||
| chr12:123598496 | C | T | 1 | a0001c0001t0020 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1767C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 4/4 | 1767 | chr12 | 123598496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:123585067 | T | A | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.180+251T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585067 | |||||||
| chr12:123585120 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(38): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.180+304A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585120 | |||||||
| chr12:123585427 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180+611G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585427 | |||||||
| chr12:123585466 | G | A | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.180+650G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585466 | |||||||
| chr12:123585667 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(37): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.180+851A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585667 | |||||||
| chr12:123585733 | C | T | 1 | a0001c0001t0006g0039 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.180+917C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585733 | |||||||
| chr12:123585746 | A | G | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.180+930A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585746 | |||||||
| chr12:123585800 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0001g0082 |
7 | HG01070.hp2 HG01981.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-947G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585800 | |||||||
| chr12:123585827 | A | G | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.181-920A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123585827 | |||||||
| chr12:123586065 | A | C | 17 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0040 others(14): Show |
39 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.181-682A>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586065 | |||||||
| chr12:123586129 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03688.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.181-618G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586129 | |||||||
| chr12:123586296 | T | C | 12 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0040 others(9): Show |
30 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.181-451T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586296 | |||||||
| chr12:123586351 | C | CT | 15 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0080 others(12): Show |
22 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.181-378dupT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 123586351 | ||||||
| chr12:123586351 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0039 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.181-388_181-378del others(11): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 123586351 | ||||||
| chr12:123586381 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.181-366C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586381 | |||||||
| chr12:123586390 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.181-357G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586390 | |||||||
| chr12:123586444 | G | A | 32 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(29): Show |
88 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.181-303G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586444 | |||||||
| chr12:123586539 | G | A | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.181-208G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586539 | |||||||
| chr12:123586597 | G | T | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.181-150G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | chr12 | 123586597 | |||||||
| chr12:123586691 | T | TA | 7 | a0001c0001t0006g0015 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-53dupA | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 123586691 | ||||||
| chr12:123586960 | AT | A | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.373+24delT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 123586960 | ||||||
| chr12:123587008 | T | C | 1 | a0001c0001t0004g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.373+69T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587008 | |||||||
| chr12:123587035 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.373+96A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587035 | |||||||
| chr12:123587181 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(37): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.373+242C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587181 | |||||||
| chr12:123587218 | C | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(73): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.373+279C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587218 | |||||||
| chr12:123587228 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.373+289T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587228 | |||||||
| chr12:123587317 | G | A | 22 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(19): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.373+378G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587317 | |||||||
| chr12:123587721 | G | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0019g0004 others(1): Show |
15 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.373+782G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587721 | |||||||
| chr12:123587808 | A | G | 2 | a0001c0001t0003g0035 a0001c0001t0007g0010 |
6 | HG02109.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+869A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587808 | |||||||
| chr12:123587875 | A | G | 4 | a0001c0001t0005g0005 a0001c0001t0005g0045 a0001c0001t0005g0046 others(1): Show |
12 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.373+936A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123587875 | |||||||
| chr12:123588076 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.373+1137G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588076 | |||||||
| chr12:123588100 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.373+1161C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588100 | |||||||
| chr12:123588146 | T | G | 2 | a0001c0001t0004g0013 a0001c0001t0007g0013 |
4 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+1207T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588146 | |||||||
| chr12:123588187 | GT | G | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.373+1257delT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 123588187 | ||||||
| chr12:123588469 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.373+1530G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588469 | |||||||
| chr12:123588654 | A | G | 1 | a0001c0001t0004g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.374-1688A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588654 | |||||||
| chr12:123588922 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.374-1420A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588922 | |||||||
| chr12:123588989 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.374-1353C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123588989 | |||||||
| chr12:123589174 | G | C | 32 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(29): Show |
88 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.374-1168G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589174 | |||||||
| chr12:123589191 | G | A | 5 | a0001c0001t0009g0008 a0001c0001t0009g0057 a0001c0001t0009g0058 others(2): Show |
9 | HG01243.hp1 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.374-1151G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589191 | |||||||
| chr12:123589254 | T | A | 3 | a0001c0001t0005g0022 a0001c0001t0012g0048 a0001c0001t0012g0049 |
4 | HG02970.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.374-1088T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589254 | |||||||
| chr12:123589272 | G | A | 1 | a0001c0001t0009g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.374-1070G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589272 | |||||||
| chr12:123589364 | C | T | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.374-978C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589364 | |||||||
| chr12:123589400 | T | C | 1 | a0001c0001t0005g0023 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.374-942T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589400 | |||||||
| chr12:123589773 | A | T | 7 | a0001c0001t0006g0015 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.374-569A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589773 | |||||||
| chr12:123589818 | C | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(6): Show |
35 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.374-524C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589818 | |||||||
| chr12:123589903 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.374-439T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123589903 | |||||||
| chr12:123589985 | G | GA | 22 | a0001c0001t0003g0035 a0001c0001t0003g0051 a0001c0001t0004g0006 others(19): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.374-345dupA | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 123589985 | ||||||
| chr12:123590197 | C | G | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.374-145C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123590197 | |||||||
| chr12:123590284 | C | CA | 6 | a0001c0001t0001g0065 a0001c0001t0003g0052 a0001c0001t0004g0014 others(3): Show |
8 | HG01074.hp1 HG01243.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-41dupA | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 123590284 | ||||||
| chr12:123590301 | A | T | 7 | a0001c0001t0006g0015 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.374-41A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 2/3 | chr12 | 123590301 | |||||||
| chr12:123590516 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.481+67C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590516 | |||||||
| chr12:123590564 | A | G | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.481+115A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590564 | |||||||
| chr12:123590721 | C | A | 7 | a0001c0001t0006g0015 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+272C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590721 | |||||||
| chr12:123590809 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.481+360C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590809 | |||||||
| chr12:123590964 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(94): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.481+515T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590964 | |||||||
| chr12:123590965 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.481+516G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123590965 | |||||||
| chr12:123591056 | TAAATC | T | 8 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0021 others(5): Show |
28 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.481+609_481+613del others(5): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 123591056 | ||||||
| chr12:123591176 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481+727G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591176 | |||||||
| chr12:123591327 | G | A | 1 | a0001c0001t0005g0022 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.481+878G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591327 | |||||||
| chr12:123591368 | G | T | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.481+919G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591368 | |||||||
| chr12:123591374 | T | C | 10 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0040 others(7): Show |
28 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.481+925T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591374 | |||||||
| chr12:123591478 | T | C | 1 | a0001c0002t0001g0066 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.481+1029T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591478 | |||||||
| chr12:123591521 | C | T | 1 | a0001c0001t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.481+1072C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591521 | |||||||
| chr12:123591639 | G | A | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481+1190G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591639 | |||||||
| chr12:123591707 | C | T | 22 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(19): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.481+1258C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123591707 | |||||||
| chr12:123592075 | C | A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0040 a0001c0001t0003g0050 |
6 | HG00733.hp1 HG01934.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+1626C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592075 | |||||||
| chr12:123592259 | T | C | 21 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.481+1810T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592259 | |||||||
| chr12:123592347 | G | T | 1 | a0001c0001t0003g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481+1898G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592347 | |||||||
| chr12:123592348 | G | A | 1 | a0001c0001t0004g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481+1899G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592348 | |||||||
| chr12:123592450 | C | CA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(94): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.481+2001_481+2002i others(3): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592450 | |||||||
| chr12:123592617 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.481+2168T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592617 | |||||||
| chr12:123592650 | C | T | 5 | a0001c0001t0009g0008 a0001c0001t0009g0057 a0001c0001t0009g0058 others(2): Show |
9 | HG01243.hp1 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+2201C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592650 | |||||||
| chr12:123592665 | T | C | 4 | a0001c0001t0004g0014 a0001c0001t0004g0031 a0001c0001t0004g0032 others(1): Show |
6 | HG01243.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.481+2216T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592665 | |||||||
| chr12:123592703 | A | G | 1 | a0001c0001t0005g0023 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.481+2254A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123592703 | |||||||
| chr12:123593207 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0023g0033 |
4 | HG01109.hp2 HG01256.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+2758C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593207 | |||||||
| chr12:123593240 | A | AT | 20 | a0001c0001t0004g0006 a0001c0001t0004g0013 a0001c0001t0004g0014 others(17): Show |
39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.481+2791_481+2792i others(3): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593240 | |||||||
| chr12:123593260 | TG | T | 18 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0017 others(15): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+2812delG | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593260 | |||||||
| chr12:123593276 | G | A | 1 | a0001c0001t0005g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.481+2827G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593276 | |||||||
| chr12:123593314 | G | A | 1 | a0001c0001t0004g0017 | 3 | HG01109.hp2 HG01256.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.481+2865G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593314 | |||||||
| chr12:123593339 | A | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0029 |
5 | HG00099.hp1 HG00323.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+2890A>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593339 | |||||||
| chr12:123593355 | C | T | 14 | a0001c0001t0004g0006 a0001c0001t0004g0013 a0001c0001t0004g0014 others(11): Show |
33 | HG00099.hp1 HG00323.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.481+2906C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593355 | |||||||
| chr12:123593379 | A | G | 2 | a0001c0001t0012g0048 a0001c0001t0012g0049 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.481+2930A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593379 | |||||||
| chr12:123593513 | G | C | 1 | a0001c0001t0005g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.481+3064G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593513 | |||||||
| chr12:123593519 | T | C | 4 | a0001c0001t0005g0022 a0001c0001t0005g0060 a0001c0001t0012g0048 others(1): Show |
5 | HG02970.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+3070T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593519 | |||||||
| chr12:123593625 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.482-2980G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123593625 | |||||||
| chr12:123593962 | A | AT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0079 others(1): Show |
7 | HG00140.hp1 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2625dupT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 123593962 | ||||||
| chr12:123593962 | A | ATT | 18 | a0001c0001t0004g0006 a0001c0001t0004g0013 a0001c0001t0004g0014 others(15): Show |
37 | HG00099.hp1 HG00323.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.482-2626_482-2625d others(4): Show |
TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 123593962 | ||||||
| chr12:123594029 | A | T | 1 | a0001c0001t0002g0020 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.482-2576A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594029 | |||||||
| chr12:123594038 | C | G | 13 | a0001c0001t0004g0006 a0001c0001t0004g0013 a0001c0001t0004g0014 others(10): Show |
29 | HG01109.hp2 HG01243.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.482-2567C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594038 | |||||||
| chr12:123594137 | A | AT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(37): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.482-2453dupT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 123594137 | ||||||
| chr12:123594137 | AT | A | 21 | a0001c0001t0003g0053 a0001c0001t0004g0006 a0001c0001t0004g0013 others(18): Show |
40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.482-2453delT | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr12 | 123594137 | ||||||
| chr12:123594235 | C | T | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.482-2370C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594235 | |||||||
| chr12:123594244 | C | A | 7 | a0001c0001t0006g0015 a0001c0001t0006g0028 a0001c0001t0006g0029 others(4): Show |
10 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-2361C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594244 | |||||||
| chr12:123594253 | G | C | 1 | a0001c0001t0005g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.482-2352G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594253 | |||||||
| chr12:123594259 | C | T | 1 | a0001c0001t0001g0009 | 6 | HG00544.hp2 HG00597.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-2346C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594259 | |||||||
| chr12:123594324 | C | T | 4 | a0001c0001t0005g0005 a0001c0001t0005g0045 a0001c0001t0005g0046 others(1): Show |
12 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.482-2281C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594324 | |||||||
| chr12:123594386 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.482-2219G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594386 | |||||||
| chr12:123594500 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.482-2105G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594500 | |||||||
| chr12:123594536 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2069T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594536 | |||||||
| chr12:123594537 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2068T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594537 | |||||||
| chr12:123594538 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2067G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594538 | |||||||
| chr12:123594539 | T | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2066T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594539 | |||||||
| chr12:123594540 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2065T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594540 | |||||||
| chr12:123594540 | T | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2065T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594540 | |||||||
| chr12:123594541 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2064T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594541 | |||||||
| chr12:123594544 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2061G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594544 | |||||||
| chr12:123594545 | G | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2060G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594545 | |||||||
| chr12:123594545 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2060G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594545 | |||||||
| chr12:123594546 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2059T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594546 | |||||||
| chr12:123594550 | G | T | 11 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0035 others(8): Show |
29 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-2055G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594550 | |||||||
| chr12:123594553 | C | G | 1 | a0001c0001t0004g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.482-2052C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594553 | |||||||
| chr12:123594557 | A | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0046 |
2 | HG03486.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482-2048A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594557 | |||||||
| chr12:123594559 | A | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0046 |
2 | HG03486.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482-2046A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594559 | |||||||
| chr12:123594565 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2040C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594565 | |||||||
| chr12:123594567 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2038G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594567 | |||||||
| chr12:123594567 | G | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2038G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594567 | |||||||
| chr12:123594569 | G | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0046 |
2 | HG03486.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482-2036G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594569 | |||||||
| chr12:123594574 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2031A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594574 | |||||||
| chr12:123594576 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2029G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594576 | |||||||
| chr12:123594578 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2027G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594578 | |||||||
| chr12:123594580 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2025C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594580 | |||||||
| chr12:123594582 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2023G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594582 | |||||||
| chr12:123594588 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2017A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594588 | |||||||
| chr12:123594592 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2013A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594592 | |||||||
| chr12:123594594 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2011A>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594594 | |||||||
| chr12:123594598 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2007A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594598 | |||||||
| chr12:123594599 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2006A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594599 | |||||||
| chr12:123594602 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2003A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594602 | |||||||
| chr12:123594603 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2002A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594603 | |||||||
| chr12:123594605 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-2000T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594605 | |||||||
| chr12:123594615 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1990T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594615 | |||||||
| chr12:123594616 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1989G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594616 | |||||||
| chr12:123594617 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1988A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594617 | |||||||
| chr12:123594621 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.482-1984C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594621 | |||||||
| chr12:123594647 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1958G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594647 | |||||||
| chr12:123594652 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0046 |
2 | HG03486.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482-1953C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594652 | |||||||
| chr12:123594683 | T | A | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1922T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594683 | |||||||
| chr12:123594693 | G | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0046 |
2 | HG03486.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.482-1912G>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594693 | |||||||
| chr12:123594698 | A | G | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1907A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594698 | |||||||
| chr12:123594706 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1899G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594706 | |||||||
| chr12:123594708 | A | T | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1897A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594708 | |||||||
| chr12:123594715 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1890G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594715 | |||||||
| chr12:123594716 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1889C>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594716 | |||||||
| chr12:123594717 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1888A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594717 | |||||||
| chr12:123594738 | T | A | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1867T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594738 | |||||||
| chr12:123594740 | A | T | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1865A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594740 | |||||||
| chr12:123594741 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1864G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594741 | |||||||
| chr12:123594742 | T | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-1863T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594742 | |||||||
| chr12:123594747 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1858T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594747 | |||||||
| chr12:123594748 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1857A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594748 | |||||||
| chr12:123594755 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1850T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594755 | |||||||
| chr12:123594756 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1849A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594756 | |||||||
| chr12:123594804 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1801T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594804 | |||||||
| chr12:123594812 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1793A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594812 | |||||||
| chr12:123594815 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1790A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594815 | |||||||
| chr12:123594816 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1789G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594816 | |||||||
| chr12:123594818 | T | G | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1787T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594818 | |||||||
| chr12:123594839 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1766A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594839 | |||||||
| chr12:123594845 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1760T>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594845 | |||||||
| chr12:123594848 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1757T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594848 | |||||||
| chr12:123594857 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.482-1748A>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594857 | |||||||
| chr12:123594983 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.482-1622C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123594983 | |||||||
| chr12:123595280 | T | G | 1 | a0001c0002t0015g0072 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.482-1325T>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595280 | |||||||
| chr12:123595284 | G | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(6): Show |
35 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-1321G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595284 | |||||||
| chr12:123595373 | A | G | 20 | a0001c0001t0004g0006 a0001c0001t0004g0013 a0001c0001t0004g0014 others(17): Show |
39 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.482-1232A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595373 | |||||||
| chr12:123595397 | C | G | 1 | a0001c0002t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.482-1208C>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595397 | |||||||
| chr12:123595548 | T | C | 1 | a0001c0001t0012g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482-1057T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595548 | |||||||
| chr12:123595889 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.482-716T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123595889 | |||||||
| chr12:123596072 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(30): Show |
89 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.482-533G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596072 | |||||||
| chr12:123596080 | G | C | 1 | a0001c0001t0002g0041 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.482-525G>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596080 | |||||||
| chr12:123596135 | A | G | 13 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0035 others(10): Show |
31 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.482-470A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596135 | |||||||
| chr12:123596277 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0076 |
3 | HG01168.hp1 HG01169.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.482-328A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596277 | |||||||
| chr12:123596352 | G | A | 9 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0020 others(6): Show |
35 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-253G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596352 | |||||||
| chr12:123596422 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.482-183T>C | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596422 | |||||||
| chr12:123596541 | A | G | 1 | a0001c0001t0004g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.482-64A>G | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596541 | |||||||
| chr12:123596547 | C | T | 13 | a0001c0001t0003g0003 a0001c0001t0003g0016 a0001c0001t0003g0035 others(10): Show |
31 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.482-58C>T | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596547 | |||||||
| chr12:123596581 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.482-24G>A | TMED2 | ENSG00000086598.11 | transcript | ENST00000262225.8 | protein_coding | 3/3 | chr12 | 123596581 |