Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51290 |
| ensemblid | ENSG00000087502.19 |
| hgncid | 30208 |
| symbol | ERGIC2 |
| name | ERGIC and golgi 2 |
| refseq_nuc | NM_016570.3 |
| refseq_prot | NP_057654.2 |
| ensembl_nuc | ENST00000360150.9 |
| ensembl_prot | ENSP00000353270.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 29337352 |
| end | 29381172 |
| strand | - |
| ver | v1.2 |
| region | chr12:29337352-29381172 |
| region5000 | chr12:29332352-29386172 |
| regionname0 | ERGIC2_chr12_29337352_29381172 |
| regionname5000 | ERGIC2_chr12_29332352_29386172 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1131 | 327 | 77 | 56 | 147 | 10 | 37 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | ATGAG others(1126): Show |
chr12 | 29332352 | 29386172 | ||
| a0001c0002 | 0/0 | 1131 | 77 | 11 | 16 | 47 | 2 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | ATGAG others(1126): Show |
chr12 | 29332352 | 29386172 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5033 | 171 | 18 | 38 | 83 | 8 | 24 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0003 | 0/0 | 5034 | 19 | 1 | 4 | 13 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0004 | 0/0 | 5033 | 17 | 0 | 0 | 16 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0005 | 0/0 | 5035 | 16 | 12 | 2 | 0 | 0 | 2 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0006 | 0/0 | 5035 | 14 | 1 | 2 | 8 | 1 | 2 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0007 | 0/0 | 5035 | 11 | 5 | 0 | 5 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0008 | 0/0 | 5036 | 10 | 8 | 2 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5031): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0009 | 0/0 | 5032 | 8 | 0 | 3 | 4 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0010 | 0/0 | 5033 | 9 | 8 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0011 | 0/0 | 5035 | 8 | 0 | 0 | 6 | 0 | 2 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0012 | 0/0 | 5035 | 7 | 7 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0013 | 0/0 | 5035 | 7 | 7 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0015 | 0/0 | 5034 | 4 | 1 | 1 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0019 | 0/0 | 5036 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5031): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0022 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0023 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0024 | 0/0 | 5034 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0025 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0026 | 0/0 | 5035 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0027 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0028 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0029 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0030 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0031 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0032 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0033 | 0/0 | 5034 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0036 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0037 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0038 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0039 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0041 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5031): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0042 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0043 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0044 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5031): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0046 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0047 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0049 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0001t0050 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0002 | 0/0 | 5035 | 56 | 3 | 14 | 36 | 2 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0009 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5027): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0014 | 0/0 | 5034 | 5 | 0 | 0 | 5 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0016 | 0/0 | 5034 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0017 | 0/0 | 5036 | 3 | 0 | 0 | 3 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5031): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0018 | 0/0 | 5034 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5029): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0020 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5028): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0021 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0034 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0035 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0040 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0045 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| a0001c0002t0048 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | AGCCC others(5030): Show |
chr12 | 29332352 | 29386172 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 0 | 8 | 19 | 0 | 7 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0003 | 0/0 | 22 | 1 | 12 | 3 | 2 | 4 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0005 | 0/0 | 10 | 7 | 3 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0010 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0009g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0009g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0010g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0011g0012 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0012g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0013g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0015g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0015g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0015g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0019g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0023g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0024g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0025g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0026g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0027g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0028g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0030g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0031g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0032g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0033g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0036g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0037g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0038g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0039g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0041g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0042g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0043g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0044g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0046g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0047g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0049g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0001t0050g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0002 | 0/0 | 32 | 1 | 3 | 27 | 0 | 1 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0020 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0021 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0014g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0014g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0016g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0017g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0018g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0020g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0034g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0035g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0040g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0045g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| a0001c0002t0048g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0020 | EUR | GBR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00558 | hp1 | a0001 | c0002 | t0014 | g0043 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00609 | hp2 | a0001 | c0002 | t0017 | g0044 | EAS | CHS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00642 | hp2 | a0001 | c0001 | t0038 | g0062 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0064 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0097 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01106 | hp1 | a0001 | c0001 | t0015 | g0111 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01168 | hp1 | a0001 | c0002 | t0045 | g0177 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0053 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0161 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01358 | hp1 | a0001 | c0001 | t0043 | g0092 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01891 | hp2 | a0001 | c0001 | t0041 | g0052 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01978 | hp1 | a0001 | c0001 | t0028 | g0144 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02015 | hp1 | a0001 | c0002 | t0014 | g0176 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02055 | hp1 | a0001 | c0002 | t0016 | g0029 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02074 | hp2 | a0001 | c0001 | t0011 | g0143 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0084 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0118 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02258 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0147 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02300 | hp1 | a0001 | c0002 | t0040 | g0165 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02523 | hp2 | a0001 | c0002 | t0009 | g0173 | EAS | KHV | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0012 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0140 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0197 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02622 | hp1 | a0001 | c0002 | t0021 | g0055 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0198 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0157 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02717 | hp1 | a0001 | c0001 | t0042 | g0184 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02717 | hp2 | a0001 | c0002 | t0018 | g0030 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0185 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02723 | hp2 | a0001 | c0002 | t0018 | g0030 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0017 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02735 | hp2 | a0001 | c0001 | t0036 | g0078 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02886 | hp1 | a0001 | c0002 | t0016 | g0029 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0141 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0194 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0026 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0117 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03098 | hp1 | a0001 | c0001 | t0044 | g0196 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0138 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0191 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0163 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03486 | hp1 | a0001 | c0001 | t0046 | g0187 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03491 | hp2 | a0001 | c0001 | t0026 | g0158 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0149 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | GWD | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03579 | hp1 | a0001 | c0001 | t0050 | g0200 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0047 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0125 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03942 | hp1 | a0001 | c0001 | t0032 | g0122 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0012 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0151 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0039 | SAS | STU | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0195 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | CHB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18939 | hp1 | a0001 | c0001 | t0009 | g0066 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18946 | hp1 | a0001 | c0001 | t0037 | g0079 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18946 | hp2 | a0001 | c0002 | t0014 | g0168 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18952 | hp1 | a0001 | c0002 | t0017 | g0044 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18975 | hp1 | a0001 | c0001 | t0015 | g0106 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18975 | hp2 | a0001 | c0001 | t0027 | g0156 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18982 | hp1 | a0001 | c0001 | t0011 | g0135 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18986 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18997 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19000 | hp2 | a0001 | c0001 | t0015 | g0091 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19002 | hp2 | a0001 | c0001 | t0011 | g0136 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19009 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19010 | hp1 | a0001 | c0002 | t0035 | g0169 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19012 | hp2 | a0001 | c0001 | t0023 | g0183 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19043 | hp2 | a0001 | c0002 | t0020 | g0056 | AFR | LWK | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19056 | hp1 | a0001 | c0002 | t0014 | g0166 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19056 | hp2 | a0001 | c0001 | t0049 | g0108 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19063 | hp1 | a0001 | c0001 | t0022 | g0088 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19072 | hp1 | a0001 | c0001 | t0039 | g0090 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19074 | hp2 | a0001 | c0001 | t0024 | g0189 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19076 | hp1 | a0001 | c0001 | t0047 | g0107 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19076 | hp2 | a0001 | c0002 | t0017 | g0180 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19078 | hp1 | a0001 | c0001 | t0033 | g0119 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19081 | hp2 | a0001 | c0002 | t0014 | g0043 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19086 | hp1 | a0001 | c0001 | t0030 | g0137 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19086 | hp2 | a0001 | c0001 | t0009 | g0017 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19089 | hp1 | a0001 | c0002 | t0034 | g0170 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19090 | hp1 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA19240 | hp2 | a0001 | c0002 | t0016 | g0054 | AFR | YRI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ASW | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0046 | EUR | TSI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20805 | hp1 | a0001 | c0001 | t0031 | g0089 | EUR | TSI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0082 | EUR | TSI | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0039 | SAS | GIH | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02559 | hp1 | a0001 | c0001 | t0025 | g0190 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG02559 | hp2 | a0001 | c0002 | t0048 | g0171 | AFR | ACB | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0192 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG06807 | hp1 | a0001 | c0001 | t0029 | g0132 | AFR | USA | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | USA | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | LWK | ERGIC2_chr12_29332352_29386172 | ERGIC2 | chr12 | 29332352 | 29386172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:29368260 | A | G | 1 | a0001c0002 | 77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
synonymous_variant | LOW | c.243T>C | p.Thr81Thr | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/14 | 338/5033 | 243/1134 | 81/377 | chr12 | 29368260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:29337403 | A | T | 1 | a0001c0002t0034 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3753T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3753 | chr12 | 29337403 | ||||||
| chr12:29337408 | T | TTA | 34 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(31): Show |
183 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3747_*3748insTA | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3747 | chr12 | 29337408 | ||||||
| chr12:29337410 | G | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3746C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3746 | chr12 | 29337410 | ||||||
| chr12:29337411 | T | G | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3745A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3745 | chr12 | 29337411 | ||||||
| chr12:29337563 | G | A | 1 | a0001c0001t0030 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3593 | chr12 | 29337563 | ||||||
| chr12:29337640 | C | G | 1 | a0001c0001t0037 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3516G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3516 | chr12 | 29337640 | ||||||
| chr12:29337658 | G | C | 1 | a0001c0001t0037 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3498C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3498 | chr12 | 29337658 | ||||||
| chr12:29337665 | A | C | 1 | a0001c0001t0036 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3491 | chr12 | 29337665 | ||||||
| chr12:29337726 | T | G | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3430A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3430 | chr12 | 29337726 | ||||||
| chr12:29337949 | G | A | 1 | a0001c0001t0038 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3207C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3207 | chr12 | 29337949 | ||||||
| chr12:29337954 | A | G | 1 | a0001c0001t0027 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3202T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3202 | chr12 | 29337954 | ||||||
| chr12:29337970 | G | A | 1 | a0001c0001t0039 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3186C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3186 | chr12 | 29337970 | ||||||
| chr12:29337974 | C | G | 3 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0030 |
10 | HG01978.hp1 HG02074.hp2 HG02602.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3182G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3182 | chr12 | 29337974 | ||||||
| chr12:29337992 | T | C | 6 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0028 others(3): Show |
28 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3164A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3164 | chr12 | 29337992 | ||||||
| chr12:29338045 | G | A | 2 | a0001c0001t0025 a0001c0001t0046 |
2 | HG02559.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3111C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3111 | chr12 | 29338045 | ||||||
| chr12:29338125 | G | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3031C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 3031 | chr12 | 29338125 | ||||||
| chr12:29338163 | G | C | 1 | a0001c0001t0019 | 2 | HG03453.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2993C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2993 | chr12 | 29338163 | ||||||
| chr12:29338173 | C | CA | 8 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(5): Show |
23 | HG00609.hp2 HG01106.hp1 HG01167.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2982dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2982 | chr12 | 29338173 | ||||||
| chr12:29338173 | CA | C | 12 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0022 others(9): Show |
41 | HG00558.hp1 HG00639.hp2 HG01069.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2982delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2982 | chr12 | 29338173 | ||||||
| chr12:29338198 | A | T | 34 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(31): Show |
183 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2958T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2958 | chr12 | 29338198 | ||||||
| chr12:29338358 | T | C | 1 | a0001c0002t0035 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2798A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2798 | chr12 | 29338358 | ||||||
| chr12:29338435 | G | A | 33 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(30): Show |
182 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2721C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2721 | chr12 | 29338435 | ||||||
| chr12:29338595 | A | G | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(30): Show |
195 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2561T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2561 | chr12 | 29338595 | ||||||
| chr12:29338630 | C | T | 1 | a0001c0001t0026 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2526G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2526 | chr12 | 29338630 | ||||||
| chr12:29338631 | G | A | 1 | a0001c0002t0040 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2525 | chr12 | 29338631 | ||||||
| chr12:29338775 | A | G | 1 | a0001c0001t0041 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2381T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2381 | chr12 | 29338775 | ||||||
| chr12:29339008 | C | G | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0026 others(2): Show |
36 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2148G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2148 | chr12 | 29339008 | ||||||
| chr12:29339014 | C | A | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2142G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2142 | chr12 | 29339014 | ||||||
| chr12:29339015 | T | C | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2141A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2141 | chr12 | 29339015 | ||||||
| chr12:29339016 | C | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2140G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2140 | chr12 | 29339016 | ||||||
| chr12:29339066 | G | A | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0024 others(4): Show |
26 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2090C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2090 | chr12 | 29339066 | ||||||
| chr12:29339075 | A | G | 1 | a0001c0001t0031 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2081T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2081 | chr12 | 29339075 | ||||||
| chr12:29339088 | C | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2068G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2068 | chr12 | 29339088 | ||||||
| chr12:29339089 | A | C | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2067T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2067 | chr12 | 29339089 | ||||||
| chr12:29339112 | G | A | 1 | a0001c0001t0043 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2044C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2044 | chr12 | 29339112 | ||||||
| chr12:29339119 | A | G | 1 | a0001c0001t0010 | 9 | HG01167.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2037T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2037 | chr12 | 29339119 | ||||||
| chr12:29339144 | G | T | 13 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(10): Show |
78 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2012C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 2012 | chr12 | 29339144 | ||||||
| chr12:29339296 | C | T | 4 | a0001c0002t0016 a0001c0002t0018 a0001c0002t0020 others(1): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1860G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1860 | chr12 | 29339296 | ||||||
| chr12:29339323 | A | G | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1833T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1833 | chr12 | 29339323 | ||||||
| chr12:29339324 | G | A | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1832C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1832 | chr12 | 29339324 | ||||||
| chr12:29339325 | A | G | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1831T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1831 | chr12 | 29339325 | ||||||
| chr12:29339519 | T | A | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1637 | chr12 | 29339519 | ||||||
| chr12:29339521 | A | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1635 | chr12 | 29339521 | ||||||
| chr12:29339776 | G | T | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1380 | chr12 | 29339776 | ||||||
| chr12:29339777 | A | G | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1379T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1379 | chr12 | 29339777 | ||||||
| chr12:29339830 | T | C | 2 | a0001c0001t0013 a0001c0001t0044 |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1326 | chr12 | 29339830 | ||||||
| chr12:29339969 | T | A | 1 | a0001c0002t0045 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1187 | chr12 | 29339969 | ||||||
| chr12:29340041 | A | G | 5 | a0001c0001t0007 a0001c0001t0023 a0001c0001t0024 others(2): Show |
15 | HG00438.hp1 HG02559.hp1 HG02976.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1115T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1115 | chr12 | 29340041 | ||||||
| chr12:29340107 | C | T | 2 | a0001c0002t0018 a0001c0002t0020 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1049G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 1049 | chr12 | 29340107 | ||||||
| chr12:29340175 | A | C | 1 | a0001c0001t0022 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*981T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 981 | chr12 | 29340175 | ||||||
| chr12:29340190 | T | C | 1 | a0001c0001t0046 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 966 | chr12 | 29340190 | ||||||
| chr12:29340316 | G | A | 1 | a0001c0001t0047 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*840C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 840 | chr12 | 29340316 | ||||||
| chr12:29340420 | G | A | 5 | a0001c0001t0010 a0001c0002t0016 a0001c0002t0018 others(2): Show |
16 | HG01167.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 736 | chr12 | 29340420 | ||||||
| chr12:29340517 | T | C | 4 | a0001c0002t0016 a0001c0002t0018 a0001c0002t0020 others(1): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*639A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 639 | chr12 | 29340517 | ||||||
| chr12:29340652 | GT | G | 4 | a0001c0002t0016 a0001c0002t0018 a0001c0002t0020 others(1): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*503delA | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 503 | chr12 | 29340652 | ||||||
| chr12:29340855 | T | C | 1 | a0001c0002t0048 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 301 | chr12 | 29340855 | ||||||
| chr12:29340939 | C | T | 4 | a0001c0002t0016 a0001c0002t0018 a0001c0002t0020 others(1): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 217 | chr12 | 29340939 | ||||||
| chr12:29341125 | C | A | 1 | a0001c0001t0049 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 14/14 | 31 | chr12 | 29341125 | ||||||
| chr12:29381139 | G | A | 1 | a0001c0001t0050 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-62C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/14 | 9506 | chr12 | 29381139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:29341496 | A | C | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1071+238T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 13/13 | chr12 | 29341496 | |||||||
| chr12:29341619 | C | T | 2 | a0001c0002t0002g0042 a0001c0002t0014g0168 |
3 | HG02135.hp1 NA18946.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1071+115G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 13/13 | chr12 | 29341619 | |||||||
| chr12:29341898 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.989-82G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29341898 | |||||||
| chr12:29341950 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.989-134T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29341950 | |||||||
| chr12:29342124 | G | C | 1 | a0001c0001t0013g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.989-308C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342124 | |||||||
| chr12:29342170 | C | A | 10 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(7): Show |
19 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.989-354G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342170 | |||||||
| chr12:29342173 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.989-357C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342173 | |||||||
| chr12:29342423 | G | A | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.989-607C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342423 | |||||||
| chr12:29342520 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0114 |
3 | NA18945.hp2 NA18971.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.988+600T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342520 | |||||||
| chr12:29342543 | T | C | 5 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(2): Show |
7 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+577A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342543 | |||||||
| chr12:29342555 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.988+565T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342555 | |||||||
| chr12:29342590 | C | T | 2 | a0001c0001t0025g0190 a0001c0001t0046g0187 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+530G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342590 | |||||||
| chr12:29342655 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG01891.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.988+465A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342655 | |||||||
| chr12:29342915 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(1): Show |
7 | HG01884.hp2 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+205A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342915 | |||||||
| chr12:29342925 | C | T | 2 | a0001c0001t0025g0190 a0001c0001t0046g0187 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.988+195G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342925 | |||||||
| chr12:29342931 | T | G | 1 | a0001c0001t0001g0036 | 2 | NA18612.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.988+189A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 12/13 | chr12 | 29342931 | |||||||
| chr12:29343291 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(47): Show |
113 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.826-9C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29343291 | |||||||
| chr12:29343307 | G | A | 1 | a0001c0002t0045g0177 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.826-25C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29343307 | |||||||
| chr12:29343628 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(1): Show |
7 | HG01884.hp2 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.826-346A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29343628 | |||||||
| chr12:29343670 | C | T | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.826-388G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29343670 | |||||||
| chr12:29344058 | C | T | 112 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(109): Show |
201 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.826-776G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344058 | |||||||
| chr12:29344192 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.826-910G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344192 | |||||||
| chr12:29344201 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.826-919T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344201 | |||||||
| chr12:29344399 | A | G | 2 | a0001c0001t0013g0195 a0001c0001t0013g0197 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.825+1044T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344399 | |||||||
| chr12:29344573 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(49): Show |
115 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.825+870C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344573 | |||||||
| chr12:29344668 | C | CA | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.825+774dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344668 | |||||||
| chr12:29344757 | T | A | 1 | a0001c0001t0001g0025 | 3 | HG01243.hp1 HG01358.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.825+686A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344757 | |||||||
| chr12:29344768 | C | G | 16 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(13): Show |
27 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.825+675G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29344768 | |||||||
| chr12:29345108 | C | G | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.825+335G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29345108 | |||||||
| chr12:29345115 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.825+328A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 11/13 | chr12 | 29345115 | |||||||
| chr12:29345556 | A | C | 2 | a0001c0001t0005g0133 a0001c0001t0005g0134 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.728-16T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29345556 | |||||||
| chr12:29345746 | G | A | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.728-206C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29345746 | |||||||
| chr12:29345987 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.728-447C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29345987 | |||||||
| chr12:29346018 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.728-478T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346018 | |||||||
| chr12:29346080 | A | G | 2 | a0001c0001t0005g0127 a0001c0001t0050g0200 |
2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.728-540T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346080 | |||||||
| chr12:29346212 | AG | A | 16 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(13): Show |
27 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.728-673delC | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346212 | |||||||
| chr12:29346277 | T | C | 16 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(13): Show |
27 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.728-737A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346277 | |||||||
| chr12:29346303 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0115 others(1): Show |
9 | HG01081.hp1 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-763G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346303 | |||||||
| chr12:29346395 | G | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(2): Show |
7 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-855C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346395 | |||||||
| chr12:29346645 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(24): Show |
69 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.728-1105T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346645 | |||||||
| chr12:29346834 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.728-1294G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29346834 | |||||||
| chr12:29347079 | T | A | 32 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(29): Show |
76 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.728-1539A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347079 | |||||||
| chr12:29347380 | G | A | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+1699C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347380 | |||||||
| chr12:29347578 | C | T | 1 | a0001c0002t0002g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.727+1501G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347578 | |||||||
| chr12:29347583 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.727+1496C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347583 | |||||||
| chr12:29347767 | A | G | 1 | a0001c0001t0006g0013 | 5 | HG02015.hp2 NA18953.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+1312T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347767 | |||||||
| chr12:29347788 | T | C | 1 | a0001c0001t0007g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.727+1291A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29347788 | |||||||
| chr12:29348096 | T | C | 1 | a0001c0001t0008g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.727+983A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29348096 | |||||||
| chr12:29348624 | G | A | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+455C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29348624 | |||||||
| chr12:29348719 | C | A | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+360G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29348719 | |||||||
| chr12:29348972 | G | T | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+107C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29348972 | |||||||
| chr12:29348973 | A | G | 96 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(93): Show |
176 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.727+106T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29348973 | |||||||
| chr12:29349008 | A | G | 37 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(34): Show |
84 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.727+71T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 10/13 | chr12 | 29349008 | |||||||
| chr12:29349303 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(48): Show |
114 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.629-126A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 9/13 | chr12 | 29349303 | |||||||
| chr12:29349502 | C | T | 1 | a0001c0001t0004g0031 | 2 | NA18988.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.629-325G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 9/13 | chr12 | 29349502 | |||||||
| chr12:29349538 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.629-361T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 9/13 | chr12 | 29349538 | |||||||
| chr12:29349919 | A | G | 1 | a0001c0001t0001g0011 | 5 | NA18971.hp2 NA18972.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+94T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 9/13 | chr12 | 29349919 | |||||||
| chr12:29350219 | T | G | 1 | a0001c0002t0034g0170 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.573-151A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350219 | |||||||
| chr12:29350366 | A | G | 2 | a0001c0001t0013g0195 a0001c0001t0013g0197 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.573-298T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350366 | |||||||
| chr12:29350375 | A | G | 1 | a0001c0002t0014g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.573-307T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350375 | |||||||
| chr12:29350459 | T | G | 2 | a0001c0001t0008g0028 a0001c0001t0008g0053 |
3 | HG01167.hp2 HG01169.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.573-391A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350459 | |||||||
| chr12:29350554 | C | T | 1 | a0001c0001t0012g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.573-486G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350554 | |||||||
| chr12:29350699 | T | C | 32 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(29): Show |
76 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.573-631A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350699 | |||||||
| chr12:29350743 | C | T | 32 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(29): Show |
76 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.573-675G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350743 | |||||||
| chr12:29350754 | G | A | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.573-686C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350754 | |||||||
| chr12:29350812 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.573-744G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350812 | |||||||
| chr12:29350843 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573-775G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350843 | |||||||
| chr12:29350982 | A | G | 1 | a0001c0001t0046g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.573-914T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29350982 | |||||||
| chr12:29351075 | C | A | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573-1007G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351075 | |||||||
| chr12:29351228 | C | T | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.573-1160G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351228 | |||||||
| chr12:29351260 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0009g0097 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.573-1192A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351260 | |||||||
| chr12:29351419 | T | G | 1 | a0001c0001t0006g0142 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.573-1351A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351419 | |||||||
| chr12:29351420 | C | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.573-1352G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351420 | |||||||
| chr12:29351449 | G | A | 68 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(65): Show |
106 | HG00438.hp1 HG00639.hp2 HG01074.hp1 others(103): Show |
intron_variant | MODIFIER | c.573-1381C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351449 | |||||||
| chr12:29351544 | G | A | 27 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(24): Show |
69 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.573-1476C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351544 | |||||||
| chr12:29351621 | C | T | 48 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(45): Show |
78 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.573-1553G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351621 | |||||||
| chr12:29351622 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.573-1554G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351622 | |||||||
| chr12:29351623 | A | G | 113 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(110): Show |
202 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.573-1555T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351623 | |||||||
| chr12:29351800 | G | A | 1 | a0001c0001t0012g0139 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573-1732C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29351800 | |||||||
| chr12:29352146 | C | A | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.573-2078G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352146 | |||||||
| chr12:29352237 | A | T | 1 | a0001c0001t0010g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.573-2169T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352237 | |||||||
| chr12:29352248 | A | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.573-2180T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352248 | |||||||
| chr12:29352358 | A | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(28): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.573-2290T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352358 | |||||||
| chr12:29352523 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.573-2455G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352523 | |||||||
| chr12:29352757 | A | G | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-2689T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352757 | |||||||
| chr12:29352784 | G | A | 2 | a0001c0002t0002g0020 a0001c0002t0048g0171 |
5 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-2716C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352784 | |||||||
| chr12:29352837 | T | TA | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(28): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.573-2770dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352837 | |||||||
| chr12:29352988 | T | C | 2 | a0001c0001t0010g0006 a0001c0001t0010g0118 |
8 | HG01167.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.573-2920A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29352988 | |||||||
| chr12:29353022 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.573-2954A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353022 | |||||||
| chr12:29353039 | T | C | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.573-2971A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353039 | |||||||
| chr12:29353067 | G | A | 1 | a0001c0001t0015g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.573-2999C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353067 | |||||||
| chr12:29353140 | T | C | 2 | a0001c0001t0008g0028 a0001c0001t0008g0053 |
3 | HG01167.hp2 HG01169.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.573-3072A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353140 | |||||||
| chr12:29353321 | A | C | 101 | a0001c0001t0001g0087 a0001c0001t0003g0010 a0001c0001t0003g0014 others(98): Show |
183 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.572+3061T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353321 | |||||||
| chr12:29353429 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.572+2953G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353429 | |||||||
| chr12:29353632 | G | A | 1 | a0001c0001t0041g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.572+2750C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353632 | |||||||
| chr12:29353687 | ACT | A | 8 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(5): Show |
12 | HG00438.hp1 HG02976.hp2 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.572+2693_572+2694d others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353687 | |||||||
| chr12:29353725 | C | CCTT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.572+2654_572+2656d others(5): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353725 | |||||||
| chr12:29353729 | C | CTTCT | 39 | a0001c0001t0001g0087 a0001c0001t0001g0116 a0001c0001t0013g0022 others(36): Show |
86 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.572+2652_572+2653i others(6): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353729 | |||||||
| chr12:29353730 | T | TTC | 13 | a0001c0001t0001g0035 a0001c0001t0004g0007 a0001c0001t0004g0031 others(10): Show |
21 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.572+2651_572+2652i others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353730 | |||||||
| chr12:29353993 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.572+2389C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29353993 | |||||||
| chr12:29354091 | T | C | 1 | a0001c0001t0012g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+2291A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354091 | |||||||
| chr12:29354172 | T | C | 1 | a0001c0001t0011g0136 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.572+2210A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354172 | |||||||
| chr12:29354352 | C | T | 10 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(7): Show |
14 | HG00438.hp1 HG02559.hp1 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.572+2030G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354352 | |||||||
| chr12:29354378 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.572+2004A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354378 | |||||||
| chr12:29354417 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.572+1965A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354417 | |||||||
| chr12:29354443 | C | T | 1 | a0001c0002t0002g0082 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.572+1939G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354443 | |||||||
| chr12:29354485 | T | C | 1 | a0001c0001t0005g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.572+1897A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354485 | |||||||
| chr12:29354576 | G | A | 2 | a0001c0001t0025g0190 a0001c0001t0046g0187 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.572+1806C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354576 | |||||||
| chr12:29354749 | A | G | 1 | a0001c0001t0005g0128 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.572+1633T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354749 | |||||||
| chr12:29354988 | C | A | 1 | a0001c0002t0002g0167 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.572+1394G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29354988 | |||||||
| chr12:29355149 | G | A | 1 | a0001c0001t0001g0011 | 5 | NA18971.hp2 NA18972.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+1233C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355149 | |||||||
| chr12:29355381 | A | C | 1 | a0001c0002t0002g0167 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.572+1001T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355381 | |||||||
| chr12:29355384 | C | T | 1 | a0001c0002t0002g0167 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.572+998G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355384 | |||||||
| chr12:29355395 | T | C | 1 | a0001c0001t0013g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.572+987A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355395 | |||||||
| chr12:29355519 | T | C | 1 | a0001c0001t0001g0024 | 3 | NA18959.hp1 NA18988.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.572+863A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355519 | |||||||
| chr12:29355551 | A | C | 5 | a0001c0001t0007g0047 a0001c0001t0007g0048 a0001c0001t0007g0182 others(2): Show |
7 | HG00438.hp1 HG03669.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+831T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355551 | |||||||
| chr12:29355709 | A | G | 113 | a0001c0001t0001g0087 a0001c0001t0003g0010 a0001c0001t0003g0014 others(110): Show |
202 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.572+673T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355709 | |||||||
| chr12:29355814 | T | C | 1 | a0001c0001t0019g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.572+568A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355814 | |||||||
| chr12:29355962 | T | G | 4 | a0001c0001t0008g0185 a0001c0001t0025g0190 a0001c0001t0042g0184 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+420A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29355962 | |||||||
| chr12:29356027 | C | CT | 17 | a0001c0001t0001g0116 a0001c0001t0007g0027 a0001c0001t0007g0047 others(14): Show |
24 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.572+354dupA | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 8/13 | chr12 | 29356027 | |||||||
| chr12:29356517 | C | T | 109 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(106): Show |
198 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.477-40G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29356517 | |||||||
| chr12:29356580 | A | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0063 others(105): Show |
202 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.477-103T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29356580 | |||||||
| chr12:29357050 | C | CT | 113 | a0001c0001t0001g0033 a0001c0001t0003g0010 a0001c0001t0003g0014 others(110): Show |
203 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.476+572_476+573ins others(1): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357050 | |||||||
| chr12:29357213 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.476+410C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357213 | |||||||
| chr12:29357232 | A | C | 1 | a0001c0001t0005g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.476+391T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357232 | |||||||
| chr12:29357250 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.476+373C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357250 | |||||||
| chr12:29357297 | G | A | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+326C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357297 | |||||||
| chr12:29357388 | T | C | 20 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(17): Show |
28 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.476+235A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357388 | |||||||
| chr12:29357436 | T | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
95 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.476+187A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357436 | |||||||
| chr12:29357616 | A | C | 13 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(10): Show |
17 | HG00438.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.476+7T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 7/13 | chr12 | 29357616 | |||||||
| chr12:29357756 | A | G | 2 | a0001c0001t0008g0185 a0001c0001t0042g0184 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.375-32T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29357756 | |||||||
| chr12:29357927 | T | C | 2 | a0001c0001t0012g0138 a0001c0001t0012g0139 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.375-203A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29357927 | |||||||
| chr12:29357928 | G | A | 2 | a0001c0001t0012g0138 a0001c0001t0012g0139 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.375-204C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29357928 | |||||||
| chr12:29358136 | T | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.375-412A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358136 | |||||||
| chr12:29358153 | T | G | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.375-429A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358153 | |||||||
| chr12:29358367 | T | C | 69 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(66): Show |
107 | HG00438.hp1 HG00639.hp2 HG01074.hp1 others(104): Show |
intron_variant | MODIFIER | c.375-643A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358367 | |||||||
| chr12:29358403 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.375-679C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358403 | |||||||
| chr12:29358465 | C | A | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.375-741G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358465 | |||||||
| chr12:29358492 | T | C | 1 | a0001c0001t0005g0039 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.375-768A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358492 | |||||||
| chr12:29358497 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.375-773C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358497 | |||||||
| chr12:29358608 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(28): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.375-884C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358608 | |||||||
| chr12:29358665 | G | A | 38 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(35): Show |
63 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(60): Show |
intron_variant | MODIFIER | c.375-941C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358665 | |||||||
| chr12:29358930 | G | T | 2 | a0001c0001t0025g0190 a0001c0001t0046g0187 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.375-1206C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29358930 | |||||||
| chr12:29359122 | T | A | 1 | a0001c0001t0007g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.375-1398A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359122 | |||||||
| chr12:29359331 | A | C | 2 | a0001c0001t0008g0185 a0001c0001t0042g0184 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.375-1607T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359331 | |||||||
| chr12:29359432 | G | A | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-1708C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359432 | |||||||
| chr12:29359774 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.374+1871C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359774 | |||||||
| chr12:29359977 | A | C | 1 | a0001c0001t0026g0158 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.374+1668T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359977 | |||||||
| chr12:29359981 | T | A | 1 | a0001c0001t0037g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.374+1664A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29359981 | |||||||
| chr12:29360007 | C | T | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.374+1638G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360007 | |||||||
| chr12:29360156 | T | C | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.374+1489A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360156 | |||||||
| chr12:29360300 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.374+1345A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360300 | |||||||
| chr12:29360454 | T | C | 1 | a0001c0001t0047g0107 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.374+1191A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360454 | |||||||
| chr12:29360545 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(28): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.374+1100A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360545 | |||||||
| chr12:29360768 | T | C | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+877A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360768 | |||||||
| chr12:29360903 | T | C | 1 | a0001c0002t0002g0175 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.374+742A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360903 | |||||||
| chr12:29360915 | G | A | 1 | a0001c0001t0007g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.374+730C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360915 | |||||||
| chr12:29360916 | A | G | 1 | a0001c0001t0007g0186 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.374+729T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360916 | |||||||
| chr12:29360999 | C | A | 1 | a0001c0001t0038g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.374+646G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29360999 | |||||||
| chr12:29361016 | A | G | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.374+629T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361016 | |||||||
| chr12:29361155 | G | C | 1 | a0001c0001t0003g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.374+490C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361155 | |||||||
| chr12:29361178 | T | G | 69 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(66): Show |
107 | HG00438.hp1 HG00639.hp2 HG01074.hp1 others(104): Show |
intron_variant | MODIFIER | c.374+467A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361178 | |||||||
| chr12:29361181 | G | A | 5 | a0001c0001t0003g0014 a0001c0001t0003g0145 a0001c0001t0003g0152 others(2): Show |
9 | NA18945.hp1 NA18953.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.374+464C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361181 | |||||||
| chr12:29361532 | T | C | 1 | a0001c0002t0002g0174 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.374+113A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361532 | |||||||
| chr12:29361552 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.374+93A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361552 | |||||||
| chr12:29361565 | G | A | 1 | a0001c0001t0030g0137 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.374+80C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 6/13 | chr12 | 29361565 | |||||||
| chr12:29361768 | A | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0115 others(1): Show |
9 | HG01081.hp1 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-83T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29361768 | |||||||
| chr12:29361900 | C | T | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.334-215G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29361900 | |||||||
| chr12:29362031 | C | G | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.334-346G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362031 | |||||||
| chr12:29362120 | T | G | 16 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(13): Show |
27 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.334-435A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362120 | |||||||
| chr12:29362504 | C | T | 9 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(6): Show |
16 | HG01074.hp1 HG01257.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.334-819G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362504 | |||||||
| chr12:29362507 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.334-822C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362507 | |||||||
| chr12:29362595 | C | CA | 6 | a0001c0001t0001g0071 a0001c0001t0003g0155 a0001c0001t0004g0124 others(3): Show |
7 | HG02818.hp1 NA18967.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.334-911dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362595 | |||||||
| chr12:29362595 | CA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(51): Show |
119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.334-911delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362595 | |||||||
| chr12:29362642 | T | G | 1 | a0001c0001t0013g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-957A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362642 | |||||||
| chr12:29362646 | G | A | 1 | a0001c0001t0012g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.334-961C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362646 | |||||||
| chr12:29362681 | G | T | 10 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(7): Show |
15 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.334-996C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362681 | |||||||
| chr12:29362774 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.334-1089G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362774 | |||||||
| chr12:29362794 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0009g0097 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.334-1109A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362794 | |||||||
| chr12:29362843 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.334-1158T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362843 | |||||||
| chr12:29362932 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.334-1247A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362932 | |||||||
| chr12:29362995 | T | A | 16 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(13): Show |
27 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.334-1310A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29362995 | |||||||
| chr12:29363159 | G | A | 28 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(25): Show |
70 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.334-1474C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363159 | |||||||
| chr12:29363258 | T | C | 1 | a0001c0002t0002g0175 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.334-1573A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363258 | |||||||
| chr12:29363282 | A | C | 1 | a0001c0002t0014g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.334-1597T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363282 | |||||||
| chr12:29363282 | A | G | 27 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(24): Show |
69 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.334-1597T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363282 | |||||||
| chr12:29363679 | C | T | 15 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0039 others(12): Show |
26 | HG01074.hp1 HG01257.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.334-1994G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363679 | |||||||
| chr12:29363835 | G | GA | 16 | a0001c0001t0001g0085 a0001c0001t0001g0099 a0001c0001t0004g0007 others(13): Show |
23 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.334-2151dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363835 | |||||||
| chr12:29363835 | GA | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(63): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.334-2151delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29363835 | |||||||
| chr12:29364210 | T | G | 1 | a0001c0001t0013g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.334-2525A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364210 | |||||||
| chr12:29364222 | A | C | 1 | a0001c0001t0019g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.334-2537T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364222 | |||||||
| chr12:29364355 | G | A | 2 | a0001c0001t0006g0046 a0001c0001t0025g0190 |
3 | HG01433.hp1 HG02559.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.333+2522C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364355 | |||||||
| chr12:29364364 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.333+2513G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364364 | |||||||
| chr12:29364493 | A | T | 2 | a0001c0001t0012g0138 a0001c0001t0012g0139 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.333+2384T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364493 | |||||||
| chr12:29364596 | A | G | 10 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(7): Show |
15 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.333+2281T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364596 | |||||||
| chr12:29364764 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.333+2113C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364764 | |||||||
| chr12:29364926 | G | A | 10 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(7): Show |
15 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.333+1951C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364926 | |||||||
| chr12:29364949 | GA | G | 10 | a0001c0001t0001g0086 a0001c0001t0008g0053 a0001c0001t0013g0022 others(7): Show |
14 | HG01168.hp1 HG01169.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+1927delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364949 | |||||||
| chr12:29364949 | GAA | G | 24 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(21): Show |
65 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.333+1926_333+1927d others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364949 | |||||||
| chr12:29364987 | A | T | 1 | a0001c0002t0002g0181 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.333+1890T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364987 | |||||||
| chr12:29364991 | G | C | 50 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(47): Show |
80 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(77): Show |
intron_variant | MODIFIER | c.333+1886C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29364991 | |||||||
| chr12:29365069 | G | A | 5 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(2): Show |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.333+1808C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365069 | |||||||
| chr12:29365080 | T | C | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+1797A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365080 | |||||||
| chr12:29365086 | C | A | 10 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(7): Show |
15 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.333+1791G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365086 | |||||||
| chr12:29365219 | T | A | 21 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0145 others(18): Show |
35 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.333+1658A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365219 | |||||||
| chr12:29365386 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0063 others(8): Show |
25 | HG01256.hp1 HG02056.hp1 HG02071.hp2 others(22): Show |
intron_variant | MODIFIER | c.333+1491T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365386 | |||||||
| chr12:29365497 | A | G | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.333+1380T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365497 | |||||||
| chr12:29365673 | TA | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.333+1203delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365673 | |||||||
| chr12:29365674 | A | T | 2 | a0001c0002t0016g0054 a0001c0002t0021g0055 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.333+1203T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365674 | |||||||
| chr12:29365675 | A | T | 112 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(109): Show |
201 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.333+1202T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365675 | |||||||
| chr12:29365741 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.333+1136A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365741 | |||||||
| chr12:29365895 | T | C | 11 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(8): Show |
15 | HG00438.hp1 HG02559.hp1 HG02976.hp2 others(12): Show |
intron_variant | MODIFIER | c.333+982A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365895 | |||||||
| chr12:29365938 | A | G | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+939T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365938 | |||||||
| chr12:29365979 | A | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0009g0064 |
4 | HG00280.hp1 HG01069.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+898T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29365979 | |||||||
| chr12:29366044 | C | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.333+833G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29366044 | |||||||
| chr12:29366231 | A | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0085 others(115): Show |
218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.333+646T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29366231 | |||||||
| chr12:29366714 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.333+163A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29366714 | |||||||
| chr12:29366826 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+51C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 5/13 | chr12 | 29366826 | |||||||
| chr12:29367047 | C | CA | 22 | a0001c0001t0001g0102 a0001c0001t0003g0154 a0001c0001t0003g0155 others(19): Show |
33 | HG01074.hp1 HG01169.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.263-101dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367047 | |||||||
| chr12:29367081 | A | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-134T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367081 | |||||||
| chr12:29367083 | T | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-136A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367083 | |||||||
| chr12:29367084 | A | C | 113 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(110): Show |
202 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.263-137T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367084 | |||||||
| chr12:29367084 | A | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-137T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367084 | |||||||
| chr12:29367085 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-138T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367085 | |||||||
| chr12:29367089 | C | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-142G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367089 | |||||||
| chr12:29367090 | C | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-143G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367090 | |||||||
| chr12:29367091 | G | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-144C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367091 | |||||||
| chr12:29367092 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-145T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367092 | |||||||
| chr12:29367094 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-147T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367094 | |||||||
| chr12:29367096 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-149T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367096 | |||||||
| chr12:29367103 | C | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-156G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367103 | |||||||
| chr12:29367105 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-158T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367105 | |||||||
| chr12:29367106 | A | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-159T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367106 | |||||||
| chr12:29367112 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-165T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367112 | |||||||
| chr12:29367116 | A | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-169T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367116 | |||||||
| chr12:29367117 | G | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-170C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367117 | |||||||
| chr12:29367119 | A | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-172T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367119 | |||||||
| chr12:29367126 | T | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-179A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367126 | |||||||
| chr12:29367127 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-180T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367127 | |||||||
| chr12:29367131 | C | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-184G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367131 | |||||||
| chr12:29367135 | G | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-188C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367135 | |||||||
| chr12:29367136 | G | A | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-189C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367136 | |||||||
| chr12:29367140 | A | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-193T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367140 | |||||||
| chr12:29367145 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-198T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367145 | |||||||
| chr12:29367147 | T | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-200A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367147 | |||||||
| chr12:29367150 | A | T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-203T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367150 | |||||||
| chr12:29367151 | A | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-204T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367151 | |||||||
| chr12:29367152 | A | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-205T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367152 | |||||||
| chr12:29367154 | T | A | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-207A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367154 | |||||||
| chr12:29367156 | T | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-209A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367156 | |||||||
| chr12:29367159 | T | G | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-212A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367159 | |||||||
| chr12:29367164 | TTTTTTCT others(7): Show |
T | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-231_263-218del others(14): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367164 | |||||||
| chr12:29367174 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.263-227G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367174 | |||||||
| chr12:29367180 | A | C | 1 | a0001c0002t0017g0180 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.263-233T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367180 | |||||||
| chr12:29367194 | C | T | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.263-247G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367194 | |||||||
| chr12:29367198 | T | TA | 74 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(71): Show |
114 | HG00438.hp1 HG00639.hp2 HG01074.hp1 others(111): Show |
intron_variant | MODIFIER | c.263-252dupT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367198 | |||||||
| chr12:29367382 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.263-435A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367382 | |||||||
| chr12:29367533 | T | C | 1 | a0001c0002t0002g0041 | 2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.263-586A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367533 | |||||||
| chr12:29367748 | G | T | 4 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(1): Show |
7 | HG01884.hp2 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.262+493C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367748 | |||||||
| chr12:29367773 | T | C | 114 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(111): Show |
203 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.262+468A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367773 | |||||||
| chr12:29367968 | T | C | 11 | a0001c0001t0006g0013 a0001c0001t0006g0046 a0001c0001t0006g0142 others(8): Show |
16 | HG01433.hp1 HG02015.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.262+273A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 4/13 | chr12 | 29367968 | |||||||
| chr12:29368400 | G | A | 1 | a0001c0001t0006g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.216-113C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29368400 | |||||||
| chr12:29368457 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.216-170A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29368457 | |||||||
| chr12:29368518 | T | A | 21 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0145 others(18): Show |
35 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.216-231A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29368518 | |||||||
| chr12:29368852 | A | G | 2 | a0001c0002t0018g0030 a0001c0002t0020g0056 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.216-565T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29368852 | |||||||
| chr12:29368909 | C | T | 1 | a0001c0001t0006g0149 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.216-622G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29368909 | |||||||
| chr12:29369008 | A | T | 1 | a0001c0001t0003g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.216-721T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369008 | |||||||
| chr12:29369023 | T | G | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.216-736A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369023 | |||||||
| chr12:29369214 | T | C | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.215+900A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369214 | |||||||
| chr12:29369274 | A | G | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.215+840T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369274 | |||||||
| chr12:29369302 | T | C | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.215+812A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369302 | |||||||
| chr12:29369465 | C | G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.215+649G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369465 | |||||||
| chr12:29369744 | A | G | 1 | a0001c0001t0012g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.215+370T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 3/13 | chr12 | 29369744 | |||||||
| chr12:29370929 | C | T | 2 | a0001c0001t0019g0163 a0001c0001t0019g0192 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+599G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29370929 | |||||||
| chr12:29371024 | T | C | 114 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(111): Show |
203 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.106+504A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29371024 | |||||||
| chr12:29371226 | T | C | 28 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(25): Show |
70 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.106+302A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29371226 | |||||||
| chr12:29371432 | TA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(46): Show |
112 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.106+95delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29371432 | |||||||
| chr12:29371439 | T | C | 1 | a0001c0001t0004g0059 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.106+89A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29371439 | |||||||
| chr12:29371499 | C | T | 2 | a0001c0002t0002g0041 a0001c0002t0040g0165 |
3 | HG01361.hp1 HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.106+29G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 2/13 | chr12 | 29371499 | |||||||
| chr12:29371828 | C | A | 1 | a0001c0001t0012g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37-158G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29371828 | |||||||
| chr12:29372092 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-37-422A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372092 | |||||||
| chr12:29372156 | A | G | 19 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(16): Show |
27 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37-486T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372156 | |||||||
| chr12:29372230 | C | G | 1 | a0001c0001t0006g0147 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-37-560G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372230 | |||||||
| chr12:29372434 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-37-764C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372434 | |||||||
| chr12:29372443 | AAAG | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-776_-37-774del others(3): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372443 | |||||||
| chr12:29372457 | C | A | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-787G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372457 | |||||||
| chr12:29372503 | T | G | 114 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(111): Show |
203 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.-37-833A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372503 | |||||||
| chr12:29372597 | T | C | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-927A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372597 | |||||||
| chr12:29372654 | C | CT | 7 | a0001c0001t0003g0145 a0001c0001t0006g0146 a0001c0001t0011g0143 others(4): Show |
7 | HG01978.hp1 HG02074.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-985dupA | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372654 | |||||||
| chr12:29372664 | TC | T | 32 | a0001c0001t0013g0195 a0001c0002t0002g0002 a0001c0002t0002g0020 others(29): Show |
76 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-37-995delG | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372664 | |||||||
| chr12:29372665 | C | T | 70 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(67): Show |
108 | HG00438.hp1 HG00639.hp2 HG01074.hp1 others(105): Show |
intron_variant | MODIFIER | c.-37-995G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372665 | |||||||
| chr12:29372680 | G | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0065 others(2): Show |
11 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-1010C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372680 | |||||||
| chr12:29372787 | C | G | 1 | a0001c0001t0001g0016 | 4 | HG02056.hp1 NA18957.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-1117G>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372787 | |||||||
| chr12:29372976 | TA | T | 6 | a0001c0001t0004g0121 a0001c0001t0012g0026 a0001c0001t0012g0138 others(3): Show |
8 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-1307delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372976 | |||||||
| chr12:29372976 | TAA | T | 5 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(2): Show |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-1308_-37-1307d others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29372976 | |||||||
| chr12:29373180 | T | C | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37-1510A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373180 | |||||||
| chr12:29373219 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-37-1549C>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373219 | |||||||
| chr12:29373522 | A | G | 3 | a0001c0001t0004g0037 a0001c0001t0004g0120 a0001c0001t0033g0119 |
4 | NA18978.hp1 NA19000.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-1852T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373522 | |||||||
| chr12:29373573 | T | C | 1 | a0001c0001t0007g0191 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-37-1903A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373573 | |||||||
| chr12:29373675 | C | A | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-2005G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373675 | |||||||
| chr12:29373698 | T | C | 5 | a0001c0001t0012g0026 a0001c0001t0012g0138 a0001c0001t0012g0139 others(2): Show |
7 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-2028A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373698 | |||||||
| chr12:29373828 | T | G | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.-37-2158A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29373828 | |||||||
| chr12:29374045 | C | T | 1 | a0001c0001t0007g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-37-2375G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374045 | |||||||
| chr12:29374219 | G | A | 3 | a0001c0001t0010g0006 a0001c0001t0010g0117 a0001c0001t0010g0118 |
9 | HG01167.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-2549C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374219 | |||||||
| chr12:29374300 | C | T | 6 | a0001c0001t0008g0015 a0001c0001t0008g0028 a0001c0001t0008g0051 others(3): Show |
10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-2630G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374300 | |||||||
| chr12:29374353 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.-37-2683T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374353 | |||||||
| chr12:29374387 | C | T | 1 | a0001c0002t0002g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-37-2717G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374387 | |||||||
| chr12:29374421 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-37-2751G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374421 | |||||||
| chr12:29374862 | G | A | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37-3192C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29374862 | |||||||
| chr12:29375154 | G | GT | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-3485dupA | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375154 | |||||||
| chr12:29375321 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0199 others(3): Show |
10 | NA18612.hp2 NA18943.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.-37-3651A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375321 | |||||||
| chr12:29375525 | C | A | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(1): Show |
4 | HG01106.hp1 HG01175.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-3855G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375525 | |||||||
| chr12:29375586 | A | C | 2 | a0001c0001t0006g0013 a0001c0001t0006g0142 |
6 | HG02015.hp2 NA18953.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-3916T>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375586 | |||||||
| chr12:29375662 | C | T | 33 | a0001c0002t0002g0002 a0001c0002t0002g0020 a0001c0002t0002g0021 others(30): Show |
77 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-3992G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375662 | |||||||
| chr12:29375786 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.-37-4116C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375786 | |||||||
| chr12:29375788 | T | C | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-4118A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29375788 | |||||||
| chr12:29376146 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-37-4476T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376146 | |||||||
| chr12:29376266 | T | G | 22 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0145 others(19): Show |
36 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.-37-4596A>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376266 | |||||||
| chr12:29376317 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-37-4647C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376317 | |||||||
| chr12:29376504 | C | T | 50 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(47): Show |
80 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(77): Show |
intron_variant | MODIFIER | c.-38+4611G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376504 | |||||||
| chr12:29376520 | C | T | 1 | a0001c0001t0038g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-38+4595G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376520 | |||||||
| chr12:29376590 | C | T | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38+4525G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376590 | |||||||
| chr12:29376759 | T | C | 2 | a0001c0002t0002g0021 a0001c0002t0002g0181 |
5 | HG01070.hp1 HG01106.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+4356A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376759 | |||||||
| chr12:29376797 | T | A | 3 | a0001c0001t0010g0006 a0001c0001t0010g0117 a0001c0001t0010g0118 |
9 | HG01167.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38+4318A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376797 | |||||||
| chr12:29376810 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-38+4305A>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376810 | |||||||
| chr12:29376927 | T | TTG | 102 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(99): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38+4186_-38+4187d others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376927 | |||||||
| chr12:29376966 | G | T | 2 | a0001c0002t0018g0030 a0001c0002t0020g0056 |
3 | HG02717.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-38+4149C>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29376966 | |||||||
| chr12:29377531 | A | G | 48 | a0001c0001t0003g0010 a0001c0001t0003g0014 a0001c0001t0003g0131 others(45): Show |
78 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.-38+3584T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29377531 | |||||||
| chr12:29377784 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-38+3331A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29377784 | |||||||
| chr12:29377818 | C | A | 1 | a0001c0001t0006g0046 | 2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-38+3297G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29377818 | |||||||
| chr12:29377824 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0115 others(1): Show |
9 | HG01081.hp1 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+3291A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29377824 | |||||||
| chr12:29378286 | T | C | 1 | a0001c0001t0005g0038 | 2 | HG01074.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-38+2829A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29378286 | |||||||
| chr12:29378349 | C | A | 3 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0021g0055 |
4 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+2766G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29378349 | |||||||
| chr12:29378363 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38+2752T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29378363 | |||||||
| chr12:29378877 | C | T | 2 | a0001c0002t0016g0054 a0001c0002t0021g0055 |
2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-38+2238G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29378877 | |||||||
| chr12:29378894 | T | C | 19 | a0001c0001t0007g0027 a0001c0001t0007g0047 a0001c0001t0007g0048 others(16): Show |
27 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-38+2221A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29378894 | |||||||
| chr12:29379033 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-38+2082T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379033 | |||||||
| chr12:29379056 | C | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(47): Show |
113 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-38+2059G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379056 | |||||||
| chr12:29379212 | G | A | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-38+1903C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379212 | |||||||
| chr12:29379454 | C | A | 1 | a0001c0001t0019g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+1661G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379454 | |||||||
| chr12:29379552 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(9): Show |
19 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+1563C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379552 | |||||||
| chr12:29379850 | GA | G | 7 | a0001c0001t0005g0009 a0001c0001t0005g0038 a0001c0001t0005g0127 others(4): Show |
13 | HG01074.hp1 HG01257.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+1264delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29379850 | |||||||
| chr12:29380057 | TA | T | 15 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0037 others(12): Show |
28 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.-38+1057delT | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380057 | |||||||
| chr12:29380057 | TAA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-38+1056_-38+1057d others(4): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380057 | |||||||
| chr12:29380137 | TTCC | T | 3 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0021g0055 |
4 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+975_-38+977del others(3): Show |
ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380137 | |||||||
| chr12:29380226 | G | A | 1 | a0001c0002t0002g0193 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-38+889C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380226 | |||||||
| chr12:29380284 | C | A | 1 | a0001c0001t0008g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-38+831G>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380284 | |||||||
| chr12:29380354 | T | C | 5 | a0001c0001t0013g0022 a0001c0001t0013g0195 a0001c0001t0013g0197 others(2): Show |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+761A>G | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380354 | |||||||
| chr12:29380369 | A | T | 3 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0004g0059 |
9 | HG00408.hp2 HG00438.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+746T>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380369 | |||||||
| chr12:29380921 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-38+194G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380921 | |||||||
| chr12:29380975 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-38+140C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29380975 | |||||||
| chr12:29381027 | G | A | 1 | a0001c0001t0001g0050 | 2 | NA18990.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-38+88C>T | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29381027 | |||||||
| chr12:29381087 | A | G | 5 | a0001c0002t0016g0029 a0001c0002t0016g0054 a0001c0002t0018g0030 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+28T>C | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29381087 | |||||||
| chr12:29381091 | C | T | 5 | a0001c0001t0008g0015 a0001c0001t0008g0028 a0001c0001t0008g0051 others(2): Show |
9 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+24G>A | ERGIC2 | ENSG00000087502.19 | transcript | ENST00000360150.9 | protein_coding | 1/13 | chr12 | 29381091 |