Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4939 |
| ensemblid | ENSG00000111335.14 |
| hgncid | 8087 |
| symbol | OAS2 |
| name | 2'-5'-oligoadenylate synthetase 2 |
| refseq_nuc | NM_002535.3 |
| refseq_prot | NP_002526.2 |
| ensembl_nuc | ENST00000392583.7 |
| ensembl_prot | ENSP00000376362.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 112978519 |
| end | 113011723 |
| strand | + |
| ver | v1.2 |
| region | chr12:112978519-113011723 |
| region5000 | chr12:112973519-113016723 |
| regionname0 | OAS2_chr12_112978519_113011723 |
| regionname5000 | OAS2_chr12_112973519_113016723 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 687 | 375 | 89 | 67 | 160 | 14 | 43 | 120 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(682): Show |
chr12 | 112973519 | 113016723 |
| a0002 | 0/0 | 687 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(682): Show |
chr12 | 112973519 | 113016723 |
| a0003 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(682): Show |
chr12 | 112973519 | 113016723 |
| a0004 | 0/0 | 687 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(682): Show |
chr12 | 112973519 | 113016723 |
| a0005 | 0/0 | 382 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(377): Show |
chr12 | 112973519 | 113016723 |
| a0006 | 0/0 | 687 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | MGNGE others(682): Show |
chr12 | 112973519 | 113016723 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2061 | 242 | 42 | 28 | 134 | 5 | 33 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0002 | 0/0 | 2061 | 69 | 16 | 23 | 21 | 4 | 5 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0003 | 1/1 | 2061 | 19 | 1 | 8 | 0 | 4 | 4 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0004 | 0/0 | 2061 | 17 | 12 | 5 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0005 | 0/0 | 2061 | 9 | 8 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0006 | 0/0 | 2061 | 7 | 5 | 2 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0007 | 0/0 | 2061 | 5 | 4 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0008 | 0/0 | 2061 | 4 | 0 | 0 | 4 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0010 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0013 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0001c0014 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0002c0009 | 0/0 | 2061 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0003c0011 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0004c0015 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0005c0012 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 | ||
| a0006c0016 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | ATGGG others(2056): Show |
chr12 | 112973519 | 113016723 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4621 | 88 | 6 | 8 | 58 | 3 | 13 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0002 | 0/0 | 4619 | 80 | 3 | 12 | 55 | 0 | 10 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0003 | 0/0 | 4621 | 17 | 15 | 2 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0004 | 0/0 | 4622 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4617): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0005 | 0/0 | 4621 | 3 | 1 | 1 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0006 | 0/0 | 4619 | 10 | 0 | 0 | 10 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0007 | 0/0 | 4622 | 9 | 0 | 5 | 0 | 0 | 4 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4617): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0008 | 0/0 | 4620 | 7 | 0 | 0 | 6 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0010 | 0/0 | 4620 | 7 | 7 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0012 | 0/0 | 4620 | 4 | 1 | 0 | 1 | 0 | 2 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0014 | 0/0 | 4621 | 3 | 3 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0015 | 0/0 | 4620 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0016 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0017 | 0/0 | 4619 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0018 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0019 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4633): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0020 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0022 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0024 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0025 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0026 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0027 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0001t0028 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0001 | 0/0 | 4621 | 44 | 4 | 21 | 14 | 2 | 3 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0002 | 0/0 | 4619 | 9 | 0 | 2 | 5 | 2 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0003 | 0/0 | 4621 | 9 | 8 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0004 | 0/0 | 4622 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4617): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0008 | 0/0 | 4620 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0012 | 0/0 | 4620 | 3 | 3 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0002t0023 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0003t0001 | 0/0 | 4621 | 3 | 0 | 1 | 0 | 0 | 2 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0003t0004 | 1/1 | 4622 | 16 | 1 | 7 | 0 | 4 | 2 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4617): Show |
chr12 | 112973519 | 113016723 |
| a0001c0004t0001 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0004t0003 | 0/0 | 4621 | 9 | 6 | 3 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0004t0011 | 0/0 | 4620 | 7 | 6 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0005t0009 | 0/0 | 4621 | 8 | 7 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0005t0021 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0006t0005 | 0/0 | 4621 | 4 | 3 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0006t0013 | 0/0 | 4620 | 3 | 2 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0007t0005 | 0/0 | 4621 | 4 | 3 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0007t0013 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4615): Show |
chr12 | 112973519 | 113016723 |
| a0001c0008t0001 | 0/0 | 4621 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0001c0008t0002 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0008t0006 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0010t0002 | 0/0 | 4619 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0013t0002 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4614): Show |
chr12 | 112973519 | 113016723 |
| a0001c0014t0003 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0002c0009t0001 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0003c0011t0003 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0004c0015t0005 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0005c0012t0001 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| a0006c0016t0001 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | AGTTT others(4616): Show |
chr12 | 112973519 | 113016723 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 2 | 22 | 0 | 4 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0002 | 0/0 | 20 | 2 | 5 | 8 | 0 | 5 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0007g0005 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0012g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0014g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0015g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0016g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0019g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0022g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0024g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0025g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0026g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0027g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0001t0028g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0003 | 0/0 | 9 | 0 | 5 | 1 | 2 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0004 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0002t0023g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0020 | 0/1 | 3 | 1 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0023 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0004t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0005t0009g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0005t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0005t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0005t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0005t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0006t0005g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0006t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0006t0013g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0006t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0006t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0007t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0007t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0007t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0007t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0007t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0008t0006g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0010t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0013t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0001c0014t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0002c0009t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0003c0011t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0004c0015t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0005c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| a0006c0016t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00099 | hp2 | a0001 | c0003 | t0004 | g0020 | EUR | GBR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0023 | EUR | GBR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00140 | hp2 | a0001 | c0007 | t0005 | g0183 | EUR | GBR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00323 | hp2 | a0001 | c0003 | t0004 | g0043 | EUR | FIN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00438 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0218 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00639 | hp1 | a0002 | c0009 | t0001 | g0150 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0182 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG00738 | hp2 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01081 | hp2 | a0001 | c0004 | t0003 | g0066 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01099 | hp1 | a0001 | c0006 | t0005 | g0026 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01106 | hp2 | a0001 | c0003 | t0004 | g0023 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0015 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01167 | hp2 | a0001 | c0004 | t0011 | g0037 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01168 | hp1 | a0001 | c0004 | t0003 | g0041 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0197 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01169 | hp2 | a0001 | c0004 | t0003 | g0198 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0022 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01358 | hp2 | a0001 | c0003 | t0004 | g0022 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01361 | hp2 | a0001 | c0005 | t0009 | g0054 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0030 | EUR | IBS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0174 | EUR | IBS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0030 | EUR | IBS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0027 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01884 | hp2 | a0001 | c0006 | t0005 | g0026 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01891 | hp1 | a0001 | c0004 | t0003 | g0119 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0084 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01943 | hp2 | a0001 | c0006 | t0013 | g0025 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02040 | hp1 | a0001 | c0001 | t0016 | g0124 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02055 | hp2 | a0001 | c0002 | t0012 | g0057 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02074 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02074 | hp2 | a0001 | c0001 | t0008 | g0222 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02132 | hp2 | a0001 | c0008 | t0001 | g0209 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0008 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0105 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CDX | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CDX | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0137 | EAS | CDX | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02257 | hp1 | a0001 | c0004 | t0003 | g0041 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0060 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02258 | hp2 | a0001 | c0005 | t0009 | g0055 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02280 | hp2 | a0001 | c0005 | t0009 | g0007 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02572 | hp2 | a0001 | c0004 | t0011 | g0067 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02602 | hp1 | a0001 | c0003 | t0004 | g0022 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02615 | hp1 | a0001 | c0006 | t0013 | g0059 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02615 | hp2 | a0003 | c0011 | t0003 | g0013 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02622 | hp1 | a0001 | c0004 | t0003 | g0107 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0118 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02698 | hp1 | a0001 | c0010 | t0002 | g0148 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02698 | hp2 | a0001 | c0001 | t0022 | g0204 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0120 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0172 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0180 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0220 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0115 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02818 | hp2 | a0001 | c0006 | t0013 | g0091 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02886 | hp2 | a0001 | c0005 | t0009 | g0007 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02896 | hp1 | a0001 | c0002 | t0012 | g0025 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02897 | hp1 | a0001 | c0002 | t0012 | g0058 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02897 | hp2 | a0001 | c0004 | t0011 | g0098 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0019 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02970 | hp2 | a0001 | c0007 | t0005 | g0116 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02976 | hp1 | a0001 | c0006 | t0005 | g0031 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0106 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03130 | hp1 | a0001 | c0006 | t0005 | g0031 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0104 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03195 | hp1 | a0001 | c0004 | t0011 | g0061 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03195 | hp2 | a0001 | c0007 | t0013 | g0019 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03209 | hp1 | a0001 | c0014 | t0003 | g0121 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0158 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03225 | hp2 | a0001 | c0005 | t0009 | g0007 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03453 | hp1 | a0001 | c0005 | t0009 | g0007 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0013 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03486 | hp1 | a0001 | c0004 | t0011 | g0068 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03486 | hp2 | a0001 | c0001 | t0028 | g0064 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03490 | hp1 | a0001 | c0001 | t0012 | g0160 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03516 | hp1 | a0001 | c0005 | t0009 | g0024 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | ESN | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | GWD | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03579 | hp1 | a0001 | c0001 | t0020 | g0110 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03579 | hp2 | a0001 | c0001 | t0025 | g0193 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0221 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03669 | hp1 | a0001 | c0001 | t0017 | g0212 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0072 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0190 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03704 | hp2 | a0001 | c0002 | t0008 | g0003 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03831 | hp1 | a0004 | c0015 | t0005 | g0165 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18522 | hp1 | a0001 | c0005 | t0021 | g0024 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0050 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18906 | hp2 | a0001 | c0002 | t0023 | g0083 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18940 | hp2 | a0001 | c0001 | t0027 | g0036 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18941 | hp1 | a0005 | c0012 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18949 | hp1 | a0001 | c0008 | t0002 | g0215 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18957 | hp2 | a0001 | c0001 | t0019 | g0033 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18961 | hp1 | a0001 | c0013 | t0002 | g0151 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18975 | hp2 | a0001 | c0008 | t0001 | g0211 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0200 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19043 | hp1 | a0001 | c0007 | t0005 | g0179 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0079 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19055 | hp2 | a0001 | c0008 | t0006 | g0006 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19062 | hp2 | a0006 | c0016 | t0001 | g0018 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19077 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA19240 | hp2 | a0001 | c0005 | t0009 | g0007 | AFR | YRI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20752 | hp2 | a0001 | c0003 | t0004 | g0043 | EUR | TSI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20805 | hp2 | a0001 | c0001 | t0026 | g0173 | EUR | TSI | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20905 | hp1 | a0001 | c0003 | t0004 | g0205 | SAS | GIH | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02109 | hp1 | a0001 | c0004 | t0011 | g0037 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02109 | hp2 | a0001 | c0007 | t0005 | g0053 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0100 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0103 | AFR | ACB | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0196 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| HG06807 | hp2 | a0001 | c0004 | t0011 | g0069 | AFR | USA | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | USA | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0004 | g0020 | REF | REF | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0023 | REF | REF | OAS2_chr12_112973519_113016723 | OAS2 | chr12 | 112973519 | 113016723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112978652 | A | C | 1 | a0006 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.44A>C | p.Lys15Thr | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/10 | 134/4622 | 44/2064 | 15/687 | chr12 | 112978652 | |||
| chr12:112978760 | T | C | 1 | a0002 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.152T>C | p.Phe51Ser | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/10 | 242/4622 | 152/2064 | 51/687 | chr12 | 112978760 | |||
| chr12:112987053 | C | T | 1 | a0004 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.193C>T | p.Arg65Trp | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/10 | 283/4622 | 193/2064 | 65/687 | chr12 | 112987053 | |||
| chr12:113003070 | C | T | 1 | a0005 | 1 | NA18941.hp1 | stop_gained | HIGH | c.1147C>T | p.Arg383* | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/10 | 1237/4622 | 1147/2064 | 383/687 | chr12 | 113003070 | |||
| chr12:113007826 | G | A | 1 | a0003 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1778G>A | p.Arg593Gln | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/10 | 1868/4622 | 1778/2064 | 593/687 | chr12 | 113007826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112978758 | G | A | 1 | a0001c0008 | 4 | HG02132.hp2 NA18949.hp1 NA18975.hp2 others(1): Show |
synonymous_variant | LOW | c.150G>A | p.Gln50Gln | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/10 | 240/4622 | 150/2064 | 50/687 | chr12 | 112978758 | |||
| chr12:112987088 | C | G | 2 | a0001c0002 a0001c0006 |
76 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
synonymous_variant | LOW | c.228C>G | p.Thr76Thr | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/10 | 318/4622 | 228/2064 | 76/687 | chr12 | 112987088 | |||
| chr12:112987280 | C | T | 1 | a0001c0014 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.420C>T | p.Phe140Phe | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/10 | 510/4622 | 420/2064 | 140/687 | chr12 | 112987280 | |||
| chr12:112997645 | A | T | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
synonymous_variant | LOW | c.753A>T | p.Val251Val | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 4/10 | 843/4622 | 753/2064 | 251/687 | chr12 | 112997645 | |||
| chr12:113002949 | G | T | 1 | a0001c0013 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.1026G>T | p.Thr342Thr | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/10 | 1116/4622 | 1026/2064 | 342/687 | chr12 | 113002949 | |||
| chr12:113006480 | C | T | 1 | a0001c0005 | 9 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
synonymous_variant | LOW | c.1536C>T | p.Ser512Ser | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/10 | 1626/4622 | 1536/2064 | 512/687 | chr12 | 113006480 | |||
| chr12:113006525 | G | A | 1 | a0001c0010 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1581G>A | p.Leu527Leu | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/10 | 1671/4622 | 1581/2064 | 527/687 | chr12 | 113006525 | |||
| chr12:113007800 | G | A | 2 | a0001c0004 a0001c0014 |
18 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(15): Show |
synonymous_variant | LOW | c.1752G>A | p.Pro584Pro | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/10 | 1842/4622 | 1752/2064 | 584/687 | chr12 | 113007800 | |||
| chr12:113009207 | G | T | 2 | a0001c0006 a0001c0007 |
12 | HG00140.hp2 HG01099.hp1 HG01884.hp2 others(9): Show |
synonymous_variant | LOW | c.2016G>T | p.Gly672Gly | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 2106/4622 | 2016/2064 | 672/687 | chr12 | 113009207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112978570 | C | T | 1 | a0001c0001t0028 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/10 | 39 | chr12 | 112978570 | ||||||
| chr12:113009263 | G | T | 1 | a0001c0001t0027 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 8 | chr12 | 113009263 | ||||||
| chr12:113009298 | A | G | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(5): Show |
28 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*43A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 43 | chr12 | 113009298 | ||||||
| chr12:113009394 | GC | G | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(14): Show |
132 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*144delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 144 | INFO_REALIGN_3_PRIME | chr12 | 113009394 | |||||
| chr12:113009437 | T | C | 3 | a0001c0001t0020 a0001c0005t0009 a0001c0005t0021 |
10 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*182T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 182 | chr12 | 113009437 | ||||||
| chr12:113009438 | G | T | 1 | a0001c0005t0021 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 183 | chr12 | 113009438 | ||||||
| chr12:113009632 | G | A | 1 | a0001c0001t0016 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 377 | chr12 | 113009632 | ||||||
| chr12:113009767 | C | T | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
352 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*512C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 512 | chr12 | 113009767 | ||||||
| chr12:113010155 | C | T | 1 | a0001c0001t0026 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*900C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 900 | chr12 | 113010155 | ||||||
| chr12:113010196 | C | A | 1 | a0001c0001t0015 | 2 | HG01884.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*941C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 941 | chr12 | 113010196 | ||||||
| chr12:113010232 | A | G | 3 | a0001c0001t0006 a0001c0001t0027 a0001c0008t0006 |
12 | NA18940.hp2 NA18955.hp1 NA18978.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*977A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 977 | chr12 | 113010232 | ||||||
| chr12:113010483 | A | G | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
352 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1228 | chr12 | 113010483 | ||||||
| chr12:113010539 | C | G | 1 | a0001c0001t0025 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1284 | chr12 | 113010539 | ||||||
| chr12:113010847 | C | A | 18 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0014 others(15): Show |
166 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*1592C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1592 | chr12 | 113010847 | ||||||
| chr12:113010936 | T | C | 1 | a0001c0001t0017 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1681 | chr12 | 113010936 | ||||||
| chr12:113011014 | T | C | 1 | a0001c0001t0022 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1759 | chr12 | 113011014 | ||||||
| chr12:113011052 | TC | T | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
352 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1804delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1804 | INFO_REALIGN_3_PRIME | chr12 | 113011052 | |||||
| chr12:113011059 | C | A | 1 | a0001c0001t0018 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1804C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1804 | chr12 | 113011059 | ||||||
| chr12:113011092 | CT | C | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(13): Show |
119 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1842delT | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 1842 | INFO_REALIGN_3_PRIME | chr12 | 113011092 | |||||
| chr12:113011311 | G | C | 48 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(45): Show |
352 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 2056 | chr12 | 113011311 | ||||||
| chr12:113011365 | G | C | 3 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0024 |
10 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2110G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 2110 | chr12 | 113011365 | ||||||
| chr12:113011508 | A | G | 2 | a0001c0001t0025 a0001c0002t0023 |
2 | HG03579.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2253A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 2253 | chr12 | 113011508 | ||||||
| chr12:113011715 | A | AGTAAAAG others(12): Show |
1 | a0001c0001t0019 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463_*2464insAAAG others(15): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 10/10 | 2464 | INFO_REALIGN_3_PRIME | chr12 | 113011715 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112978804 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.177+19T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112978804 | |||||||
| chr12:112978848 | G | A | 72 | a0001c0001t0001g0056 a0001c0001t0001g0065 a0001c0001t0001g0070 others(69): Show |
99 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.177+63G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112978848 | |||||||
| chr12:112979000 | T | C | 15 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(12): Show |
21 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.177+215T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979000 | |||||||
| chr12:112979156 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.177+371G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979156 | |||||||
| chr12:112979434 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.177+649C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979434 | |||||||
| chr12:112979449 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.177+664C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979449 | |||||||
| chr12:112979561 | C | T | 1 | a0001c0002t0004g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.177+776C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979561 | |||||||
| chr12:112979580 | G | A | 1 | a0001c0002t0003g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.177+795G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979580 | |||||||
| chr12:112979617 | A | AT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
17 | HG02056.hp2 HG02074.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+841dupT | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 112979617 | ||||||
| chr12:112979654 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.177+869C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979654 | |||||||
| chr12:112979737 | C | A | 1 | a0001c0002t0002g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.177+952C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979737 | |||||||
| chr12:112979747 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.177+962C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979747 | |||||||
| chr12:112979752 | C | T | 1 | a0001c0002t0003g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.177+967C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979752 | |||||||
| chr12:112979787 | C | G | 1 | a0001c0002t0001g0099 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.177+1002C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112979787 | |||||||
| chr12:112980074 | C | A | 1 | a0001c0002t0001g0049 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.177+1289C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980074 | |||||||
| chr12:112980202 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0003g0114 a0001c0001t0010g0115 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1417G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980202 | |||||||
| chr12:112980363 | G | A | 4 | a0001c0004t0003g0118 a0001c0004t0003g0119 a0001c0004t0003g0120 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+1578G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980363 | |||||||
| chr12:112980775 | T | A | 1 | a0001c0001t0002g0122 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.177+1990T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980775 | |||||||
| chr12:112980917 | G | A | 9 | a0001c0001t0003g0051 a0001c0001t0010g0050 a0001c0001t0012g0052 others(6): Show |
13 | HG01361.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+2132G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980917 | |||||||
| chr12:112980992 | C | G | 1 | a0001c0004t0011g0098 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.177+2207C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112980992 | |||||||
| chr12:112981045 | G | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.177+2260G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981045 | |||||||
| chr12:112981094 | G | A | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(58): Show |
96 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.177+2309G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981094 | |||||||
| chr12:112981208 | C | A | 4 | a0001c0004t0003g0118 a0001c0004t0003g0119 a0001c0004t0003g0120 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+2423C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981208 | |||||||
| chr12:112981295 | A | C | 1 | a0001c0002t0001g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+2510A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981295 | |||||||
| chr12:112981372 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.177+2587C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981372 | |||||||
| chr12:112981852 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.177+3067A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981852 | |||||||
| chr12:112981935 | A | AGTTAAAT others(18): Show |
2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA18946.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.177+3158_177+3182d others(27): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 112981935 | ||||||
| chr12:112981951 | A | C | 1 | a0001c0002t0001g0021 | 3 | HG02280.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+3166A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112981951 | |||||||
| chr12:112982086 | T | C | 9 | a0001c0001t0003g0051 a0001c0001t0010g0050 a0001c0001t0012g0052 others(6): Show |
13 | HG01361.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+3301T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982086 | |||||||
| chr12:112982202 | A | G | 43 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0049 others(40): Show |
65 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.177+3417A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982202 | |||||||
| chr12:112982282 | A | G | 16 | a0001c0002t0001g0004 a0001c0002t0001g0085 a0001c0002t0001g0086 others(13): Show |
27 | HG00609.hp2 HG01081.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.177+3497A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982282 | |||||||
| chr12:112982387 | T | C | 1 | a0001c0001t0010g0050 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.177+3602T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982387 | |||||||
| chr12:112982550 | C | T | 17 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0199 others(14): Show |
21 | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.177+3765C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982550 | |||||||
| chr12:112982583 | TG | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(77): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.177+3799delG | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982583 | |||||||
| chr12:112982623 | C | T | 1 | a0001c0004t0011g0037 | 2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.177+3838C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982623 | |||||||
| chr12:112982746 | T | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(61): Show |
99 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.177+3961T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982746 | |||||||
| chr12:112982799 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.177+4014A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112982799 | |||||||
| chr12:112983091 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.178-3947G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983091 | |||||||
| chr12:112983123 | C | T | 2 | a0001c0001t0014g0158 a0001c0004t0011g0037 |
3 | HG01167.hp2 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.178-3915C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983123 | |||||||
| chr12:112983312 | GC | G | 3 | a0001c0004t0001g0197 a0001c0004t0003g0041 a0001c0004t0003g0198 |
4 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-3721delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 112983312 | ||||||
| chr12:112983469 | C | T | 2 | a0001c0001t0014g0158 a0001c0004t0011g0037 |
3 | HG01167.hp2 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.178-3569C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983469 | |||||||
| chr12:112983490 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.178-3548A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983490 | |||||||
| chr12:112983557 | G | A | 51 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0021 others(48): Show |
76 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.178-3481G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983557 | |||||||
| chr12:112983624 | G | C | 4 | a0001c0001t0001g0117 a0001c0001t0003g0114 a0001c0001t0010g0115 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-3414G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112983624 | |||||||
| chr12:112984058 | A | G | 1 | a0001c0004t0003g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.178-2980A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984058 | |||||||
| chr12:112984064 | A | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(60): Show |
98 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.178-2974A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984064 | |||||||
| chr12:112984172 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(78): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-2866A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984172 | |||||||
| chr12:112984452 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.178-2586T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984452 | |||||||
| chr12:112984508 | T | A | 4 | a0001c0001t0022g0204 a0001c0003t0001g0206 a0001c0003t0004g0022 others(1): Show |
6 | HG01175.hp2 HG01346.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-2530T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984508 | |||||||
| chr12:112984609 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.178-2429G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984609 | |||||||
| chr12:112984782 | C | T | 4 | a0001c0004t0003g0118 a0001c0004t0003g0119 a0001c0004t0003g0120 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-2256C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984782 | |||||||
| chr12:112984879 | A | G | 43 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0049 others(40): Show |
65 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.178-2159A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984879 | |||||||
| chr12:112984945 | G | GT | 57 | a0001c0001t0001g0070 a0001c0002t0001g0003 a0001c0002t0001g0004 others(54): Show |
82 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.178-2084dupT | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 112984945 | ||||||
| chr12:112984946 | T | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(140): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.178-2092T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112984946 | |||||||
| chr12:112985198 | TA | T | 9 | a0001c0001t0003g0062 a0001c0001t0010g0027 a0001c0001t0010g0103 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-1838delA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 112985198 | ||||||
| chr12:112985227 | TC | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(58): Show |
96 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.178-1810delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985227 | |||||||
| chr12:112985303 | T | C | 6 | a0001c0001t0001g0070 a0001c0004t0003g0066 a0001c0004t0011g0067 others(3): Show |
6 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-1735T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985303 | |||||||
| chr12:112985398 | A | C | 11 | a0001c0001t0001g0065 a0001c0001t0001g0199 a0001c0001t0003g0051 others(8): Show |
15 | HG01243.hp1 HG01361.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-1640A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985398 | |||||||
| chr12:112985618 | T | G | 77 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0199 others(74): Show |
106 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.178-1420T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985618 | |||||||
| chr12:112985738 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.178-1300T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985738 | |||||||
| chr12:112985895 | G | A | 9 | a0001c0001t0003g0062 a0001c0001t0010g0027 a0001c0001t0010g0103 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-1143G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985895 | |||||||
| chr12:112985955 | G | A | 9 | a0001c0001t0003g0062 a0001c0001t0010g0027 a0001c0001t0010g0103 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-1083G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112985955 | |||||||
| chr12:112986086 | T | A | 4 | a0001c0004t0003g0118 a0001c0004t0003g0119 a0001c0004t0003g0120 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-952T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986086 | |||||||
| chr12:112986166 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(78): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-872A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986166 | |||||||
| chr12:112986198 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(77): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.178-840G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986198 | |||||||
| chr12:112986255 | C | T | 51 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0021 others(48): Show |
76 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.178-783C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986255 | |||||||
| chr12:112986482 | G | A | 6 | a0001c0001t0001g0070 a0001c0004t0003g0066 a0001c0004t0011g0067 others(3): Show |
6 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-556G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986482 | |||||||
| chr12:112986607 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.178-431C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986607 | |||||||
| chr12:112986636 | G | A | 1 | a0001c0004t0003g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.178-402G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986636 | |||||||
| chr12:112986653 | C | T | 51 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0021 others(48): Show |
76 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.178-385C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986653 | |||||||
| chr12:112986670 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(77): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.178-368G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986670 | |||||||
| chr12:112986679 | C | T | 7 | a0001c0001t0010g0050 a0001c0005t0009g0007 a0001c0005t0009g0024 others(4): Show |
11 | HG01361.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-359C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986679 | |||||||
| chr12:112986686 | G | A | 6 | a0001c0001t0001g0070 a0001c0004t0003g0066 a0001c0004t0011g0067 others(3): Show |
6 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-352G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986686 | |||||||
| chr12:112986696 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.178-342T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986696 | |||||||
| chr12:112986846 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.178-192C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 1/9 | chr12 | 112986846 | |||||||
| chr12:112987349 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(225): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.448+41C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987349 | |||||||
| chr12:112987360 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448+52C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987360 | |||||||
| chr12:112987477 | T | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(60): Show |
98 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.448+169T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987477 | |||||||
| chr12:112987568 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.448+260G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987568 | |||||||
| chr12:112987669 | G | A | 6 | a0001c0001t0001g0128 a0001c0001t0002g0123 a0001c0001t0002g0126 others(3): Show |
6 | HG00597.hp2 HG02040.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.448+361G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987669 | |||||||
| chr12:112987688 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.448+380T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987688 | |||||||
| chr12:112987732 | G | A | 44 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0021 others(41): Show |
68 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.448+424G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987732 | |||||||
| chr12:112987761 | C | A | 1 | a0001c0001t0002g0129 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.448+453C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987761 | |||||||
| chr12:112987874 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(217): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.448+566T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112987874 | |||||||
| chr12:112988156 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.448+848A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988156 | |||||||
| chr12:112988177 | AG | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(60): Show |
98 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.448+870delG | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988177 | |||||||
| chr12:112988375 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0038 others(76): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.448+1067G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988375 | |||||||
| chr12:112988633 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.448+1325A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988633 | |||||||
| chr12:112988639 | C | G | 1 | a0001c0001t0012g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.448+1331C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988639 | |||||||
| chr12:112988717 | C | T | 9 | a0001c0001t0003g0062 a0001c0001t0010g0027 a0001c0001t0010g0103 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.448+1409C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988717 | |||||||
| chr12:112988827 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(54): Show |
91 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.448+1519T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988827 | |||||||
| chr12:112988983 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.448+1675C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112988983 | |||||||
| chr12:112989148 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.448+1840G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989148 | |||||||
| chr12:112989158 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.448+1850C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989158 | |||||||
| chr12:112989173 | T | C | 5 | a0001c0001t0001g0208 a0001c0001t0022g0204 a0001c0003t0001g0206 others(2): Show |
7 | HG01175.hp2 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+1865T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989173 | |||||||
| chr12:112989179 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0003g0114 a0001c0001t0010g0115 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+1871T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989179 | |||||||
| chr12:112989290 | G | A | 1 | a0001c0002t0003g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.448+1982G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989290 | |||||||
| chr12:112989375 | G | A | 1 | a0001c0002t0003g0072 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.448+2067G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989375 | |||||||
| chr12:112989419 | C | T | 1 | a0001c0004t0003g0118 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.448+2111C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989419 | |||||||
| chr12:112989800 | G | A | 1 | a0001c0004t0003g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.448+2492G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989800 | |||||||
| chr12:112989821 | T | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(240): Show |
360 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.448+2513T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989821 | |||||||
| chr12:112989999 | T | A | 1 | a0001c0001t0014g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448+2691T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112989999 | |||||||
| chr12:112990241 | G | C | 1 | a0001c0001t0014g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448+2933G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112990241 | |||||||
| chr12:112990618 | A | G | 18 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0002g0039 others(15): Show |
20 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.448+3310A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112990618 | |||||||
| chr12:112990815 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.448+3507T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112990815 | |||||||
| chr12:112990844 | G | T | 2 | a0001c0001t0003g0051 a0001c0001t0012g0052 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.448+3536G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112990844 | |||||||
| chr12:112990912 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(37): Show |
75 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.448+3604G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112990912 | |||||||
| chr12:112991103 | T | A | 1 | a0001c0001t0002g0032 | 2 | NA18941.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.448+3795T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991103 | |||||||
| chr12:112991164 | A | G | 18 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0002g0039 others(15): Show |
20 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.448+3856A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991164 | |||||||
| chr12:112991256 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.448+3948G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991256 | |||||||
| chr12:112991258 | T | C | 2 | a0001c0001t0014g0019 a0001c0007t0013g0019 |
3 | HG02965.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.448+3950T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991258 | |||||||
| chr12:112991297 | G | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(237): Show |
357 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.448+3989G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991297 | |||||||
| chr12:112991521 | T | A | 14 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(11): Show |
22 | HG00609.hp2 HG01081.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.449-3775T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991521 | |||||||
| chr12:112991524 | G | A | 67 | a0001c0001t0001g0133 a0001c0001t0001g0157 a0001c0001t0001g0194 others(64): Show |
92 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.449-3772G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991524 | |||||||
| chr12:112991526 | AAAGGC | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(102): Show |
177 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.449-3769_449-3765d others(7): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991526 | |||||||
| chr12:112991663 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(237): Show |
357 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.449-3633A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991663 | |||||||
| chr12:112991891 | A | G | 11 | a0001c0001t0001g0117 a0001c0001t0001g0214 a0001c0001t0003g0051 others(8): Show |
15 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.449-3405A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991891 | |||||||
| chr12:112991924 | T | C | 18 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0002g0039 others(15): Show |
20 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.449-3372T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112991924 | |||||||
| chr12:112992038 | GTAGA | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(48): Show |
92 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.449-3252_449-3249d others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112992038 | ||||||
| chr12:112992098 | A | AC | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
193 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.449-3197dupC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112992098 | ||||||
| chr12:112992266 | C | T | 18 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0002g0039 others(15): Show |
20 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.449-3030C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112992266 | |||||||
| chr12:112992372 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0002g0010 a0001c0001t0002g0152 others(2): Show |
7 | HG00423.hp2 HG02040.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-2924C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112992372 | |||||||
| chr12:112992393 | G | GAAA | 7 | a0001c0001t0010g0027 a0001c0001t0010g0103 a0001c0001t0010g0104 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2893_449-2891d others(5): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112992393 | ||||||
| chr12:112992393 | GA | G | 49 | a0001c0001t0001g0133 a0001c0001t0001g0157 a0001c0001t0001g0208 others(46): Show |
73 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.449-2891delA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112992393 | ||||||
| chr12:112992398 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(37): Show |
75 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.449-2898A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112992398 | |||||||
| chr12:112992989 | C | T | 1 | a0001c0002t0003g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.449-2307C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112992989 | |||||||
| chr12:112993031 | T | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(200): Show |
310 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.449-2265T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993031 | |||||||
| chr12:112993090 | C | T | 3 | a0001c0001t0003g0114 a0001c0001t0010g0115 a0001c0007t0005g0116 |
3 | HG02809.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.449-2206C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993090 | |||||||
| chr12:112993106 | AC | A | 21 | a0001c0001t0001g0046 a0001c0001t0001g0113 a0001c0001t0001g0194 others(18): Show |
29 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.449-2188delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112993106 | ||||||
| chr12:112993108 | C | T | 1 | a0001c0001t0028g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.449-2188C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993108 | |||||||
| chr12:112993135 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(240): Show |
360 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.449-2161C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993135 | |||||||
| chr12:112993220 | C | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0080 a0001c0002t0001g0081 others(1): Show |
4 | HG00558.hp2 HG02523.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2076C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993220 | |||||||
| chr12:112993258 | C | G | 1 | a0001c0001t0026g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.449-2038C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993258 | |||||||
| chr12:112993268 | C | T | 2 | a0001c0001t0008g0190 a0001c0001t0022g0204 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.449-2028C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993268 | |||||||
| chr12:112993398 | C | T | 7 | a0001c0001t0010g0027 a0001c0001t0010g0103 a0001c0001t0010g0104 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1898C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993398 | |||||||
| chr12:112993476 | G | A | 1 | a0001c0001t0028g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.449-1820G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993476 | |||||||
| chr12:112993613 | C | G | 19 | a0001c0001t0001g0065 a0001c0001t0001g0188 a0001c0001t0001g0192 others(16): Show |
21 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.449-1683C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993613 | |||||||
| chr12:112993618 | G | A | 21 | a0001c0001t0001g0065 a0001c0001t0001g0188 a0001c0001t0001g0192 others(18): Show |
23 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.449-1678G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993618 | |||||||
| chr12:112993623 | TA | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0214 a0001c0001t0003g0051 others(8): Show |
15 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.449-1671delA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112993623 | ||||||
| chr12:112993773 | G | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(201): Show |
311 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.449-1523G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993773 | |||||||
| chr12:112993838 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(238): Show |
358 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.449-1458A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993838 | |||||||
| chr12:112993851 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.449-1445C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112993851 | |||||||
| chr12:112993962 | TGG | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(239): Show |
359 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.449-1326_449-1325d others(4): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 112993962 | ||||||
| chr12:112994119 | C | T | 3 | a0001c0001t0007g0180 a0001c0001t0007g0181 a0001c0001t0007g0182 |
3 | HG00733.hp2 HG00735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.449-1177C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994119 | |||||||
| chr12:112994189 | G | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0214 a0001c0001t0003g0051 others(8): Show |
15 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.449-1107G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994189 | |||||||
| chr12:112994514 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(37): Show |
75 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.449-782C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994514 | |||||||
| chr12:112994665 | G | A | 9 | a0001c0001t0001g0070 a0001c0001t0028g0064 a0001c0002t0023g0083 others(6): Show |
9 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.449-631G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994665 | |||||||
| chr12:112994890 | T | A | 1 | a0001c0002t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.449-406T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994890 | |||||||
| chr12:112994944 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.449-352T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112994944 | |||||||
| chr12:112995079 | T | C | 21 | a0001c0001t0001g0046 a0001c0001t0001g0113 a0001c0001t0001g0194 others(18): Show |
28 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.449-217T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112995079 | |||||||
| chr12:112995210 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.449-86A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 2/9 | chr12 | 112995210 | |||||||
| chr12:112995759 | T | C | 11 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(8): Show |
17 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.627+285T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112995759 | |||||||
| chr12:112995782 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(194): Show |
301 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.627+308T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112995782 | |||||||
| chr12:112995836 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0214 a0001c0001t0003g0051 others(8): Show |
15 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+362C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112995836 | |||||||
| chr12:112995885 | C | A | 1 | a0001c0008t0002g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.627+411C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112995885 | |||||||
| chr12:112995965 | C | A | 9 | a0001c0001t0001g0070 a0001c0001t0028g0064 a0001c0002t0023g0083 others(6): Show |
9 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.627+491C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112995965 | |||||||
| chr12:112996197 | G | A | 1 | a0001c0001t0007g0005 | 6 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+723G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996197 | |||||||
| chr12:112996351 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(185): Show |
292 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.627+877A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996351 | |||||||
| chr12:112996441 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.627+967G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996441 | |||||||
| chr12:112996515 | A | T | 3 | a0001c0001t0003g0114 a0001c0001t0010g0115 a0001c0007t0005g0116 |
3 | HG02809.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.628-1005A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996515 | |||||||
| chr12:112996713 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.628-807A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996713 | |||||||
| chr12:112996786 | C | T | 7 | a0001c0001t0010g0027 a0001c0001t0010g0103 a0001c0001t0010g0104 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-734C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996786 | |||||||
| chr12:112996818 | T | G | 20 | a0001c0001t0001g0070 a0001c0001t0001g0117 a0001c0001t0001g0214 others(17): Show |
24 | HG01081.hp2 HG01361.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.628-702T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112996818 | |||||||
| chr12:112997051 | T | C | 1 | a0001c0001t0028g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.628-469T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112997051 | |||||||
| chr12:112997208 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.628-312C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112997208 | |||||||
| chr12:112997304 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.628-216A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112997304 | |||||||
| chr12:112997488 | C | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.628-32C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 3/9 | chr12 | 112997488 | |||||||
| chr12:112997889 | A | G | 2 | a0001c0001t0002g0231 a0001c0010t0002g0148 |
2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.863+134A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 4/9 | chr12 | 112997889 | |||||||
| chr12:112998047 | G | A | 4 | a0001c0001t0002g0123 a0001c0001t0002g0207 a0001c0001t0006g0125 others(1): Show |
4 | HG00597.hp2 HG02040.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.864-219G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 4/9 | chr12 | 112998047 | |||||||
| chr12:112998450 | G | A | 5 | a0001c0005t0009g0007 a0001c0005t0009g0024 a0001c0005t0009g0054 others(2): Show |
9 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+40G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998450 | |||||||
| chr12:112998467 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1008+57C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998467 | |||||||
| chr12:112998649 | C | T | 18 | a0001c0001t0001g0046 a0001c0001t0001g0113 a0001c0001t0001g0194 others(15): Show |
25 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1008+239C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998649 | |||||||
| chr12:112998673 | G | T | 1 | a0001c0001t0002g0147 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1008+263G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998673 | |||||||
| chr12:112998731 | A | G | 3 | a0001c0001t0003g0114 a0001c0001t0010g0115 a0001c0007t0005g0116 |
3 | HG02809.hp2 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1008+321A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998731 | |||||||
| chr12:112998777 | G | A | 1 | a0001c0004t0003g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1008+367G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998777 | |||||||
| chr12:112998792 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.1008+382T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998792 | |||||||
| chr12:112998828 | G | A | 3 | a0001c0004t0003g0041 a0001c0004t0003g0107 a0001c0004t0003g0198 |
4 | HG01168.hp1 HG01169.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+418G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112998828 | |||||||
| chr12:112999018 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(42): Show |
80 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.1008+608A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999018 | |||||||
| chr12:112999164 | G | A | 12 | a0001c0001t0001g0117 a0001c0001t0001g0214 a0001c0001t0003g0051 others(9): Show |
16 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1008+754G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999164 | |||||||
| chr12:112999171 | A | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0082 |
2 | HG00558.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1008+761A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999171 | |||||||
| chr12:112999359 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0019g0033 |
2 | HG02083.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1008+949T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999359 | |||||||
| chr12:112999394 | G | A | 2 | a0001c0001t0001g0011 a0001c0008t0001g0209 |
6 | HG02132.hp2 HG02135.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+984G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999394 | |||||||
| chr12:112999445 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1008+1035T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999445 | |||||||
| chr12:112999901 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1008+1491C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999901 | |||||||
| chr12:112999939 | A | T | 9 | a0001c0001t0001g0070 a0001c0001t0028g0064 a0001c0002t0023g0083 others(6): Show |
9 | HG01081.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+1529A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 112999939 | |||||||
| chr12:112999952 | GC | G | 4 | a0001c0001t0001g0046 a0001c0001t0002g0175 a0001c0001t0004g0174 others(1): Show |
5 | HG00738.hp1 HG01516.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+1544delC | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 112999952 | ||||||
| chr12:113000009 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1008+1599C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000009 | |||||||
| chr12:113000025 | G | A | 3 | a0001c0004t0003g0041 a0001c0004t0003g0107 a0001c0004t0003g0198 |
4 | HG01168.hp1 HG01169.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1615G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000025 | |||||||
| chr12:113000029 | G | C | 33 | a0001c0001t0001g0056 a0001c0001t0003g0012 a0001c0001t0003g0013 others(30): Show |
46 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1008+1619G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000029 | |||||||
| chr12:113000038 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1008+1628C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000038 | |||||||
| chr12:113000173 | T | C | 36 | a0001c0001t0001g0056 a0001c0001t0003g0012 a0001c0001t0003g0013 others(33): Show |
49 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1008+1763T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000173 | |||||||
| chr12:113000234 | C | T | 1 | a0001c0007t0005g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1008+1824C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000234 | |||||||
| chr12:113000416 | GA | G | 10 | a0001c0004t0001g0197 a0001c0004t0003g0041 a0001c0004t0003g0107 others(7): Show |
12 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1008+2008delA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000416 | ||||||
| chr12:113000439 | C | T | 20 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(17): Show |
26 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1008+2029C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000439 | |||||||
| chr12:113000462 | T | C | 20 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(17): Show |
26 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1008+2052T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000462 | |||||||
| chr12:113000481 | TAC | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(239): Show |
359 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.1008+2088_1008+208 others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000481 | ||||||
| chr12:113000532 | T | TCA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(149): Show |
224 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1008+2127_1008+212 others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000532 | ||||||
| chr12:113000532 | TCACACAT others(3): Show |
T | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1008+2131_1008+214 others(14): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000532 | ||||||
| chr12:113000570 | C | T | 5 | a0001c0001t0006g0009 a0001c0001t0006g0036 a0001c0001t0006g0125 others(2): Show |
9 | NA18940.hp2 NA18978.hp1 NA18986.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+2160C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000570 | |||||||
| chr12:113000578 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1008+2168C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000578 | |||||||
| chr12:113000608 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1008+2198T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000608 | |||||||
| chr12:113000672 | GCACACAT others(11): Show |
G | 1 | a0001c0001t0016g0124 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1009-2249_1009-223 others(22): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000672 | ||||||
| chr12:113000680 | GCACTCAT others(7): Show |
G | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1009-2249_1009-223 others(18): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113000680 | ||||||
| chr12:113000869 | C | G | 1 | a0001c0001t0015g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1009-2063C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000869 | |||||||
| chr12:113000869 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1009-2063C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000869 | |||||||
| chr12:113000906 | C | A | 1 | a0001c0002t0001g0021 | 3 | HG02280.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1009-2026C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000906 | |||||||
| chr12:113000913 | A | T | 92 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0128 others(89): Show |
137 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.1009-2019A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000913 | |||||||
| chr12:113000989 | C | G | 10 | a0001c0004t0001g0197 a0001c0004t0003g0041 a0001c0004t0003g0107 others(7): Show |
12 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009-1943C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113000989 | |||||||
| chr12:113001383 | T | C | 7 | a0001c0001t0028g0064 a0001c0004t0003g0066 a0001c0004t0011g0061 others(4): Show |
7 | HG01081.hp2 HG02572.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1009-1549T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001383 | |||||||
| chr12:113001389 | C | CAT | 244 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
361 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.1009-1535_1009-153 others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001389 | ||||||
| chr12:113001431 | T | TATATATA others(11): Show |
1 | a0001c0001t0008g0222 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1009-1463_1009-144 others(22): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001431 | ||||||
| chr12:113001431 | TATATATA others(11): Show |
T | 53 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0113 others(50): Show |
73 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1009-1463_1009-144 others(22): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001431 | ||||||
| chr12:113001441 | CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0033 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1009-1485_1009-147 others(14): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001441 | ||||||
| chr12:113001449 | C | CATATATA others(33): Show |
3 | a0001c0001t0001g0070 a0001c0002t0001g0021 a0001c0002t0023g0083 |
5 | HG02280.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1009-1449_1009-144 others(44): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001449 | ||||||
| chr12:113001763 | C | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0128 others(85): Show |
128 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1009-1169C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001763 | |||||||
| chr12:113001817 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1009-1115A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001817 | |||||||
| chr12:113001887 | A | AAAT | 11 | a0001c0001t0001g0070 a0001c0001t0001g0113 a0001c0001t0001g0228 others(8): Show |
13 | HG00609.hp2 HG01978.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009-1044_1009-104 others(7): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001887 | ||||||
| chr12:113001887 | A | AAT | 59 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0046 others(56): Show |
85 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1009-1044_1009-104 others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 113001887 | ||||||
| chr12:113001887 | A | AT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(73): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1009-1045_1009-104 others(5): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001887 | |||||||
| chr12:113001887 | A | T | 99 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0117 others(96): Show |
146 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1009-1045A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001887 | |||||||
| chr12:113001895 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(91): Show |
144 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1009-1037C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001895 | |||||||
| chr12:113001948 | T | A | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1009-984T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001948 | |||||||
| chr12:113001961 | G | A | 1 | a0001c0007t0005g0179 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1009-971G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113001961 | |||||||
| chr12:113002022 | G | A | 14 | a0001c0001t0001g0056 a0001c0001t0003g0012 a0001c0001t0003g0013 others(11): Show |
21 | HG00140.hp2 HG01109.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1009-910G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002022 | |||||||
| chr12:113002076 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1009-856G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002076 | |||||||
| chr12:113002132 | C | T | 2 | a0001c0001t0001g0184 a0001c0002t0001g0085 |
2 | HG00609.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1009-800C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002132 | |||||||
| chr12:113002230 | A | G | 2 | a0001c0001t0003g0114 a0001c0001t0010g0115 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1009-702A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002230 | |||||||
| chr12:113002427 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1009-505C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002427 | |||||||
| chr12:113002460 | C | A | 1 | a0001c0003t0001g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1009-472C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002460 | |||||||
| chr12:113002478 | C | T | 1 | a0001c0001t0002g0035 | 2 | HG01433.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1009-454C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002478 | |||||||
| chr12:113002686 | C | T | 1 | a0001c0002t0003g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1009-246C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002686 | |||||||
| chr12:113002765 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1009-167G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 5/9 | chr12 | 113002765 | |||||||
| chr12:113003116 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(77): Show |
132 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1179+14T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003116 | |||||||
| chr12:113003210 | A | G | 1 | a0001c0006t0005g0026 | 2 | HG01099.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1179+108A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003210 | |||||||
| chr12:113003399 | T | C | 8 | a0001c0001t0003g0062 a0001c0001t0010g0050 a0001c0001t0012g0160 others(5): Show |
12 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+297T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003399 | |||||||
| chr12:113003644 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1179+542G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003644 | |||||||
| chr12:113003687 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1179+585A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003687 | |||||||
| chr12:113003792 | A | G | 1 | a0001c0013t0002g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1179+690A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003792 | |||||||
| chr12:113003986 | C | A | 1 | a0001c0002t0001g0021 | 3 | HG02280.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+884C>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003986 | |||||||
| chr12:113003987 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1179+885T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113003987 | |||||||
| chr12:113004009 | A | T | 1 | a0001c0013t0002g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1179+907A>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004009 | |||||||
| chr12:113004033 | G | T | 3 | a0001c0001t0003g0051 a0001c0001t0012g0052 a0001c0001t0014g0158 |
3 | HG03209.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1180-901G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004033 | |||||||
| chr12:113004328 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1180-606T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004328 | |||||||
| chr12:113004452 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1180-482C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004452 | |||||||
| chr12:113004671 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0003g0063 others(11): Show |
17 | HG00558.hp2 HG00673.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.1180-263C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004671 | |||||||
| chr12:113004808 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1180-126A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004808 | |||||||
| chr12:113004816 | CT | C | 3 | a0001c0001t0003g0051 a0001c0001t0012g0052 a0001c0001t0014g0158 |
3 | HG03209.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1180-117delT | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004816 | |||||||
| chr12:113004873 | C | T | 3 | a0001c0001t0003g0051 a0001c0001t0012g0052 a0001c0001t0014g0158 |
3 | HG03209.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1180-61C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 6/9 | chr12 | 113004873 | |||||||
| chr12:113005376 | G | T | 8 | a0001c0001t0003g0062 a0001c0001t0010g0050 a0001c0001t0012g0160 others(5): Show |
12 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468+154G>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005376 | |||||||
| chr12:113005415 | G | A | 11 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0005g0178 others(8): Show |
17 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1468+193G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005415 | |||||||
| chr12:113005417 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(228): Show |
342 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.1468+195C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005417 | |||||||
| chr12:113005420 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(141): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1468+198T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005420 | |||||||
| chr12:113005475 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG02080.hp2 NA18959.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1468+253G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005475 | |||||||
| chr12:113005495 | C | T | 8 | a0001c0001t0003g0062 a0001c0001t0010g0050 a0001c0001t0012g0160 others(5): Show |
12 | HG01361.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468+273C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005495 | |||||||
| chr12:113005702 | A | AAAAT | 10 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0017 others(7): Show |
16 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1468+507_1468+510d others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005702 | ||||||
| chr12:113005702 | AAAAT | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0149 others(98): Show |
144 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1468+507_1468+510d others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005702 | ||||||
| chr12:113005702 | AAAATAAA others(5): Show |
A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(77): Show |
131 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1468+499_1468+510d others(14): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005702 | ||||||
| chr12:113005903 | A | AAAC | 8 | a0001c0001t0001g0145 a0001c0001t0003g0063 a0001c0001t0005g0177 others(5): Show |
9 | HG02129.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1469-495_1469-493d others(5): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005903 | ||||||
| chr12:113005903 | A | AAACAAC | 25 | a0001c0001t0001g0008 a0001c0001t0001g0149 a0001c0001t0002g0008 others(22): Show |
29 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1469-498_1469-493d others(8): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005903 | ||||||
| chr12:113005903 | A | AAACAACA others(8): Show |
2 | a0001c0001t0003g0062 a0001c0001t0010g0050 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1469-507_1469-493d others(17): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005903 | ||||||
| chr12:113005903 | A | C | 1 | a0001c0001t0002g0127 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1469-510A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005903 | |||||||
| chr12:113005918 | C | CA | 3 | a0001c0002t0004g0230 a0001c0003t0004g0020 a0001c0003t0004g0022 |
6 | HG00099.hp2 HG01175.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469-462dupA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | C | CAACAAAA others(3): Show |
1 | a0001c0007t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1469-493_1469-492i others(12): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | C | CAACAACA others(4): Show |
2 | a0001c0001t0003g0051 a0001c0007t0005g0053 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1469-493_1469-492i others(13): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | C | CAACAACA others(5): Show |
1 | a0001c0001t0012g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1469-493_1469-492i others(14): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | CA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(67): Show |
123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1469-462delA | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | CAA | C | 9 | a0001c0001t0001g0070 a0001c0001t0001g0117 a0001c0001t0001g0135 others(6): Show |
11 | HG01109.hp1 HG01167.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1469-463_1469-462d others(4): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | CAAA | C | 8 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0108 others(5): Show |
12 | HG01433.hp1 HG02055.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1469-464_1469-462d others(5): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | CAAAA | C | 6 | a0001c0001t0003g0111 a0001c0001t0028g0064 a0001c0004t0011g0061 others(3): Show |
6 | HG02572.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469-465_1469-462d others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005918 | CAAAAAAA others(3): Show |
C | 1 | a0001c0006t0005g0031 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1469-471_1469-462d others(12): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005918 | ||||||
| chr12:113005919 | A | AAC | 8 | a0001c0001t0001g0018 a0001c0002t0001g0049 a0001c0002t0001g0080 others(5): Show |
10 | HG00558.hp2 HG00673.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-493_1469-492i others(4): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005919 | ||||||
| chr12:113005919 | A | AACAAC | 58 | a0001c0001t0001g0010 a0001c0001t0002g0002 a0001c0001t0002g0006 others(55): Show |
99 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1469-493_1469-492i others(7): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 113005919 | ||||||
| chr12:113005920 | A | AC | 2 | a0001c0004t0003g0041 a0001c0004t0003g0120 |
3 | HG01168.hp1 HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1469-493_1469-492i others(3): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005920 | |||||||
| chr12:113005920 | A | ACAAC | 11 | a0001c0001t0002g0154 a0001c0001t0002g0229 a0001c0001t0005g0178 others(8): Show |
16 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1469-493_1469-492i others(6): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005920 | |||||||
| chr12:113005920 | A | ACAACAAC | 4 | a0001c0001t0001g0214 a0001c0001t0002g0127 a0001c0001t0002g0143 others(1): Show |
4 | HG03669.hp1 HG04228.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-493_1469-492i others(9): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005920 | |||||||
| chr12:113005920 | A | ACAACAAC others(9): Show |
1 | a0001c0001t0012g0160 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1469-493_1469-492i others(18): Show |
OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005920 | |||||||
| chr12:113005921 | A | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0065 others(39): Show |
51 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1469-492A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005921 | |||||||
| chr12:113005922 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(120): Show |
215 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.1469-491A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005922 | |||||||
| chr12:113005923 | A | C | 20 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0001g0167 others(17): Show |
22 | HG01099.hp2 HG01109.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1469-490A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005923 | |||||||
| chr12:113005924 | A | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0065 others(38): Show |
51 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1469-489A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005924 | |||||||
| chr12:113005925 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): Show |
213 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1469-488A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005925 | |||||||
| chr12:113005926 | A | C | 12 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0001g0167 others(9): Show |
12 | HG01081.hp2 HG01099.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1469-487A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005926 | |||||||
| chr12:113005927 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0159 others(6): Show |
10 | HG00423.hp2 HG01928.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-486A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005927 | |||||||
| chr12:113005928 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(71): Show |
126 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1469-485A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005928 | |||||||
| chr12:113005929 | A | C | 7 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0001g0167 others(4): Show |
7 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469-484A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005929 | |||||||
| chr12:113005930 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1469-483A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005930 | |||||||
| chr12:113005931 | A | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0102 a0001c0001t0001g0232 others(1): Show |
5 | HG02976.hp1 HG03130.hp1 NA19088.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-482A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005931 | |||||||
| chr12:113005932 | A | C | 3 | a0001c0001t0002g0139 a0001c0001t0006g0146 a0001c0002t0001g0076 |
3 | HG01106.hp1 HG01243.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1469-481A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005932 | |||||||
| chr12:113005933 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1469-480A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005933 | |||||||
| chr12:113005935 | A | C | 2 | a0001c0001t0002g0139 a0001c0002t0001g0076 |
2 | HG01106.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1469-478A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005935 | |||||||
| chr12:113005939 | A | C | 5 | a0001c0001t0001g0157 a0001c0001t0012g0172 a0001c0001t0026g0173 others(2): Show |
5 | HG02735.hp1 NA18949.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-474A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113005939 | |||||||
| chr12:113006062 | T | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0003g0063 others(12): Show |
18 | HG00558.hp2 HG00673.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1469-351T>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113006062 | |||||||
| chr12:113006219 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(242): Show |
362 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.1469-194T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113006219 | |||||||
| chr12:113006312 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(125): Show |
197 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1469-101C>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 7/9 | chr12 | 113006312 | |||||||
| chr12:113006613 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(219): Show |
330 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.1656+13T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113006613 | |||||||
| chr12:113006661 | T | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
13 | HG02056.hp2 HG02132.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1656+61T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113006661 | |||||||
| chr12:113006664 | G | C | 1 | a0001c0001t0012g0137 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1656+64G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113006664 | |||||||
| chr12:113006738 | C | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0145 a0001c0001t0003g0063 others(10): Show |
16 | HG00558.hp2 HG00673.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1656+138C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113006738 | |||||||
| chr12:113007003 | C | T | 1 | a0001c0008t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1656+403C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007003 | |||||||
| chr12:113007040 | G | A | 99 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0149 others(96): Show |
142 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1656+440G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007040 | |||||||
| chr12:113007299 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1657-406G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007299 | |||||||
| chr12:113007383 | G | A | 10 | a0001c0004t0001g0197 a0001c0004t0003g0041 a0001c0004t0003g0107 others(7): Show |
12 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1657-322G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007383 | |||||||
| chr12:113007437 | G | C | 1 | a0001c0014t0003g0121 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1657-268G>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007437 | |||||||
| chr12:113007588 | C | T | 23 | a0001c0001t0001g0070 a0001c0001t0003g0062 a0001c0001t0005g0176 others(20): Show |
35 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1657-117C>T | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007588 | |||||||
| chr12:113007680 | G | A | 1 | a0001c0001t0008g0218 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1657-25G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 8/9 | chr12 | 113007680 | |||||||
| chr12:113007963 | G | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0149 others(81): Show |
126 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1895+20G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113007963 | |||||||
| chr12:113008007 | T | C | 17 | a0001c0002t0003g0100 a0001c0004t0001g0197 a0001c0004t0003g0041 others(14): Show |
19 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1895+64T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008007 | |||||||
| chr12:113008141 | A | C | 11 | a0001c0002t0012g0025 a0001c0002t0012g0057 a0001c0002t0012g0058 others(8): Show |
12 | HG00140.hp2 HG01943.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1895+198A>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008141 | |||||||
| chr12:113008204 | T | C | 31 | a0001c0001t0003g0051 a0001c0001t0012g0052 a0001c0001t0014g0158 others(28): Show |
34 | HG00140.hp2 HG01081.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1895+261T>C | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008204 | |||||||
| chr12:113008230 | T | A | 14 | a0001c0001t0003g0051 a0001c0001t0012g0052 a0001c0001t0014g0158 others(11): Show |
15 | HG00140.hp2 HG01943.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1895+287T>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008230 | |||||||
| chr12:113008393 | G | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0149 others(83): Show |
128 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1895+450G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008393 | |||||||
| chr12:113008461 | G | A | 4 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0111 others(1): Show |
9 | HG01109.hp1 HG02055.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1895+518G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008461 | |||||||
| chr12:113008575 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1896-512A>G | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008575 | |||||||
| chr12:113008719 | G | A | 16 | a0001c0004t0001g0197 a0001c0004t0003g0041 a0001c0004t0003g0066 others(13): Show |
18 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1896-368G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008719 | |||||||
| chr12:113008760 | G | A | 1 | a0001c0002t0003g0028 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1896-327G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008760 | |||||||
| chr12:113008922 | G | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0149 others(83): Show |
128 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1896-165G>A | OAS2 | ENSG00000111335.14 | transcript | ENST00000392583.7 | protein_coding | 9/9 | chr12 | 113008922 |