Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10678 |
| ensemblid | ENSG00000170340.11 |
| hgncid | 15629 |
| symbol | B3GNT2 |
| name | UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 |
| refseq_nuc | NM_006577.6 |
| refseq_prot | NP_006568.2 |
| ensembl_nuc | ENST00000301998.5 |
| ensembl_prot | ENSP00000305595.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 62196115 |
| end | 62224731 |
| strand | + |
| ver | v1.2 |
| region | chr2:62196115-62224731 |
| region5000 | chr2:62191115-62229731 |
| regionname0 | B3GNT2_chr2_62196115_62224731 |
| regionname5000 | B3GNT2_chr2_62191115_62229731 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 397 | 390 | 82 | 69 | 173 | 18 | 46 | 132 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| a0002 | 0/0 | 397 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| a0003 | 0/0 | 397 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| a0004 | 0/0 | 397 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| a0005 | 0/0 | 397 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| a0006 | 0/0 | 397 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | MSVGR others(392): Show |
chr2 | 62191115 | 62229731 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1191 | 381 | 80 | 65 | 171 | 18 | 45 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0004 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0005 | 0/0 | 1191 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0006 | 0/0 | 1191 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0007 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0009 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0001c0010 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0002c0002 | 0/0 | 1191 | 8 | 7 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0002c0003 | 0/0 | 1191 | 4 | 4 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0003c0008 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0004c0011 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0005c0013 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 | ||
| a0006c0012 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | ATGAG others(1186): Show |
chr2 | 62191115 | 62229731 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2761 | 227 | 17 | 48 | 108 | 13 | 39 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0002 | 0/0 | 2761 | 73 | 6 | 11 | 46 | 4 | 6 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0003 | 0/0 | 2761 | 36 | 33 | 3 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0004 | 0/0 | 2757 | 7 | 0 | 0 | 7 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2752): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0005 | 0/0 | 2761 | 7 | 7 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0006 | 0/0 | 2761 | 5 | 5 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0007 | 0/0 | 2762 | 4 | 0 | 0 | 4 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2757): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0008 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0009 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0010 | 0/0 | 2761 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0012 | 0/0 | 2762 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2757): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0013 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0014 | 0/0 | 2767 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2762): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0015 | 0/0 | 2761 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0016 | 0/0 | 2761 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0018 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0019 | 0/0 | 2761 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0020 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0021 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0022 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0001t0024 | 0/0 | 2761 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0004t0011 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0005t0001 | 0/0 | 2761 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0006t0002 | 0/0 | 2761 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0007t0001 | 0/0 | 2761 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0009t0001 | 0/0 | 2761 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0001c0010t0001 | 0/0 | 2761 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0002c0002t0003 | 0/0 | 2761 | 7 | 6 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0002c0002t0017 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0002c0003t0003 | 0/0 | 2761 | 3 | 3 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0002c0003t0006 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0003c0008t0001 | 0/0 | 2761 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0004c0011t0023 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2762): Show |
chr2 | 62191115 | 62229731 |
| a0005c0013t0001 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| a0006c0012t0002 | 0/0 | 2761 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | AGCCT others(2756): Show |
chr2 | 62191115 | 62229731 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 1 | 6 | 7 | 2 | 3 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0070 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0072 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0060 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0071 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0004g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0004g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0005g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0006g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0007g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0010g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0018g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0020g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0021g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0001t0024g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0004t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0004t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0005t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0006t0002g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0007t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0009t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0001c0010t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0002t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0003t0003g0068 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0002c0003t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0003c0008t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0004c0011t0023g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0005c0013t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| a0006c0012t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | FIN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01070 | hp1 | a0001 | c0009 | t0001 | g0014 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01070 | hp2 | a0001 | c0006 | t0002 | g0062 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01071 | hp2 | a0001 | c0006 | t0002 | g0062 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01109 | hp1 | a0002 | c0002 | t0003 | g0049 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0049 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01934 | hp1 | a0001 | c0010 | t0001 | g0018 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01981 | hp1 | a0001 | c0001 | t0024 | g0208 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02027 | hp2 | a0003 | c0008 | t0001 | g0004 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0036 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02280 | hp1 | a0004 | c0011 | t0023 | g0207 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02622 | hp2 | a0005 | c0013 | t0001 | g0173 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02647 | hp2 | a0001 | c0001 | t0022 | g0069 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02809 | hp1 | a0002 | c0003 | t0003 | g0153 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0069 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0044 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0102 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0250 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0141 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03041 | hp1 | a0001 | c0004 | t0011 | g0228 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0214 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0246 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0068 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03195 | hp1 | a0002 | c0003 | t0006 | g0236 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ESN | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03486 | hp2 | a0002 | c0003 | t0003 | g0068 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0226 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03834 | hp1 | a0001 | c0007 | t0001 | g0123 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18940 | hp1 | a0001 | c0001 | t0016 | g0096 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18944 | hp2 | a0001 | c0005 | t0001 | g0042 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18948 | hp1 | a0001 | c0005 | t0001 | g0042 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18971 | hp1 | a0001 | c0001 | t0012 | g0090 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18988 | hp2 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18993 | hp2 | a0001 | c0001 | t0016 | g0161 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0211 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19067 | hp2 | a0001 | c0001 | t0015 | g0097 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19087 | hp1 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19087 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19240 | hp1 | a0001 | c0004 | t0011 | g0075 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0235 | AFR | YRI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ASW | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ASW | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0126 | EUR | TSI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | GIH | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | ACB | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0215 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | USA | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | USA | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA20300 | hp2 | a0006 | c0012 | t0002 | g0006 | AFR | USA | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA21309 | hp1 | a0002 | c0002 | t0017 | g0044 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0099 | REF | REF | B3GNT2_chr2_62191115_62229731 | B3GNT2 | chr2 | 62191115 | 62229731 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:62222293 | A | G | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.73A>G | p.Met25Val | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 323/2761 | 73/1194 | 25/397 | chr2 | 62222293 | |||
| chr2:62222381 | C | G | 1 | a0006 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.161C>G | p.Pro54Arg | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 411/2761 | 161/1194 | 54/397 | chr2 | 62222381 | |||
| chr2:62222446 | A | G | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.226A>G | p.Met76Val | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 476/2761 | 226/1194 | 76/397 | chr2 | 62222446 | |||
| chr2:62222628 | T | A | 1 | a0002 | 8 | HG01109.hp1 HG01884.hp1 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.408T>A | p.Asp136Glu | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 658/2761 | 408/1194 | 136/397 | chr2 | 62222628 | |||
| chr2:62222628 | T | G | 1 | a0002 | 4 | HG02809.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.408T>G | p.Asp136Glu | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 658/2761 | 408/1194 | 136/397 | chr2 | 62222628 | |||
| chr2:62223338 | T | C | 1 | a0003 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1118T>C | p.Met373Thr | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1368/2761 | 1118/1194 | 373/397 | chr2 | 62223338 | |||
| chr2:62223414 | A | G | 1 | a0001 | 1 | HG02970.hp2 | stop_retained_variant | LOW | c.1194A>G | p.Ter398Ter | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1444/2761 | 1194/1194 | 398/397 | chr2 | 62223414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:62222449 | C | T | 1 | a0001c0010 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.229C>T | p.Leu77Leu | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 479/2761 | 229/1194 | 77/397 | chr2 | 62222449 | |||
| chr2:62222463 | G | A | 1 | a0001c0007 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.243G>A | p.Thr81Thr | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 493/2761 | 243/1194 | 81/397 | chr2 | 62222463 | |||
| chr2:62222529 | G | A | 1 | a0001c0004 | 2 | HG03041.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.309G>A | p.Thr103Thr | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 559/2761 | 309/1194 | 103/397 | chr2 | 62222529 | |||
| chr2:62222658 | G | A | 1 | a0001c0005 | 2 | NA18944.hp2 NA18948.hp1 |
synonymous_variant | LOW | c.438G>A | p.Leu146Leu | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 688/2761 | 438/1194 | 146/397 | chr2 | 62222658 | |||
| chr2:62222730 | C | T | 1 | a0001c0009 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.510C>T | p.Asn170Asn | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 760/2761 | 510/1194 | 170/397 | chr2 | 62222730 | |||
| chr2:62222952 | C | T | 1 | a0001c0006 | 2 | HG01070.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.732C>T | p.Gly244Gly | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 982/2761 | 732/1194 | 244/397 | chr2 | 62222952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:62196129 | C | CGCAGCG | 2 | a0001c0001t0014 a0004c0011t0023 |
3 | HG02258.hp2 HG02280.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-224_-219dupGGCAGC | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/2 | 26074 | INFO_REALIGN_3_PRIME | chr2 | 62196129 | |||||
| chr2:62196130 | G | T | 2 | a0001c0001t0015 a0001c0001t0016 |
4 | NA18940.hp1 NA18988.hp2 NA18993.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-235G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/2 | 26091 | chr2 | 62196130 | ||||||
| chr2:62196144 | A | C | 1 | a0001c0001t0024 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/2 | 26077 | chr2 | 62196144 | ||||||
| chr2:62196179 | A | G | 5 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(2): Show |
10 | HG01891.hp2 HG02486.hp1 HG02647.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-186A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/2 | 26042 | chr2 | 62196179 | ||||||
| chr2:62196323 | C | CG | 2 | a0001c0001t0007 a0001c0001t0012 |
6 | NA18971.hp1 NA18971.hp2 NA18977.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-41dupG | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/2 | 25896 | INFO_REALIGN_3_PRIME | chr2 | 62196323 | |||||
| chr2:62223445 | G | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 31 | chr2 | 62223445 | ||||||
| chr2:62223446 | G | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 32 | chr2 | 62223446 | ||||||
| chr2:62223448 | G | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 34 | chr2 | 62223448 | ||||||
| chr2:62223449 | T | G | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 35 | chr2 | 62223449 | ||||||
| chr2:62223451 | T | G | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 37 | chr2 | 62223451 | ||||||
| chr2:62223456 | A | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 42 | chr2 | 62223456 | ||||||
| chr2:62223465 | C | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 51 | chr2 | 62223465 | ||||||
| chr2:62223468 | G | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 54 | chr2 | 62223468 | ||||||
| chr2:62223472 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*58T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 58 | chr2 | 62223472 | ||||||
| chr2:62223473 | G | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 59 | chr2 | 62223473 | ||||||
| chr2:62223476 | C | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 62 | chr2 | 62223476 | ||||||
| chr2:62223478 | C | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 64 | chr2 | 62223478 | ||||||
| chr2:62223480 | C | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 66 | chr2 | 62223480 | ||||||
| chr2:62223488 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 74 | chr2 | 62223488 | ||||||
| chr2:62223490 | A | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 76 | chr2 | 62223490 | ||||||
| chr2:62223492 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 78 | chr2 | 62223492 | ||||||
| chr2:62223494 | C | G | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*80C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 80 | chr2 | 62223494 | ||||||
| chr2:62223495 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 81 | chr2 | 62223495 | ||||||
| chr2:62223496 | A | G | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(5): Show |
86 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*82A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 82 | chr2 | 62223496 | ||||||
| chr2:62223497 | T | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 83 | chr2 | 62223497 | ||||||
| chr2:62223498 | A | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 84 | chr2 | 62223498 | ||||||
| chr2:62223500 | T | G | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 86 | chr2 | 62223500 | ||||||
| chr2:62223502 | A | G | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 88 | chr2 | 62223502 | ||||||
| chr2:62223508 | G | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 94 | chr2 | 62223508 | ||||||
| chr2:62223509 | A | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 95 | chr2 | 62223509 | ||||||
| chr2:62223510 | A | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 96 | chr2 | 62223510 | ||||||
| chr2:62223514 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 100 | chr2 | 62223514 | ||||||
| chr2:62223515 | G | A | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*101G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 101 | chr2 | 62223515 | ||||||
| chr2:62223516 | C | T | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 102 | chr2 | 62223516 | ||||||
| chr2:62223519 | T | C | 1 | a0002c0002t0017 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 105 | chr2 | 62223519 | ||||||
| chr2:62223534 | A | G | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0004t0011 others(4): Show |
55 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*120A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 120 | chr2 | 62223534 | ||||||
| chr2:62223597 | AT | A | 1 | a0001c0001t0004 | 7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*192delT | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 192 | INFO_REALIGN_3_PRIME | chr2 | 62223597 | |||||
| chr2:62223608 | T | C | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
158 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*194T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 194 | chr2 | 62223608 | ||||||
| chr2:62223748 | C | T | 1 | a0001c0001t0022 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*334C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 334 | chr2 | 62223748 | ||||||
| chr2:62223831 | C | T | 1 | a0001c0001t0019 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 417 | chr2 | 62223831 | ||||||
| chr2:62223980 | G | A | 1 | a0001c0001t0008 | 2 | HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*566G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 566 | chr2 | 62223980 | ||||||
| chr2:62224031 | T | A | 1 | a0001c0001t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 617 | chr2 | 62224031 | ||||||
| chr2:62224207 | A | G | 1 | a0001c0001t0010 | 2 | HG01257.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*793A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 793 | chr2 | 62224207 | ||||||
| chr2:62224287 | A | G | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(5): Show |
86 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*873A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 873 | chr2 | 62224287 | ||||||
| chr2:62224493 | CATG | C | 1 | a0001c0001t0004 | 7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1082_*1084delGAT | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1082 | INFO_REALIGN_3_PRIME | chr2 | 62224493 | |||||
| chr2:62224614 | A | C | 1 | a0001c0001t0009 | 2 | HG02630.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1200A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1200 | chr2 | 62224614 | ||||||
| chr2:62224633 | A | G | 1 | a0001c0001t0021 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1219A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1219 | chr2 | 62224633 | ||||||
| chr2:62224642 | T | G | 6 | a0001c0001t0003 a0001c0001t0006 a0002c0002t0003 others(3): Show |
53 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1228T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 2/2 | 1228 | chr2 | 62224642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:62196384 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0252 |
4 | HG02523.hp1 NA18980.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+29C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196384 | |||||||
| chr2:62196463 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+108T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196463 | |||||||
| chr2:62196521 | C | G | 2 | a0001c0001t0003g0251 a0002c0002t0003g0250 |
2 | HG01167.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10+166C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196521 | |||||||
| chr2:62196614 | G | C | 1 | a0001c0001t0002g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+259G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196614 | |||||||
| chr2:62196671 | C | G | 1 | a0001c0001t0003g0251 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-10+316C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196671 | |||||||
| chr2:62196676 | C | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0002g0249 others(2): Show |
7 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+321C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196676 | |||||||
| chr2:62196788 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0018g0246 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-10+433C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196788 | |||||||
| chr2:62196841 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-10+486G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196841 | |||||||
| chr2:62196846 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10+491C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62196846 | |||||||
| chr2:62197092 | GGGGGTGG others(8): Show |
G | 1 | a0001c0001t0005g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10+751_-10+765del others(15): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62197092 | ||||||
| chr2:62197225 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-10+870C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197225 | |||||||
| chr2:62197244 | G | T | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+889G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197244 | |||||||
| chr2:62197349 | T | A | 1 | a0001c0004t0011g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+994T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197349 | |||||||
| chr2:62197699 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0003g0027 |
3 | HG02572.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-10+1344G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197699 | |||||||
| chr2:62197707 | A | T | 1 | a0001c0001t0002g0241 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-10+1352A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197707 | |||||||
| chr2:62197738 | A | C | 1 | a0001c0001t0001g0070 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+1383A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197738 | |||||||
| chr2:62197788 | T | C | 3 | a0001c0001t0001g0245 a0001c0001t0003g0251 a0002c0002t0003g0250 |
3 | HG01167.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-10+1433T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197788 | |||||||
| chr2:62197833 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10+1478G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197833 | |||||||
| chr2:62197920 | T | C | 2 | a0001c0001t0003g0251 a0002c0002t0003g0250 |
2 | HG01167.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10+1565T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62197920 | |||||||
| chr2:62198504 | C | G | 112 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(109): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-10+2149C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198504 | |||||||
| chr2:62198788 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-10+2433A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198788 | |||||||
| chr2:62198805 | T | A | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+2450T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198805 | |||||||
| chr2:62198806 | A | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0076 a0001c0001t0001g0171 others(1): Show |
6 | HG02572.hp2 HG02735.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+2451A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198806 | |||||||
| chr2:62198899 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0003g0071 others(1): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+2544T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198899 | |||||||
| chr2:62198978 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-10+2623C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62198978 | |||||||
| chr2:62199064 | C | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0003g0071 others(2): Show |
7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+2709C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199064 | |||||||
| chr2:62199203 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0078 |
3 | NA18943.hp1 NA18983.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-10+2848T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199203 | |||||||
| chr2:62199212 | T | G | 1 | a0001c0001t0001g0070 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+2857T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199212 | |||||||
| chr2:62199828 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-10+3473A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199828 | |||||||
| chr2:62199937 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-10+3582A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199937 | |||||||
| chr2:62199945 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0003g0027 |
3 | HG02572.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-10+3590G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199945 | |||||||
| chr2:62199993 | T | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(65): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.-10+3638T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62199993 | |||||||
| chr2:62200010 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-10+3655G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200010 | |||||||
| chr2:62200112 | G | A | 2 | a0001c0001t0003g0251 a0002c0002t0003g0250 |
2 | HG01167.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10+3757G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200112 | |||||||
| chr2:62200269 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-10+3914C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200269 | |||||||
| chr2:62200285 | TA | T | 11 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+3938delA | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62200285 | ||||||
| chr2:62200429 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0168 a0001c0001t0001g0169 |
4 | NA18955.hp2 NA19077.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+4074C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200429 | |||||||
| chr2:62200731 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0080 |
3 | HG02027.hp1 NA19060.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-10+4376T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200731 | |||||||
| chr2:62200917 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-10+4562C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200917 | |||||||
| chr2:62200982 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10+4627A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62200982 | |||||||
| chr2:62201135 | A | C | 1 | a0001c0001t0001g0070 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+4780A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62201135 | |||||||
| chr2:62202001 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-10+5646G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202001 | |||||||
| chr2:62202060 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-10+5705C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202060 | |||||||
| chr2:62202114 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18943.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-10+5759C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202114 | |||||||
| chr2:62202488 | G | T | 3 | a0001c0001t0006g0237 a0001c0001t0013g0069 a0001c0001t0022g0069 |
3 | HG02647.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-10+6133G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202488 | |||||||
| chr2:62202512 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-10+6157A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202512 | |||||||
| chr2:62202678 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10+6323C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202678 | |||||||
| chr2:62202875 | C | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(37): Show |
52 | HG00558.hp1 HG01109.hp1 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.-10+6520C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202875 | |||||||
| chr2:62202898 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-10+6543A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202898 | |||||||
| chr2:62202905 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-10+6550C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202905 | |||||||
| chr2:62202947 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-10+6592G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202947 | |||||||
| chr2:62202963 | A | G | 1 | a0001c0001t0006g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-10+6608A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202963 | |||||||
| chr2:62202976 | G | C | 74 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(71): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-10+6621G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202976 | |||||||
| chr2:62202978 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-10+6623G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202978 | |||||||
| chr2:62202993 | T | C | 3 | a0001c0001t0006g0237 a0001c0001t0013g0069 a0001c0001t0022g0069 |
3 | HG02647.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-10+6638T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62202993 | |||||||
| chr2:62203002 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-10+6647A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203002 | |||||||
| chr2:62203073 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-10+6718A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203073 | |||||||
| chr2:62203242 | TGTTTGGA others(7): Show |
T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0125 |
2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-10+6889_-10+6902d others(16): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62203242 | ||||||
| chr2:62203267 | A | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(83): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-10+6912A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203267 | |||||||
| chr2:62203346 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0006g0230 a0001c0001t0018g0246 others(1): Show |
4 | HG02809.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6991G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203346 | |||||||
| chr2:62203361 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(136): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-10+7006C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203361 | |||||||
| chr2:62203446 | T | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0231 a0001c0001t0019g0126 |
3 | HG01168.hp1 HG01255.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-10+7091T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203446 | |||||||
| chr2:62203800 | T | G | 1 | a0002c0003t0003g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-10+7445T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203800 | |||||||
| chr2:62203801 | G | C | 1 | a0001c0001t0002g0160 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-10+7446G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203801 | |||||||
| chr2:62203855 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-10+7500G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203855 | |||||||
| chr2:62203917 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+7562A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203917 | |||||||
| chr2:62203934 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0166 |
2 | HG00280.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-10+7579T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203934 | |||||||
| chr2:62203996 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0003g0071 others(1): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+7641A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62203996 | |||||||
| chr2:62204169 | G | A | 3 | a0001c0001t0002g0055 a0001c0001t0002g0175 a0001c0001t0002g0183 |
4 | HG00609.hp2 NA18965.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7814G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204169 | |||||||
| chr2:62204280 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0058 others(61): Show |
99 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10+7925C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204280 | |||||||
| chr2:62204285 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10+7930C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204285 | |||||||
| chr2:62204288 | A | T | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-10+7933A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204288 | |||||||
| chr2:62204302 | AT | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-10+7952delT | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62204302 | ||||||
| chr2:62204469 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-10+8114C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204469 | |||||||
| chr2:62204661 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10+8306A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204661 | |||||||
| chr2:62204886 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10+8531C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204886 | |||||||
| chr2:62204998 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(136): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-10+8643G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62204998 | |||||||
| chr2:62205067 | C | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+8712C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205067 | |||||||
| chr2:62205171 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0003g0251 a0002c0002t0003g0049 others(2): Show |
6 | HG00741.hp1 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+8816G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205171 | |||||||
| chr2:62205461 | G | C | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+9106G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205461 | |||||||
| chr2:62205785 | C | T | 1 | a0001c0001t0001g0070 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10+9430C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205785 | |||||||
| chr2:62205873 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-10+9518A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205873 | |||||||
| chr2:62205962 | T | C | 14 | a0001c0001t0001g0186 a0001c0001t0001g0245 a0001c0001t0002g0241 others(11): Show |
20 | HG00735.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-10+9607T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62205962 | |||||||
| chr2:62206073 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+9718C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206073 | |||||||
| chr2:62206212 | G | A | 1 | a0001c0004t0011g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-10+9857G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206212 | |||||||
| chr2:62206219 | G | C | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+9864G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206219 | |||||||
| chr2:62206259 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-10+9904G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206259 | |||||||
| chr2:62206309 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-10+9954A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206309 | |||||||
| chr2:62206420 | CCTCACTC others(4): Show |
C | 1 | a0001c0001t0002g0060 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-10+10066_-10+1007 others(15): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206420 | |||||||
| chr2:62206482 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-10+10127T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206482 | |||||||
| chr2:62206482 | T | G | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10+10127T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206482 | |||||||
| chr2:62206505 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0002g0061 a0001c0001t0002g0150 others(1): Show |
5 | HG00140.hp1 HG01243.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+10150T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206505 | |||||||
| chr2:62206574 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-10+10219T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206574 | |||||||
| chr2:62206794 | C | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0162 |
2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-10+10439C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206794 | |||||||
| chr2:62206805 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+10450C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206805 | |||||||
| chr2:62206806 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-10+10451A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206806 | |||||||
| chr2:62206878 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0002g0241 |
2 | HG01943.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-10+10523C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206878 | |||||||
| chr2:62206956 | C | T | 1 | a0004c0011t0023g0207 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10+10601C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62206956 | |||||||
| chr2:62207146 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0142 a0001c0001t0001g0145 others(1): Show |
8 | HG02055.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+10791G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207146 | |||||||
| chr2:62207197 | T | A | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10+10842T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207197 | |||||||
| chr2:62207202 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-10+10847C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207202 | |||||||
| chr2:62207235 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0003g0071 others(2): Show |
7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+10880C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207235 | |||||||
| chr2:62207304 | C | T | 3 | a0001c0001t0003g0212 a0001c0001t0005g0025 a0002c0002t0003g0211 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+10949C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207304 | |||||||
| chr2:62207436 | A | G | 1 | a0001c0001t0005g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-10+11081A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207436 | |||||||
| chr2:62207514 | T | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0248 a0001c0001t0003g0071 others(2): Show |
7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+11159T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207514 | |||||||
| chr2:62207565 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+11210C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207565 | |||||||
| chr2:62207582 | G | T | 1 | a0001c0001t0005g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-10+11227G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207582 | |||||||
| chr2:62207647 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10+11292A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207647 | |||||||
| chr2:62207696 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-10+11341C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62207696 | |||||||
| chr2:62208085 | T | A | 6 | a0001c0001t0003g0015 a0001c0001t0003g0066 a0001c0001t0003g0213 others(3): Show |
10 | HG01167.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+11730T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208085 | |||||||
| chr2:62208101 | T | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0186 a0001c0001t0002g0241 others(1): Show |
4 | HG01943.hp1 HG01952.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+11746T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208101 | |||||||
| chr2:62208243 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-10+11888A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208243 | |||||||
| chr2:62208384 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0002g0026 a0001c0001t0002g0085 others(1): Show |
6 | HG02523.hp1 NA18980.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+12029A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208384 | |||||||
| chr2:62208521 | T | A | 1 | a0001c0001t0002g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-10+12166T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208521 | |||||||
| chr2:62208593 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10+12238G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208593 | |||||||
| chr2:62208789 | T | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0024 others(19): Show |
38 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-10+12434T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208789 | |||||||
| chr2:62208881 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-10+12526C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208881 | |||||||
| chr2:62208927 | A | G | 5 | a0001c0001t0003g0220 a0001c0001t0003g0227 a0001c0001t0009g0226 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+12572A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62208927 | |||||||
| chr2:62209002 | T | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10+12647T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209002 | |||||||
| chr2:62209040 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-10+12685G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209040 | |||||||
| chr2:62209137 | A | G | 1 | a0001c0004t0011g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-10+12782A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209137 | |||||||
| chr2:62209207 | T | C | 50 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0001g0127 others(47): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+12852T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209207 | |||||||
| chr2:62209378 | T | A | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9-12834T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209378 | |||||||
| chr2:62209556 | A | C | 8 | a0001c0001t0001g0076 a0001c0001t0003g0212 a0001c0001t0003g0229 others(5): Show |
10 | HG01243.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-12656A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209556 | |||||||
| chr2:62209571 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-9-12641G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209571 | |||||||
| chr2:62209682 | G | T | 1 | a0001c0001t0002g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-9-12530G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209682 | |||||||
| chr2:62209965 | G | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0022 others(39): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-9-12247G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62209965 | |||||||
| chr2:62210009 | G | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-12203G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210009 | |||||||
| chr2:62210083 | G | T | 2 | a0001c0001t0020g0141 a0001c0001t0021g0215 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-9-12129G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210083 | |||||||
| chr2:62210108 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-9-12104G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210108 | |||||||
| chr2:62210420 | T | TGAAAAGA others(334): Show |
1 | a0001c0001t0005g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9-11778_-9-11777i others(343): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62210420 | ||||||
| chr2:62210420 | T | TGAAAAGA others(347): Show |
1 | a0001c0001t0005g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9-11778_-9-11777i others(356): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62210420 | ||||||
| chr2:62210436 | A | G | 1 | a0001c0001t0002g0175 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-9-11776A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210436 | |||||||
| chr2:62210466 | A | G | 1 | a0001c0001t0003g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9-11746A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210466 | |||||||
| chr2:62210505 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-9-11707A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210505 | |||||||
| chr2:62210572 | C | A | 10 | a0001c0001t0003g0051 a0001c0001t0003g0148 a0001c0001t0003g0149 others(7): Show |
12 | HG00735.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-11640C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210572 | |||||||
| chr2:62210574 | T | C | 131 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(128): Show |
195 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.-9-11638T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210574 | |||||||
| chr2:62210617 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0131 |
3 | NA18951.hp1 NA18977.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-9-11595A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210617 | |||||||
| chr2:62210643 | G | A | 3 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-11569G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210643 | |||||||
| chr2:62210760 | C | G | 2 | a0001c0001t0005g0216 a0001c0001t0005g0217 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-11452C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210760 | |||||||
| chr2:62210768 | C | CA | 66 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(63): Show |
97 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-9-11436dupA | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62210768 | ||||||
| chr2:62210777 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(133): Show |
203 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.-9-11435T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210777 | |||||||
| chr2:62210780 | T | A | 2 | a0001c0001t0002g0006 a0006c0012t0002g0006 |
6 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-11432T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210780 | |||||||
| chr2:62210845 | G | A | 1 | a0001c0001t0018g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9-11367G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210845 | |||||||
| chr2:62210882 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9-11330A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210882 | |||||||
| chr2:62210968 | C | T | 1 | a0001c0001t0009g0226 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-11244C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62210968 | |||||||
| chr2:62211077 | T | C | 1 | a0002c0002t0003g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-9-11135T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211077 | |||||||
| chr2:62211168 | C | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(59): Show |
91 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-9-11044C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211168 | |||||||
| chr2:62211267 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0040 others(7): Show |
18 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-10945C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211267 | |||||||
| chr2:62211288 | T | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0071 a0001c0001t0003g0116 others(1): Show |
6 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-10924T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211288 | |||||||
| chr2:62211365 | C | T | 3 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-10847C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211365 | |||||||
| chr2:62211522 | T | C | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-10690T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211522 | |||||||
| chr2:62211546 | G | A | 117 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(114): Show |
179 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-9-10666G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211546 | |||||||
| chr2:62211655 | T | C | 13 | a0001c0001t0003g0051 a0001c0001t0003g0148 a0001c0001t0003g0149 others(10): Show |
15 | HG00735.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-10557T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211655 | |||||||
| chr2:62211783 | ACG | A | 77 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-9-10427_-9-10426d others(4): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62211783 | ||||||
| chr2:62211785 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0018 others(35): Show |
63 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.-9-10427G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211785 | |||||||
| chr2:62211787 | T | A | 77 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-9-10425T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211787 | |||||||
| chr2:62211906 | G | A | 1 | a0001c0004t0011g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9-10306G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62211906 | |||||||
| chr2:62212076 | C | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-10136C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212076 | |||||||
| chr2:62212300 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9-9912T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212300 | |||||||
| chr2:62212309 | G | C | 1 | a0001c0001t0001g0045 | 2 | NA18966.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-9-9903G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212309 | |||||||
| chr2:62212344 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0205 |
2 | HG00423.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-9-9868T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212344 | |||||||
| chr2:62212397 | G | A | 4 | a0001c0001t0003g0213 a0001c0001t0005g0025 a0001c0001t0005g0219 others(1): Show |
6 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-9815G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212397 | |||||||
| chr2:62212405 | C | T | 6 | a0001c0001t0002g0105 a0001c0001t0013g0069 a0001c0001t0022g0069 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-9807C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212405 | |||||||
| chr2:62212480 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-9-9732G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212480 | |||||||
| chr2:62212497 | A | C | 1 | a0001c0001t0001g0052 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-9-9715A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212497 | |||||||
| chr2:62212502 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-9-9710G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212502 | |||||||
| chr2:62212514 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-9698C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212514 | |||||||
| chr2:62212568 | G | C | 41 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0022 others(38): Show |
62 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9-9644G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212568 | |||||||
| chr2:62212722 | A | G | 4 | a0001c0001t0009g0226 a0001c0004t0011g0075 a0001c0004t0011g0228 others(1): Show |
4 | HG02622.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-9490A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212722 | |||||||
| chr2:62212956 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-9-9256G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62212956 | |||||||
| chr2:62213076 | C | G | 1 | a0005c0013t0001g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9-9136C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213076 | |||||||
| chr2:62213089 | G | C | 1 | a0001c0001t0002g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-9-9123G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213089 | |||||||
| chr2:62213140 | G | C | 9 | a0001c0001t0002g0105 a0001c0001t0013g0069 a0001c0001t0022g0069 others(6): Show |
10 | HG01109.hp1 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-9072G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213140 | |||||||
| chr2:62213153 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9-9059A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213153 | |||||||
| chr2:62213158 | A | T | 3 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-9054A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213158 | |||||||
| chr2:62213259 | T | G | 55 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(52): Show |
81 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-8953T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213259 | |||||||
| chr2:62213398 | G | T | 1 | a0001c0001t0002g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-9-8814G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213398 | |||||||
| chr2:62213441 | A | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0149 a0001c0001t0003g0221 |
4 | HG00735.hp1 HG01884.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-8771A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213441 | |||||||
| chr2:62213452 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-9-8760A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213452 | |||||||
| chr2:62213554 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0050 others(8): Show |
17 | HG00544.hp2 HG02040.hp1 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-8658A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213554 | |||||||
| chr2:62213588 | T | G | 1 | a0001c0001t0013g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-9-8624T>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213588 | |||||||
| chr2:62213737 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9-8475C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213737 | |||||||
| chr2:62213794 | CAT | C | 3 | a0001c0004t0011g0075 a0001c0004t0011g0228 a0005c0013t0001g0173 |
3 | HG02622.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-8417_-9-8416del others(2): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213794 | |||||||
| chr2:62213901 | A | G | 1 | a0001c0001t0009g0226 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-9-8311A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213901 | |||||||
| chr2:62213941 | A | G | 2 | a0001c0001t0003g0224 a0001c0001t0003g0244 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-9-8271A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213941 | |||||||
| chr2:62213985 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0064 a0001c0001t0018g0246 others(2): Show |
10 | HG02970.hp2 HG03130.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-8227C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62213985 | |||||||
| chr2:62214083 | A | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(41): Show |
75 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-9-8129A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214083 | |||||||
| chr2:62214154 | A | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-8058A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214154 | |||||||
| chr2:62214161 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-8051C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214161 | |||||||
| chr2:62214375 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-9-7837A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214375 | |||||||
| chr2:62214380 | AGCACCTG | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(49): Show |
78 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9-7829_-9-7823del others(7): Show |
B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62214380 | ||||||
| chr2:62214725 | A | G | 24 | a0001c0001t0003g0005 a0001c0001t0003g0015 a0001c0001t0003g0027 others(21): Show |
36 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9-7487A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214725 | |||||||
| chr2:62214902 | A | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0085 a0001c0001t0002g0252 |
5 | HG02523.hp1 NA18980.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-7310A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214902 | |||||||
| chr2:62214998 | G | A | 101 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(98): Show |
149 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.-9-7214G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62214998 | |||||||
| chr2:62215154 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9-7058G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215154 | |||||||
| chr2:62215194 | C | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-7018C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215194 | |||||||
| chr2:62215249 | C | A | 1 | a0001c0001t0002g0191 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-9-6963C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215249 | |||||||
| chr2:62215299 | G | A | 1 | a0002c0003t0003g0068 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-6913G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215299 | |||||||
| chr2:62215303 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(85): Show |
129 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-9-6909G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215303 | |||||||
| chr2:62215373 | G | A | 18 | a0001c0001t0003g0005 a0001c0001t0003g0027 a0001c0001t0003g0066 others(15): Show |
27 | HG01167.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9-6839G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215373 | |||||||
| chr2:62215443 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0122 |
2 | HG00408.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-9-6769T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215443 | |||||||
| chr2:62215485 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-6727C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215485 | |||||||
| chr2:62215597 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-9-6615A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215597 | |||||||
| chr2:62215750 | T | C | 53 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(50): Show |
79 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-6462T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215750 | |||||||
| chr2:62215776 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-9-6436G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215776 | |||||||
| chr2:62215829 | A | C | 9 | a0001c0001t0002g0105 a0001c0001t0013g0069 a0001c0001t0022g0069 others(6): Show |
10 | HG01109.hp1 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-6383A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215829 | |||||||
| chr2:62215926 | A | G | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-6286A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215926 | |||||||
| chr2:62215994 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9-6218G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62215994 | |||||||
| chr2:62216011 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0002g0172 |
2 | HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-9-6201C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216011 | |||||||
| chr2:62216154 | T | C | 1 | a0001c0001t0001g0035 | 2 | NA18984.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-9-6058T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216154 | |||||||
| chr2:62216271 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-9-5941A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216271 | |||||||
| chr2:62216315 | G | C | 53 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0006 others(50): Show |
79 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-5897G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216315 | |||||||
| chr2:62216356 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.-9-5856G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216356 | |||||||
| chr2:62216411 | TG | T | 85 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0006 others(82): Show |
124 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-9-5800delG | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216411 | |||||||
| chr2:62216460 | C | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-5752C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216460 | |||||||
| chr2:62216515 | C | T | 1 | a0002c0002t0003g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-9-5697C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216515 | |||||||
| chr2:62216643 | A | G | 4 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 others(1): Show |
6 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5569A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216643 | |||||||
| chr2:62216653 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-5559C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216653 | |||||||
| chr2:62216939 | C | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-5273C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62216939 | |||||||
| chr2:62217210 | C | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-5002C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217210 | |||||||
| chr2:62217224 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-9-4988G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217224 | |||||||
| chr2:62217352 | A | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9-4860A>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217352 | |||||||
| chr2:62217382 | C | A | 2 | a0001c0001t0002g0188 a0001c0001t0002g0197 |
2 | NA18970.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-9-4830C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217382 | |||||||
| chr2:62217389 | C | G | 2 | a0001c0004t0011g0075 a0001c0004t0011g0228 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9-4823C>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217389 | |||||||
| chr2:62217416 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-9-4796G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217416 | |||||||
| chr2:62217563 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9-4649T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217563 | |||||||
| chr2:62217603 | C | T | 2 | a0001c0001t0005g0216 a0001c0001t0005g0217 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-4609C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217603 | |||||||
| chr2:62217671 | C | T | 9 | a0001c0001t0002g0105 a0001c0001t0005g0025 a0001c0001t0005g0219 others(6): Show |
11 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-4541C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217671 | |||||||
| chr2:62217689 | G | A | 9 | a0001c0001t0002g0105 a0001c0001t0005g0025 a0001c0001t0005g0219 others(6): Show |
11 | HG02451.hp2 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-4523G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62217689 | |||||||
| chr2:62218005 | T | C | 6 | a0001c0001t0002g0043 a0001c0001t0002g0128 a0001c0001t0002g0132 others(3): Show |
7 | HG00323.hp1 HG01943.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-4207T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218005 | |||||||
| chr2:62218012 | A | G | 1 | a0001c0001t0012g0090 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-9-4200A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218012 | |||||||
| chr2:62218049 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9-4163T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218049 | |||||||
| chr2:62218188 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-9-4024G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218188 | |||||||
| chr2:62218249 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-9-3963G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218249 | |||||||
| chr2:62218616 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-3596C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218616 | |||||||
| chr2:62218636 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-9-3576C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218636 | |||||||
| chr2:62218969 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9-3243G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62218969 | |||||||
| chr2:62219028 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-9-3184A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219028 | |||||||
| chr2:62219133 | C | T | 2 | a0001c0001t0002g0057 a0001c0006t0002g0062 |
4 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-3079C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219133 | |||||||
| chr2:62219296 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-9-2916G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219296 | |||||||
| chr2:62219557 | G | T | 1 | a0001c0001t0021g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-9-2655G>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219557 | |||||||
| chr2:62219578 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-9-2634C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219578 | |||||||
| chr2:62219594 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-9-2618T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219594 | |||||||
| chr2:62219602 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-9-2610T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219602 | |||||||
| chr2:62219637 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9-2575C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219637 | |||||||
| chr2:62219676 | G | A | 1 | a0001c0001t0001g0065 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-9-2536G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219676 | |||||||
| chr2:62219695 | T | C | 1 | a0001c0001t0001g0040 | 2 | HG00558.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-9-2517T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219695 | |||||||
| chr2:62219748 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-9-2464A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219748 | |||||||
| chr2:62219779 | C | T | 96 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(93): Show |
142 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-9-2433C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219779 | |||||||
| chr2:62219963 | A | G | 3 | a0001c0001t0003g0223 a0001c0001t0003g0227 a0001c0001t0003g0251 |
3 | HG01167.hp1 HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-2249A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62219963 | |||||||
| chr2:62220099 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-2113C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220099 | |||||||
| chr2:62220282 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1930C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220282 | |||||||
| chr2:62220329 | T | C | 2 | a0001c0001t0005g0216 a0001c0001t0005g0217 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-1883T>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220329 | |||||||
| chr2:62220613 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-9-1599A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220613 | |||||||
| chr2:62220620 | A | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0015 a0001c0001t0003g0027 others(18): Show |
33 | HG01167.hp1 HG01884.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9-1592A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220620 | |||||||
| chr2:62220749 | GA | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0015 a0001c0001t0003g0027 others(18): Show |
33 | HG01167.hp1 HG01884.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.-9-1459delA | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 62220749 | ||||||
| chr2:62220781 | T | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0213 |
5 | HG02109.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1431T>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220781 | |||||||
| chr2:62220910 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9-1302C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62220910 | |||||||
| chr2:62221143 | C | A | 1 | a0001c0001t0002g0241 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-9-1069C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221143 | |||||||
| chr2:62221264 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(165): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-9-948A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221264 | |||||||
| chr2:62221480 | G | C | 1 | a0001c0001t0003g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-9-732G>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221480 | |||||||
| chr2:62221520 | A | G | 3 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-692A>G | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221520 | |||||||
| chr2:62221546 | C | A | 2 | a0001c0001t0004g0010 a0001c0001t0004g0064 |
7 | NA18961.hp1 NA18966.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-666C>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221546 | |||||||
| chr2:62221657 | A | C | 3 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0005g0243 |
5 | HG02451.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-555A>C | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221657 | |||||||
| chr2:62221720 | G | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0007 others(90): Show |
141 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-9-492G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221720 | |||||||
| chr2:62221849 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0088 others(3): Show |
9 | HG00408.hp2 HG00544.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9-363C>T | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62221849 | |||||||
| chr2:62222135 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0142 a0001c0001t0001g0145 |
7 | HG02055.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-77G>A | B3GNT2 | ENSG00000170340.11 | transcript | ENST00000301998.5 | protein_coding | 1/1 | chr2 | 62222135 |