Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11282 |
| ensemblid | ENSG00000161013.17 |
| hgncid | 7048 |
| symbol | MGAT4B |
| name | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B |
| refseq_nuc | NM_014275.5 |
| refseq_prot | NP_055090.1 |
| ensembl_nuc | ENST00000292591.12 |
| ensembl_prot | ENSP00000292591.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 179797610 |
| end | 179806866 |
| strand | - |
| ver | v1.2 |
| region | chr5:179797610-179806866 |
| region5000 | chr5:179792610-179811866 |
| regionname0 | MGAT4B_chr5_179797610_179806866 |
| regionname5000 | MGAT4B_chr5_179792610_179811866 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 395 | 92 | 74 | 171 | 14 | 42 | 125 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0002 | 0/0 | 548 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0003 | 0/0 | 548 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0004 | 0/0 | 548 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0005 | 0/0 | 548 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0006 | 0/0 | 548 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0007 | 0/0 | 548 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0008 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0009 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| a0010 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | MRLRN others(543): Show |
chr5 | 179792610 | 179811866 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 347 | 53 | 71 | 166 | 14 | 41 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0002 | 0/0 | 1644 | 18 | 16 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0003 | 0/0 | 1644 | 16 | 15 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0005 | 0/0 | 1644 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0006 | 0/0 | 1644 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0009 | 0/0 | 1644 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0013 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0014 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0016 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0001c0019 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0002c0004 | 0/0 | 1644 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0003c0010 | 0/0 | 1644 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0004c0008 | 0/0 | 1644 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0005c0007 | 0/0 | 1644 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0006c0018 | 0/0 | 1644 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0007c0017 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0008c0015 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0009c0011 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 | ||
| a0010c0012 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | ATGAG others(1639): Show |
chr5 | 179792610 | 179811866 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2365 | 286 | 43 | 64 | 125 | 14 | 38 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0002 | 0/0 | 2368 | 43 | 4 | 7 | 30 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2363): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0003 | 0/0 | 2365 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0004 | 0/0 | 2368 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2363): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0005 | 0/0 | 2365 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0006 | 0/0 | 2365 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0007 | 0/0 | 2365 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0008 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0010 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0011 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0012 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0013 | 0/0 | 2365 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0001t0014 | 0/0 | 2365 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0002t0001 | 0/0 | 2365 | 10 | 8 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0002t0002 | 0/0 | 2368 | 8 | 8 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2363): Show |
chr5 | 179792610 | 179811866 |
| a0001c0003t0001 | 0/0 | 2365 | 16 | 15 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0005t0001 | 0/0 | 2365 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0006t0002 | 0/0 | 2368 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2363): Show |
chr5 | 179792610 | 179811866 |
| a0001c0009t0001 | 0/0 | 2365 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0013t0001 | 0/0 | 2365 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0014t0001 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0016t0001 | 0/0 | 2365 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0001c0019t0001 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0002c0004t0001 | 0/0 | 2365 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0003c0010t0001 | 0/0 | 2365 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0004c0008t0001 | 0/0 | 2365 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0004c0008t0002 | 0/0 | 2368 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2363): Show |
chr5 | 179792610 | 179811866 |
| a0005c0007t0001 | 0/0 | 2365 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0006c0018t0001 | 0/0 | 2365 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0007c0017t0001 | 0/0 | 2365 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0008c0015t0009 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0009c0011t0003 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| a0010c0012t0001 | 0/0 | 2365 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | AGTGT others(2360): Show |
chr5 | 179792610 | 179811866 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 103 | 14 | 29 | 42 | 3 | 15 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0002 | 0/0 | 41 | 1 | 13 | 15 | 6 | 6 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0004 | 0/1 | 33 | 3 | 9 | 16 | 1 | 3 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0005 | 0/0 | 17 | 0 | 2 | 13 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0012 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0003 | 0/0 | 34 | 1 | 7 | 25 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0007g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0010g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0011g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0012g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0001t0014g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0002g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0005t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0006t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0009t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0013t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0014t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0016t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0001c0019t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0002c0004t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0003c0010t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0003c0010t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0004c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0004c0008t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0005c0007t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0006c0018t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0007c0017t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0008c0015t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0009c0011t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| a0010c0012t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01106 | hp1 | a0006 | c0018 | t0001 | g0073 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01884 | hp2 | a0003 | c0010 | t0001 | g0098 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02083 | hp2 | a0001 | c0001 | t0010 | g0118 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02129 | hp2 | a0001 | c0019 | t0001 | g0067 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0018 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02280 | hp1 | a0007 | c0017 | t0001 | g0114 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02300 | hp2 | a0003 | c0010 | t0001 | g0101 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0099 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02698 | hp1 | a0001 | c0001 | t0014 | g0132 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02965 | hp1 | a0001 | c0013 | t0001 | g0079 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0112 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02970 | hp2 | a0001 | c0009 | t0001 | g0038 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03195 | hp1 | a0001 | c0009 | t0001 | g0038 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03669 | hp1 | a0001 | c0016 | t0001 | g0087 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03704 | hp1 | a0004 | c0008 | t0002 | g0041 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03942 | hp2 | a0004 | c0008 | t0001 | g0085 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18612 | hp1 | a0001 | c0014 | t0001 | g0111 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18942 | hp2 | a0005 | c0007 | t0001 | g0030 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18947 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18956 | hp2 | a0002 | c0004 | t0001 | g0091 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18961 | hp1 | a0005 | c0007 | t0001 | g0030 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18979 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18993 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18993 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19003 | hp2 | a0008 | c0015 | t0009 | g0063 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19064 | hp2 | a0009 | c0011 | t0003 | g0039 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19078 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19080 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19085 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19086 | hp2 | a0010 | c0012 | t0001 | g0083 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19087 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19087 | hp2 | a0001 | c0001 | t0012 | g0070 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0086 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0018 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | MGAT4B_chr5_179792610_179811866 | MGAT4B | chr5 | 179792610 | 179811866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179798386 | G | A | 1 | a0003 | 2 | HG01884.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.1471C>T | p.Leu491Phe | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/15 | 1754/2365 | 1471/1647 | 491/548 | chr5 | 179798386 | |||
| chr5:179798409 | A | C | 1 | a0004 | 2 | HG03704.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.1448T>G | p.Leu483Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/15 | 1731/2365 | 1448/1647 | 483/548 | chr5 | 179798409 | |||
| chr5:179798976 | G | C | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1295C>G | p.Ala432Gly | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1578/2365 | 1295/1647 | 432/548 | chr5 | 179798976 | |||
| chr5:179798977 | C | G | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1294G>C | p.Ala432Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1577/2365 | 1294/1647 | 432/548 | chr5 | 179798977 | |||
| chr5:179799549 | T | G | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.998A>C | p.Asp333Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1281/2365 | 998/1647 | 333/548 | chr5 | 179799549 | |||
| chr5:179799585 | A | C | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.962T>G | p.Met321Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1245/2365 | 962/1647 | 321/548 | chr5 | 179799585 | |||
| chr5:179799586 | T | A | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.961A>T | p.Met321Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1244/2365 | 961/1647 | 321/548 | chr5 | 179799586 | |||
| chr5:179799591 | A | C | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.956T>G | p.Ile319Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1239/2365 | 956/1647 | 319/548 | chr5 | 179799591 | |||
| chr5:179799624 | T | G | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.923A>C | p.Lys308Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1206/2365 | 923/1647 | 308/548 | chr5 | 179799624 | |||
| chr5:179799959 | A | C | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.905T>G | p.Phe302Cys | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1188/2365 | 905/1647 | 302/548 | chr5 | 179799959 | |||
| chr5:179800031 | C | G | 1 | a0010 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.833G>C | p.Ser278Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1116/2365 | 833/1647 | 278/548 | chr5 | 179800031 | |||
| chr5:179800040 | T | C | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.824A>G | p.Asn275Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1107/2365 | 824/1647 | 275/548 | chr5 | 179800040 | |||
| chr5:179800213 | C | T | 1 | a0009 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.766G>A | p.Ala256Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/15 | 1049/2365 | 766/1647 | 256/548 | chr5 | 179800213 | |||
| chr5:179801559 | G | T | 1 | a0005 | 2 | NA18942.hp2 NA18961.hp1 |
missense_variant | MODERATE | c.419C>A | p.Thr140Asn | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 702/2365 | 419/1647 | 140/548 | chr5 | 179801559 | |||
| chr5:179801641 | G | A | 1 | a0006 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.337C>T | p.Pro113Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 620/2365 | 337/1647 | 113/548 | chr5 | 179801641 | |||
| chr5:179801891 | T | C | 1 | a0002 | 6 | NA18956.hp2 NA18979.hp2 NA18993.hp2 others(3): Show |
missense_variant | MODERATE | c.176A>G | p.Lys59Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 459/2365 | 176/1647 | 59/548 | chr5 | 179801891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179798978 | G | A | 1 | a0001c0016 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1293C>T | p.Ala431Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1576/2365 | 1293/1647 | 431/548 | chr5 | 179798978 | |||
| chr5:179798978 | G | C | 1 | a0008c0015 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1293C>G | p.Ala431Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1576/2365 | 1293/1647 | 431/548 | chr5 | 179798978 | |||
| chr5:179799074 | C | T | 1 | a0001c0014 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1197G>A | p.Pro399Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1480/2365 | 1197/1647 | 399/548 | chr5 | 179799074 | |||
| chr5:179799518 | G | A | 1 | a0001c0002 | 18 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
synonymous_variant | LOW | c.1029C>T | p.Pro343Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1312/2365 | 1029/1647 | 343/548 | chr5 | 179799518 | |||
| chr5:179799620 | C | T | 1 | a0001c0013 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.927G>A | p.Ser309Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1210/2365 | 927/1647 | 309/548 | chr5 | 179799620 | |||
| chr5:179801430 | C | T | 1 | a0001c0006 | 3 | NA18947.hp1 NA18993.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.462G>A | p.Glu154Glu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/15 | 745/2365 | 462/1647 | 154/548 | chr5 | 179801430 | |||
| chr5:179801585 | G | A | 1 | a0001c0009 | 2 | HG02970.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.393C>T | p.Pro131Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 676/2365 | 393/1647 | 131/548 | chr5 | 179801585 | |||
| chr5:179801623 | G | A | 2 | a0001c0002 a0001c0003 |
34 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
synonymous_variant | LOW | c.355C>T | p.Leu119Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 638/2365 | 355/1647 | 119/548 | chr5 | 179801623 | |||
| chr5:179801893 | G | C | 2 | a0001c0005 a0003c0010 |
7 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
synonymous_variant | LOW | c.174C>G | p.Leu58Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 457/2365 | 174/1647 | 58/548 | chr5 | 179801893 | |||
| chr5:179801926 | G | A | 1 | a0001c0019 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.141C>T | p.Arg47Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 424/2365 | 141/1647 | 47/548 | chr5 | 179801926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179797680 | G | A | 1 | a0001c0001t0005 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*365C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 365 | chr5 | 179797680 | ||||||
| chr5:179797708 | A | G | 1 | a0001c0001t0010 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 337 | chr5 | 179797708 | ||||||
| chr5:179797750 | G | C | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 295 | chr5 | 179797750 | ||||||
| chr5:179797751 | C | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 294 | chr5 | 179797751 | ||||||
| chr5:179797784 | C | A | 1 | a0001c0001t0011 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 261 | chr5 | 179797784 | ||||||
| chr5:179797796 | G | A | 2 | a0001c0001t0004 a0001c0001t0012 |
4 | NA18966.hp2 NA18997.hp2 NA19072.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 249 | chr5 | 179797796 | ||||||
| chr5:179797857 | G | A | 1 | a0001c0001t0014 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 188 | chr5 | 179797857 | ||||||
| chr5:179797863 | C | G | 1 | a0008c0015t0009 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*182G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 182 | chr5 | 179797863 | ||||||
| chr5:179797945 | T | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 100 | chr5 | 179797945 | ||||||
| chr5:179797949 | C | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 96 | chr5 | 179797949 | ||||||
| chr5:179797950 | G | A | 1 | a0001c0001t0013 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 95 | chr5 | 179797950 | ||||||
| chr5:179797976 | G | A | 1 | a0001c0001t0007 | 2 | NA18974.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*69C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 69 | chr5 | 179797976 | ||||||
| chr5:179806663 | A | AGGC | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(2): Show |
58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
5_prime_UTR_variant | MODIFIER | c.-83_-81dupGCC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 81 | chr5 | 179806663 | ||||||
| chr5:179806666 | C | G | 1 | a0001c0001t0006 | 2 | HG03225.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-83G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 83 | chr5 | 179806666 | ||||||
| chr5:179806725 | C | T | 2 | a0001c0001t0003 a0009c0011t0003 |
3 | NA18950.hp2 NA18997.hp1 NA19064.hp2 |
5_prime_UTR_variant | MODIFIER | c.-142G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 142 | chr5 | 179806725 | ||||||
| chr5:179806740 | G | A | 1 | a0001c0001t0014 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 157 | chr5 | 179806740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179798099 | C | A | 4 | a0001c0005t0001g0099 a0001c0005t0001g0100 a0003c0010t0001g0098 others(1): Show |
4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-31G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 14/14 | chr5 | 179798099 | |||||||
| chr5:179798324 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0068 a0001c0003t0001g0103 others(1): Show |
7 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510+23C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/14 | chr5 | 179798324 | |||||||
| chr5:179798480 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0068 a0001c0005t0001g0018 |
6 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+33C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798480 | |||||||
| chr5:179798499 | C | A | 4 | a0001c0005t0001g0099 a0001c0005t0001g0100 a0003c0010t0001g0098 others(1): Show |
4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+14G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798499 | |||||||
| chr5:179798504 | C | T | 5 | a0001c0001t0001g0057 a0001c0003t0001g0009 a0001c0003t0001g0024 others(2): Show |
10 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1422+9G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798504 | |||||||
| chr5:179798768 | C | G | 8 | a0001c0002t0001g0010 a0001c0002t0001g0017 a0001c0002t0001g0059 others(5): Show |
18 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1343+160G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798768 | |||||||
| chr5:179798811 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0068 |
3 | HG01433.hp1 HG02040.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1343+117G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798811 | |||||||
| chr5:179798814 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1343+114C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798814 | |||||||
| chr5:179798830 | G | A | 1 | a0001c0001t0005g0023 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1343+98C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798830 | |||||||
| chr5:179798912 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0071 |
3 | NA18974.hp2 NA19055.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1343+16A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798912 | |||||||
| chr5:179799161 | G | C | 1 | a0001c0003t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1150-40C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 10/14 | chr5 | 179799161 | |||||||
| chr5:179799188 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1149+15A>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 10/14 | chr5 | 179799188 | |||||||
| chr5:179799341 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0124 |
2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1042-31C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799341 | |||||||
| chr5:179799365 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1042-55C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799365 | |||||||
| chr5:179799393 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1042-83G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799393 | |||||||
| chr5:179799464 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0068 a0001c0003t0001g0103 others(1): Show |
7 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+42G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799464 | |||||||
| chr5:179799639 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.911-3C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799639 | |||||||
| chr5:179799703 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0009t0001g0038 |
5 | HG02257.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.911-67G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799703 | |||||||
| chr5:179799774 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0096 others(2): Show |
10 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-138A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799774 | |||||||
| chr5:179799786 | ACATGTCT others(23): Show |
A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0096 others(2): Show |
10 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.910+138_911-151del others(30): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799786 | |||||||
| chr5:179799847 | A | T | 1 | a0010c0012t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.910+107T>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799847 | |||||||
| chr5:179799850 | G | C | 1 | a0010c0012t0001g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.910+104C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799850 | |||||||
| chr5:179799915 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.910+39C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799915 | |||||||
| chr5:179800096 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.796-28C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800096 | |||||||
| chr5:179800097 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.796-29G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800097 | |||||||
| chr5:179800099 | G | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0061 others(12): Show |
24 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.796-31C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800099 | |||||||
| chr5:179800129 | T | TCGCAGGG others(8): Show |
4 | a0001c0005t0001g0099 a0001c0005t0001g0100 a0003c0010t0001g0098 others(1): Show |
4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+40_795+54dupCC others(13): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800129 | |||||||
| chr5:179800146 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.795+38C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800146 | |||||||
| chr5:179800154 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0029 others(12): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.795+30C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800154 | |||||||
| chr5:179800274 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.720-15C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800274 | |||||||
| chr5:179800286 | G | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(36): Show |
105 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.720-27C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800286 | |||||||
| chr5:179800307 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.720-48A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800307 | |||||||
| chr5:179800327 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720-68G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800327 | |||||||
| chr5:179800398 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0116 others(1): Show |
8 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.719+86C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800398 | |||||||
| chr5:179800616 | T | C | 1 | a0001c0001t0006g0020 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.606-19A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800616 | |||||||
| chr5:179800622 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.606-25C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800622 | |||||||
| chr5:179800701 | C | A | 2 | a0001c0002t0001g0108 a0007c0017t0001g0114 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606-104G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800701 | |||||||
| chr5:179800826 | A | G | 1 | a0001c0001t0001g0016 | 3 | HG02055.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605+81T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800826 | |||||||
| chr5:179800844 | G | T | 1 | a0001c0005t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.605+63C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800844 | |||||||
| chr5:179800847 | AGCACAAC others(20): Show |
A | 1 | a0002c0004t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.605+33_605+59delGG others(25): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800847 | |||||||
| chr5:179800865 | G | A | 10 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0003t0001g0009 others(7): Show |
15 | HG01243.hp2 HG01884.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.605+42C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800865 | |||||||
| chr5:179801011 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.559-58C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801011 | |||||||
| chr5:179801018 | G | A | 1 | a0001c0001t0006g0020 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.559-65C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801018 | |||||||
| chr5:179801149 | C | CG | 7 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0069 others(4): Show |
9 | HG01884.hp2 HG02523.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+184dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801149 | |||||||
| chr5:179801150 | G | A | 2 | a0001c0003t0001g0103 a0001c0005t0001g0018 |
4 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+184C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801150 | |||||||
| chr5:179801162 | TA | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0096 others(1): Show |
9 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+171delT | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801162 | |||||||
| chr5:179801173 | G | A | 1 | a0001c0003t0001g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.558+161C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801173 | |||||||
| chr5:179801215 | C | G | 1 | a0001c0013t0001g0079 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.558+119G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801215 | |||||||
| chr5:179801473 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0128 |
2 | HG01192.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.425-6C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801473 | |||||||
| chr5:179801478 | C | T | 1 | a0001c0002t0002g0021 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-11G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801478 | |||||||
| chr5:179801501 | T | C | 2 | a0001c0001t0006g0020 a0001c0003t0001g0103 |
3 | HG02145.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.425-34A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801501 | |||||||
| chr5:179801522 | C | A | 2 | a0001c0003t0001g0011 a0001c0003t0001g0053 |
5 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+32G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801522 | |||||||
| chr5:179802005 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.98-36A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802005 | |||||||
| chr5:179802032 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG00733.hp2 HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.98-63C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802032 | |||||||
| chr5:179802039 | A | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0003t0001g0009 others(3): Show |
11 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-70T>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802039 | |||||||
| chr5:179802151 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0001t0006g0020 others(1): Show |
8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-182T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802151 | |||||||
| chr5:179802296 | G | A | 1 | a0001c0003t0001g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.98-327C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802296 | |||||||
| chr5:179802303 | T | C | 1 | a0001c0009t0001g0038 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.98-334A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802303 | |||||||
| chr5:179802315 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.98-346C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802315 | |||||||
| chr5:179802348 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0001t0006g0020 |
5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-379C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802348 | |||||||
| chr5:179802367 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-398C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802367 | |||||||
| chr5:179802396 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98-427A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802396 | |||||||
| chr5:179802419 | G | A | 1 | a0001c0009t0001g0038 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.98-450C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802419 | |||||||
| chr5:179802464 | C | CG | 7 | a0001c0001t0001g0057 a0001c0001t0001g0078 a0001c0001t0001g0121 others(4): Show |
12 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-496dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802464 | |||||||
| chr5:179802641 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0109 |
2 | HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.98-672C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802641 | |||||||
| chr5:179802649 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-680G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802649 | |||||||
| chr5:179802688 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98-719A>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802688 | |||||||
| chr5:179802717 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-748A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802717 | |||||||
| chr5:179802767 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA19000.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.98-798G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802767 | |||||||
| chr5:179802817 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18970.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.98-848C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802817 | |||||||
| chr5:179802987 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0068 |
5 | HG01433.hp1 HG02040.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-1018G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802987 | |||||||
| chr5:179803238 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.98-1269G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803238 | |||||||
| chr5:179803291 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.98-1322G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803291 | |||||||
| chr5:179803320 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98-1351G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803320 | |||||||
| chr5:179803321 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(41): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.98-1352A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803321 | |||||||
| chr5:179803448 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.98-1479C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803448 | |||||||
| chr5:179803529 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.98-1560C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803529 | |||||||
| chr5:179803556 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0001t0006g0020 |
5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-1587G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803556 | |||||||
| chr5:179803598 | C | G | 1 | a0001c0001t0001g0035 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.98-1629G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803598 | |||||||
| chr5:179803617 | G | C | 1 | a0001c0001t0001g0034 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.98-1648C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803617 | |||||||
| chr5:179803669 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1700C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803669 | |||||||
| chr5:179803860 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1891A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803860 | |||||||
| chr5:179803892 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.98-1923A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803892 | |||||||
| chr5:179803939 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.98-1970C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803939 | |||||||
| chr5:179804248 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(50): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.97+2239A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804248 | |||||||
| chr5:179804255 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.97+2232T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804255 | |||||||
| chr5:179804257 | A | ATCAGGCC others(43): Show |
1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.97+2180_97+2229dup others(50): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804257 | |||||||
| chr5:179804353 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0001t0006g0020 |
5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2134T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804353 | |||||||
| chr5:179804424 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA18943.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.97+2063C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804424 | |||||||
| chr5:179804554 | G | A | 4 | a0001c0005t0001g0099 a0001c0005t0001g0100 a0003c0010t0001g0098 others(1): Show |
4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+1933C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804554 | |||||||
| chr5:179804600 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG00621.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.97+1887C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804600 | |||||||
| chr5:179804753 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97+1734C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804753 | |||||||
| chr5:179804884 | C | T | 10 | a0001c0002t0001g0010 a0001c0002t0001g0017 a0001c0002t0001g0059 others(7): Show |
23 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+1603G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804884 | |||||||
| chr5:179804907 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.97+1580C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804907 | |||||||
| chr5:179805064 | A | T | 2 | a0001c0005t0001g0018 a0001c0009t0001g0038 |
5 | HG01891.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+1423T>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805064 | |||||||
| chr5:179805342 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.97+1145T>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805342 | |||||||
| chr5:179805387 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97+1100C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805387 | |||||||
| chr5:179805603 | T | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0126 a0001c0001t0006g0020 others(2): Show |
10 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+884A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805603 | |||||||
| chr5:179805780 | G | A | 1 | a0001c0003t0001g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97+707C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805780 | |||||||
| chr5:179805825 | G | A | 1 | a0001c0003t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+662C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805825 | |||||||
| chr5:179805833 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97+654C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805833 | |||||||
| chr5:179805866 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97+621C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805866 | |||||||
| chr5:179805966 | G | A | 7 | a0001c0001t0001g0057 a0001c0003t0001g0009 a0001c0003t0001g0024 others(4): Show |
15 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.97+521C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805966 | |||||||
| chr5:179805976 | GCCTC | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.97+507_97+510delGA others(2): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805976 | |||||||
| chr5:179805977 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97+510G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805977 | |||||||
| chr5:179805993 | C | T | 3 | a0001c0001t0001g0057 a0001c0003t0001g0024 a0001c0003t0001g0058 |
4 | HG01243.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+494G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805993 | |||||||
| chr5:179806106 | T | TG | 10 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
11 | HG01192.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+380dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806106 | |||||||
| chr5:179806140 | C | CG | 4 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0005g0023 others(1): Show |
5 | HG03195.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+346dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806140 | |||||||
| chr5:179806172 | G | A | 2 | a0001c0005t0001g0018 a0001c0009t0001g0038 |
5 | HG01891.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+315C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806172 | |||||||
| chr5:179806213 | C | T | 1 | a0001c0003t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97+274G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806213 | |||||||
| chr5:179806273 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.97+214C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806273 | |||||||
| chr5:179806292 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+195G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806292 | |||||||
| chr5:179806295 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+192C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806295 | |||||||
| chr5:179806371 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.97+116C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806371 | |||||||
| chr5:179806372 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.97+115G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806372 |