Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11226 |
| ensemblid | ENSG00000139629.16 |
| hgncid | 4128 |
| symbol | GALNT6 |
| name | polypeptide N-acetylgalactosaminyltransferase 6 |
| refseq_nuc | NM_007210.4 |
| refseq_prot | NP_009141.2 |
| ensembl_nuc | ENST00000356317.8 |
| ensembl_prot | ENSP00000348668.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51351252 |
| end | 51391406 |
| strand | - |
| ver | v1.2 |
| region | chr12:51351252-51391406 |
| region5000 | chr12:51346252-51396406 |
| regionname0 | GALNT6_chr12_51351252_51391406 |
| regionname5000 | GALNT6_chr12_51346252_51396406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 622 | 407 | 78 | 76 | 190 | 14 | 47 | 145 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0002 | 0/0 | 622 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0003 | 0/0 | 622 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0004 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0005 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0006 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0007 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0008 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0009 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0010 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0011 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| a0012 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | MRLLR others(617): Show |
chr12 | 51346252 | 51396406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1866 | 307 | 66 | 60 | 130 | 13 | 36 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0002 | 0/0 | 1866 | 54 | 5 | 11 | 35 | 0 | 3 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0003 | 0/0 | 1866 | 33 | 2 | 4 | 21 | 1 | 5 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0006 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0007 | 0/0 | 1866 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0008 | 0/0 | 1866 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0017 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0019 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0020 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0021 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0001c0022 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0002c0004 | 0/0 | 1866 | 9 | 9 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0003c0005 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0004c0012 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0005c0013 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0006c0014 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0007c0016 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0008c0011 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0009c0010 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0010c0018 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0011c0009 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 | ||
| a0012c0015 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | ATGAG others(1861): Show |
chr12 | 51346252 | 51396406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5303 | 33 | 14 | 9 | 7 | 0 | 3 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0002 | 0/0 | 5303 | 31 | 7 | 8 | 7 | 1 | 8 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0003 | 0/0 | 5307 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0004 | 0/0 | 5307 | 7 | 1 | 0 | 5 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0005 | 0/0 | 5303 | 22 | 0 | 6 | 11 | 3 | 2 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0006 | 0/0 | 5307 | 23 | 0 | 4 | 13 | 2 | 4 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0007 | 0/1 | 5307 | 17 | 1 | 0 | 13 | 0 | 2 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0008 | 0/0 | 5303 | 21 | 2 | 7 | 3 | 2 | 7 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0009 | 1/0 | 5307 | 9 | 2 | 0 | 6 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0010 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0011 | 0/0 | 5303 | 17 | 2 | 7 | 2 | 1 | 5 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0012 | 0/0 | 5303 | 16 | 0 | 0 | 16 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0013 | 0/0 | 5303 | 12 | 1 | 4 | 7 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0014 | 0/0 | 5303 | 8 | 0 | 2 | 4 | 2 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0015 | 0/0 | 5303 | 3 | 1 | 2 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0016 | 0/0 | 5303 | 7 | 0 | 0 | 7 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0017 | 0/0 | 5303 | 4 | 1 | 1 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0018 | 0/0 | 5307 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0019 | 0/0 | 5303 | 3 | 0 | 0 | 1 | 0 | 2 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0020 | 0/0 | 5307 | 3 | 2 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0021 | 0/0 | 5307 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0022 | 0/0 | 5303 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0023 | 0/0 | 5303 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0024 | 0/0 | 5303 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0026 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0027 | 0/0 | 5307 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0028 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0029 | 0/0 | 5303 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0030 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0031 | 0/0 | 5303 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0032 | 0/0 | 5305 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0033 | 0/0 | 5304 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5299): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0034 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0035 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5297): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0036 | 0/0 | 5303 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0038 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0039 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0040 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0043 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0046 | 0/0 | 5307 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0047 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0049 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0051 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0052 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0053 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0054 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0055 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0056 | 0/0 | 5303 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0057 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0058 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0059 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0060 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0061 | 0/0 | 5302 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5297): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0062 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5297): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0063 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0064 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0065 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5299): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0066 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0067 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0068 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0071 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0078 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0079 | 0/0 | 5302 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5297): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0080 | 0/0 | 5306 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0081 | 0/0 | 5306 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0082 | 0/0 | 5305 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0083 | 0/0 | 5305 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0084 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0086 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0087 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0088 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0089 | 0/0 | 5305 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5300): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0090 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5299): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0091 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0001t0092 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0003 | 0/0 | 5307 | 24 | 0 | 7 | 17 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0004 | 0/0 | 5307 | 2 | 1 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0007 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0010 | 0/0 | 5307 | 18 | 0 | 3 | 12 | 0 | 3 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0025 | 0/0 | 5307 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0037 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0042 | 0/0 | 5308 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5303): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0045 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0048 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0050 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0072 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0002t0073 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0001 | 0/0 | 5303 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0004 | 0/0 | 5307 | 14 | 0 | 3 | 10 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0007 | 0/0 | 5307 | 3 | 0 | 0 | 0 | 0 | 3 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0009 | 0/0 | 5307 | 9 | 0 | 1 | 8 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0015 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0044 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0070 | 0/0 | 5307 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0074 | 0/0 | 5306 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0077 | 0/0 | 5304 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5299): Show |
chr12 | 51346252 | 51396406 |
| a0001c0003t0085 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0006t0019 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0006t0028 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0006t0041 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0007t0005 | 0/0 | 5303 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0008t0003 | 0/0 | 5307 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0017t0069 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0001c0019t0001 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0020t0001 | 0/0 | 5303 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0001c0021t0075 | 0/0 | 5306 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5301): Show |
chr12 | 51346252 | 51396406 |
| a0001c0022t0003 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0002c0004t0004 | 0/0 | 5307 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0002c0004t0009 | 0/0 | 5307 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0002c0004t0015 | 0/0 | 5303 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0002c0004t0026 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0002c0004t0030 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0003c0005t0001 | 0/0 | 5303 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0003c0005t0002 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0004c0012t0008 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0005c0013t0014 | 0/0 | 5303 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0006c0014t0013 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0007c0016t0007 | 0/0 | 5307 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| a0008c0011t0001 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0009c0010t0076 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5299): Show |
chr12 | 51346252 | 51396406 |
| a0010c0018t0015 | 0/0 | 5303 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0011c0009t0013 | 0/0 | 5303 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5298): Show |
chr12 | 51346252 | 51396406 |
| a0012c0015t0006 | 0/0 | 5307 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | CCCTC others(5302): Show |
chr12 | 51346252 | 51396406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0001g0408 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0397 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0403 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0005g0409 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0402 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0007g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0008g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0009g0375 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0014g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0015g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0015g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0016g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0017g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0017g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0017g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0018g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0018g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0018g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0018g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0019g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0019g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0020g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0020g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0020g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0021g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0021g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0022g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0022g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0023g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0024g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0024g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0026g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0027g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0027g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0028g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0029g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0029g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0030g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0031g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0031g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0032g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0032g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0033g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0033g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0034g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0035g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0036g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0038g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0039g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0040g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0043g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0046g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0047g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0049g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0051g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0052g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0053g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0054g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0055g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0056g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0057g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0058g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0059g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0060g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0061g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0062g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0063g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0064g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0065g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0066g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0067g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0068g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0071g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0078g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0079g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0080g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0081g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0082g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0083g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0084g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0086g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0087g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0088g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0089g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0090g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0091g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0001t0092g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0003g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0007g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0025g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0025g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0037g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0042g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0045g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0048g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0050g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0072g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0002t0073g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0001g0391 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0007g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0007g0407 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0007g0412 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0009g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0044g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0070g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0074g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0077g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0003t0085g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0006t0019g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0006t0028g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0006t0041g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0007t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0007t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0007t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0008t0003g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0008t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0017t0069g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0019t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0020t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0021t0075g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0001c0022t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0009g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0009g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0015g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0015g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0026g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0002c0004t0030g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0003c0005t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0003c0005t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0003c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0004c0012t0008g0405 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0005c0013t0014g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0006c0014t0013g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0007c0016t0007g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0008c0011t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0009c0010t0076g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0010c0018t0015g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0011c0009t0013g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| a0012c0015t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0271 | EUR | GBR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0123 | EUR | GBR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0155 | EUR | GBR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0245 | EUR | GBR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0403 | EUR | FIN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0391 | EUR | FIN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0150 | EUR | FIN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | FIN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00408 | hp2 | a0001 | c0001 | t0022 | g0017 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00423 | hp1 | a0001 | c0003 | t0004 | g0091 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0055 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00438 | hp1 | a0001 | c0003 | t0044 | g0186 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0273 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00544 | hp2 | a0001 | c0001 | t0018 | g0291 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00558 | hp1 | a0001 | c0003 | t0004 | g0070 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00558 | hp2 | a0001 | c0002 | t0010 | g0094 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00597 | hp1 | a0001 | c0007 | t0005 | g0258 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00597 | hp2 | a0001 | c0002 | t0010 | g0074 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00609 | hp1 | a0001 | c0001 | t0022 | g0158 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0337 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00621 | hp1 | a0001 | c0003 | t0009 | g0283 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00621 | hp2 | a0001 | c0002 | t0072 | g0310 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0247 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0251 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0305 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00673 | hp2 | a0001 | c0001 | t0029 | g0339 | EAS | CHS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0250 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00738 | hp1 | a0004 | c0012 | t0008 | g0405 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00738 | hp2 | a0001 | c0001 | t0057 | g0047 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00741 | hp1 | a0001 | c0008 | t0003 | g0376 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01070 | hp1 | a0001 | c0001 | t0040 | g0108 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0001 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0001 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0122 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01081 | hp1 | a0001 | c0001 | t0014 | g0199 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01081 | hp2 | a0001 | c0003 | t0004 | g0049 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01099 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0115 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01106 | hp2 | a0001 | c0001 | t0059 | g0131 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01109 | hp1 | a0001 | c0003 | t0009 | g0290 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01109 | hp2 | a0001 | c0001 | t0060 | g0037 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01167 | hp1 | a0001 | c0002 | t0042 | g0165 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0229 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0398 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0228 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01175 | hp2 | a0001 | c0001 | t0046 | g0154 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0149 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0237 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0401 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01243 | hp2 | a0001 | c0001 | t0081 | g0254 | AMR | PUR | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01255 | hp1 | a0005 | c0013 | t0014 | g0071 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01255 | hp2 | a0001 | c0001 | t0082 | g0399 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0221 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01257 | hp1 | a0001 | c0001 | t0011 | g0142 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0220 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0325 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0198 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01346 | hp1 | a0001 | c0001 | t0032 | g0354 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0408 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0085 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01361 | hp2 | a0001 | c0001 | t0017 | g0059 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0219 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0306 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0246 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0397 | EUR | IBS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0119 | EUR | IBS | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01884 | hp1 | a0002 | c0004 | t0026 | g0350 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01884 | hp2 | a0001 | c0001 | t0023 | g0053 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0387 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01928 | hp1 | a0001 | c0001 | t0013 | g0050 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0340 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0311 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01952 | hp2 | a0001 | c0002 | t0010 | g0078 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0248 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0400 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01978 | hp2 | a0001 | c0003 | t0004 | g0057 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0395 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0212 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02015 | hp1 | a0006 | c0014 | t0013 | g0088 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02015 | hp2 | a0001 | c0003 | t0009 | g0313 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02040 | hp1 | a0001 | c0003 | t0004 | g0178 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0360 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02055 | hp2 | a0001 | c0001 | t0052 | g0044 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02056 | hp1 | a0001 | c0002 | t0073 | g0373 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02056 | hp2 | a0001 | c0007 | t0005 | g0274 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02071 | hp2 | a0001 | c0002 | t0010 | g0196 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02074 | hp1 | a0001 | c0001 | t0019 | g0328 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02080 | hp2 | a0001 | c0003 | t0004 | g0191 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02083 | hp2 | a0001 | c0001 | t0013 | g0097 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02129 | hp1 | a0001 | c0001 | t0039 | g0130 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0312 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0379 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0404 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0243 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02155 | hp1 | a0001 | c0001 | t0018 | g0343 | EAS | CDX | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02155 | hp2 | a0001 | c0003 | t0009 | g0326 | EAS | CDX | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02165 | hp1 | a0001 | c0001 | t0011 | g0058 | EAS | CDX | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02165 | hp2 | a0001 | c0019 | t0001 | g0223 | EAS | CDX | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02257 | hp1 | a0001 | c0001 | t0034 | g0015 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0300 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02258 | hp1 | a0001 | c0001 | t0053 | g0023 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02258 | hp2 | a0001 | c0001 | t0068 | g0296 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02273 | hp1 | a0001 | c0003 | t0004 | g0060 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02273 | hp2 | a0001 | c0002 | t0010 | g0156 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02280 | hp1 | a0002 | c0004 | t0009 | g0348 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02293 | hp2 | a0001 | c0002 | t0010 | g0028 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02300 | hp2 | a0001 | c0001 | t0083 | g0213 | AMR | PEL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0038 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02523 | hp1 | a0001 | c0003 | t0009 | g0336 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0054 | EAS | KHV | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02572 | hp2 | a0002 | c0004 | t0009 | g0385 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0065 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02615 | hp1 | a0001 | c0006 | t0041 | g0035 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02615 | hp2 | a0001 | c0002 | t0037 | g0098 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02622 | hp1 | a0001 | c0001 | t0079 | g0349 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02630 | hp2 | a0001 | c0001 | t0088 | g0389 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0063 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02647 | hp2 | a0001 | c0008 | t0003 | g0370 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0255 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02683 | hp2 | a0007 | c0016 | t0007 | g0287 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0256 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0240 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0386 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02723 | hp2 | a0001 | c0003 | t0085 | g0388 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02735 | hp1 | a0001 | c0003 | t0007 | g0407 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02735 | hp2 | a0001 | c0001 | t0008 | g0332 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02809 | hp1 | a0002 | c0004 | t0030 | g0249 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0320 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02895 | hp1 | a0001 | c0002 | t0025 | g0393 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02896 | hp2 | a0008 | c0011 | t0001 | g0206 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02922 | hp1 | a0009 | c0010 | t0076 | g0369 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02922 | hp2 | a0001 | c0001 | t0089 | g0382 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02965 | hp1 | a0002 | c0004 | t0004 | g0110 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02965 | hp2 | a0001 | c0006 | t0028 | g0207 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0026 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02970 | hp2 | a0010 | c0018 | t0015 | g0411 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0355 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02976 | hp2 | a0002 | c0004 | t0015 | g0410 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0141 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03041 | hp1 | a0001 | c0001 | t0055 | g0056 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03041 | hp2 | a0001 | c0001 | t0090 | g0299 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03098 | hp1 | a0001 | c0001 | t0063 | g0083 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03098 | hp2 | a0001 | c0002 | t0025 | g0361 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03139 | hp1 | a0001 | c0001 | t0062 | g0024 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03139 | hp2 | a0001 | c0001 | t0033 | g0205 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03195 | hp1 | a0001 | c0001 | t0038 | g0084 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03195 | hp2 | a0001 | c0001 | t0086 | g0353 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03209 | hp1 | a0001 | c0001 | t0026 | g0384 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03209 | hp2 | a0001 | c0003 | t0015 | g0288 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03225 | hp1 | a0001 | c0006 | t0019 | g0377 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03225 | hp2 | a0001 | c0001 | t0087 | g0356 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0010 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0406 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03453 | hp1 | a0001 | c0001 | t0058 | g0109 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0204 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03486 | hp1 | a0002 | c0004 | t0009 | g0319 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03486 | hp2 | a0001 | c0001 | t0031 | g0352 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0138 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03491 | hp2 | a0001 | c0002 | t0010 | g0006 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03492 | hp1 | a0001 | c0002 | t0010 | g0006 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0137 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03516 | hp1 | a0001 | c0002 | t0045 | g0041 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0381 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03540 | hp2 | a0001 | c0001 | t0023 | g0067 | AFR | GWD | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03579 | hp2 | a0001 | c0001 | t0054 | g0039 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03654 | hp1 | a0001 | c0001 | t0056 | g0043 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0076 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0270 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03688 | hp1 | a0001 | c0021 | t0075 | g0231 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03688 | hp2 | a0001 | c0001 | t0043 | g0188 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03704 | hp1 | a0001 | c0003 | t0007 | g0330 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03710 | hp1 | a0001 | c0002 | t0010 | g0124 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0162 | SAS | PJL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0409 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0147 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03834 | hp1 | a0001 | c0022 | t0003 | g0302 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0143 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03927 | hp1 | a0001 | c0001 | t0008 | g0214 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03942 | hp1 | a0001 | c0020 | t0001 | g0308 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03942 | hp2 | a0001 | c0003 | t0007 | g0412 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0396 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0172 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0010 | SAS | BEB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04199 | hp2 | a0001 | c0003 | t0077 | g0394 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0182 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | STU | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18522 | hp1 | a0001 | c0001 | t0032 | g0362 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0380 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18612 | hp1 | a0001 | c0002 | t0007 | g0346 | EAS | CHB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0257 | EAS | CHB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18747 | hp1 | a0001 | c0002 | t0048 | g0061 | EAS | CHB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0307 | EAS | CHB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0358 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18939 | hp1 | a0001 | c0001 | t0027 | g0342 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18939 | hp2 | a0001 | c0001 | t0018 | g0323 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18941 | hp1 | a0001 | c0001 | t0014 | g0100 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18941 | hp2 | a0001 | c0001 | t0012 | g0187 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18942 | hp1 | a0001 | c0001 | t0013 | g0166 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18942 | hp2 | a0001 | c0001 | t0021 | g0168 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0157 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18943 | hp2 | a0001 | c0001 | t0013 | g0117 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0192 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18945 | hp1 | a0001 | c0001 | t0029 | g0235 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18945 | hp2 | a0001 | c0001 | t0018 | g0239 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18946 | hp1 | a0001 | c0003 | t0004 | g0132 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18946 | hp2 | a0001 | c0001 | t0012 | g0169 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18947 | hp1 | a0001 | c0003 | t0009 | g0222 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18948 | hp2 | a0001 | c0002 | t0010 | g0202 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18950 | hp1 | a0001 | c0001 | t0017 | g0093 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18950 | hp2 | a0001 | c0001 | t0049 | g0146 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18952 | hp2 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18953 | hp1 | a0001 | c0001 | t0016 | g0390 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18957 | hp2 | a0001 | c0001 | t0017 | g0159 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18959 | hp2 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18963 | hp2 | a0001 | c0001 | t0047 | g0080 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18964 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18966 | hp2 | a0001 | c0002 | t0010 | g0099 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0260 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0324 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18973 | hp2 | a0001 | c0001 | t0008 | g0236 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0372 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18977 | hp2 | a0001 | c0001 | t0013 | g0045 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18978 | hp1 | a0001 | c0003 | t0004 | g0040 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18978 | hp2 | a0001 | c0001 | t0013 | g0081 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0298 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18980 | hp2 | a0001 | c0002 | t0010 | g0160 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18982 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18982 | hp2 | a0001 | c0003 | t0009 | g0253 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18983 | hp1 | a0001 | c0001 | t0021 | g0096 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18984 | hp2 | a0001 | c0001 | t0012 | g0195 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18985 | hp1 | a0001 | c0002 | t0010 | g0185 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18987 | hp1 | a0001 | c0001 | t0013 | g0092 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18988 | hp1 | a0001 | c0001 | t0020 | g0105 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0284 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18990 | hp2 | a0001 | c0001 | t0071 | g0242 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18994 | hp1 | a0001 | c0007 | t0005 | g0225 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18994 | hp2 | a0001 | c0001 | t0024 | g0145 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18995 | hp1 | a0001 | c0001 | t0016 | g0233 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18997 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18997 | hp2 | a0001 | c0001 | t0012 | g0101 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0133 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19000 | hp1 | a0001 | c0001 | t0012 | g0189 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0089 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19002 | hp1 | a0001 | c0002 | t0010 | g0170 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19002 | hp2 | a0001 | c0001 | t0066 | g0197 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0338 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19004 | hp1 | a0001 | c0001 | t0012 | g0075 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0297 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19005 | hp2 | a0001 | c0003 | t0009 | g0276 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19007 | hp2 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19009 | hp1 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0392 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19030 | hp1 | a0001 | c0001 | t0020 | g0111 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19030 | hp2 | a0001 | c0001 | t0033 | g0318 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19043 | hp1 | a0001 | c0001 | t0065 | g0031 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19043 | hp2 | a0002 | c0004 | t0004 | g0021 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19054 | hp1 | a0001 | c0002 | t0010 | g0079 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19054 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19057 | hp1 | a0001 | c0003 | t0004 | g0171 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0347 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19058 | hp1 | a0001 | c0001 | t0051 | g0167 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19058 | hp2 | a0001 | c0003 | t0004 | g0018 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19060 | hp1 | a0001 | c0001 | t0012 | g0033 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0267 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19062 | hp1 | a0001 | c0003 | t0004 | g0181 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19062 | hp2 | a0001 | c0001 | t0078 | g0227 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19065 | hp1 | a0001 | c0001 | t0016 | g0263 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19066 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19066 | hp2 | a0001 | c0002 | t0010 | g0077 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19067 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19067 | hp2 | a0001 | c0001 | t0014 | g0104 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19068 | hp1 | a0001 | c0002 | t0050 | g0107 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19074 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0345 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19077 | hp1 | a0011 | c0009 | t0013 | g0136 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19077 | hp2 | a0001 | c0003 | t0009 | g0252 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19078 | hp1 | a0001 | c0001 | t0084 | g0279 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19078 | hp2 | a0001 | c0001 | t0024 | g0173 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19080 | hp2 | a0001 | c0002 | t0010 | g0180 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0134 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0052 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19084 | hp2 | a0001 | c0001 | t0091 | g0218 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19086 | hp2 | a0001 | c0001 | t0027 | g0309 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19087 | hp1 | a0001 | c0001 | t0067 | g0265 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19088 | hp1 | a0001 | c0003 | t0070 | g0285 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19088 | hp2 | a0001 | c0002 | t0010 | g0174 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19090 | hp1 | a0001 | c0001 | t0016 | g0209 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19091 | hp1 | a0001 | c0001 | t0016 | g0264 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19091 | hp2 | a0001 | c0003 | t0074 | g0277 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19240 | hp1 | a0001 | c0001 | t0030 | g0383 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA19240 | hp2 | a0001 | c0001 | t0064 | g0030 | AFR | YRI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0153 | EUR | TSI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0140 | EUR | TSI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20805 | hp1 | a0001 | c0001 | t0036 | g0121 | EUR | TSI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0295 | EUR | TSI | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | GIH | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0329 | SAS | GIH | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01123 | hp1 | a0001 | c0001 | t0013 | g0082 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0118 | AMR | CLM | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0368 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02486 | hp1 | a0002 | c0004 | t0015 | g0367 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02486 | hp2 | a0001 | c0017 | t0069 | g0378 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02559 | hp1 | a0003 | c0005 | t0001 | g0374 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG02559 | hp2 | a0001 | c0001 | t0031 | g0351 | AFR | ACB | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG03471 | hp2 | a0003 | c0005 | t0002 | g0020 | AFR | MSL | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG06807 | hp1 | a0001 | c0001 | t0028 | g0365 | AFR | USA | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| HG06807 | hp2 | a0001 | c0001 | t0035 | g0016 | AFR | USA | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18955 | hp1 | a0001 | c0001 | t0061 | g0106 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA18955 | hp2 | a0001 | c0001 | t0009 | g0268 | EAS | JPT | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | USA | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA20300 | hp2 | a0012 | c0015 | t0006 | g0163 | AFR | USA | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA21309 | hp1 | a0001 | c0001 | t0080 | g0366 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| NA21309 | hp2 | a0001 | c0001 | t0092 | g0232 | AFR | LWK | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0402 | REF | REF | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0375 | REF | REF | GALNT6_chr12_51346252_51396406 | GALNT6 | chr12 | 51346252 | 51396406 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51357402 | G | A | 1 | a0012 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1549C>T | p.Arg517Cys | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/12 | 1860/5307 | 1549/1869 | 517/622 | chr12 | 51357402 | |||
| chr12:51359187 | C | T | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1313G>A | p.Ser438Asn | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/12 | 1624/5307 | 1313/1869 | 438/622 | chr12 | 51359187 | |||
| chr12:51359233 | C | T | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1267G>A | p.Val423Ile | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/12 | 1578/5307 | 1267/1869 | 423/622 | chr12 | 51359233 | |||
| chr12:51364245 | C | T | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.925G>A | p.Ala309Thr | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/12 | 1236/5307 | 925/1869 | 309/622 | chr12 | 51364245 | |||
| chr12:51364293 | C | A | 1 | a0007 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.877G>T | p.Val293Leu | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/12 | 1188/5307 | 877/1869 | 293/622 | chr12 | 51364293 | |||
| chr12:51377335 | G | T | 2 | a0003 a0008 |
4 | HG02559.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.524C>A | p.Pro175Gln | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/12 | 835/5307 | 524/1869 | 175/622 | chr12 | 51377335 | |||
| chr12:51379336 | C | T | 1 | a0004 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.446G>A | p.Arg149Gln | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 757/5307 | 446/1869 | 149/622 | chr12 | 51379336 | |||
| chr12:51379368 | C | G | 1 | a0002 | 9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
missense_variant | MODERATE | c.414G>C | p.Lys138Asn | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 725/5307 | 414/1869 | 138/622 | chr12 | 51379368 | |||
| chr12:51379438 | G | T | 1 | a0008 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.344C>A | p.Ala115Glu | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 655/5307 | 344/1869 | 115/622 | chr12 | 51379438 | |||
| chr12:51379559 | C | T | 1 | a0009 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.223G>A | p.Ala75Thr | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 534/5307 | 223/1869 | 75/622 | chr12 | 51379559 | |||
| chr12:51379625 | C | T | 1 | a0011 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.157G>A | p.Val53Ile | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 468/5307 | 157/1869 | 53/622 | chr12 | 51379625 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51355827 | G | A | 1 | a0001c0021 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/12 | 2045/5307 | 1734/1869 | 578/622 | chr12 | 51355827 | |||
| chr12:51360829 | C | T | 1 | a0001c0007 | 3 | HG00597.hp1 HG02056.hp2 NA18994.hp1 |
synonymous_variant | LOW | c.1059G>A | p.Thr353Thr | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/12 | 1370/5307 | 1059/1869 | 353/622 | chr12 | 51360829 | |||
| chr12:51365458 | C | T | 1 | a0001c0017 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.786G>A | p.Ala262Ala | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/12 | 1097/5307 | 786/1869 | 262/622 | chr12 | 51365458 | |||
| chr12:51377256 | T | C | 6 | a0001c0002 a0001c0008 a0001c0017 others(3): Show |
60 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(57): Show |
synonymous_variant | LOW | c.603A>G | p.Leu201Leu | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/12 | 914/5307 | 603/1869 | 201/622 | chr12 | 51377256 | |||
| chr12:51377316 | C | T | 1 | a0001c0006 | 3 | HG02615.hp1 HG02965.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.543G>A | p.Val181Val | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/12 | 854/5307 | 543/1869 | 181/622 | chr12 | 51377316 | |||
| chr12:51377361 | C | A | 1 | a0001c0019 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.498G>T | p.Val166Val | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/12 | 809/5307 | 498/1869 | 166/622 | chr12 | 51377361 | |||
| chr12:51379530 | G | A | 1 | a0001c0020 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.252C>T | p.Ser84Ser | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 563/5307 | 252/1869 | 84/622 | chr12 | 51379530 | |||
| chr12:51379671 | G | A | 1 | a0001c0008 | 2 | HG00741.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.111C>T | p.Ala37Ala | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 422/5307 | 111/1869 | 37/622 | chr12 | 51379671 | |||
| chr12:51379773 | G | A | 3 | a0001c0003 a0001c0021 a0001c0022 |
35 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(32): Show |
synonymous_variant | LOW | c.9C>T | p.Leu3Leu | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 320/5307 | 9/1869 | 3/622 | chr12 | 51379773 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51351523 | A | G | 1 | a0001c0001t0059 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2856T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2856 | chr12 | 51351523 | ||||||
| chr12:51351694 | G | C | 18 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0012 others(15): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2685C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2685 | chr12 | 51351694 | ||||||
| chr12:51351814 | G | T | 1 | a0001c0001t0038 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2565C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2565 | chr12 | 51351814 | ||||||
| chr12:51351906 | T | C | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*2473A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2473 | chr12 | 51351906 | ||||||
| chr12:51351965 | C | T | 1 | a0001c0001t0087 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2414G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2414 | chr12 | 51351965 | ||||||
| chr12:51352011 | G | T | 8 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0022 others(5): Show |
30 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2368C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2368 | chr12 | 51352011 | ||||||
| chr12:51352038 | T | C | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*2341A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2341 | chr12 | 51352038 | ||||||
| chr12:51352050 | C | T | 32 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0012 others(29): Show |
97 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2329G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2329 | chr12 | 51352050 | ||||||
| chr12:51352100 | C | T | 1 | a0001c0001t0091 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2279G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2279 | chr12 | 51352100 | ||||||
| chr12:51352101 | C | G | 1 | a0001c0001t0091 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2278 | chr12 | 51352101 | ||||||
| chr12:51352321 | G | A | 2 | a0001c0001t0027 a0001c0001t0047 |
3 | NA18939.hp1 NA18963.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2058C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2058 | chr12 | 51352321 | ||||||
| chr12:51352349 | G | T | 1 | a0001c0002t0072 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2030C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 2030 | chr12 | 51352349 | ||||||
| chr12:51352480 | G | A | 40 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(37): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1899C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1899 | chr12 | 51352480 | ||||||
| chr12:51352675 | C | T | 1 | a0001c0001t0092 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1704G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1704 | chr12 | 51352675 | ||||||
| chr12:51352734 | C | T | 1 | a0001c0001t0056 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1645 | chr12 | 51352734 | ||||||
| chr12:51352735 | G | A | 1 | a0001c0001t0055 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1644 | chr12 | 51352735 | ||||||
| chr12:51352910 | T | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
144 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1469A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1469 | chr12 | 51352910 | ||||||
| chr12:51353173 | C | T | 1 | a0001c0001t0043 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1206 | chr12 | 51353173 | ||||||
| chr12:51353221 | C | T | 4 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0066 others(1): Show |
25 | HG02129.hp2 HG02523.hp2 NA18612.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1158G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1158 | chr12 | 51353221 | ||||||
| chr12:51353364 | CT | C | 6 | a0001c0001t0049 a0001c0001t0082 a0001c0001t0083 others(3): Show |
6 | HG01255.hp2 HG02300.hp2 HG03688.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1014delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1014 | chr12 | 51353364 | ||||||
| chr12:51353364 | CTTT | C | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(58): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1014delAAA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1012 | chr12 | 51353364 | ||||||
| chr12:51353364 | CTTTT | C | 8 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0035 others(5): Show |
29 | HG02129.hp2 HG02523.hp2 HG02622.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1011_*1014delAAAA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 1011 | chr12 | 51353364 | ||||||
| chr12:51353400 | G | A | 1 | a0001c0001t0051 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 979 | chr12 | 51353400 | ||||||
| chr12:51353681 | T | C | 7 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0033 others(4): Show |
29 | HG02129.hp2 HG02523.hp2 HG03041.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*698A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 698 | chr12 | 51353681 | ||||||
| chr12:51353824 | A | G | 1 | a0001c0001t0079 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 555 | chr12 | 51353824 | ||||||
| chr12:51353851 | G | A | 3 | a0001c0001t0018 a0001c0001t0021 a0001c0001t0078 |
7 | HG00544.hp2 HG02155.hp1 NA18939.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*528C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 528 | chr12 | 51353851 | ||||||
| chr12:51353913 | C | CT | 6 | a0001c0001t0032 a0001c0001t0063 a0001c0001t0064 others(3): Show |
7 | HG01167.hp1 HG01346.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*465dupA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 465 | chr12 | 51353913 | ||||||
| chr12:51353913 | CT | C | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(57): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*465delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 465 | chr12 | 51353913 | ||||||
| chr12:51353935 | G | A | 5 | a0001c0001t0032 a0001c0001t0063 a0001c0001t0064 others(2): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*444C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 444 | chr12 | 51353935 | ||||||
| chr12:51354130 | G | A | 7 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0033 others(4): Show |
29 | HG02129.hp2 HG02523.hp2 HG03041.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 249 | chr12 | 51354130 | ||||||
| chr12:51354148 | C | T | 1 | a0001c0006t0041 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 231 | chr12 | 51354148 | ||||||
| chr12:51354156 | C | T | 1 | a0001c0001t0040 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 223 | chr12 | 51354156 | ||||||
| chr12:51354261 | G | C | 1 | a0001c0001t0092 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 118 | chr12 | 51354261 | ||||||
| chr12:51354284 | C | T | 1 | a0001c0001t0039 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 12/12 | 95 | chr12 | 51354284 | ||||||
| chr12:51379791 | C | T | 3 | a0001c0001t0038 a0001c0002t0025 a0001c0002t0037 |
4 | HG02615.hp2 HG02895.hp1 HG03098.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 10 | chr12 | 51379791 | ||||||
| chr12:51379854 | C | T | 1 | a0001c0001t0036 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/12 | 73 | chr12 | 51379854 | ||||||
| chr12:51391326 | G | T | 56 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(53): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(201): Show |
5_prime_UTR_variant | MODIFIER | c.-231C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 1/12 | 11545 | chr12 | 51391326 | ||||||
| chr12:51391400 | A | G | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02257.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-305T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 1/12 | 11619 | chr12 | 51391400 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51354542 | G | A | 201 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1756-50C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51354542 | |||||||
| chr12:51354611 | G | A | 393 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(390): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1756-119C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51354611 | |||||||
| chr12:51354929 | TTGAGCTC others(7): Show |
T | 58 | a0001c0001t0008g0010 a0001c0001t0008g0212 a0001c0001t0008g0214 others(55): Show |
61 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1756-451_1756-438d others(16): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51354929 | |||||||
| chr12:51354969 | G | A | 4 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0065g0031 others(1): Show |
4 | HG03041.hp2 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756-477C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51354969 | |||||||
| chr12:51355021 | G | C | 1 | a0009c0010t0076g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1756-529C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355021 | |||||||
| chr12:51355235 | T | C | 1 | a0001c0001t0091g0218 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1755+571A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355235 | |||||||
| chr12:51355411 | C | T | 1 | a0003c0005t0001g0374 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1755+395G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355411 | |||||||
| chr12:51355455 | C | A | 2 | a0001c0001t0024g0145 a0001c0001t0024g0173 |
2 | NA18994.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1755+351G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355455 | |||||||
| chr12:51355635 | A | T | 1 | a0001c0001t0092g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1755+171T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355635 | |||||||
| chr12:51355688 | C | T | 3 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0065g0031 |
3 | HG03139.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1755+118G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355688 | |||||||
| chr12:51355799 | G | A | 3 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0065g0031 |
3 | HG03139.hp2 NA19030.hp2 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.1755+7C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 11/11 | chr12 | 51355799 | |||||||
| chr12:51356051 | G | A | 1 | a0001c0001t0011g0142 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1603-93C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356051 | |||||||
| chr12:51356160 | A | G | 3 | a0001c0001t0001g0357 a0001c0001t0001g0371 a0001c0001t0002g0069 |
3 | HG02717.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1603-202T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356160 | |||||||
| chr12:51356182 | G | A | 225 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1603-224C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356182 | |||||||
| chr12:51356241 | A | G | 1 | a0009c0010t0076g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1603-283T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356241 | |||||||
| chr12:51356353 | CT | C | 302 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0230 others(299): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-396delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356353 | |||||||
| chr12:51356353 | CTT | C | 27 | a0001c0001t0001g0281 a0001c0001t0001g0331 a0001c0001t0002g0200 others(24): Show |
27 | HG01167.hp2 HG01256.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.1603-397_1603-396d others(4): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356353 | |||||||
| chr12:51356356 | T | C | 1 | a0001c0003t0009g0336 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1603-398A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356356 | |||||||
| chr12:51356394 | C | T | 140 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(137): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1603-436G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356394 | |||||||
| chr12:51356531 | T | A | 3 | a0001c0001t0005g0245 a0001c0001t0013g0042 a0001c0001t0013g0082 |
3 | HG00140.hp2 HG01123.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1603-573A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356531 | |||||||
| chr12:51356531 | TA | T | 7 | a0001c0001t0018g0239 a0001c0001t0018g0291 a0001c0001t0018g0323 others(4): Show |
7 | HG00544.hp2 HG02155.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-574delT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356531 | |||||||
| chr12:51356631 | T | G | 2 | a0001c0002t0010g0079 a0001c0002t0010g0185 |
2 | NA18985.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1603-673A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356631 | |||||||
| chr12:51356716 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+633A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356716 | |||||||
| chr12:51356771 | TTAAAA | T | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1602+573_1602+577d others(7): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356771 | |||||||
| chr12:51356801 | C | T | 3 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0090g0299 |
3 | HG03041.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1602+548G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356801 | |||||||
| chr12:51356895 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1602+454G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356895 | |||||||
| chr12:51356941 | C | T | 1 | a0001c0001t0079g0349 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1602+408G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 10/11 | chr12 | 51356941 | |||||||
| chr12:51357737 | G | A | 90 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(87): Show |
94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1501-287C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 9/11 | chr12 | 51357737 | |||||||
| chr12:51357837 | T | G | 342 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(339): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1500+293A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 9/11 | chr12 | 51357837 | |||||||
| chr12:51357900 | T | C | 1 | a0001c0001t0006g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1500+230A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 9/11 | chr12 | 51357900 | |||||||
| chr12:51357980 | C | T | 2 | a0001c0001t0055g0056 a0001c0006t0041g0035 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1500+150G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 9/11 | chr12 | 51357980 | |||||||
| chr12:51358301 | GT | G | 65 | a0001c0001t0001g0282 a0001c0001t0001g0363 a0001c0001t0001g0364 others(62): Show |
68 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1369-41delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358301 | |||||||
| chr12:51358301 | GTT | G | 24 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0054 others(21): Show |
25 | HG02129.hp2 HG02523.hp2 NA18612.hp2 others(22): Show |
intron_variant | MODIFIER | c.1369-42_1369-41del others(2): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358301 | |||||||
| chr12:51358447 | C | T | 24 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0054 others(21): Show |
25 | HG02129.hp2 HG02523.hp2 NA18612.hp2 others(22): Show |
intron_variant | MODIFIER | c.1369-186G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358447 | |||||||
| chr12:51358538 | T | C | 1 | a0001c0001t0008g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1369-277A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358538 | |||||||
| chr12:51358824 | C | T | 3 | a0001c0001t0064g0030 a0001c0001t0088g0389 a0001c0001t0089g0382 |
3 | HG02630.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1368+308G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358824 | |||||||
| chr12:51358836 | A | G | 60 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 others(57): Show |
63 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1368+296T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51358836 | |||||||
| chr12:51359044 | G | A | 1 | a0001c0001t0092g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1368+88C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51359044 | |||||||
| chr12:51359112 | C | T | 1 | a0001c0001t0003g0335 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1368+20G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51359112 | |||||||
| chr12:51359113 | G | A | 149 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1368+19C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 8/11 | chr12 | 51359113 | |||||||
| chr12:51359477 | T | C | 3 | a0001c0001t0017g0038 a0001c0001t0031g0352 a0001c0001t0060g0037 |
3 | HG01109.hp2 HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1168-145A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51359477 | |||||||
| chr12:51359481 | G | A | 7 | a0001c0001t0006g0048 a0001c0001t0006g0114 a0001c0001t0006g0183 others(4): Show |
7 | NA18939.hp1 NA18948.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-149C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51359481 | |||||||
| chr12:51359548 | A | C | 10 | a0001c0001t0002g0087 a0001c0001t0012g0003 a0001c0001t0012g0101 others(7): Show |
11 | NA18612.hp2 NA18943.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-216T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51359548 | |||||||
| chr12:51359868 | G | A | 84 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(81): Show |
88 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1168-536C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51359868 | |||||||
| chr12:51360001 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1168-669G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360001 | |||||||
| chr12:51360029 | G | A | 1 | a0008c0011t0001g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1167+692C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360029 | |||||||
| chr12:51360145 | G | T | 6 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0065g0031 others(3): Show |
6 | HG02622.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+576C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360145 | |||||||
| chr12:51360295 | C | T | 82 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1167+426G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360295 | |||||||
| chr12:51360430 | A | G | 3 | a0001c0001t0001g0359 a0001c0001t0002g0025 a0001c0001t0002g0068 |
3 | HG02109.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1167+291T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360430 | |||||||
| chr12:51360586 | A | G | 227 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 others(224): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1167+135T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360586 | |||||||
| chr12:51360587 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1167+134G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 7/11 | chr12 | 51360587 | |||||||
| chr12:51360845 | A | G | 188 | a0001c0001t0003g0335 a0001c0001t0004g0008 a0001c0001t0004g0034 others(185): Show |
193 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
splice_region_variant&intron_variant | LOW | c.1050-7T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51360845 | |||||||
| chr12:51360986 | A | C | 1 | a0001c0001t0001g0327 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1050-148T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51360986 | |||||||
| chr12:51361003 | T | C | 2 | a0001c0003t0015g0288 a0001c0003t0085g0388 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1050-165A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361003 | |||||||
| chr12:51361033 | G | A | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-195C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361033 | |||||||
| chr12:51361118 | G | A | 1 | a0001c0001t0053g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1050-280C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361118 | |||||||
| chr12:51361163 | C | A | 1 | a0001c0003t0001g0391 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1050-325G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361163 | |||||||
| chr12:51361509 | G | A | 264 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1050-671C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361509 | |||||||
| chr12:51361610 | T | A | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-772A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361610 | |||||||
| chr12:51361630 | A | G | 2 | a0001c0001t0028g0365 a0001c0001t0092g0232 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1050-792T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361630 | |||||||
| chr12:51361657 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1050-819C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361657 | |||||||
| chr12:51361665 | G | T | 95 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(92): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1050-827C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361665 | |||||||
| chr12:51361685 | G | A | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-847C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361685 | |||||||
| chr12:51361695 | C | G | 1 | a0001c0001t0014g0122 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1050-857G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361695 | |||||||
| chr12:51361742 | G | A | 1 | a0001c0002t0003g0260 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1050-904C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361742 | |||||||
| chr12:51361745 | C | T | 1 | a0001c0006t0041g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1050-907G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361745 | |||||||
| chr12:51361807 | G | T | 1 | a0001c0001t0012g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1050-969C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361807 | |||||||
| chr12:51361938 | C | T | 1 | a0001c0001t0008g0247 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1050-1100G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51361938 | |||||||
| chr12:51362006 | T | C | 351 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(348): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1050-1168A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362006 | |||||||
| chr12:51362112 | G | A | 258 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 others(255): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1050-1274C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362112 | |||||||
| chr12:51362244 | T | C | 1 | a0001c0001t0021g0168 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1050-1406A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362244 | |||||||
| chr12:51362270 | C | A | 2 | a0001c0001t0001g0404 a0001c0001t0009g0204 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-1432G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362270 | |||||||
| chr12:51362289 | A | C | 2 | a0001c0006t0019g0377 a0001c0006t0028g0207 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1050-1451T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362289 | |||||||
| chr12:51362405 | G | A | 1 | a0006c0014t0013g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1050-1567C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362405 | |||||||
| chr12:51362434 | G | A | 87 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1050-1596C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362434 | |||||||
| chr12:51362485 | T | C | 162 | a0001c0001t0001g0303 a0001c0001t0003g0335 a0001c0001t0004g0008 others(159): Show |
166 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1049+1636A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362485 | |||||||
| chr12:51362490 | G | A | 2 | a0001c0001t0005g0259 a0001c0001t0013g0090 |
2 | HG02040.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1049+1631C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362490 | |||||||
| chr12:51362541 | A | T | 1 | a0001c0001t0008g0295 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1049+1580T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362541 | |||||||
| chr12:51362602 | C | A | 2 | a0001c0003t0015g0288 a0001c0003t0085g0388 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1049+1519G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362602 | |||||||
| chr12:51362853 | GT | G | 162 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 others(159): Show |
167 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1049+1267delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362853 | |||||||
| chr12:51362853 | GTT | G | 79 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(76): Show |
83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1049+1266_1049+126 others(6): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362853 | |||||||
| chr12:51362983 | G | A | 1 | a0001c0001t0012g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1049+1138C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51362983 | |||||||
| chr12:51363071 | C | A | 3 | a0001c0001t0008g0214 a0001c0001t0008g0220 a0001c0001t0008g0221 |
3 | HG01256.hp1 HG01258.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1049+1050G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363071 | |||||||
| chr12:51363104 | AC | A | 27 | a0001c0001t0005g0210 a0001c0001t0005g0278 a0001c0001t0012g0003 others(24): Show |
28 | HG02129.hp2 HG02523.hp2 NA18612.hp2 others(25): Show |
intron_variant | MODIFIER | c.1049+1016delG | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363104 | |||||||
| chr12:51363119 | C | T | 1 | a0001c0006t0019g0377 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1049+1002G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363119 | |||||||
| chr12:51363213 | G | A | 1 | a0001c0001t0007g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1049+908C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363213 | |||||||
| chr12:51363479 | A | T | 1 | a0001c0003t0009g0252 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1049+642T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363479 | |||||||
| chr12:51363763 | T | C | 1 | a0001c0001t0024g0173 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1049+358A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51363763 | |||||||
| chr12:51364081 | C | T | 1 | a0001c0001t0026g0384 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1049+40G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51364081 | |||||||
| chr12:51364112 | G | A | 1 | a0001c0001t0019g0256 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1049+9C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 6/11 | chr12 | 51364112 | |||||||
| chr12:51364688 | G | T | 3 | a0001c0002t0025g0361 a0001c0002t0025g0393 a0001c0002t0037g0098 |
3 | HG02615.hp2 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.815-333C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51364688 | |||||||
| chr12:51364712 | C | T | 1 | a0002c0004t0030g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.815-357G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51364712 | |||||||
| chr12:51364728 | C | T | 151 | a0001c0001t0001g0303 a0001c0001t0003g0335 a0001c0001t0004g0034 others(148): Show |
155 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.815-373G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51364728 | |||||||
| chr12:51364752 | T | C | 358 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(355): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.815-397A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51364752 | |||||||
| chr12:51364910 | T | A | 1 | a0001c0001t0047g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.814+520A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51364910 | |||||||
| chr12:51365148 | A | G | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.814+282T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51365148 | |||||||
| chr12:51365289 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0002g0164 |
2 | HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.814+141C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51365289 | |||||||
| chr12:51365341 | G | A | 1 | a0001c0001t0007g0329 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.814+89C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51365341 | |||||||
| chr12:51365413 | G | A | 3 | a0001c0001t0068g0296 a0001c0002t0045g0041 a0001c0017t0069g0378 |
3 | HG02258.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.814+17C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 5/11 | chr12 | 51365413 | |||||||
| chr12:51365624 | A | G | 1 | a0001c0001t0008g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.665-45T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51365624 | |||||||
| chr12:51365631 | A | G | 1 | a0001c0022t0003g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.665-52T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51365631 | |||||||
| chr12:51365679 | G | C | 1 | a0001c0001t0005g0409 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.665-100C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51365679 | |||||||
| chr12:51365727 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.665-148G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51365727 | |||||||
| chr12:51365979 | G | A | 1 | a0001c0001t0008g0270 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.665-400C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51365979 | |||||||
| chr12:51366074 | T | C | 38 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(35): Show |
39 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(36): Show |
intron_variant | MODIFIER | c.665-495A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366074 | |||||||
| chr12:51366143 | C | T | 3 | a0001c0001t0001g0359 a0001c0001t0002g0025 a0001c0001t0002g0068 |
3 | HG02109.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.665-564G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366143 | |||||||
| chr12:51366209 | C | T | 1 | a0001c0001t0016g0264 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.665-630G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366209 | |||||||
| chr12:51366254 | C | T | 1 | a0001c0001t0008g0010 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.665-675G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366254 | |||||||
| chr12:51366319 | G | A | 32 | a0001c0001t0002g0087 a0001c0001t0012g0003 a0001c0001t0012g0033 others(29): Show |
33 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(30): Show |
intron_variant | MODIFIER | c.665-740C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366319 | |||||||
| chr12:51366371 | G | A | 52 | a0001c0001t0004g0034 a0001c0002t0003g0237 a0001c0002t0003g0243 others(49): Show |
53 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.665-792C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366371 | |||||||
| chr12:51366399 | A | G | 36 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(33): Show |
37 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.665-820T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366399 | |||||||
| chr12:51366424 | A | G | 36 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(33): Show |
37 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.665-845T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366424 | |||||||
| chr12:51366480 | G | A | 36 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(33): Show |
37 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.665-901C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366480 | |||||||
| chr12:51366543 | C | T | 354 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(351): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.665-964G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366543 | |||||||
| chr12:51366593 | A | C | 2 | a0001c0001t0005g0397 a0001c0001t0005g0409 |
2 | HG01515.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.665-1014T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366593 | |||||||
| chr12:51366652 | A | G | 36 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(33): Show |
37 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.665-1073T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366652 | |||||||
| chr12:51366746 | G | A | 36 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(33): Show |
37 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.665-1167C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366746 | |||||||
| chr12:51366902 | T | C | 38 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(35): Show |
39 | HG00438.hp1 HG01346.hp1 HG02129.hp2 others(36): Show |
intron_variant | MODIFIER | c.665-1323A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366902 | |||||||
| chr12:51366989 | C | T | 1 | a0001c0001t0001g0381 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.665-1410G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366989 | |||||||
| chr12:51366991 | C | T | 1 | a0002c0004t0030g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.665-1412G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51366991 | |||||||
| chr12:51367062 | G | A | 1 | a0001c0003t0009g0326 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.665-1483C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367062 | |||||||
| chr12:51367099 | A | G | 1 | a0001c0001t0007g0208 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.665-1520T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367099 | |||||||
| chr12:51367125 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.665-1546G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367125 | |||||||
| chr12:51367192 | G | A | 316 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(313): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.665-1613C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367192 | |||||||
| chr12:51367252 | C | T | 2 | a0001c0001t0079g0349 a0001c0001t0092g0232 |
2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.665-1673G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367252 | |||||||
| chr12:51367267 | A | C | 1 | a0001c0001t0012g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.665-1688T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367267 | |||||||
| chr12:51367421 | C | A | 2 | a0001c0001t0001g0371 a0001c0001t0002g0069 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.665-1842G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367421 | |||||||
| chr12:51367448 | A | G | 319 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(316): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.665-1869T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367448 | |||||||
| chr12:51367450 | G | C | 355 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(352): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.665-1871C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367450 | |||||||
| chr12:51367748 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0005g0392 |
3 | HG01168.hp2 HG01169.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.665-2169C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367748 | |||||||
| chr12:51367755 | A | G | 2 | a0001c0001t0006g0113 a0001c0001t0006g0201 |
2 | NA18985.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.665-2176T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367755 | |||||||
| chr12:51367846 | A | C | 116 | a0001c0001t0001g0303 a0001c0001t0003g0335 a0001c0001t0006g0032 others(113): Show |
119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.665-2267T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51367846 | |||||||
| chr12:51368017 | AT | A | 41 | a0001c0001t0001g0331 a0001c0001t0002g0087 a0001c0001t0004g0184 others(38): Show |
42 | HG01256.hp2 HG01346.hp1 HG02129.hp2 others(39): Show |
intron_variant | MODIFIER | c.665-2439delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368017 | |||||||
| chr12:51368031 | T | A | 20 | a0001c0001t0006g0032 a0001c0001t0006g0036 a0001c0001t0006g0051 others(17): Show |
21 | HG02074.hp2 HG03688.hp2 NA18747.hp2 others(18): Show |
intron_variant | MODIFIER | c.665-2452A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368031 | |||||||
| chr12:51368141 | A | T | 37 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(34): Show |
38 | HG01346.hp1 HG02129.hp2 HG02630.hp2 others(35): Show |
intron_variant | MODIFIER | c.665-2562T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368141 | |||||||
| chr12:51368145 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.665-2566A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368145 | |||||||
| chr12:51368231 | C | T | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-2652G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368231 | |||||||
| chr12:51368233 | C | CA | 116 | a0001c0001t0001g0303 a0001c0001t0003g0335 a0001c0001t0006g0032 others(113): Show |
119 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.665-2655dupT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368233 | |||||||
| chr12:51368395 | GT | G | 230 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(227): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.665-2817delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368395 | |||||||
| chr12:51368395 | GTT | G | 118 | a0001c0001t0001g0303 a0001c0001t0002g0129 a0001c0001t0003g0335 others(115): Show |
121 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.665-2818_665-2817d others(4): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368395 | |||||||
| chr12:51368397 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.665-2818A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368397 | |||||||
| chr12:51368561 | C | T | 1 | a0001c0001t0008g0212 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.665-2982G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368561 | |||||||
| chr12:51368586 | T | G | 30 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(27): Show |
31 | HG00438.hp1 HG02129.hp2 NA18612.hp2 others(28): Show |
intron_variant | MODIFIER | c.665-3007A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368586 | |||||||
| chr12:51368674 | G | C | 1 | a0001c0001t0006g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.665-3095C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368674 | |||||||
| chr12:51368699 | C | A | 1 | a0001c0002t0003g0314 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.665-3120G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368699 | |||||||
| chr12:51368738 | CAGGTG | C | 200 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(197): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.665-3164_665-3160d others(7): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368738 | |||||||
| chr12:51368758 | T | C | 80 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
84 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.665-3179A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368758 | |||||||
| chr12:51368830 | A | G | 200 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(197): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.665-3251T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368830 | |||||||
| chr12:51368839 | C | T | 1 | a0001c0008t0003g0376 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.665-3260G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51368839 | |||||||
| chr12:51369050 | C | T | 30 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(27): Show |
31 | HG00438.hp1 HG02129.hp2 NA18612.hp2 others(28): Show |
intron_variant | MODIFIER | c.665-3471G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51369050 | |||||||
| chr12:51369132 | C | G | 1 | a0001c0002t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.665-3553G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51369132 | |||||||
| chr12:51369874 | A | G | 3 | a0001c0003t0004g0040 a0001c0003t0004g0132 a0001c0003t0004g0171 |
3 | NA18946.hp1 NA18978.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.665-4295T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51369874 | |||||||
| chr12:51369883 | C | T | 1 | a0001c0001t0012g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.665-4304G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51369883 | |||||||
| chr12:51369974 | T | C | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-4395A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51369974 | |||||||
| chr12:51370324 | C | T | 1 | a0001c0008t0003g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.665-4745G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370324 | |||||||
| chr12:51370362 | C | T | 200 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(197): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.665-4783G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370362 | |||||||
| chr12:51370475 | C | T | 1 | a0001c0001t0008g0010 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.665-4896G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370475 | |||||||
| chr12:51370491 | C | T | 1 | a0001c0001t0043g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665-4912G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370491 | |||||||
| chr12:51370497 | T | C | 1 | a0001c0001t0003g0335 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.665-4918A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370497 | |||||||
| chr12:51370593 | A | C | 1 | a0001c0001t0014g0100 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.665-5014T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370593 | |||||||
| chr12:51370600 | A | G | 9 | a0001c0001t0055g0056 a0001c0006t0041g0035 a0002c0004t0004g0021 others(6): Show |
9 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.665-5021T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370600 | |||||||
| chr12:51370634 | T | C | 1 | a0001c0001t0051g0167 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.665-5055A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370634 | |||||||
| chr12:51370701 | G | A | 1 | a0001c0001t0008g0355 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.665-5122C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370701 | |||||||
| chr12:51370724 | T | C | 1 | a0001c0001t0014g0122 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.665-5145A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370724 | |||||||
| chr12:51370761 | T | C | 2 | a0001c0003t0015g0288 a0001c0003t0085g0388 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.665-5182A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51370761 | |||||||
| chr12:51371054 | A | AATTT | 58 | a0001c0001t0006g0147 a0001c0001t0012g0134 a0001c0001t0012g0169 others(55): Show |
58 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.665-5476_665-5475i others(6): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | A | AATTTATT | 39 | a0001c0001t0001g0303 a0001c0001t0006g0032 a0001c0001t0006g0036 others(36): Show |
42 | HG00323.hp1 HG00544.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.665-5476_665-5475i others(9): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | A | AATTTATT others(3): Show |
17 | a0001c0001t0006g0064 a0001c0001t0006g0095 a0001c0001t0006g0103 others(14): Show |
17 | HG00741.hp2 HG02074.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.665-5476_665-5475i others(12): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | A | AATTTATT others(6): Show |
8 | a0001c0001t0006g0072 a0001c0001t0006g0141 a0001c0001t0007g0300 others(5): Show |
8 | HG01074.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-5476_665-5475i others(15): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | A | AATTTATT others(9): Show |
1 | a0001c0001t0006g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.665-5476_665-5475i others(18): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATT | A | 3 | a0001c0001t0002g0112 a0001c0001t0079g0349 a0002c0004t0030g0249 |
3 | HG02622.hp1 HG02809.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665-5478_665-5476d others(5): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATT | A | 64 | a0001c0001t0001g0244 a0001c0001t0001g0281 a0001c0001t0001g0282 others(61): Show |
67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.665-5481_665-5476d others(8): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATTA others(2): Show |
A | 5 | a0001c0001t0013g0050 a0001c0001t0017g0059 a0001c0003t0015g0288 others(2): Show |
5 | HG00738.hp1 HG01361.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.665-5484_665-5476d others(11): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATTA others(5): Show |
A | 51 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(48): Show |
55 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.665-5487_665-5476d others(14): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATTA others(8): Show |
A | 119 | a0001c0001t0001g0322 a0001c0001t0001g0363 a0001c0001t0001g0364 others(116): Show |
123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.665-5490_665-5476d others(17): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATTA others(11): Show |
A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0321 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.665-5493_665-5476d others(20): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371054 | AATTATTA others(14): Show |
A | 9 | a0001c0001t0004g0034 a0001c0001t0015g0228 a0001c0001t0015g0229 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-5496_665-5476d others(23): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371054 | |||||||
| chr12:51371055 | A | AT | 24 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(21): Show |
25 | HG00099.hp2 HG00438.hp1 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.665-5477dupA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371055 | |||||||
| chr12:51371065 | T | A | 1 | a0001c0001t0012g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.665-5486A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371065 | |||||||
| chr12:51371135 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.665-5556C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371135 | |||||||
| chr12:51371170 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(19): Show |
24 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.665-5591C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371170 | |||||||
| chr12:51371193 | T | C | 352 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(349): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.665-5614A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371193 | |||||||
| chr12:51371233 | A | G | 344 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(341): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.665-5654T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371233 | |||||||
| chr12:51371282 | C | G | 2 | a0001c0003t0015g0288 a0001c0003t0085g0388 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.665-5703G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371282 | |||||||
| chr12:51371442 | C | T | 1 | a0001c0001t0008g0332 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.664+5753G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371442 | |||||||
| chr12:51371540 | C | T | 1 | a0001c0001t0005g0305 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.664+5655G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371540 | |||||||
| chr12:51371563 | C | T | 1 | a0001c0001t0079g0349 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.664+5632G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371563 | |||||||
| chr12:51371726 | C | T | 2 | a0001c0006t0019g0377 a0001c0006t0028g0207 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.664+5469G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371726 | |||||||
| chr12:51371757 | G | C | 1 | a0001c0001t0092g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664+5438C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371757 | |||||||
| chr12:51371920 | T | C | 3 | a0001c0001t0009g0267 a0001c0001t0009g0268 a0001c0001t0067g0265 |
3 | NA18955.hp2 NA19060.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.664+5275A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371920 | |||||||
| chr12:51371938 | G | A | 1 | a0001c0001t0022g0017 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.664+5257C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51371938 | |||||||
| chr12:51372230 | C | G | 4 | a0001c0001t0053g0023 a0001c0006t0019g0377 a0001c0006t0028g0207 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+4965G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372230 | |||||||
| chr12:51372500 | C | T | 1 | a0002c0004t0030g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.664+4695G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372500 | |||||||
| chr12:51372533 | G | A | 1 | a0009c0010t0076g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.664+4662C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372533 | |||||||
| chr12:51372570 | T | A | 1 | a0001c0001t0053g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664+4625A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372570 | |||||||
| chr12:51372735 | G | C | 114 | a0001c0001t0001g0303 a0001c0001t0006g0032 a0001c0001t0006g0036 others(111): Show |
117 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.664+4460C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372735 | |||||||
| chr12:51372768 | C | T | 1 | a0001c0001t0006g0051 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.664+4427G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372768 | |||||||
| chr12:51372831 | C | T | 1 | a0001c0001t0079g0349 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.664+4364G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51372831 | |||||||
| chr12:51373015 | C | T | 25 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0073 others(22): Show |
26 | HG02129.hp2 HG02922.hp1 NA18612.hp2 others(23): Show |
intron_variant | MODIFIER | c.664+4180G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373015 | |||||||
| chr12:51373033 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.664+4162T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373033 | |||||||
| chr12:51373102 | C | T | 1 | a0001c0001t0031g0351 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.664+4093G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373102 | |||||||
| chr12:51373279 | G | A | 3 | a0001c0006t0019g0377 a0001c0006t0028g0207 a0001c0006t0041g0035 |
3 | HG02615.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.664+3916C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373279 | |||||||
| chr12:51373391 | T | C | 5 | a0001c0001t0004g0034 a0001c0001t0015g0228 a0001c0001t0015g0229 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+3804A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373391 | |||||||
| chr12:51373403 | G | A | 131 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(128): Show |
137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.664+3792C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373403 | |||||||
| chr12:51373491 | T | C | 1 | a0001c0001t0012g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.664+3704A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373491 | |||||||
| chr12:51373529 | A | C | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+3666T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373529 | |||||||
| chr12:51373835 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.664+3360G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373835 | |||||||
| chr12:51373851 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.664+3344G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373851 | |||||||
| chr12:51373918 | G | A | 24 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0073 others(21): Show |
25 | HG02129.hp2 NA18612.hp2 NA18941.hp2 others(22): Show |
intron_variant | MODIFIER | c.664+3277C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373918 | |||||||
| chr12:51373921 | G | A | 1 | a0001c0001t0080g0366 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664+3274C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51373921 | |||||||
| chr12:51374331 | C | A | 6 | a0001c0001t0032g0354 a0001c0001t0032g0362 a0001c0001t0063g0083 others(3): Show |
6 | HG01346.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+2864G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374331 | |||||||
| chr12:51374488 | C | T | 47 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0281 others(44): Show |
49 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.664+2707G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374488 | |||||||
| chr12:51374494 | T | C | 1 | a0001c0001t0005g0397 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.664+2701A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374494 | |||||||
| chr12:51374524 | A | G | 2 | a0001c0003t0015g0288 a0001c0003t0085g0388 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.664+2671T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374524 | |||||||
| chr12:51374599 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.664+2596C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374599 | |||||||
| chr12:51374697 | C | G | 1 | a0001c0002t0003g0248 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.664+2498G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374697 | |||||||
| chr12:51374813 | G | A | 132 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(129): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.664+2382C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374813 | |||||||
| chr12:51374841 | C | T | 1 | a0001c0001t0053g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664+2354G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374841 | |||||||
| chr12:51374880 | G | A | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.664+2315C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374880 | |||||||
| chr12:51374933 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0030g0383 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.664+2262A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51374933 | |||||||
| chr12:51375132 | T | C | 1 | a0001c0001t0079g0349 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.664+2063A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375132 | |||||||
| chr12:51375240 | T | C | 3 | a0001c0002t0003g0280 a0001c0002t0010g0079 a0001c0002t0010g0185 |
3 | NA18985.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.664+1955A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375240 | |||||||
| chr12:51375249 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.664+1946G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375249 | |||||||
| chr12:51375282 | C | A | 1 | a0001c0001t0013g0081 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.664+1913G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375282 | |||||||
| chr12:51375337 | G | T | 24 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0073 others(21): Show |
25 | HG02129.hp2 NA18612.hp2 NA18941.hp2 others(22): Show |
intron_variant | MODIFIER | c.664+1858C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375337 | |||||||
| chr12:51375342 | G | C | 1 | a0001c0001t0024g0173 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.664+1853C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375342 | |||||||
| chr12:51375433 | G | A | 1 | a0001c0001t0036g0121 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.664+1762C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375433 | |||||||
| chr12:51375450 | G | T | 3 | a0001c0006t0019g0377 a0001c0006t0028g0207 a0001c0006t0041g0035 |
3 | HG02615.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.664+1745C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375450 | |||||||
| chr12:51375560 | C | CT | 26 | a0001c0001t0012g0003 a0001c0001t0012g0033 a0001c0001t0012g0073 others(23): Show |
27 | HG00741.hp1 HG02129.hp2 HG02922.hp1 others(24): Show |
intron_variant | MODIFIER | c.664+1634dupA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375560 | |||||||
| chr12:51375560 | CT | C | 61 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0281 others(58): Show |
63 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.664+1634delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375560 | |||||||
| chr12:51375627 | G | A | 39 | a0001c0001t0004g0128 a0001c0001t0005g0002 a0001c0001t0005g0210 others(36): Show |
42 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.664+1568C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375627 | |||||||
| chr12:51375644 | G | A | 2 | a0001c0001t0002g0120 a0001c0003t0001g0391 |
2 | HG00280.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.664+1551C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375644 | |||||||
| chr12:51375718 | T | C | 1 | a0001c0001t0053g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664+1477A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375718 | |||||||
| chr12:51375764 | G | A | 3 | a0001c0002t0003g0280 a0001c0002t0010g0079 a0001c0002t0010g0185 |
3 | NA18985.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.664+1431C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375764 | |||||||
| chr12:51375800 | G | C | 2 | a0001c0001t0008g0255 a0001c0001t0081g0254 |
2 | HG01243.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.664+1395C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375800 | |||||||
| chr12:51375913 | AGCAGTGG others(3): Show |
A | 1 | a0001c0002t0003g0280 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.664+1272_664+1281d others(12): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375913 | |||||||
| chr12:51375946 | C | T | 1 | a0001c0001t0008g0010 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.664+1249G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375946 | |||||||
| chr12:51375989 | C | T | 261 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(258): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.664+1206G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51375989 | |||||||
| chr12:51376111 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.664+1084G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376111 | |||||||
| chr12:51376112 | G | A | 28 | a0001c0001t0005g0210 a0001c0001t0005g0278 a0001c0001t0012g0003 others(25): Show |
29 | HG02129.hp2 HG02922.hp1 NA18612.hp2 others(26): Show |
intron_variant | MODIFIER | c.664+1083C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376112 | |||||||
| chr12:51376113 | C | A | 4 | a0001c0001t0005g0245 a0001c0001t0005g0398 a0001c0001t0013g0042 others(1): Show |
4 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1082G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376113 | |||||||
| chr12:51376146 | T | G | 1 | a0001c0001t0079g0349 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.664+1049A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376146 | |||||||
| chr12:51376173 | T | A | 1 | a0001c0001t0012g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.664+1022A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376173 | |||||||
| chr12:51376355 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.664+840G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376355 | |||||||
| chr12:51376361 | C | T | 1 | a0001c0001t0055g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.664+834G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376361 | |||||||
| chr12:51376543 | G | A | 10 | a0001c0001t0004g0034 a0001c0001t0015g0228 a0001c0001t0015g0229 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.664+652C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376543 | |||||||
| chr12:51376569 | G | A | 1 | a0001c0001t0055g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.664+626C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376569 | |||||||
| chr12:51376633 | C | CA | 9 | a0001c0001t0003g0368 a0001c0001t0006g0201 a0001c0001t0014g0104 others(6): Show |
9 | HG00544.hp1 HG01928.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.664+561dupT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376633 | |||||||
| chr12:51376633 | CA | C | 249 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(246): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.664+561delT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376633 | |||||||
| chr12:51376821 | T | C | 1 | a0001c0001t0066g0197 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.664+374A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376821 | |||||||
| chr12:51376864 | G | A | 1 | a0001c0002t0003g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.664+331C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51376864 | |||||||
| chr12:51377143 | T | G | 1 | a0001c0003t0004g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.664+52A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 4/11 | chr12 | 51377143 | |||||||
| chr12:51377430 | G | A | 1 | a0001c0003t0004g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.492-63C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377430 | |||||||
| chr12:51377646 | C | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0281 others(45): Show |
50 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.492-279G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377646 | |||||||
| chr12:51377657 | C | T | 1 | a0001c0002t0010g0074 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.492-290G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377657 | |||||||
| chr12:51377857 | T | A | 28 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(25): Show |
29 | HG02129.hp2 NA18612.hp2 NA18941.hp2 others(26): Show |
intron_variant | MODIFIER | c.492-490A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377857 | |||||||
| chr12:51377954 | T | C | 1 | a0001c0003t0007g0407 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.492-587A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377954 | |||||||
| chr12:51377987 | ACT | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0321 |
3 | HG02572.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.492-622_492-621del others(2): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51377987 | |||||||
| chr12:51378277 | T | C | 1 | a0001c0001t0009g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.492-910A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378277 | |||||||
| chr12:51378461 | T | C | 29 | a0001c0001t0001g0303 a0001c0001t0004g0190 a0001c0001t0006g0032 others(26): Show |
30 | HG00423.hp2 HG00639.hp1 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.491+830A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378461 | |||||||
| chr12:51378498 | T | C | 51 | a0001c0002t0003g0237 a0001c0002t0003g0243 a0001c0002t0003g0248 others(48): Show |
52 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.491+793A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378498 | |||||||
| chr12:51378568 | T | C | 1 | a0010c0018t0015g0411 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491+723A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378568 | |||||||
| chr12:51378570 | ACG | A | 3 | a0001c0001t0033g0205 a0001c0001t0033g0318 a0001c0001t0090g0299 |
3 | HG03041.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.491+719_491+720del others(2): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378570 | |||||||
| chr12:51378572 | G | A | 6 | a0001c0001t0004g0034 a0001c0001t0015g0228 a0001c0001t0015g0229 others(3): Show |
6 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+719C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378572 | |||||||
| chr12:51378577 | C | A | 1 | a0010c0018t0015g0411 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491+714G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378577 | |||||||
| chr12:51378619 | A | G | 2 | a0001c0001t0032g0354 a0001c0001t0053g0023 |
2 | HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.491+672T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378619 | |||||||
| chr12:51378882 | A | ACCC | 19 | a0001c0001t0001g0303 a0001c0001t0004g0190 a0001c0001t0006g0032 others(16): Show |
19 | HG01167.hp1 HG02895.hp1 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.491+406_491+408dup others(3): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378882 | |||||||
| chr12:51378882 | A | ACCCC | 16 | a0001c0001t0006g0051 a0001c0001t0006g0064 a0001c0001t0006g0113 others(13): Show |
17 | HG00423.hp2 HG01243.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.491+405_491+408dup others(4): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378882 | |||||||
| chr12:51378882 | A | ACCCCC | 19 | a0001c0001t0008g0247 a0001c0001t0071g0242 a0001c0002t0003g0237 others(16): Show |
19 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.491+404_491+408dup others(5): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378882 | |||||||
| chr12:51378882 | A | ACCCCCC | 26 | a0001c0002t0003g0243 a0001c0002t0003g0260 a0001c0002t0003g0275 others(23): Show |
27 | HG00609.hp2 HG01928.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.491+403_491+408dup others(6): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378882 | |||||||
| chr12:51378884 | C | CG | 102 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0281 others(99): Show |
106 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.491+406_491+407ins others(1): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378884 | |||||||
| chr12:51378888 | C | T | 5 | a0001c0001t0032g0362 a0001c0001t0063g0083 a0001c0001t0064g0030 others(2): Show |
5 | HG02630.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.491+403G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378888 | |||||||
| chr12:51378890 | C | T | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(119): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.491+401G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378890 | |||||||
| chr12:51378891 | C | G | 63 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0281 others(60): Show |
66 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.491+400G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378891 | |||||||
| chr12:51378993 | C | T | 4 | a0001c0001t0014g0122 a0001c0001t0014g0155 a0001c0001t0014g0199 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+298G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51378993 | |||||||
| chr12:51379208 | C | G | 1 | a0010c0018t0015g0411 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491+83G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51379208 | |||||||
| chr12:51379284 | T | C | 1 | a0001c0001t0081g0254 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.491+7A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 3/11 | chr12 | 51379284 | |||||||
| chr12:51379908 | G | A | 1 | a0002c0004t0030g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-103-24C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51379908 | |||||||
| chr12:51380024 | C | T | 2 | a0001c0001t0018g0291 a0001c0001t0021g0168 |
2 | HG00544.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-103-140G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380024 | |||||||
| chr12:51380048 | C | T | 27 | a0001c0001t0002g0087 a0001c0001t0005g0210 a0001c0001t0005g0278 others(24): Show |
28 | HG02129.hp2 NA18612.hp2 NA18941.hp2 others(25): Show |
intron_variant | MODIFIER | c.-103-164G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380048 | |||||||
| chr12:51380138 | T | G | 1 | a0001c0001t0012g0101 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-103-254A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380138 | |||||||
| chr12:51380270 | C | G | 46 | a0001c0001t0001g0303 a0001c0001t0001g0381 a0001c0001t0004g0128 others(43): Show |
50 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-103-386G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380270 | |||||||
| chr12:51380302 | C | G | 1 | a0009c0010t0076g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-103-418G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380302 | |||||||
| chr12:51380350 | T | C | 141 | a0001c0001t0001g0303 a0001c0001t0001g0322 a0001c0001t0001g0381 others(138): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-103-466A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380350 | |||||||
| chr12:51380387 | C | T | 28 | a0001c0001t0005g0210 a0001c0001t0005g0278 a0001c0001t0008g0219 others(25): Show |
29 | HG01433.hp1 HG01496.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.-103-503G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380387 | |||||||
| chr12:51380514 | T | C | 148 | a0001c0001t0001g0322 a0001c0001t0002g0019 a0001c0001t0002g0027 others(145): Show |
152 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-103-630A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380514 | |||||||
| chr12:51380534 | A | G | 1 | a0001c0001t0087g0356 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-103-650T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380534 | |||||||
| chr12:51380657 | A | G | 3 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0379 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-103-773T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380657 | |||||||
| chr12:51380664 | G | A | 37 | a0001c0001t0002g0203 a0001c0001t0004g0034 a0001c0001t0005g0210 others(34): Show |
37 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.-103-780C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380664 | |||||||
| chr12:51380703 | G | A | 285 | a0001c0001t0001g0012 a0001c0001t0001g0281 a0001c0001t0001g0282 others(282): Show |
291 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(288): Show |
intron_variant | MODIFIER | c.-103-819C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380703 | |||||||
| chr12:51380869 | T | G | 387 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(384): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.-103-985A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380869 | |||||||
| chr12:51380911 | C | T | 243 | a0001c0001t0001g0293 a0001c0001t0001g0303 a0001c0001t0001g0321 others(240): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-103-1027G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380911 | |||||||
| chr12:51380981 | G | A | 32 | a0001c0001t0001g0304 a0001c0001t0001g0333 a0001c0001t0001g0359 others(29): Show |
34 | HG00597.hp2 HG00673.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.-103-1097C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51380981 | |||||||
| chr12:51381024 | G | A | 3 | a0001c0002t0003g0280 a0001c0002t0010g0079 a0001c0002t0010g0185 |
3 | NA18985.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-103-1140C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381024 | |||||||
| chr12:51381054 | C | T | 2 | a0001c0001t0005g0002 a0001c0001t0005g0211 |
4 | NA18947.hp2 NA18966.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-1170G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381054 | |||||||
| chr12:51381055 | G | A | 1 | a0001c0006t0028g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-1171C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381055 | |||||||
| chr12:51381175 | G | C | 1 | a0001c0001t0008g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-103-1291C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381175 | |||||||
| chr12:51381218 | C | T | 1 | a0001c0001t0009g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-103-1334G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381218 | |||||||
| chr12:51381244 | T | A | 1 | a0001c0003t0004g0191 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-103-1360A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381244 | |||||||
| chr12:51381256 | A | G | 2 | a0001c0001t0001g0012 a0003c0005t0002g0020 |
3 | HG02896.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-103-1372T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381256 | |||||||
| chr12:51381379 | G | A | 1 | a0001c0002t0004g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-1495C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381379 | |||||||
| chr12:51381441 | C | T | 56 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0331 others(53): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.-103-1557G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381441 | |||||||
| chr12:51381492 | C | T | 177 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(174): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-103-1608G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381492 | |||||||
| chr12:51381534 | G | GT | 9 | a0001c0001t0001g0357 a0001c0001t0015g0320 a0001c0001t0023g0067 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-103-1651dupA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381534 | |||||||
| chr12:51381544 | T | C | 3 | a0001c0001t0005g0002 a0001c0001t0005g0211 a0001c0001t0005g0241 |
5 | NA18947.hp2 NA18951.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-1660A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381544 | |||||||
| chr12:51381698 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-1814C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381698 | |||||||
| chr12:51381729 | T | C | 1 | a0001c0001t0080g0366 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-103-1845A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381729 | |||||||
| chr12:51381906 | T | C | 2 | a0001c0001t0032g0354 a0001c0002t0025g0361 |
2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-103-2022A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381906 | |||||||
| chr12:51381957 | C | T | 2 | a0001c0001t0001g0404 a0001c0001t0038g0084 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-103-2073G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51381957 | |||||||
| chr12:51382018 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-103-2134C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382018 | |||||||
| chr12:51382036 | G | C | 346 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(343): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-103-2152C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382036 | |||||||
| chr12:51382039 | G | C | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-103-2155C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382039 | |||||||
| chr12:51382100 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-103-2216C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382100 | |||||||
| chr12:51382133 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.-103-2249T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382133 | |||||||
| chr12:51382233 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-103-2349C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382233 | |||||||
| chr12:51382311 | A | G | 1 | a0001c0001t0032g0362 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-103-2427T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382311 | |||||||
| chr12:51382360 | C | T | 15 | a0001c0001t0001g0344 a0001c0001t0001g0359 a0001c0001t0002g0102 others(12): Show |
15 | HG00408.hp1 HG00673.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103-2476G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382360 | |||||||
| chr12:51382374 | C | T | 15 | a0001c0001t0001g0344 a0001c0001t0001g0359 a0001c0001t0002g0102 others(12): Show |
15 | HG00408.hp1 HG00673.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103-2490G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382374 | |||||||
| chr12:51382447 | G | A | 1 | a0001c0001t0006g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-103-2563C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382447 | |||||||
| chr12:51382677 | G | A | 13 | a0001c0001t0001g0344 a0001c0001t0001g0359 a0001c0001t0002g0102 others(10): Show |
13 | HG00408.hp1 HG02055.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103-2793C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382677 | |||||||
| chr12:51382710 | A | C | 108 | a0001c0001t0001g0014 a0001c0001t0001g0234 a0001c0001t0001g0293 others(105): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103-2826T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382710 | |||||||
| chr12:51382788 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0341 |
3 | NA19003.hp1 NA19011.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-103-2904C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382788 | |||||||
| chr12:51382816 | G | A | 1 | a0001c0001t0006g0064 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-103-2932C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382816 | |||||||
| chr12:51382817 | A | G | 1 | a0001c0001t0006g0064 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-103-2933T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382817 | |||||||
| chr12:51382921 | T | C | 14 | a0001c0001t0001g0404 a0001c0001t0002g0025 a0001c0001t0002g0027 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-3037A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382921 | |||||||
| chr12:51382941 | C | T | 191 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0234 others(188): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-103-3057G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51382941 | |||||||
| chr12:51383151 | G | A | 1 | a0001c0001t0008g0251 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-103-3267C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383151 | |||||||
| chr12:51383329 | C | T | 1 | a0001c0003t0009g0326 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-103-3445G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383329 | |||||||
| chr12:51383330 | G | A | 4 | a0001c0001t0001g0359 a0001c0001t0008g0386 a0001c0001t0009g0360 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-3446C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383330 | |||||||
| chr12:51383344 | G | A | 218 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0234 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.-103-3460C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383344 | |||||||
| chr12:51383636 | C | T | 11 | a0001c0001t0001g0344 a0001c0001t0002g0102 a0001c0001t0002g0193 others(8): Show |
11 | HG00408.hp1 HG00673.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103-3752G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383636 | |||||||
| chr12:51383698 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103-3814T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383698 | |||||||
| chr12:51383851 | C | T | 258 | a0001c0001t0001g0014 a0001c0001t0001g0234 a0001c0001t0001g0281 others(255): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-103-3967G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383851 | |||||||
| chr12:51383912 | C | A | 1 | a0001c0001t0011g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-103-4028G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51383912 | |||||||
| chr12:51384083 | C | G | 2 | a0001c0001t0003g0368 a0003c0005t0002g0020 |
2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-103-4199G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384083 | |||||||
| chr12:51384134 | T | C | 12 | a0001c0001t0001g0344 a0001c0001t0002g0102 a0001c0001t0002g0193 others(9): Show |
12 | HG00408.hp1 HG00673.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103-4250A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384134 | |||||||
| chr12:51384217 | G | C | 66 | a0001c0001t0001g0244 a0001c0001t0001g0387 a0001c0001t0002g0120 others(63): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-103-4333C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384217 | |||||||
| chr12:51384456 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-103-4572G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384456 | |||||||
| chr12:51384529 | TA | T | 128 | a0001c0001t0001g0244 a0001c0001t0001g0281 a0001c0001t0001g0282 others(125): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-103-4646delT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384529 | |||||||
| chr12:51384537 | C | T | 113 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0327 others(110): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-103-4653G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384537 | |||||||
| chr12:51384561 | A | T | 78 | a0001c0001t0001g0234 a0001c0001t0001g0357 a0001c0001t0001g0359 others(75): Show |
82 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-103-4677T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384561 | |||||||
| chr12:51384562 | T | G | 232 | a0001c0001t0001g0012 a0001c0001t0001g0234 a0001c0001t0001g0244 others(229): Show |
239 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-103-4678A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384562 | |||||||
| chr12:51384651 | C | G | 11 | a0001c0001t0001g0321 a0001c0001t0002g0066 a0001c0001t0002g0069 others(8): Show |
11 | HG01346.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-4767G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384651 | |||||||
| chr12:51384691 | C | CA | 238 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0281 others(235): Show |
246 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-103-4808dupT | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384691 | |||||||
| chr12:51384691 | C | CAA | 41 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0380 others(38): Show |
42 | HG01175.hp1 HG01884.hp1 HG02145.hp2 others(39): Show |
intron_variant | MODIFIER | c.-103-4809_-103-480 others(6): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384691 | |||||||
| chr12:51384691 | C | CAAAA | 27 | a0001c0001t0001g0014 a0001c0001t0001g0408 a0001c0001t0002g0148 others(24): Show |
30 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.-103-4811_-103-480 others(8): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384691 | |||||||
| chr12:51384762 | G | A | 1 | a0001c0001t0011g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-103-4878C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384762 | |||||||
| chr12:51384767 | C | A | 10 | a0001c0001t0001g0321 a0001c0001t0002g0066 a0001c0001t0002g0068 others(7): Show |
10 | HG02109.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103-4883G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384767 | |||||||
| chr12:51384771 | G | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0380 a0001c0001t0001g0381 others(16): Show |
20 | HG01884.hp1 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103-4887C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384771 | |||||||
| chr12:51384823 | T | C | 135 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0331 others(132): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-103-4939A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384823 | |||||||
| chr12:51384909 | A | T | 6 | a0001c0001t0001g0404 a0001c0001t0033g0205 a0001c0001t0038g0084 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-5025T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384909 | |||||||
| chr12:51384915 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0063g0083 a0001c0003t0015g0288 others(2): Show |
6 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-5031G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384915 | |||||||
| chr12:51384917 | A | G | 1 | a0001c0002t0010g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-103-5033T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384917 | |||||||
| chr12:51384981 | GT | G | 3 | a0001c0001t0001g0404 a0001c0001t0038g0084 a0001c0001t0090g0299 |
3 | HG02145.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-103-5098delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51384981 | |||||||
| chr12:51385172 | G | C | 2 | a0001c0001t0020g0111 a0002c0004t0004g0110 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-5288C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51385172 | |||||||
| chr12:51385341 | C | T | 3 | a0001c0001t0007g0215 a0001c0001t0009g0216 a0001c0001t0009g0217 |
3 | NA18949.hp2 NA18959.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-103-5457G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51385341 | |||||||
| chr12:51385508 | C | T | 1 | a0001c0001t0008g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-104+5342G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51385508 | |||||||
| chr12:51385537 | C | T | 349 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(346): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-104+5313G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51385537 | |||||||
| chr12:51385760 | AG | A | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0380 others(133): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-104+5089delC | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51385760 | |||||||
| chr12:51386165 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0387 a0001c0001t0008g0386 others(3): Show |
7 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-104+4685C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386165 | |||||||
| chr12:51386318 | T | C | 1 | a0001c0001t0088g0389 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-104+4532A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386318 | |||||||
| chr12:51386352 | G | GC | 102 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0244 others(99): Show |
107 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-104+4497dupG | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386352 | |||||||
| chr12:51386355 | T | C | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+4495A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386355 | |||||||
| chr12:51386398 | C | T | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+4452G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386398 | |||||||
| chr12:51386399 | T | C | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+4451A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386399 | |||||||
| chr12:51386434 | A | G | 1 | a0001c0001t0013g0117 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-104+4416T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386434 | |||||||
| chr12:51386768 | G | A | 1 | a0001c0001t0003g0368 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-104+4082C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386768 | |||||||
| chr12:51386789 | T | G | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+4061A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386789 | |||||||
| chr12:51386852 | C | T | 94 | a0001c0001t0002g0005 a0001c0001t0002g0112 a0001c0001t0002g0120 others(91): Show |
99 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-104+3998G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51386852 | |||||||
| chr12:51387018 | C | T | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+3832G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387018 | |||||||
| chr12:51387021 | A | G | 1 | a0001c0001t0008g0212 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-104+3829T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387021 | |||||||
| chr12:51387098 | C | T | 1 | a0001c0001t0011g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-104+3752G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387098 | |||||||
| chr12:51387105 | T | A | 4 | a0001c0001t0001g0321 a0001c0001t0015g0320 a0001c0001t0033g0318 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+3745A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387105 | |||||||
| chr12:51387183 | C | T | 1 | a0001c0001t0006g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-104+3667G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387183 | |||||||
| chr12:51387296 | C | T | 2 | a0001c0001t0006g0113 a0001c0001t0006g0114 |
2 | NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-104+3554G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387296 | |||||||
| chr12:51387746 | C | T | 2 | a0001c0001t0002g0019 a0001c0003t0004g0018 |
2 | NA18964.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-104+3104G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387746 | |||||||
| chr12:51387761 | G | A | 4 | a0001c0001t0001g0321 a0001c0001t0015g0320 a0001c0001t0033g0318 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+3089C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387761 | |||||||
| chr12:51387970 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0404 others(16): Show |
21 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-104+2880G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51387970 | |||||||
| chr12:51388286 | G | C | 74 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0025 others(71): Show |
76 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.-104+2564C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388286 | |||||||
| chr12:51388376 | G | A | 1 | a0001c0001t0006g0201 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-104+2474C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388376 | |||||||
| chr12:51388434 | G | A | 1 | a0001c0002t0010g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-104+2416C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388434 | |||||||
| chr12:51388497 | T | G | 47 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0357 others(44): Show |
49 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.-104+2353A>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388497 | |||||||
| chr12:51388691 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-104+2159G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388691 | |||||||
| chr12:51388793 | T | A | 1 | a0001c0001t0007g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-104+2057A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51388793 | |||||||
| chr12:51389191 | A | T | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+1659T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389191 | |||||||
| chr12:51389330 | A | G | 1 | a0001c0001t0033g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-104+1520T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389330 | |||||||
| chr12:51389378 | C | T | 1 | a0001c0003t0077g0394 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104+1472G>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389378 | |||||||
| chr12:51389523 | G | A | 1 | a0009c0010t0076g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-104+1327C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389523 | |||||||
| chr12:51389574 | G | A | 1 | a0001c0001t0005g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-104+1276C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389574 | |||||||
| chr12:51389636 | T | A | 97 | a0001c0001t0002g0005 a0001c0001t0002g0112 a0001c0001t0002g0120 others(94): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-104+1214A>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389636 | |||||||
| chr12:51389641 | G | A | 23 | a0001c0001t0001g0357 a0001c0001t0001g0359 a0001c0001t0001g0363 others(20): Show |
23 | HG01346.hp1 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-104+1209C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389641 | |||||||
| chr12:51389818 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+1032C>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389818 | |||||||
| chr12:51389877 | A | G | 338 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0230 others(335): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-104+973T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51389877 | |||||||
| chr12:51390021 | C | G | 32 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0331 others(29): Show |
33 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-104+829G>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390021 | |||||||
| chr12:51390079 | G | A | 101 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0244 others(98): Show |
105 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-104+771C>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390079 | |||||||
| chr12:51390115 | A | C | 1 | a0001c0001t0001g0322 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-104+735T>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390115 | |||||||
| chr12:51390136 | A | ATTTC | 92 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0244 others(89): Show |
96 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-104+710_-104+713d others(6): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390136 | |||||||
| chr12:51390156 | C | CT | 17 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0005g0301 others(14): Show |
17 | HG00621.hp2 HG00642.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-104+693dupA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390156 | |||||||
| chr12:51390156 | C | CTTTCT | 7 | a0001c0001t0002g0203 a0001c0001t0005g0210 a0001c0001t0005g0211 others(4): Show |
7 | HG01891.hp1 HG02074.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-104+693_-104+694i others(7): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390156 | |||||||
| chr12:51390156 | CT | C | 5 | a0001c0001t0001g0012 a0001c0001t0005g0392 a0001c0001t0016g0390 others(2): Show |
6 | HG00280.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104+693delA | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390156 | |||||||
| chr12:51390156 | CTTTTTTT others(1): Show |
C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0404 others(16): Show |
21 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-104+686_-104+693d others(10): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390156 | |||||||
| chr12:51390157 | T | TTTC | 30 | a0001c0001t0001g0293 a0001c0001t0001g0357 a0001c0001t0001g0359 others(27): Show |
30 | HG01346.hp1 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-104+692_-104+693i others(5): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390157 | |||||||
| chr12:51390158 | T | TTCTTTC | 164 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0025 others(161): Show |
169 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-104+691_-104+692i others(8): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390158 | |||||||
| chr12:51390158 | T | TTCTTTCT others(3): Show |
5 | a0001c0001t0002g0068 a0001c0001t0012g0189 a0001c0001t0023g0067 others(2): Show |
5 | HG02109.hp1 HG03139.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+691_-104+692i others(12): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390158 | |||||||
| chr12:51390158 | T | TTCTTTCT others(7): Show |
2 | a0001c0001t0002g0022 a0001c0002t0004g0063 |
2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-104+691_-104+692i others(16): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390158 | |||||||
| chr12:51390159 | T | TCTTTC | 17 | a0001c0001t0002g0148 a0001c0001t0002g0200 a0001c0001t0004g0008 others(14): Show |
18 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+690_-104+691i others(7): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390159 | |||||||
| chr12:51390160 | T | C | 7 | a0001c0001t0001g0331 a0001c0003t0007g0412 a0001c0006t0019g0377 others(4): Show |
7 | HG00741.hp1 HG01256.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-104+690A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390160 | |||||||
| chr12:51390162 | T | C | 2 | a0001c0002t0010g0079 a0012c0015t0006g0163 |
2 | NA19054.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-104+688A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390162 | |||||||
| chr12:51390168 | T | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0404 others(16): Show |
21 | HG00280.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-104+682A>G | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390168 | |||||||
| chr12:51390218 | A | T | 102 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0244 others(99): Show |
106 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-104+632T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390218 | |||||||
| chr12:51390262 | A | G | 1 | a0001c0001t0033g0205 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-104+588T>C | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390262 | |||||||
| chr12:51390324 | G | T | 1 | a0001c0001t0022g0017 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-104+526C>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390324 | |||||||
| chr12:51390475 | A | T | 1 | a0001c0001t0009g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-104+375T>A | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390475 | |||||||
| chr12:51390724 | GCA | G | 193 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0022 others(190): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-104+124_-104+125d others(4): Show |
GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 2/11 | chr12 | 51390724 | |||||||
| chr12:51390980 | C | A | 1 | a0001c0003t0007g0412 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-191-43G>T | GALNT6 | ENSG00000139629.16 | transcript | ENST00000356317.8 | protein_coding | 1/11 | chr12 | 51390980 |