Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9331 |
| ensemblid | ENSG00000118276.12 |
| hgncid | 929 |
| symbol | B4GALT6 |
| name | beta-1,4-galactosyltransferase 6 |
| refseq_nuc | NM_004775.5 |
| refseq_prot | NP_004766.2 |
| ensembl_nuc | ENST00000306851.10 |
| ensembl_prot | ENSP00000306459.5 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 31622246 |
| end | 31684581 |
| strand | - |
| ver | v1.2 |
| region | chr18:31622246-31684581 |
| region5000 | chr18:31617246-31689581 |
| regionname0 | B4GALT6_chr18_31622246_31684581 |
| regionname5000 | B4GALT6_chr18_31617246_31689581 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 382 | 298 | 73 | 57 | 132 | 10 | 24 | 96 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | MSVLR others(377): Show |
chr18 | 31617246 | 31689581 |
| a0002 | 0/0 | 382 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | MSVLR others(377): Show |
chr18 | 31617246 | 31689581 |
| a0003 | 0/0 | 382 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | MSVLR others(377): Show |
chr18 | 31617246 | 31689581 |
| a0004 | 0/0 | 382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | MSVLR others(377): Show |
chr18 | 31617246 | 31689581 |
| a0005 | 0/0 | 382 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | MSVLR others(377): Show |
chr18 | 31617246 | 31689581 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1146 | 296 | 71 | 57 | 132 | 10 | 24 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0001c0003 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0001c0005 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0002c0002 | 0/0 | 1146 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0003c0004 | 0/0 | 1146 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0004c0007 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 | ||
| a0005c0006 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | ATGTC others(1141): Show |
chr18 | 31617246 | 31689581 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4672 | 96 | 5 | 19 | 59 | 4 | 7 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0002 | 0/0 | 4672 | 66 | 10 | 9 | 38 | 3 | 6 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0003 | 0/0 | 4672 | 23 | 6 | 7 | 3 | 2 | 5 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0004 | 0/0 | 4672 | 15 | 0 | 3 | 11 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0005 | 0/0 | 4672 | 13 | 11 | 1 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0006 | 0/0 | 4672 | 14 | 0 | 8 | 6 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0007 | 0/0 | 4672 | 10 | 8 | 2 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0008 | 0/0 | 4672 | 11 | 10 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0009 | 0/0 | 4672 | 11 | 0 | 6 | 3 | 1 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0010 | 0/0 | 4672 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0011 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0012 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0013 | 0/0 | 4672 | 2 | 1 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0014 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0015 | 0/0 | 4672 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0016 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0017 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0018 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0019 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0020 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0022 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0023 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0024 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0025 | 0/0 | 4672 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0026 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0027 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0028 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0029 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0031 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0033 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0034 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0035 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0036 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0037 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0001t0038 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0003t0021 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0001c0005t0007 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0002c0002t0003 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0002c0002t0005 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0002c0002t0032 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0003c0004t0030 | 0/0 | 4672 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0004c0007t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| a0005c0006t0002 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | CTCTT others(4667): Show |
chr18 | 31617246 | 31689581 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0001g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0009g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0010g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0012g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0014g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0016g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0016g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0017g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0019g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0020g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0022g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0023g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0024g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0025g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0026g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0027g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0028g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0029g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0031g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0033g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0034g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0035g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0036g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0037g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0001t0038g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0003t0021g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0001c0005t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0002c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0002c0002t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0002c0002t0032g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0003c0004t0030g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0004c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| a0005c0006t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | FIN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | FIN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0102 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01074 | hp2 | a0001 | c0001 | t0025 | g0128 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0209 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0174 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0173 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0103 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01361 | hp1 | a0001 | c0001 | t0009 | g0256 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01496 | hp2 | a0003 | c0004 | t0030 | g0205 | AMR | CLM | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | IBS | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01884 | hp2 | a0001 | c0003 | t0021 | g0068 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0106 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0047 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02015 | hp1 | a0001 | c0001 | t0038 | g0285 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0170 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02027 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02055 | hp1 | a0001 | c0005 | t0007 | g0167 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | CDX | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CDX | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0247 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0281 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0220 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02280 | hp2 | a0001 | c0001 | t0015 | g0067 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0275 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0240 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02630 | hp1 | a0001 | c0001 | t0031 | g0171 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0237 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0069 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0016 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0279 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02809 | hp1 | a0002 | c0002 | t0005 | g0278 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0216 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0276 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0280 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0071 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0015 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03209 | hp2 | a0001 | c0001 | t0022 | g0252 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0222 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0224 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03453 | hp1 | a0001 | c0001 | t0023 | g0070 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0218 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03492 | hp2 | a0001 | c0001 | t0037 | g0284 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03540 | hp1 | a0004 | c0007 | t0001 | g0282 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03540 | hp2 | a0005 | c0006 | t0002 | g0039 | AFR | GWD | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03831 | hp1 | a0001 | c0001 | t0027 | g0043 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0194 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0214 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04204 | hp1 | a0001 | c0001 | t0033 | g0165 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04204 | hp2 | a0001 | c0001 | t0019 | g0021 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | STU | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | YRI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | YRI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | CHB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18747 | hp2 | a0001 | c0001 | t0026 | g0108 | EAS | CHB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18943 | hp2 | a0001 | c0001 | t0035 | g0243 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18953 | hp2 | a0001 | c0001 | t0014 | g0144 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18973 | hp2 | a0001 | c0001 | t0036 | g0283 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18986 | hp2 | a0001 | c0001 | t0016 | g0287 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18999 | hp2 | a0001 | c0001 | t0009 | g0157 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19005 | hp2 | a0001 | c0001 | t0016 | g0286 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19009 | hp2 | a0001 | c0001 | t0014 | g0143 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0272 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19043 | hp1 | a0001 | c0001 | t0028 | g0229 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19058 | hp2 | a0001 | c0001 | t0034 | g0085 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19085 | hp2 | a0001 | c0001 | t0020 | g0020 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19089 | hp1 | a0001 | c0001 | t0009 | g0064 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0019 | AFR | YRI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0186 | AFR | YRI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20129 | hp1 | a0001 | c0001 | t0029 | g0107 | AFR | ASW | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ASW | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | TSI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20805 | hp1 | a0001 | c0001 | t0009 | g0213 | EUR | TSI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03471 | hp1 | a0002 | c0002 | t0032 | g0277 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0266 | AFR | MSL | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0246 | AFR | USA | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | USA | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0219 | AFR | LWK | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0265 | REF | REF | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0046 | REF | REF | B4GALT6_chr18_31617246_31689581 | B4GALT6 | chr18 | 31617246 | 31689581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31622247 | C | A | 1 | a0001 | 1 | HG02723.hp1 | splice_region_variant | LOW | c.*3367G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | chr18 | 31622247 | |||||||
| chr18:31625628 | T | C | 1 | a0003 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1135A>G | p.Ile379Val | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1290/4672 | 1135/1149 | 379/382 | chr18 | 31625628 | |||
| chr18:31638730 | G | A | 1 | a0005 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.502C>T | p.His168Tyr | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/9 | 657/4672 | 502/1149 | 168/382 | chr18 | 31638730 | |||
| chr18:31684333 | T | C | 1 | a0002 | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.94A>G | p.Ile32Val | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 249/4672 | 94/1149 | 32/382 | chr18 | 31684333 | |||
| chr18:31684384 | G | A | 1 | a0004 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.43C>T | p.Leu15Phe | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 198/4672 | 43/1149 | 15/382 | chr18 | 31684384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31626324 | T | C | 1 | a0001c0005 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.960A>G | p.Ser320Ser | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/9 | 1115/4672 | 960/1149 | 320/382 | chr18 | 31626324 | |||
| chr18:31631066 | A | G | 1 | a0001c0003 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.669T>C | p.Cys223Cys | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/9 | 824/4672 | 669/1149 | 223/382 | chr18 | 31631066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31622432 | T | C | 1 | a0001c0001t0013 | 2 | HG02015.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3182A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 3182 | chr18 | 31622432 | ||||||
| chr18:31622655 | G | A | 1 | a0001c0001t0010 | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2959C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2959 | chr18 | 31622655 | ||||||
| chr18:31622678 | A | C | 1 | a0001c0001t0024 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2936T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2936 | chr18 | 31622678 | ||||||
| chr18:31622867 | C | A | 1 | a0001c0001t0034 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2747G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2747 | chr18 | 31622867 | ||||||
| chr18:31622887 | T | C | 1 | a0001c0001t0026 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2727 | chr18 | 31622887 | ||||||
| chr18:31622962 | T | C | 1 | a0001c0001t0031 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2652A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2652 | chr18 | 31622962 | ||||||
| chr18:31622988 | G | C | 1 | a0001c0001t0006 | 14 | HG01074.hp1 HG01081.hp1 HG01934.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2626C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2626 | chr18 | 31622988 | ||||||
| chr18:31622995 | A | T | 1 | a0001c0001t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2619T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2619 | chr18 | 31622995 | ||||||
| chr18:31623008 | T | C | 1 | a0001c0003t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2606A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2606 | chr18 | 31623008 | ||||||
| chr18:31623140 | G | A | 1 | a0001c0001t0035 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2474C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2474 | chr18 | 31623140 | ||||||
| chr18:31623314 | C | T | 1 | a0001c0001t0025 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2300G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2300 | chr18 | 31623314 | ||||||
| chr18:31623422 | T | G | 6 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0037 others(3): Show |
31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2192A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2192 | chr18 | 31623422 | ||||||
| chr18:31623572 | T | G | 2 | a0001c0001t0009 a0001c0001t0015 |
13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2042A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 2042 | chr18 | 31623572 | ||||||
| chr18:31623645 | T | C | 1 | a0001c0001t0014 | 2 | NA18953.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1969A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1969 | chr18 | 31623645 | ||||||
| chr18:31623922 | T | A | 1 | a0001c0001t0027 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1692A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1692 | chr18 | 31623922 | ||||||
| chr18:31624135 | T | C | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(12): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1479A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1479 | chr18 | 31624135 | ||||||
| chr18:31624157 | A | G | 1 | a0001c0001t0022 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1457T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1457 | chr18 | 31624157 | ||||||
| chr18:31624205 | T | C | 1 | a0001c0001t0029 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1409A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1409 | chr18 | 31624205 | ||||||
| chr18:31624247 | C | T | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1367G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1367 | chr18 | 31624247 | ||||||
| chr18:31624513 | T | G | 1 | a0003c0004t0030 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1101A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1101 | chr18 | 31624513 | ||||||
| chr18:31624612 | T | C | 4 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0031 others(1): Show |
16 | HG01243.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1002A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 1002 | chr18 | 31624612 | ||||||
| chr18:31624799 | A | G | 1 | a0001c0001t0004 | 15 | HG01099.hp2 HG01496.hp1 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*815T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 815 | chr18 | 31624799 | ||||||
| chr18:31624926 | T | C | 1 | a0001c0001t0033 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*688A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 688 | chr18 | 31624926 | ||||||
| chr18:31625037 | G | A | 1 | a0001c0001t0016 | 2 | NA18986.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*577C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 577 | chr18 | 31625037 | ||||||
| chr18:31625178 | G | A | 1 | a0001c0001t0004 | 15 | HG01099.hp2 HG01496.hp1 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*436C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 436 | chr18 | 31625178 | ||||||
| chr18:31625293 | C | T | 2 | a0001c0001t0012 a0001c0003t0021 |
4 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 321 | chr18 | 31625293 | ||||||
| chr18:31625396 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(7): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*218C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 9/9 | 218 | chr18 | 31625396 | ||||||
| chr18:31684445 | C | A | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG04204.hp2 NA19085.hp2 |
5_prime_UTR_variant | MODIFIER | c.-19G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 19 | chr18 | 31684445 | ||||||
| chr18:31684504 | T | C | 1 | a0001c0001t0036 | 1 | NA18973.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | chr18 | 31684504 | |||||||
| chr18:31684535 | G | T | 2 | a0001c0001t0019 a0001c0001t0020 |
2 | HG04204.hp2 NA19085.hp2 |
5_prime_UTR_variant | MODIFIER | c.-109C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 109 | chr18 | 31684535 | ||||||
| chr18:31684540 | C | A | 1 | a0001c0001t0037 | 1 | HG03492.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-114G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | chr18 | 31684540 | |||||||
| chr18:31684563 | G | C | 2 | a0001c0001t0016 a0001c0001t0038 |
3 | HG02015.hp1 NA18986.hp2 NA19005.hp2 |
5_prime_UTR_variant | MODIFIER | c.-137C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 137 | chr18 | 31684563 | ||||||
| chr18:31684572 | C | G | 3 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0018 |
5 | HG02723.hp1 HG03098.hp2 NA18522.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-146G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/9 | 146 | chr18 | 31684572 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:31625795 | A | G | 11 | a0001c0001t0005g0014 a0001c0001t0005g0169 a0001c0001t0005g0183 others(8): Show |
12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002-34T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31625795 | |||||||
| chr18:31625854 | A | G | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-93T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31625854 | |||||||
| chr18:31625969 | T | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | NA18979.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1002-208A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31625969 | |||||||
| chr18:31625971 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | NA18979.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1002-210G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31625971 | |||||||
| chr18:31626023 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1001+260C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31626023 | |||||||
| chr18:31626066 | AATATGTG others(13): Show |
A | 1 | a0001c0001t0007g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1001+197_1001+216d others(22): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31626066 | |||||||
| chr18:31626113 | A | G | 1 | a0001c0001t0005g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1001+170T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31626113 | |||||||
| chr18:31626158 | A | G | 125 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(122): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1001+125T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 8/8 | chr18 | 31626158 | |||||||
| chr18:31626396 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.900-12A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626396 | |||||||
| chr18:31626399 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.900-15T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626399 | |||||||
| chr18:31626555 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.900-171C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626555 | |||||||
| chr18:31626593 | G | A | 31 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(28): Show |
31 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.900-209C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626593 | |||||||
| chr18:31626715 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0151 |
2 | NA18956.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.899+284C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626715 | |||||||
| chr18:31626800 | G | A | 28 | a0001c0001t0002g0031 a0001c0001t0002g0036 a0001c0001t0002g0040 others(25): Show |
28 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.899+199C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626800 | |||||||
| chr18:31626870 | C | T | 129 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(126): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.899+129G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 7/8 | chr18 | 31626870 | |||||||
| chr18:31627192 | C | T | 158 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(155): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.777-71G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627192 | |||||||
| chr18:31627194 | T | C | 1 | a0001c0001t0028g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.777-73A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627194 | |||||||
| chr18:31627218 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.777-97G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627218 | |||||||
| chr18:31627232 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.777-111A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627232 | |||||||
| chr18:31627263 | C | G | 16 | a0001c0001t0008g0042 a0001c0001t0008g0186 a0001c0001t0008g0218 others(13): Show |
16 | HG01243.hp2 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.777-142G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627263 | |||||||
| chr18:31627532 | T | G | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-411A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627532 | |||||||
| chr18:31627769 | G | A | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777-648C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627769 | |||||||
| chr18:31627891 | C | G | 1 | a0001c0001t0002g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.777-770G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31627891 | |||||||
| chr18:31628072 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0160 |
2 | HG03704.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.777-951A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628072 | |||||||
| chr18:31628098 | G | A | 1 | a0004c0007t0001g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.777-977C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628098 | |||||||
| chr18:31628128 | G | A | 1 | a0001c0001t0007g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.777-1007C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628128 | |||||||
| chr18:31628222 | T | C | 11 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0100 others(8): Show |
15 | HG01099.hp2 HG01496.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.777-1101A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628222 | |||||||
| chr18:31628414 | T | C | 2 | a0001c0001t0011g0017 a0001c0001t0011g0018 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.777-1293A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628414 | |||||||
| chr18:31628625 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.777-1504A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628625 | |||||||
| chr18:31628718 | A | G | 17 | a0001c0001t0007g0217 a0001c0001t0008g0042 a0001c0001t0008g0186 others(14): Show |
17 | HG01243.hp2 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.777-1597T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628718 | |||||||
| chr18:31628804 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.777-1683G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628804 | |||||||
| chr18:31628885 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | NA18952.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.777-1764T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628885 | |||||||
| chr18:31628981 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0199 |
2 | NA19054.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.777-1860G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31628981 | |||||||
| chr18:31629024 | G | A | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.777-1903C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629024 | |||||||
| chr18:31629039 | G | A | 2 | a0001c0001t0004g0011 a0001c0001t0004g0204 |
3 | HG01099.hp2 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.777-1918C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629039 | |||||||
| chr18:31629085 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.776+1874G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629085 | |||||||
| chr18:31629201 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.776+1758G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629201 | |||||||
| chr18:31629277 | C | T | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.776+1682G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629277 | |||||||
| chr18:31629447 | A | AT | 49 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0119 others(46): Show |
50 | HG00280.hp2 HG00438.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.776+1511dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | A | ATT | 21 | a0001c0001t0002g0048 a0001c0001t0002g0062 a0001c0001t0002g0063 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.776+1510_776+1511d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | A | ATTT | 20 | a0001c0001t0001g0113 a0001c0001t0002g0013 a0001c0001t0002g0032 others(17): Show |
22 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.776+1509_776+1511d others(5): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | A | ATTTT | 9 | a0001c0001t0001g0114 a0001c0001t0002g0037 a0001c0001t0002g0051 others(6): Show |
9 | HG02486.hp1 HG04184.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.776+1508_776+1511d others(6): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0004g0181 a0001c0001t0004g0255 |
2 | HG02165.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.776+1501_776+1511d others(13): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0123 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.776+1495_776+1511d others(19): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | AT | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(58): Show |
68 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.776+1511delA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATT | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0081 others(18): Show |
23 | HG00597.hp2 HG02004.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.776+1510_776+1511d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(1): Show |
A | 10 | a0001c0001t0007g0208 a0001c0001t0007g0217 a0001c0001t0008g0186 others(7): Show |
10 | HG01243.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+1504_776+1511d others(10): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(2): Show |
A | 15 | a0001c0001t0003g0155 a0001c0001t0008g0042 a0001c0001t0008g0218 others(12): Show |
15 | HG01361.hp2 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.776+1503_776+1511d others(11): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0005g0185 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.776+1502_776+1511d others(12): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0005g0169 a0001c0001t0005g0183 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.776+1501_776+1511d others(13): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0258 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.776+1500_776+1511d others(14): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.776+1499_776+1511d others(15): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0013g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.776+1498_776+1511d others(16): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0007g0035 a0001c0001t0013g0170 |
2 | HG02015.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.776+1497_776+1511d others(17): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629447 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.776+1496_776+1511d others(18): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629447 | |||||||
| chr18:31629576 | A | G | 3 | a0001c0001t0010g0009 a0001c0001t0010g0275 a0001c0001t0010g0276 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+1383T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629576 | |||||||
| chr18:31629616 | G | A | 1 | a0001c0001t0038g0285 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.776+1343C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629616 | |||||||
| chr18:31629646 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0131 |
2 | NA18965.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.776+1313T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629646 | |||||||
| chr18:31629651 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0131 |
2 | NA18965.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.776+1308A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629651 | |||||||
| chr18:31629655 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0131 |
2 | NA18965.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.776+1304A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629655 | |||||||
| chr18:31629657 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.776+1302C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629657 | |||||||
| chr18:31629659 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.776+1300G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629659 | |||||||
| chr18:31629713 | G | T | 1 | a0001c0001t0017g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.776+1246C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629713 | |||||||
| chr18:31629829 | G | A | 3 | a0001c0001t0008g0221 a0001c0001t0008g0222 a0001c0001t0008g0225 |
3 | HG03209.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.776+1130C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629829 | |||||||
| chr18:31629830 | A | T | 2 | a0001c0001t0008g0218 a0001c0001t0031g0171 |
2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.776+1129T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629830 | |||||||
| chr18:31629849 | C | CA | 9 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0151 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.776+1109dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31629849 | |||||||
| chr18:31630078 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.776+881G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630078 | |||||||
| chr18:31630163 | A | G | 10 | a0001c0001t0001g0045 a0001c0001t0001g0089 a0001c0001t0001g0090 others(7): Show |
10 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+796T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630163 | |||||||
| chr18:31630253 | C | T | 4 | a0001c0001t0012g0069 a0001c0001t0012g0216 a0001c0001t0012g0219 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+706G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630253 | |||||||
| chr18:31630292 | C | A | 1 | a0001c0001t0008g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.776+667G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630292 | |||||||
| chr18:31630294 | A | G | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+665T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630294 | |||||||
| chr18:31630348 | A | G | 3 | a0001c0001t0007g0035 a0001c0001t0013g0170 a0001c0001t0013g0272 |
3 | HG02015.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.776+611T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630348 | |||||||
| chr18:31630417 | G | GT | 130 | a0001c0001t0001g0139 a0001c0001t0002g0013 a0001c0001t0002g0031 others(127): Show |
138 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.776+541dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630417 | |||||||
| chr18:31630427 | T | A | 2 | a0001c0001t0013g0272 a0001c0001t0024g0071 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.776+532A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630427 | |||||||
| chr18:31630888 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.776+71C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630888 | |||||||
| chr18:31630927 | G | A | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0005t0007g0167 |
3 | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.776+32C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 6/8 | chr18 | 31630927 | |||||||
| chr18:31631200 | C | CT | 136 | a0001c0001t0001g0146 a0001c0001t0001g0192 a0001c0001t0002g0013 others(133): Show |
145 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.589-55dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631200 | |||||||
| chr18:31631200 | C | CTT | 51 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0003g0030 others(48): Show |
51 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.589-56_589-55dupAA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631200 | |||||||
| chr18:31631342 | G | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.589-196C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631342 | |||||||
| chr18:31631353 | C | T | 127 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(124): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.589-207G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631353 | |||||||
| chr18:31631467 | A | G | 4 | a0001c0001t0012g0069 a0001c0001t0012g0216 a0001c0001t0012g0219 others(1): Show |
4 | HG01884.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-321T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631467 | |||||||
| chr18:31631642 | A | G | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0215 |
3 | HG00735.hp2 HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.589-496T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631642 | |||||||
| chr18:31631675 | C | T | 1 | a0001c0001t0010g0276 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.589-529G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631675 | |||||||
| chr18:31631921 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.589-775T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31631921 | |||||||
| chr18:31632271 | A | G | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.589-1125T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632271 | |||||||
| chr18:31632631 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.589-1485C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632631 | |||||||
| chr18:31632764 | A | G | 157 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(154): Show |
165 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.589-1618T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632764 | |||||||
| chr18:31632845 | T | C | 3 | a0001c0001t0010g0009 a0001c0001t0010g0275 a0001c0001t0010g0276 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-1699A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632845 | |||||||
| chr18:31632963 | C | T | 129 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(126): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.589-1817G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632963 | |||||||
| chr18:31632976 | C | T | 2 | a0001c0001t0007g0173 a0001c0001t0007g0174 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.589-1830G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31632976 | |||||||
| chr18:31633128 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.589-1982G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633128 | |||||||
| chr18:31633129 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.589-1983T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633129 | |||||||
| chr18:31633157 | A | C | 2 | a0001c0001t0003g0153 a0001c0001t0003g0154 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.589-2011T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633157 | |||||||
| chr18:31633302 | A | T | 189 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(186): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.589-2156T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633302 | |||||||
| chr18:31633753 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.589-2607A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633753 | |||||||
| chr18:31633877 | A | T | 1 | a0001c0001t0007g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.589-2731T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633877 | |||||||
| chr18:31633889 | C | T | 1 | a0001c0001t0005g0274 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.589-2743G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633889 | |||||||
| chr18:31633944 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.589-2798A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633944 | |||||||
| chr18:31633990 | G | C | 4 | a0001c0001t0003g0061 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.589-2844C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31633990 | |||||||
| chr18:31634152 | G | A | 128 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(125): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.589-3006C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634152 | |||||||
| chr18:31634192 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.589-3046G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634192 | |||||||
| chr18:31634309 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.589-3163C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634309 | |||||||
| chr18:31634342 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.589-3196C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634342 | |||||||
| chr18:31634497 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.589-3351T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634497 | |||||||
| chr18:31634593 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.589-3447A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634593 | |||||||
| chr18:31634632 | T | C | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.589-3486A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634632 | |||||||
| chr18:31634674 | T | C | 129 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(126): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.589-3528A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634674 | |||||||
| chr18:31634811 | T | C | 1 | a0001c0001t0004g0194 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.589-3665A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31634811 | |||||||
| chr18:31635250 | A | C | 190 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0001g0082 others(187): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.588+3394T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635250 | |||||||
| chr18:31635251 | A | C | 1 | a0001c0001t0002g0260 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.588+3393T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635251 | |||||||
| chr18:31635254 | A | C | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG00738.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.588+3390T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635254 | |||||||
| chr18:31635301 | T | C | 1 | a0001c0001t0017g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.588+3343A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635301 | |||||||
| chr18:31635561 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.588+3083A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635561 | |||||||
| chr18:31635655 | G | A | 26 | a0001c0001t0007g0035 a0001c0001t0007g0208 a0001c0001t0007g0217 others(23): Show |
26 | HG01243.hp2 HG01884.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.588+2989C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635655 | |||||||
| chr18:31635711 | G | A | 1 | a0001c0005t0007g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.588+2933C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635711 | |||||||
| chr18:31635772 | C | T | 3 | a0001c0001t0007g0035 a0001c0001t0013g0170 a0001c0001t0013g0272 |
3 | HG02015.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.588+2872G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31635772 | |||||||
| chr18:31636099 | G | T | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+2545C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636099 | |||||||
| chr18:31636194 | T | C | 192 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(189): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.588+2450A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636194 | |||||||
| chr18:31636277 | C | T | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2367G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636277 | |||||||
| chr18:31636351 | T | G | 1 | a0003c0004t0030g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+2293A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636351 | |||||||
| chr18:31636360 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+2284A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636360 | |||||||
| chr18:31636513 | C | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0115 a0001c0001t0002g0116 |
3 | HG01891.hp2 HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.588+2131G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636513 | |||||||
| chr18:31636545 | T | C | 4 | a0001c0001t0007g0035 a0001c0001t0007g0208 a0001c0001t0013g0170 others(1): Show |
4 | HG02015.hp2 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2099A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636545 | |||||||
| chr18:31636769 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.588+1875G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636769 | |||||||
| chr18:31636861 | G | A | 1 | a0001c0001t0010g0009 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.588+1783C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636861 | |||||||
| chr18:31636874 | C | T | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.588+1770G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636874 | |||||||
| chr18:31636982 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | NA18985.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.588+1662C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31636982 | |||||||
| chr18:31637237 | T | C | 6 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(3): Show |
6 | HG02132.hp1 NA18942.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.588+1407A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637237 | |||||||
| chr18:31637267 | C | CT | 204 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0089 others(201): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.588+1376dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637267 | |||||||
| chr18:31637390 | C | CT | 34 | a0001c0001t0001g0125 a0001c0001t0003g0030 a0001c0001t0003g0061 others(31): Show |
34 | HG00280.hp1 HG01071.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.588+1253dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637390 | |||||||
| chr18:31637400 | T | C | 2 | a0001c0001t0009g0209 a0001c0001t0009g0213 |
2 | HG01167.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.588+1244A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637400 | |||||||
| chr18:31637400 | T | TC | 128 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(125): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.588+1243_588+1244i others(3): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637400 | |||||||
| chr18:31637512 | G | GA | 167 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(164): Show |
176 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.588+1131dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637512 | |||||||
| chr18:31637684 | C | T | 1 | a0001c0001t0033g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.588+960G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637684 | |||||||
| chr18:31637696 | A | C | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.588+948T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637696 | |||||||
| chr18:31637720 | A | G | 3 | a0001c0001t0008g0186 a0001c0001t0008g0266 a0001c0001t0011g0015 |
3 | HG03098.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.588+924T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637720 | |||||||
| chr18:31637820 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0151 others(2): Show |
5 | HG00544.hp2 HG02056.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+824G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637820 | |||||||
| chr18:31637825 | C | G | 1 | a0001c0001t0004g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.588+819G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31637825 | |||||||
| chr18:31638285 | T | A | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+359A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638285 | |||||||
| chr18:31638285 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.588+359A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638285 | |||||||
| chr18:31638293 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.588+351G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638293 | |||||||
| chr18:31638344 | G | A | 2 | a0001c0001t0015g0067 a0001c0001t0015g0247 |
2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.588+300C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638344 | |||||||
| chr18:31638344 | G | T | 5 | a0001c0001t0002g0075 a0001c0001t0002g0206 a0001c0001t0002g0244 others(2): Show |
5 | HG00609.hp2 HG02074.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+300C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638344 | |||||||
| chr18:31638356 | T | C | 4 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 others(1): Show |
5 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+288A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638356 | |||||||
| chr18:31638371 | T | C | 12 | a0001c0001t0005g0014 a0001c0001t0005g0169 a0001c0001t0005g0183 others(9): Show |
13 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.588+273A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638371 | |||||||
| chr18:31638418 | T | C | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.588+226A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 5/8 | chr18 | 31638418 | |||||||
| chr18:31638910 | C | G | 160 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(157): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.472-150G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31638910 | |||||||
| chr18:31638978 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.472-218A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31638978 | |||||||
| chr18:31639209 | C | T | 160 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(157): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.472-449G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639209 | |||||||
| chr18:31639249 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.472-489C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639249 | |||||||
| chr18:31639296 | G | A | 1 | a0001c0001t0012g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.472-536C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639296 | |||||||
| chr18:31639326 | C | T | 127 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(124): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.472-566G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639326 | |||||||
| chr18:31639793 | C | T | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-1033G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639793 | |||||||
| chr18:31639813 | T | C | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.472-1053A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639813 | |||||||
| chr18:31639928 | T | C | 190 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(187): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.472-1168A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639928 | |||||||
| chr18:31639956 | A | C | 15 | a0001c0001t0008g0042 a0001c0001t0008g0186 a0001c0001t0008g0218 others(12): Show |
15 | HG01243.hp2 HG02615.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.472-1196T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31639956 | |||||||
| chr18:31640300 | C | A | 1 | a0001c0005t0007g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.472-1540G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640300 | |||||||
| chr18:31640344 | G | A | 3 | a0001c0001t0008g0221 a0001c0001t0008g0222 a0001c0001t0008g0225 |
3 | HG03209.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.472-1584C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640344 | |||||||
| chr18:31640385 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472-1625A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640385 | |||||||
| chr18:31640637 | G | C | 127 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(124): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.472-1877C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640637 | |||||||
| chr18:31640719 | G | A | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.472-1959C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640719 | |||||||
| chr18:31640793 | C | G | 191 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(188): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.472-2033G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640793 | |||||||
| chr18:31640830 | T | A | 1 | a0001c0001t0031g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.472-2070A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640830 | |||||||
| chr18:31640902 | T | C | 1 | a0001c0001t0006g0022 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.472-2142A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640902 | |||||||
| chr18:31640955 | A | G | 191 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(188): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.472-2195T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31640955 | |||||||
| chr18:31641466 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.472-2706T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31641466 | |||||||
| chr18:31641723 | A | G | 1 | a0001c0003t0021g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.472-2963T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31641723 | |||||||
| chr18:31642038 | T | C | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0215 |
3 | HG00735.hp2 HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.472-3278A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642038 | |||||||
| chr18:31642416 | T | C | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+2939A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642416 | |||||||
| chr18:31642475 | GTTC | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0192 |
3 | NA18952.hp2 NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.471+2877_471+2879d others(5): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642475 | |||||||
| chr18:31642810 | G | A | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+2545C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642810 | |||||||
| chr18:31642828 | G | A | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+2527C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642828 | |||||||
| chr18:31642841 | C | T | 129 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(126): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.471+2514G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642841 | |||||||
| chr18:31642873 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0260 |
3 | HG00423.hp2 HG00544.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.471+2482G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642873 | |||||||
| chr18:31642874 | G | A | 29 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(26): Show |
29 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.471+2481C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642874 | |||||||
| chr18:31642877 | G | T | 29 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(26): Show |
29 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.471+2478C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642877 | |||||||
| chr18:31642920 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.471+2435G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31642920 | |||||||
| chr18:31643049 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+2306A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643049 | |||||||
| chr18:31643211 | C | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+2144G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643211 | |||||||
| chr18:31643364 | T | C | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+1991A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643364 | |||||||
| chr18:31643478 | T | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0199 |
2 | NA19054.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.471+1877A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643478 | |||||||
| chr18:31643494 | T | G | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.471+1861A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643494 | |||||||
| chr18:31643545 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.471+1810G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643545 | |||||||
| chr18:31643547 | C | T | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+1808G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643547 | |||||||
| chr18:31643658 | C | T | 188 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(185): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.471+1697G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643658 | |||||||
| chr18:31643710 | C | T | 3 | a0001c0001t0007g0008 a0001c0001t0007g0172 a0001c0001t0007g0237 |
4 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+1645G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643710 | |||||||
| chr18:31643714 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.471+1641A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643714 | |||||||
| chr18:31643721 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.471+1634A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31643721 | |||||||
| chr18:31644014 | T | C | 4 | a0001c0001t0008g0186 a0001c0001t0008g0240 a0001c0001t0008g0266 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+1341A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644014 | |||||||
| chr18:31644264 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.471+1091C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644264 | |||||||
| chr18:31644303 | A | G | 32 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(29): Show |
32 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.471+1052T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644303 | |||||||
| chr18:31644378 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.471+977T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644378 | |||||||
| chr18:31644426 | T | C | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.471+929A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644426 | |||||||
| chr18:31644446 | T | G | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0005t0007g0167 |
3 | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.471+909A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644446 | |||||||
| chr18:31644613 | G | A | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.471+742C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644613 | |||||||
| chr18:31644679 | A | G | 1 | a0001c0001t0009g0158 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.471+676T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644679 | |||||||
| chr18:31644835 | T | C | 1 | a0001c0001t0005g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.471+520A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644835 | |||||||
| chr18:31644983 | T | C | 1 | a0001c0001t0003g0235 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.471+372A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31644983 | |||||||
| chr18:31645010 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0197 |
3 | NA18952.hp1 NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.471+345C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31645010 | |||||||
| chr18:31645012 | G | A | 28 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(25): Show |
28 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.471+343C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31645012 | |||||||
| chr18:31645055 | A | G | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.471+300T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31645055 | |||||||
| chr18:31645317 | G | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+38C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 4/8 | chr18 | 31645317 | |||||||
| chr18:31645489 | A | G | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0005t0007g0167 |
3 | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.347-10T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31645489 | |||||||
| chr18:31645620 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.347-141C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31645620 | |||||||
| chr18:31645910 | G | C | 3 | a0001c0001t0008g0223 a0001c0001t0008g0224 a0002c0002t0032g0277 |
3 | HG01243.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.347-431C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31645910 | |||||||
| chr18:31645936 | T | C | 1 | a0001c0001t0006g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.347-457A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31645936 | |||||||
| chr18:31646122 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.347-643A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646122 | |||||||
| chr18:31646127 | G | C | 1 | a0001c0001t0009g0012 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.347-648C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646127 | |||||||
| chr18:31646218 | G | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.347-739C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646218 | |||||||
| chr18:31646245 | A | G | 192 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(189): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.347-766T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646245 | |||||||
| chr18:31646412 | T | C | 1 | a0001c0001t0008g0042 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347-933A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646412 | |||||||
| chr18:31646481 | G | A | 122 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(119): Show |
127 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.347-1002C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646481 | |||||||
| chr18:31646723 | T | G | 4 | a0001c0001t0008g0221 a0001c0001t0008g0222 a0001c0001t0008g0225 others(1): Show |
4 | HG03209.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-1244A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646723 | |||||||
| chr18:31646937 | C | A | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-1458G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646937 | |||||||
| chr18:31646991 | T | A | 12 | a0001c0001t0009g0012 a0001c0001t0009g0064 a0001c0001t0009g0102 others(9): Show |
13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-1512A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31646991 | |||||||
| chr18:31647035 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.347-1556T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647035 | |||||||
| chr18:31647172 | G | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.347-1693C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647172 | |||||||
| chr18:31647362 | G | A | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347-1883C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647362 | |||||||
| chr18:31647527 | T | G | 1 | a0001c0001t0002g0104 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.347-2048A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647527 | |||||||
| chr18:31647566 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.347-2087C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647566 | |||||||
| chr18:31647589 | T | C | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347-2110A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647589 | |||||||
| chr18:31647688 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.347-2209G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647688 | |||||||
| chr18:31647878 | T | G | 2 | a0001c0001t0008g0223 a0001c0001t0008g0224 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.347-2399A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31647878 | |||||||
| chr18:31648001 | A | G | 1 | a0001c0001t0017g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.347-2522T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648001 | |||||||
| chr18:31648097 | G | A | 3 | a0001c0001t0010g0009 a0001c0001t0010g0275 a0001c0001t0010g0276 |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-2618C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648097 | |||||||
| chr18:31648224 | A | G | 191 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(188): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.347-2745T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648224 | |||||||
| chr18:31648424 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.347-2945A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648424 | |||||||
| chr18:31648453 | T | G | 129 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(126): Show |
137 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.347-2974A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648453 | |||||||
| chr18:31648622 | C | T | 1 | a0001c0001t0029g0107 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347-3143G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648622 | |||||||
| chr18:31648697 | A | G | 1 | a0001c0001t0006g0120 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.347-3218T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648697 | |||||||
| chr18:31648979 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.347-3500C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31648979 | |||||||
| chr18:31649190 | T | C | 189 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(186): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.347-3711A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649190 | |||||||
| chr18:31649316 | CAG | C | 127 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(124): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.347-3839_347-3838d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649316 | |||||||
| chr18:31649544 | C | T | 2 | a0001c0001t0009g0064 a0001c0001t0009g0157 |
2 | NA18999.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.347-4065G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649544 | |||||||
| chr18:31649560 | C | T | 29 | a0001c0001t0007g0008 a0001c0001t0007g0035 a0001c0001t0007g0172 others(26): Show |
30 | HG01243.hp2 HG01884.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.347-4081G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649560 | |||||||
| chr18:31649575 | C | CA | 9 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0001g0119 others(6): Show |
9 | HG00423.hp1 HG01175.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-4097dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649575 | |||||||
| chr18:31649575 | CA | C | 29 | a0001c0001t0001g0087 a0001c0001t0001g0097 a0001c0001t0001g0098 others(26): Show |
29 | HG00597.hp2 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.347-4097delT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649575 | |||||||
| chr18:31649575 | CAA | C | 76 | a0001c0001t0002g0031 a0001c0001t0002g0033 a0001c0001t0002g0034 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.347-4098_347-4097d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649575 | |||||||
| chr18:31649575 | CAAA | C | 58 | a0001c0001t0002g0013 a0001c0001t0002g0152 a0001c0001t0002g0164 others(55): Show |
66 | HG00423.hp2 HG00544.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.347-4099_347-4097d others(5): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649575 | |||||||
| chr18:31649669 | A | T | 127 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(124): Show |
135 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.347-4190T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649669 | |||||||
| chr18:31649790 | T | C | 190 | a0001c0001t0001g0132 a0001c0001t0002g0013 a0001c0001t0002g0031 others(187): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.347-4311A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31649790 | |||||||
| chr18:31650187 | T | C | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.347-4708A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650187 | |||||||
| chr18:31650242 | T | A | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-4763A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650242 | |||||||
| chr18:31650293 | C | T | 2 | a0001c0001t0003g0095 a0002c0002t0003g0281 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.347-4814G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650293 | |||||||
| chr18:31650391 | A | G | 1 | a0001c0001t0017g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.347-4912T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650391 | |||||||
| chr18:31650443 | C | T | 2 | a0001c0001t0003g0095 a0002c0002t0003g0281 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.347-4964G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650443 | |||||||
| chr18:31650448 | G | A | 179 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(176): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.347-4969C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650448 | |||||||
| chr18:31650464 | C | T | 59 | a0001c0001t0003g0030 a0001c0001t0003g0061 a0001c0001t0003g0072 others(56): Show |
60 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.347-4985G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650464 | |||||||
| chr18:31650480 | A | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.347-5001T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650480 | |||||||
| chr18:31650571 | C | T | 3 | a0001c0001t0004g0011 a0001c0001t0004g0195 a0001c0001t0004g0204 |
4 | HG01099.hp2 HG01496.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.347-5092G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650571 | |||||||
| chr18:31650572 | G | A | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0005t0007g0167 |
3 | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.347-5093C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650572 | |||||||
| chr18:31650684 | T | C | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.347-5205A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650684 | |||||||
| chr18:31650729 | G | A | 1 | a0001c0001t0014g0144 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.347-5250C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650729 | |||||||
| chr18:31650830 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.347-5351C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650830 | |||||||
| chr18:31650842 | C | T | 1 | a0001c0001t0008g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.347-5363G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650842 | |||||||
| chr18:31650862 | G | A | 16 | a0001c0001t0005g0014 a0001c0001t0005g0169 a0001c0001t0005g0183 others(13): Show |
17 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.347-5383C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650862 | |||||||
| chr18:31650865 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.347-5386A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650865 | |||||||
| chr18:31650887 | C | T | 20 | a0001c0001t0002g0013 a0001c0001t0002g0152 a0001c0001t0002g0164 others(17): Show |
21 | HG00423.hp2 HG00544.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.347-5408G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650887 | |||||||
| chr18:31650967 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.347-5488G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31650967 | |||||||
| chr18:31651014 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG01099.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-5535G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651014 | |||||||
| chr18:31651017 | C | T | 1 | a0001c0001t0004g0123 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.347-5538G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651017 | |||||||
| chr18:31651062 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0026g0108 |
3 | NA18747.hp2 NA18952.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.347-5583T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651062 | |||||||
| chr18:31651086 | G | A | 1 | a0001c0001t0014g0144 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.347-5607C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651086 | |||||||
| chr18:31651117 | A | T | 1 | a0001c0001t0006g0022 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.347-5638T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651117 | |||||||
| chr18:31651118 | T | C | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347-5639A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651118 | |||||||
| chr18:31651139 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0141 |
3 | HG00099.hp1 HG00735.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.347-5660G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651139 | |||||||
| chr18:31651232 | T | C | 5 | a0001c0001t0007g0208 a0001c0001t0007g0220 a0001c0001t0008g0221 others(2): Show |
5 | HG01496.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-5753A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651232 | |||||||
| chr18:31651319 | C | G | 8 | a0001c0001t0003g0168 a0001c0001t0003g0249 a0001c0001t0003g0250 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-5840G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651319 | |||||||
| chr18:31651369 | CT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0087 others(10): Show |
14 | HG00597.hp2 HG02135.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.347-5891delA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651369 | |||||||
| chr18:31651520 | A | G | 46 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(43): Show |
47 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.347-6041T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651520 | |||||||
| chr18:31651638 | C | G | 1 | a0001c0001t0026g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.347-6159G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651638 | |||||||
| chr18:31651752 | C | G | 4 | a0001c0001t0007g0035 a0001c0001t0011g0017 a0001c0001t0011g0018 others(1): Show |
4 | HG02723.hp1 HG02886.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+6224G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651752 | |||||||
| chr18:31651816 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.346+6160C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651816 | |||||||
| chr18:31651834 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
88 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.346+6142C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651834 | |||||||
| chr18:31651850 | C | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0135 others(82): Show |
91 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(88): Show |
intron_variant | MODIFIER | c.346+6126G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651850 | |||||||
| chr18:31651851 | A | T | 85 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0135 others(82): Show |
91 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(88): Show |
intron_variant | MODIFIER | c.346+6125T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651851 | |||||||
| chr18:31651914 | G | A | 1 | a0001c0001t0007g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.346+6062C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651914 | |||||||
| chr18:31651992 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.346+5984C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31651992 | |||||||
| chr18:31652021 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0028 |
2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.346+5955G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652021 | |||||||
| chr18:31652028 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0028 |
2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.346+5948A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652028 | |||||||
| chr18:31652059 | G | C | 1 | a0001c0001t0013g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.346+5917C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652059 | |||||||
| chr18:31652150 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.346+5826G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652150 | |||||||
| chr18:31652236 | C | T | 1 | a0001c0001t0017g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.346+5740G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652236 | |||||||
| chr18:31652237 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00741.hp2 HG01081.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+5739C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652237 | |||||||
| chr18:31652237 | G | T | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.346+5739C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652237 | |||||||
| chr18:31652257 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.346+5719A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652257 | |||||||
| chr18:31652310 | G | A | 2 | a0001c0001t0007g0220 a0001c0001t0012g0216 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.346+5666C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652310 | |||||||
| chr18:31652330 | T | C | 5 | a0001c0001t0005g0274 a0001c0001t0007g0008 a0001c0001t0007g0172 others(2): Show |
6 | HG01496.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+5646A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652330 | |||||||
| chr18:31652378 | CAA | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
135 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.346+5596_346+5597d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652378 | |||||||
| chr18:31652411 | T | C | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+5565A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652411 | |||||||
| chr18:31652481 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0056 a0001c0001t0002g0062 |
3 | HG02165.hp2 NA18984.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.346+5495C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652481 | |||||||
| chr18:31652553 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.346+5423A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652553 | |||||||
| chr18:31652972 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.346+5004C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31652972 | |||||||
| chr18:31653020 | C | CT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0058 a0001c0001t0001g0156 others(10): Show |
13 | HG01891.hp1 HG01952.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+4955dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653020 | |||||||
| chr18:31653138 | A | G | 1 | a0001c0001t0028g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.346+4838T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653138 | |||||||
| chr18:31653179 | G | A | 2 | a0001c0001t0005g0187 a0001c0001t0005g0188 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.346+4797C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653179 | |||||||
| chr18:31653199 | T | C | 1 | a0001c0001t0013g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+4777A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653199 | |||||||
| chr18:31653282 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.346+4694T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653282 | |||||||
| chr18:31653435 | C | CT | 16 | a0001c0001t0001g0059 a0001c0001t0002g0041 a0001c0001t0002g0177 others(13): Show |
16 | HG00597.hp1 HG01361.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.346+4540dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653435 | |||||||
| chr18:31653435 | CT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
152 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.346+4540delA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653435 | |||||||
| chr18:31653435 | CTT | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0060 a0001c0001t0001g0145 others(19): Show |
27 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+4539_346+4540d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653435 | |||||||
| chr18:31653474 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.346+4502C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653474 | |||||||
| chr18:31653568 | A | G | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.346+4408T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653568 | |||||||
| chr18:31653570 | T | C | 2 | a0001c0001t0007g0173 a0001c0001t0007g0174 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.346+4406A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653570 | |||||||
| chr18:31653614 | G | T | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346+4362C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653614 | |||||||
| chr18:31653649 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.346+4327C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653649 | |||||||
| chr18:31653676 | A | G | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.346+4300T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653676 | |||||||
| chr18:31653747 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.346+4229G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653747 | |||||||
| chr18:31653920 | A | AT | 8 | a0001c0001t0001g0156 a0001c0001t0007g0208 a0001c0001t0007g0217 others(5): Show |
8 | HG02015.hp2 HG02056.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+4055dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653920 | |||||||
| chr18:31653920 | AT | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0140 a0001c0001t0001g0203 others(4): Show |
8 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+4055delA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653920 | |||||||
| chr18:31653934 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.346+4042G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31653934 | |||||||
| chr18:31654173 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.346+3803G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31654173 | |||||||
| chr18:31654358 | T | C | 1 | a0001c0001t0023g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.346+3618A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31654358 | |||||||
| chr18:31654767 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.346+3209A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31654767 | |||||||
| chr18:31655095 | T | C | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.346+2881A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655095 | |||||||
| chr18:31655173 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.346+2803C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655173 | |||||||
| chr18:31655435 | C | G | 1 | a0001c0001t0023g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.346+2541G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655435 | |||||||
| chr18:31655485 | G | C | 5 | a0001c0001t0003g0168 a0001c0001t0005g0169 a0002c0002t0003g0279 others(2): Show |
5 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+2491C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655485 | |||||||
| chr18:31655508 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
134 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.346+2468C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655508 | |||||||
| chr18:31655534 | G | T | 1 | a0001c0001t0004g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.346+2442C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655534 | |||||||
| chr18:31655581 | T | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.346+2395A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655581 | |||||||
| chr18:31655626 | A | T | 1 | a0003c0004t0030g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.346+2350T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655626 | |||||||
| chr18:31655749 | T | C | 1 | a0001c0001t0031g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.346+2227A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31655749 | |||||||
| chr18:31656097 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.346+1879C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656097 | |||||||
| chr18:31656177 | A | G | 1 | a0001c0001t0023g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.346+1799T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656177 | |||||||
| chr18:31656178 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.346+1798A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656178 | |||||||
| chr18:31656211 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.346+1765C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656211 | |||||||
| chr18:31656293 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.346+1683G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656293 | |||||||
| chr18:31656422 | C | A | 4 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0001t0007g0217 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+1554G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656422 | |||||||
| chr18:31656785 | T | C | 5 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0001t0007g0217 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1191A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656785 | |||||||
| chr18:31656917 | T | A | 5 | a0001c0001t0003g0168 a0001c0001t0005g0169 a0002c0002t0003g0279 others(2): Show |
5 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+1059A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656917 | |||||||
| chr18:31656963 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.346+1013C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656963 | |||||||
| chr18:31656978 | C | G | 1 | a0001c0001t0009g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.346+998G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31656978 | |||||||
| chr18:31657007 | A | G | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+969T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657007 | |||||||
| chr18:31657136 | A | G | 62 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(59): Show |
63 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.346+840T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657136 | |||||||
| chr18:31657206 | A | AAT | 5 | a0001c0001t0001g0101 a0001c0001t0007g0173 a0001c0001t0007g0174 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+768_346+769dup others(2): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657206 | |||||||
| chr18:31657217 | A | T | 1 | a0001c0001t0019g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+759T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657217 | |||||||
| chr18:31657219 | A | T | 26 | a0001c0001t0001g0156 a0001c0001t0001g0234 a0001c0001t0002g0189 others(23): Show |
26 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.346+757T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657219 | |||||||
| chr18:31657221 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0013g0170 |
2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.346+755A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657221 | |||||||
| chr18:31657322 | C | A | 1 | a0001c0001t0005g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.346+654G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657322 | |||||||
| chr18:31657503 | A | G | 32 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0111 others(29): Show |
32 | HG00738.hp2 HG01070.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.346+473T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657503 | |||||||
| chr18:31657727 | T | C | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.346+249A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657727 | |||||||
| chr18:31657802 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.346+174A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657802 | |||||||
| chr18:31657897 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
135 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.346+79G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657897 | |||||||
| chr18:31657899 | G | T | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346+77C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 3/8 | chr18 | 31657899 | |||||||
| chr18:31658113 | C | CA | 49 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(46): Show |
50 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.233-25dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658113 | |||||||
| chr18:31658113 | CA | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
106 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.233-25delT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658113 | |||||||
| chr18:31658394 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
237 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.233-305G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658394 | |||||||
| chr18:31658459 | G | A | 61 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(58): Show |
62 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.233-370C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658459 | |||||||
| chr18:31658491 | A | C | 9 | a0001c0001t0008g0218 a0001c0001t0008g0221 a0001c0001t0008g0222 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.233-402T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658491 | |||||||
| chr18:31658587 | A | T | 4 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 others(1): Show |
4 | HG02056.hp1 HG03041.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-498T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658587 | |||||||
| chr18:31658723 | C | T | 62 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(59): Show |
63 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.233-634G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658723 | |||||||
| chr18:31658753 | C | A | 4 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 others(1): Show |
4 | HG02056.hp1 HG03041.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-664G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658753 | |||||||
| chr18:31658753 | C | T | 1 | a0001c0001t0010g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.233-664G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658753 | |||||||
| chr18:31658966 | T | G | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-877A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31658966 | |||||||
| chr18:31659164 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.233-1075C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659164 | |||||||
| chr18:31659225 | C | A | 60 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(57): Show |
61 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.233-1136G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659225 | |||||||
| chr18:31659228 | T | C | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.233-1139A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659228 | |||||||
| chr18:31659312 | C | G | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.233-1223G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659312 | |||||||
| chr18:31659425 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.233-1336G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659425 | |||||||
| chr18:31659491 | G | A | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.233-1402C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659491 | |||||||
| chr18:31659564 | T | A | 65 | a0001c0001t0001g0156 a0001c0001t0001g0234 a0001c0001t0001g0241 others(62): Show |
66 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.233-1475A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659564 | |||||||
| chr18:31659571 | C | T | 6 | a0001c0001t0008g0218 a0001c0001t0008g0221 a0001c0001t0008g0222 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-1482G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659571 | |||||||
| chr18:31659612 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.233-1523C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659612 | |||||||
| chr18:31659676 | A | C | 1 | a0001c0001t0002g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.233-1587T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659676 | |||||||
| chr18:31659865 | A | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0258 a0001c0001t0002g0259 others(7): Show |
11 | HG00423.hp2 HG00544.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-1776T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659865 | |||||||
| chr18:31659949 | C | CT | 6 | a0001c0001t0001g0078 a0001c0001t0002g0075 a0001c0001t0003g0096 others(3): Show |
6 | HG01361.hp1 HG02132.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-1861dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659949 | |||||||
| chr18:31659949 | CT | C | 50 | a0001c0001t0001g0074 a0001c0001t0001g0145 a0001c0001t0001g0156 others(47): Show |
51 | HG00280.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.233-1861delA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659949 | |||||||
| chr18:31659949 | CTT | C | 6 | a0001c0001t0008g0218 a0001c0001t0012g0069 a0001c0001t0016g0287 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-1862_233-1861d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659949 | |||||||
| chr18:31659969 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.233-1880A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31659969 | |||||||
| chr18:31660097 | T | C | 1 | a0002c0002t0032g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233-2008A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660097 | |||||||
| chr18:31660229 | G | A | 2 | a0001c0001t0007g0217 a0001c0001t0023g0070 |
2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.233-2140C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660229 | |||||||
| chr18:31660237 | C | T | 1 | a0001c0001t0006g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.233-2148G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660237 | |||||||
| chr18:31660358 | T | C | 60 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(57): Show |
61 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.233-2269A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660358 | |||||||
| chr18:31660663 | G | C | 7 | a0001c0001t0008g0218 a0001c0001t0010g0275 a0001c0001t0010g0276 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-2574C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660663 | |||||||
| chr18:31660685 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 others(1): Show |
4 | HG02056.hp1 HG03041.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2596C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660685 | |||||||
| chr18:31660711 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
168 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.233-2622A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660711 | |||||||
| chr18:31660731 | A | T | 4 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 others(1): Show |
4 | HG02056.hp1 HG03041.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-2642T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660731 | |||||||
| chr18:31660881 | C | T | 1 | a0001c0001t0008g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233-2792G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31660881 | |||||||
| chr18:31661407 | A | T | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.233-3318T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661407 | |||||||
| chr18:31661527 | T | G | 1 | a0001c0005t0007g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.233-3438A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661527 | |||||||
| chr18:31661538 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.233-3449C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661538 | |||||||
| chr18:31661546 | T | TCA | 23 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(20): Show |
28 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.233-3459_233-3458d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661546 | |||||||
| chr18:31661729 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(17): Show |
25 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(22): Show |
intron_variant | MODIFIER | c.233-3640G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661729 | |||||||
| chr18:31661768 | A | G | 2 | a0001c0001t0007g0173 a0001c0001t0007g0174 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.233-3679T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31661768 | |||||||
| chr18:31662038 | C | T | 2 | a0001c0001t0011g0017 a0001c0001t0011g0018 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.233-3949G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662038 | |||||||
| chr18:31662182 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.232+4074G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662182 | |||||||
| chr18:31662193 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0002g0164 |
2 | HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.232+4063G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662193 | |||||||
| chr18:31662326 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.232+3930A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662326 | |||||||
| chr18:31662329 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
199 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.232+3927C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662329 | |||||||
| chr18:31662375 | C | T | 1 | a0001c0001t0007g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.232+3881G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662375 | |||||||
| chr18:31662382 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.232+3874G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662382 | |||||||
| chr18:31662384 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(17): Show |
25 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(22): Show |
intron_variant | MODIFIER | c.232+3872C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662384 | |||||||
| chr18:31662449 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.232+3807A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662449 | |||||||
| chr18:31662569 | G | A | 1 | a0001c0001t0013g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.232+3687C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662569 | |||||||
| chr18:31662575 | G | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(18): Show |
26 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.232+3681C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662575 | |||||||
| chr18:31662702 | A | G | 1 | a0001c0001t0011g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.232+3554T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662702 | |||||||
| chr18:31662773 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.232+3483C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662773 | |||||||
| chr18:31662784 | T | C | 1 | a0001c0001t0002g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232+3472A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662784 | |||||||
| chr18:31662845 | A | G | 2 | a0001c0001t0007g0008 a0001c0001t0007g0172 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.232+3411T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662845 | |||||||
| chr18:31662982 | A | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0097 others(2): Show |
6 | HG00597.hp2 NA18948.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+3274T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31662982 | |||||||
| chr18:31663308 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.232+2948C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31663308 | |||||||
| chr18:31663393 | T | G | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+2863A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31663393 | |||||||
| chr18:31663807 | T | C | 2 | a0001c0001t0023g0070 a0003c0004t0030g0205 |
2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.232+2449A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31663807 | |||||||
| chr18:31663875 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.232+2381A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31663875 | |||||||
| chr18:31663913 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.232+2343A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31663913 | |||||||
| chr18:31664018 | G | T | 1 | a0001c0001t0002g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.232+2238C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664018 | |||||||
| chr18:31664078 | C | T | 1 | a0001c0001t0018g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.232+2178G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664078 | |||||||
| chr18:31664140 | T | C | 1 | a0001c0001t0008g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232+2116A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664140 | |||||||
| chr18:31664162 | C | CACCAAAA others(9): Show |
96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
105 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.232+2093_232+2094i others(18): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664162 | |||||||
| chr18:31664162 | C | CACCAAGA others(9): Show |
1 | a0001c0001t0012g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.232+2093_232+2094i others(18): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664162 | |||||||
| chr18:31664162 | C | CACCAAGA others(9): Show |
87 | a0001c0001t0001g0010 a0001c0001t0001g0156 a0001c0001t0001g0182 others(84): Show |
93 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(90): Show |
intron_variant | MODIFIER | c.232+2093_232+2094i others(18): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664162 | |||||||
| chr18:31664169 | C | G | 1 | a0005c0006t0002g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.232+2087G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664169 | |||||||
| chr18:31664529 | C | CT | 81 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(78): Show |
87 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.232+1726dupA | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664529 | |||||||
| chr18:31664564 | G | C | 8 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0191 others(5): Show |
8 | HG02818.hp2 HG02896.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.232+1692C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664564 | |||||||
| chr18:31664898 | T | G | 2 | a0001c0001t0007g0173 a0001c0001t0007g0174 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.232+1358A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31664898 | |||||||
| chr18:31665107 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.232+1149A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665107 | |||||||
| chr18:31665130 | C | G | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.232+1126G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665130 | |||||||
| chr18:31665312 | G | A | 1 | a0001c0001t0010g0009 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.232+944C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665312 | |||||||
| chr18:31665598 | C | T | 5 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0251 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+658G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665598 | |||||||
| chr18:31665671 | G | A | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+585C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665671 | |||||||
| chr18:31665728 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0038g0285 |
2 | HG02015.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.232+528G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665728 | |||||||
| chr18:31665807 | T | C | 1 | a0001c0001t0002g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.232+449A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 2/8 | chr18 | 31665807 | |||||||
| chr18:31666387 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.116-15A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666387 | |||||||
| chr18:31666489 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.116-117C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666489 | |||||||
| chr18:31666518 | T | C | 50 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(47): Show |
51 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.116-146A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666518 | |||||||
| chr18:31666569 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.116-197G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666569 | |||||||
| chr18:31666710 | G | A | 2 | a0001c0001t0007g0173 a0001c0001t0007g0174 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.116-338C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666710 | |||||||
| chr18:31666750 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.116-378T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666750 | |||||||
| chr18:31666898 | C | T | 6 | a0001c0001t0002g0152 a0001c0001t0003g0072 a0001c0001t0003g0153 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-526G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31666898 | |||||||
| chr18:31667001 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.116-629C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667001 | |||||||
| chr18:31667179 | T | C | 1 | a0001c0001t0002g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.116-807A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667179 | |||||||
| chr18:31667190 | A | G | 50 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0152 others(47): Show |
51 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.116-818T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667190 | |||||||
| chr18:31667328 | C | T | 1 | a0001c0001t0002g0086 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.116-956G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667328 | |||||||
| chr18:31667466 | A | C | 1 | a0001c0001t0002g0038 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.116-1094T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667466 | |||||||
| chr18:31667868 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0003g0030 |
2 | HG04184.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.116-1496C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667868 | |||||||
| chr18:31667920 | C | T | 1 | a0001c0001t0013g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.116-1548G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31667920 | |||||||
| chr18:31668045 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.116-1673G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668045 | |||||||
| chr18:31668053 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.116-1681G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668053 | |||||||
| chr18:31668056 | C | A | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.116-1684G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668056 | |||||||
| chr18:31668096 | C | CA | 10 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(7): Show |
10 | HG01099.hp1 HG02647.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.116-1725dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668096 | |||||||
| chr18:31668380 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.116-2008T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668380 | |||||||
| chr18:31668515 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
210 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.116-2143G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668515 | |||||||
| chr18:31668638 | A | G | 2 | a0001c0001t0010g0275 a0001c0001t0010g0276 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116-2266T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668638 | |||||||
| chr18:31668821 | G | A | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.116-2449C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668821 | |||||||
| chr18:31668828 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
95 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.116-2456G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668828 | |||||||
| chr18:31668847 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
98 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.116-2476dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668847 | |||||||
| chr18:31668913 | A | T | 3 | a0001c0001t0010g0275 a0001c0001t0010g0276 a0003c0004t0030g0205 |
3 | HG01496.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116-2541T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668913 | |||||||
| chr18:31668964 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.116-2592G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668964 | |||||||
| chr18:31668973 | G | A | 1 | a0001c0001t0009g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.116-2601C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668973 | |||||||
| chr18:31668988 | C | T | 7 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0185 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-2616G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668988 | |||||||
| chr18:31668999 | G | C | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.116-2627C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31668999 | |||||||
| chr18:31669015 | C | CA | 25 | a0001c0001t0001g0010 a0001c0001t0001g0151 a0001c0001t0001g0182 others(22): Show |
30 | HG00741.hp1 HG01099.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.116-2644dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669015 | |||||||
| chr18:31669179 | AGATT | A | 3 | a0001c0001t0001g0156 a0001c0001t0019g0021 a0001c0001t0020g0020 |
3 | HG02056.hp1 HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.116-2811_116-2808d others(6): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669179 | |||||||
| chr18:31669336 | T | C | 3 | a0001c0001t0007g0208 a0001c0001t0013g0170 a0001c0001t0024g0071 |
3 | HG02015.hp2 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.116-2964A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669336 | |||||||
| chr18:31669552 | C | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
199 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.116-3180G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669552 | |||||||
| chr18:31669594 | T | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(22): Show |
30 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.116-3222A>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669594 | |||||||
| chr18:31669744 | T | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0156 a0001c0001t0001g0182 others(25): Show |
33 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.116-3372A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669744 | |||||||
| chr18:31669823 | A | G | 1 | a0002c0002t0003g0281 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.116-3451T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31669823 | |||||||
| chr18:31670035 | CA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
105 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.116-3664delT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670035 | |||||||
| chr18:31670345 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | NA18942.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.116-3973C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670345 | |||||||
| chr18:31670428 | G | GATGA | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
201 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.116-4060_116-4057d others(6): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670428 | |||||||
| chr18:31670470 | A | G | 1 | a0001c0001t0031g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.116-4098T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670470 | |||||||
| chr18:31670670 | T | C | 1 | a0001c0003t0021g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.116-4298A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670670 | |||||||
| chr18:31670763 | TTTA | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | NA18988.hp1 NA18993.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-4394_116-4392d others(5): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670763 | |||||||
| chr18:31670787 | G | A | 2 | a0001c0001t0009g0157 a0001c0001t0009g0158 |
2 | HG02027.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.116-4415C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670787 | |||||||
| chr18:31670800 | G | C | 1 | a0001c0001t0002g0034 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.116-4428C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31670800 | |||||||
| chr18:31671157 | T | C | 1 | a0001c0001t0022g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.116-4785A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31671157 | |||||||
| chr18:31671360 | C | T | 8 | a0001c0001t0005g0014 a0001c0001t0005g0226 a0001c0001t0005g0273 others(5): Show |
9 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-4988G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31671360 | |||||||
| chr18:31671477 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.116-5105A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31671477 | |||||||
| chr18:31671598 | T | C | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.116-5226A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31671598 | |||||||
| chr18:31672377 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.116-6005T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31672377 | |||||||
| chr18:31672400 | G | A | 1 | a0001c0001t0008g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.116-6028C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31672400 | |||||||
| chr18:31672527 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.116-6155G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31672527 | |||||||
| chr18:31672869 | A | G | 2 | a0001c0001t0013g0170 a0001c0001t0024g0071 |
2 | HG02015.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.116-6497T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31672869 | |||||||
| chr18:31673115 | A | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(18): Show |
26 | HG01099.hp2 HG01496.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.116-6743T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673115 | |||||||
| chr18:31673298 | C | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(19): Show |
27 | HG01099.hp2 HG01243.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.116-6926G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673298 | |||||||
| chr18:31673497 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.116-7125G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673497 | |||||||
| chr18:31673609 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.116-7237T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673609 | |||||||
| chr18:31673889 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.116-7517A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673889 | |||||||
| chr18:31673901 | G | A | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0191 |
3 | HG02818.hp2 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.116-7529C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673901 | |||||||
| chr18:31673902 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.116-7530A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31673902 | |||||||
| chr18:31674231 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.116-7859T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31674231 | |||||||
| chr18:31674323 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.116-7951C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31674323 | |||||||
| chr18:31674473 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.116-8101G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31674473 | |||||||
| chr18:31674949 | T | A | 1 | a0001c0001t0012g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.116-8577A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31674949 | |||||||
| chr18:31675007 | T | C | 7 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0185 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-8635A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675007 | |||||||
| chr18:31675040 | C | T | 3 | a0001c0001t0005g0014 a0001c0001t0005g0273 a0001c0001t0005g0274 |
4 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-8668G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675040 | |||||||
| chr18:31675118 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.116-8746A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675118 | |||||||
| chr18:31675298 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
115 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.116-8926A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675298 | |||||||
| chr18:31675357 | G | A | 2 | a0001c0001t0016g0286 a0001c0001t0016g0287 |
2 | NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.115+8955C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675357 | |||||||
| chr18:31675700 | A | T | 48 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0175 others(45): Show |
48 | HG00609.hp2 HG01243.hp2 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.115+8612T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31675700 | |||||||
| chr18:31676155 | G | A | 20 | a0001c0001t0002g0013 a0001c0001t0002g0189 a0001c0001t0002g0190 others(17): Show |
21 | HG00423.hp2 HG00544.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.115+8157C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676155 | |||||||
| chr18:31676253 | A | C | 2 | a0001c0001t0019g0021 a0001c0001t0020g0020 |
2 | HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.115+8059T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676253 | |||||||
| chr18:31676419 | T | C | 2 | a0001c0001t0015g0067 a0001c0003t0021g0068 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.115+7893A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676419 | |||||||
| chr18:31676525 | C | G | 47 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0175 others(44): Show |
47 | HG00609.hp2 HG01243.hp2 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.115+7787G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676525 | |||||||
| chr18:31676563 | T | C | 3 | a0001c0001t0002g0244 a0001c0001t0005g0245 a0001c0001t0035g0243 |
3 | HG00609.hp2 HG02074.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.115+7749A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676563 | |||||||
| chr18:31676613 | C | T | 1 | a0001c0001t0023g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.115+7699G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31676613 | |||||||
| chr18:31677117 | T | C | 2 | a0001c0001t0019g0021 a0001c0001t0020g0020 |
2 | HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.115+7195A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677117 | |||||||
| chr18:31677218 | T | C | 12 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(9): Show |
13 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.115+7094A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677218 | |||||||
| chr18:31677391 | T | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(19): Show |
27 | HG01099.hp2 HG01243.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.115+6921A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677391 | |||||||
| chr18:31677452 | G | T | 2 | a0001c0001t0008g0223 a0001c0001t0008g0224 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.115+6860C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677452 | |||||||
| chr18:31677576 | A | G | 3 | a0001c0001t0005g0014 a0001c0001t0005g0273 a0001c0001t0005g0274 |
4 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+6736T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677576 | |||||||
| chr18:31677588 | C | T | 1 | a0001c0001t0012g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115+6724G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677588 | |||||||
| chr18:31677709 | A | C | 1 | a0001c0001t0002g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.115+6603T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677709 | |||||||
| chr18:31677809 | C | T | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115+6503G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677809 | |||||||
| chr18:31677960 | G | A | 7 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0185 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+6352C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31677960 | |||||||
| chr18:31678063 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.115+6249C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678063 | |||||||
| chr18:31678075 | G | A | 2 | a0001c0001t0005g0187 a0001c0001t0005g0188 |
2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.115+6237C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678075 | |||||||
| chr18:31678151 | A | G | 11 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(8): Show |
12 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+6161T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678151 | |||||||
| chr18:31678173 | G | C | 1 | a0001c0001t0003g0253 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+6139C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678173 | |||||||
| chr18:31678456 | GA | G | 9 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(6): Show |
10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+5855delT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678456 | |||||||
| chr18:31678532 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0008g0224 a0002c0002t0032g0277 |
3 | HG01243.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.115+5780T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678532 | |||||||
| chr18:31678584 | G | T | 1 | a0001c0001t0002g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115+5728C>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678584 | |||||||
| chr18:31678652 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01069.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.115+5660G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678652 | |||||||
| chr18:31678659 | G | A | 2 | a0001c0001t0015g0067 a0001c0003t0021g0068 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.115+5653C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678659 | |||||||
| chr18:31678684 | G | GA | 3 | a0001c0001t0008g0218 a0001c0001t0008g0221 a0001c0001t0008g0222 |
3 | HG03225.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.115+5627dupT | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678684 | |||||||
| chr18:31678704 | A | G | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+5608T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31678704 | |||||||
| chr18:31679126 | T | C | 7 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0185 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+5186A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679126 | |||||||
| chr18:31679166 | A | G | 7 | a0001c0001t0005g0183 a0001c0001t0005g0184 a0001c0001t0005g0185 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115+5146T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679166 | |||||||
| chr18:31679198 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+5114A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679198 | |||||||
| chr18:31679449 | C | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
115 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.115+4863G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679449 | |||||||
| chr18:31679510 | C | T | 1 | a0001c0001t0013g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.115+4802G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679510 | |||||||
| chr18:31679669 | ATC | A | 3 | a0001c0001t0007g0208 a0001c0001t0012g0219 a0001c0001t0024g0071 |
3 | HG03041.hp2 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.115+4641_115+4642d others(4): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679669 | |||||||
| chr18:31679688 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0004g0002 a0001c0001t0004g0181 others(1): Show |
7 | HG02165.hp1 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+4624G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679688 | |||||||
| chr18:31679784 | C | T | 2 | a0001c0001t0019g0021 a0001c0001t0020g0020 |
2 | HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.115+4528G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679784 | |||||||
| chr18:31679856 | C | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
239 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.115+4456G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679856 | |||||||
| chr18:31679895 | C | A | 1 | a0001c0001t0007g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.115+4417G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679895 | |||||||
| chr18:31679969 | A | C | 1 | a0001c0001t0013g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.115+4343T>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679969 | |||||||
| chr18:31679977 | A | G | 39 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0175 others(36): Show |
39 | HG00609.hp2 HG01243.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.115+4335T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31679977 | |||||||
| chr18:31680054 | A | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | NA18948.hp2 NA18965.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.115+4258T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680054 | |||||||
| chr18:31680321 | G | A | 9 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(6): Show |
10 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.115+3991C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680321 | |||||||
| chr18:31680468 | G | A | 1 | a0001c0001t0023g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.115+3844C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680468 | |||||||
| chr18:31680534 | A | G | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+3778T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680534 | |||||||
| chr18:31680548 | A | G | 1 | a0001c0001t0002g0031 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.115+3764T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680548 | |||||||
| chr18:31680671 | T | C | 1 | a0001c0001t0018g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.115+3641A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31680671 | |||||||
| chr18:31681116 | T | TCAAA | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
253 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.115+3195_115+3196i others(6): Show |
B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681116 | |||||||
| chr18:31681165 | T | C | 2 | a0001c0001t0007g0217 a0001c0001t0012g0216 |
2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.115+3147A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681165 | |||||||
| chr18:31681377 | C | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
177 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.115+2935G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681377 | |||||||
| chr18:31681503 | C | G | 20 | a0001c0001t0002g0013 a0001c0001t0002g0258 a0001c0001t0002g0259 others(17): Show |
22 | HG00423.hp2 HG00544.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.115+2809G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681503 | |||||||
| chr18:31681631 | G | A | 31 | a0001c0001t0001g0234 a0001c0001t0001g0241 a0001c0001t0002g0228 others(28): Show |
31 | HG00609.hp2 HG01243.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.115+2681C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681631 | |||||||
| chr18:31681952 | A | G | 1 | a0001c0001t0003g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.115+2360T>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681952 | |||||||
| chr18:31681955 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
244 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.115+2357G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31681955 | |||||||
| chr18:31682029 | G | A | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+2283C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682029 | |||||||
| chr18:31682239 | G | A | 103 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0192 others(100): Show |
111 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.115+2073C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682239 | |||||||
| chr18:31682464 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
119 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.115+1848A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682464 | |||||||
| chr18:31682479 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.115+1833C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682479 | |||||||
| chr18:31682480 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0002g0164 |
2 | HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.115+1832A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682480 | |||||||
| chr18:31682593 | T | C | 1 | a0001c0001t0033g0165 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.115+1719A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682593 | |||||||
| chr18:31682621 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.115+1691C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682621 | |||||||
| chr18:31682733 | T | C | 1 | a0001c0001t0024g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+1579A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682733 | |||||||
| chr18:31682956 | T | A | 1 | a0001c0001t0037g0284 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.115+1356A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31682956 | |||||||
| chr18:31683049 | T | A | 1 | a0001c0001t0009g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.115+1263A>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683049 | |||||||
| chr18:31683058 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.115+1254C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683058 | |||||||
| chr18:31683112 | C | A | 2 | a0001c0001t0019g0021 a0001c0001t0020g0020 |
2 | HG04204.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.115+1200G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683112 | |||||||
| chr18:31683118 | G | A | 4 | a0001c0001t0005g0014 a0001c0001t0005g0273 a0001c0001t0005g0274 others(1): Show |
5 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+1194C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683118 | |||||||
| chr18:31683349 | A | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0003g0030 others(6): Show |
9 | HG01074.hp1 HG01255.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.115+963T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683349 | |||||||
| chr18:31683351 | T | C | 1 | a0001c0001t0019g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.115+961A>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683351 | |||||||
| chr18:31683370 | G | A | 2 | a0001c0001t0010g0275 a0001c0001t0010g0276 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115+942C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683370 | |||||||
| chr18:31683409 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+903G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683409 | |||||||
| chr18:31683666 | A | T | 1 | a0001c0005t0007g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.115+646T>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683666 | |||||||
| chr18:31683955 | C | A | 1 | a0001c0001t0002g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.115+357G>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31683955 | |||||||
| chr18:31684042 | G | C | 20 | a0001c0001t0002g0013 a0001c0001t0002g0258 a0001c0001t0002g0259 others(17): Show |
22 | HG00423.hp2 HG00544.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.115+270C>G | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31684042 | |||||||
| chr18:31684065 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
115 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.115+247G>A | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31684065 | |||||||
| chr18:31684219 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
250 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.115+93C>T | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31684219 | |||||||
| chr18:31684280 | C | G | 1 | a0001c0001t0011g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.115+32G>C | B4GALT6 | ENSG00000118276.12 | transcript | ENST00000306851.10 | protein_coding | 1/8 | chr18 | 31684280 |