Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27087 |
| ensemblid | ENSG00000109956.13 |
| hgncid | 921 |
| symbol | B3GAT1 |
| name | beta-1,3-glucuronyltransferase 1 |
| refseq_nuc | NM_054025.3 |
| refseq_prot | NP_473366.1 |
| ensembl_nuc | ENST00000312527.9 |
| ensembl_prot | ENSP00000307875.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 134378508 |
| end | 134412242 |
| strand | - |
| ver | v1.2 |
| region | chr11:134378508-134412242 |
| region5000 | chr11:134373508-134417242 |
| regionname0 | B3GAT1_chr11_134378508_134412242 |
| regionname5000 | B3GAT1_chr11_134373508_134417242 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 334 | 334 | 79 | 74 | 121 | 18 | 40 | 81 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | MPKRR others(329): Show |
chr11 | 134373508 | 134417242 |
| a0002 | 0/0 | 334 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | MPKRR others(329): Show |
chr11 | 134373508 | 134417242 |
| a0003 | 0/0 | 334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | MPKRR others(329): Show |
chr11 | 134373508 | 134417242 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1002 | 328 | 73 | 74 | 121 | 18 | 40 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | ATGCC others(997): Show |
chr11 | 134373508 | 134417242 | ||
| a0001c0003 | 0/0 | 1002 | 6 | 6 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | ATGCC others(997): Show |
chr11 | 134373508 | 134417242 | ||
| a0002c0002 | 0/0 | 1002 | 17 | 15 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | ATGCC others(997): Show |
chr11 | 134373508 | 134417242 | ||
| a0003c0004 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | ATGCC others(997): Show |
chr11 | 134373508 | 134417242 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3996 | 123 | 9 | 23 | 67 | 8 | 16 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0002 | 0/0 | 3976 | 31 | 9 | 14 | 6 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0003 | 0/1 | 3996 | 30 | 13 | 7 | 3 | 0 | 6 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0004 | 0/0 | 4011 | 17 | 10 | 2 | 5 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0005 | 1/0 | 3976 | 18 | 7 | 3 | 3 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0006 | 0/0 | 3997 | 13 | 0 | 2 | 7 | 1 | 3 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0007 | 0/0 | 3996 | 11 | 0 | 5 | 4 | 0 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0008 | 0/0 | 4015 | 8 | 1 | 3 | 0 | 2 | 2 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4010): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0009 | 0/0 | 3992 | 6 | 0 | 0 | 5 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3987): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0010 | 0/0 | 3996 | 5 | 3 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0011 | 0/0 | 3997 | 4 | 2 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0012 | 0/0 | 4011 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0013 | 0/0 | 3995 | 4 | 3 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3990): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0014 | 0/0 | 4012 | 3 | 1 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4007): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0015 | 0/0 | 3977 | 3 | 1 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3972): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0016 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3993): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0017 | 0/0 | 3997 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0018 | 0/0 | 4012 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4007): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0019 | 0/0 | 3997 | 2 | 1 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0020 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0021 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0022 | 0/0 | 4011 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0023 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0024 | 0/0 | 3976 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0025 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3993): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0026 | 0/0 | 3995 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3990): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0027 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0028 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0029 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0030 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3972): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0031 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3972): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0032 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0033 | 0/0 | 3993 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3988): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0034 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3993): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0035 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0036 | 0/0 | 4016 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4011): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0037 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0038 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3988): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0039 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0040 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0041 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0042 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0043 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4010): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0044 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4010): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0045 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0046 | 0/0 | 3992 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3987): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0047 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0049 | 0/0 | 3976 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0050 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3972): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0051 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3972): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0052 | 0/0 | 3995 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3990): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0053 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0054 | 0/0 | 3976 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0055 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0001c0001t0056 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0003t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0001c0003t0004 | 0/0 | 4011 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0001c0003t0048 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(4006): Show |
chr11 | 134373508 | 134417242 |
| a0002c0002t0001 | 0/0 | 3996 | 10 | 9 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| a0002c0002t0002 | 0/0 | 3976 | 4 | 4 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3971): Show |
chr11 | 134373508 | 134417242 |
| a0002c0002t0006 | 0/0 | 3997 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3992): Show |
chr11 | 134373508 | 134417242 |
| a0002c0002t0016 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3993): Show |
chr11 | 134373508 | 134417242 |
| a0003c0004t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | AGAGC others(3991): Show |
chr11 | 134373508 | 134417242 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0302 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0010g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0013g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0013g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0014g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0015g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0015g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0016g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0017g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0018g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0018g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0019g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0020g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0020g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0021g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0021g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0022g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0022g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0023g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0023g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0024g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0024g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0025g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0026g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0027g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0028g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0029g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0030g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0031g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0032g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0033g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0034g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0035g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0036g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0037g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0038g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0039g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0040g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0041g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0042g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0043g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0044g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0045g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0046g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0047g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0049g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0050g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0051g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0052g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0053g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0054g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0055g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0001t0056g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0001c0003t0048g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0002c0002t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00099 | hp2 | a0001 | c0001 | t0049 | g0246 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0019 | EUR | GBR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00280 | hp1 | a0001 | c0001 | t0052 | g0276 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0138 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00408 | hp1 | a0001 | c0001 | t0028 | g0037 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0289 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00438 | hp2 | a0001 | c0001 | t0020 | g0125 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00544 | hp2 | a0001 | c0001 | t0027 | g0034 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0248 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0101 | EAS | CHS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0139 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0170 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0066 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01106 | hp1 | a0001 | c0001 | t0024 | g0280 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01109 | hp2 | a0001 | c0001 | t0050 | g0247 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01168 | hp2 | a0001 | c0001 | t0054 | g0260 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01169 | hp1 | a0001 | c0001 | t0031 | g0044 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01169 | hp2 | a0001 | c0001 | t0029 | g0038 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0055 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01256 | hp1 | a0001 | c0001 | t0022 | g0232 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01261 | hp1 | a0001 | c0001 | t0016 | g0035 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01261 | hp2 | a0001 | c0001 | t0018 | g0042 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01358 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0300 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0023 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0290 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0264 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01934 | hp1 | a0001 | c0001 | t0018 | g0041 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0053 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02015 | hp2 | a0001 | c0001 | t0009 | g0219 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0258 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02056 | hp2 | a0001 | c0001 | t0046 | g0220 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02080 | hp1 | a0001 | c0001 | t0056 | g0309 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02129 | hp2 | a0001 | c0001 | t0032 | g0045 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0250 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02257 | hp2 | a0001 | c0001 | t0039 | g0200 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02258 | hp1 | a0002 | c0002 | t0016 | g0036 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0224 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0291 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0153 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02622 | hp2 | a0001 | c0001 | t0021 | g0072 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02630 | hp2 | a0001 | c0001 | t0053 | g0294 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02647 | hp1 | a0002 | c0002 | t0006 | g0067 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0056 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0292 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02717 | hp1 | a0001 | c0003 | t0048 | g0243 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0245 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0057 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02738 | hp2 | a0001 | c0001 | t0022 | g0233 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0075 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0174 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0303 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0070 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02897 | hp1 | a0001 | c0001 | t0044 | g0073 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0238 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0283 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0052 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0065 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0287 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0208 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03239 | hp2 | a0001 | c0001 | t0015 | g0251 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0242 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03492 | hp1 | a0001 | c0001 | t0024 | g0263 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0225 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | GWD | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0286 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0058 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03688 | hp2 | a0001 | c0001 | t0033 | g0046 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03710 | hp2 | a0001 | c0001 | t0019 | g0051 | SAS | PJL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03831 | hp2 | a0001 | c0001 | t0036 | g0061 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03927 | hp1 | a0001 | c0001 | t0025 | g0032 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0199 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | BEB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04199 | hp2 | a0001 | c0001 | t0035 | g0048 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04204 | hp1 | a0001 | c0001 | t0008 | g0192 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0226 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | CHB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18940 | hp2 | a0001 | c0001 | t0051 | g0249 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18942 | hp2 | a0001 | c0001 | t0041 | g0107 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18948 | hp2 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18949 | hp2 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0060 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18951 | hp2 | a0001 | c0001 | t0040 | g0133 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18954 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18964 | hp2 | a0001 | c0001 | t0026 | g0033 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18982 | hp1 | a0001 | c0001 | t0023 | g0272 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19000 | hp1 | a0001 | c0001 | t0030 | g0043 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19000 | hp2 | a0001 | c0001 | t0014 | g0069 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19010 | hp1 | a0001 | c0001 | t0009 | g0218 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19011 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19043 | hp2 | a0001 | c0001 | t0047 | g0222 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19054 | hp2 | a0001 | c0001 | t0017 | g0040 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19074 | hp1 | a0001 | c0001 | t0020 | g0083 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19079 | hp1 | a0001 | c0001 | t0014 | g0071 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19081 | hp1 | a0001 | c0001 | t0034 | g0047 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19084 | hp2 | a0001 | c0001 | t0038 | g0068 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19087 | hp2 | a0001 | c0001 | t0037 | g0064 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19091 | hp2 | a0001 | c0001 | t0009 | g0215 | EAS | JPT | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19240 | hp1 | a0001 | c0001 | t0055 | g0262 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | YRI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ASW | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0008 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20752 | hp2 | a0001 | c0001 | t0042 | g0168 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0271 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | TSI | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20905 | hp2 | a0001 | c0001 | t0009 | g0217 | SAS | GIH | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0285 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG02559 | hp2 | a0001 | c0001 | t0045 | g0202 | AFR | ACB | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG06807 | hp1 | a0001 | c0001 | t0012 | g0240 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| HG06807 | hp2 | a0001 | c0001 | t0043 | g0149 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | USA | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA21309 | hp1 | a0001 | c0001 | t0021 | g0105 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0080 | REF | REF | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0302 | REF | REF | B3GAT1_chr11_134373508_134417242 | B3GAT1 | chr11 | 134373508 | 134417242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:134383910 | C | T | 1 | a0002 | 17 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(14): Show |
missense_variant | MODERATE | c.391G>A | p.Ala131Thr | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 1108/3976 | 391/1005 | 131/334 | chr11 | 134383910 | |||
| chr11:134384040 | G | T | 1 | a0003 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.261C>A | p.His87Gln | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 978/3976 | 261/1005 | 87/334 | chr11 | 134384040 | |||
| chr11:134384041 | T | G | 1 | a0003 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.260A>C | p.His87Pro | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/6 | 977/3976 | 260/1005 | 87/334 | chr11 | 134384041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:134382947 | G | A | 1 | a0001c0003 | 6 | HG02258.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
synonymous_variant | LOW | c.681C>T | p.Tyr227Tyr | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/6 | 1398/3976 | 681/1005 | 227/334 | chr11 | 134382947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:134378669 | C | T | 1 | a0001c0001t0044 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 3269 | chr11 | 134378669 | ||||||
| chr11:134379100 | C | T | 1 | a0001c0001t0022 | 2 | HG01256.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1662G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2838 | chr11 | 134379100 | ||||||
| chr11:134379161 | A | T | 2 | a0001c0001t0045 a0001c0001t0053 |
2 | HG02559.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1601T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2777 | chr11 | 134379161 | ||||||
| chr11:134379404 | G | A | 1 | a0001c0001t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2534 | chr11 | 134379404 | ||||||
| chr11:134379427 | T | C | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*1335A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2511 | chr11 | 134379427 | ||||||
| chr11:134379428 | G | A | 10 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0019 others(7): Show |
19 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1334C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2510 | chr11 | 134379428 | ||||||
| chr11:134379455 | T | C | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1307A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2483 | chr11 | 134379455 | ||||||
| chr11:134379510 | G | A | 1 | a0001c0001t0024 | 2 | HG01106.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1252C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2428 | chr11 | 134379510 | ||||||
| chr11:134379656 | C | T | 5 | a0001c0001t0007 a0001c0001t0023 a0001c0001t0024 others(2): Show |
17 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1106G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2282 | chr11 | 134379656 | ||||||
| chr11:134379712 | G | A | 4 | a0001c0001t0008 a0001c0001t0036 a0001c0001t0043 others(1): Show |
11 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1050C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2226 | chr11 | 134379712 | ||||||
| chr11:134379781 | A | ACCTTGCC others(12): Show |
6 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0036 others(3): Show |
16 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*962_*980dupCGGTGG others(13): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2156 | chr11 | 134379781 | ||||||
| chr11:134379933 | G | A | 2 | a0001c0001t0021 a0001c0001t0055 |
3 | HG02622.hp2 NA19240.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 2005 | chr11 | 134379933 | ||||||
| chr11:134379954 | C | T | 1 | a0001c0001t0047 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1984 | chr11 | 134379954 | ||||||
| chr11:134380056 | G | C | 1 | a0001c0001t0027 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*706C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1882 | chr11 | 134380056 | ||||||
| chr11:134380113 | C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1825 | chr11 | 134380113 | ||||||
| chr11:134380172 | C | T | 1 | a0001c0001t0042 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1766 | chr11 | 134380172 | ||||||
| chr11:134380255 | C | T | 1 | a0001c0001t0041 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1683 | chr11 | 134380255 | ||||||
| chr11:134380377 | T | G | 1 | a0001c0003t0048 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1561 | chr11 | 134380377 | ||||||
| chr11:134380455 | A | G | 1 | a0001c0001t0040 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 6/6 | 1483 | chr11 | 134380455 | ||||||
| chr11:134387723 | C | T | 2 | a0001c0001t0020 a0001c0001t0039 |
3 | HG00438.hp2 HG02257.hp2 NA19074.hp1 |
5_prime_UTR_variant | MODIFIER | c.-64G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/6 | 64 | chr11 | 134387723 | ||||||
| chr11:134411915 | C | T | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-390G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24256 | chr11 | 134411915 | ||||||
| chr11:134411916 | T | C | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-391A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24257 | chr11 | 134411916 | ||||||
| chr11:134411920 | C | G | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-395G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24261 | chr11 | 134411920 | ||||||
| chr11:134411971 | CCGCG | C | 5 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0033 others(2): Show |
10 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-450_-447delCGCG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24313 | chr11 | 134411971 | ||||||
| chr11:134411984 | C | CGCCCGCC others(8): Show |
8 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0014 others(5): Show |
34 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-460_-459insTGCGGG others(9): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24326 | chr11 | 134411984 | ||||||
| chr11:134412093 | C | CG | 5 | a0001c0001t0015 a0001c0001t0026 a0001c0001t0034 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG02145.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-569dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24435 | chr11 | 134412093 | ||||||
| chr11:134412093 | C | G | 2 | a0001c0001t0027 a0001c0001t0035 |
2 | HG00544.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-568G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24434 | chr11 | 134412093 | ||||||
| chr11:134412098 | G | GGGCGGGG others(7): Show |
10 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0014 others(7): Show |
29 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-574_-573insTCCCCC others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24440 | chr11 | 134412098 | ||||||
| chr11:134412100 | C | A | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-575G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24441 | chr11 | 134412100 | ||||||
| chr11:134412105 | A | G | 1 | a0001c0001t0049 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-580T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24446 | chr11 | 134412105 | ||||||
| chr11:134412106 | G | GGGGGAGC others(13): Show |
1 | a0001c0001t0056 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-601_-582dupGCTCCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24448 | chr11 | 134412106 | ||||||
| chr11:134412108 | G | GGGAGCGG others(13): Show |
31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | ||||||
| chr11:134412108 | G | GGGAGCGG others(14): Show |
2 | a0001c0001t0025 a0001c0001t0033 |
2 | HG03688.hp2 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(15): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | ||||||
| chr11:134412108 | G | GGGAGCGG others(13): Show |
1 | a0001c0001t0032 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | ||||||
| chr11:134412108 | G | GGGGAGCG others(14): Show |
2 | a0001c0001t0026 a0001c0001t0034 |
2 | NA18964.hp2 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(15): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | ||||||
| chr11:134412108 | G | GGGGAGGT | 10 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0014 others(7): Show |
29 | HG00735.hp2 HG00738.hp2 HG01074.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-584_-583insACCTCC others(1): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24450 | chr11 | 134412108 | ||||||
| chr11:134412156 | A | AG | 11 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0018 others(8): Show |
13 | HG00408.hp1 HG00544.hp2 HG01169.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-632dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/6 | 24498 | chr11 | 134412156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:134380857 | T | G | 1 | a0001c0001t0021g0105 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*15-110A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380857 | |||||||
| chr11:134380880 | G | C | 15 | a0001c0001t0047g0222 a0002c0002t0001g0027 a0002c0002t0001g0095 others(12): Show |
16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.*15-133C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380880 | |||||||
| chr11:134380924 | G | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.*15-177C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380924 | |||||||
| chr11:134380946 | C | T | 27 | a0001c0001t0008g0019 a0001c0001t0008g0023 a0001c0001t0008g0138 others(24): Show |
30 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.*15-199G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380946 | |||||||
| chr11:134380964 | C | G | 1 | a0001c0001t0003g0191 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.*15-217G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134380964 | |||||||
| chr11:134381358 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.*14+566G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381358 | |||||||
| chr11:134381450 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.*14+474C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381450 | |||||||
| chr11:134381599 | C | T | 27 | a0001c0001t0008g0019 a0001c0001t0008g0023 a0001c0001t0008g0138 others(24): Show |
30 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.*14+325G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381599 | |||||||
| chr11:134381700 | A | G | 9 | a0001c0001t0008g0019 a0001c0001t0008g0023 a0001c0001t0008g0138 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.*14+224T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381700 | |||||||
| chr11:134381850 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.*14+74C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381850 | |||||||
| chr11:134381883 | C | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
151 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.*14+41G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 5/5 | chr11 | 134381883 | |||||||
| chr11:134382123 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-99G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382123 | |||||||
| chr11:134382124 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-100G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382124 | |||||||
| chr11:134382137 | G | A | 2 | a0001c0001t0045g0202 a0001c0001t0053g0294 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.919-113C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382137 | |||||||
| chr11:134382146 | T | A | 1 | a0001c0001t0034g0047 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.919-122A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382146 | |||||||
| chr11:134382227 | T | G | 10 | a0001c0001t0003g0084 a0001c0001t0008g0019 a0001c0001t0008g0023 others(7): Show |
12 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.919-203A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382227 | |||||||
| chr11:134382233 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.919-209C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382233 | |||||||
| chr11:134382244 | G | A | 8 | a0001c0001t0013g0287 a0001c0001t0013g0290 a0001c0001t0013g0291 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-220C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382244 | |||||||
| chr11:134382269 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919-245G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382269 | |||||||
| chr11:134382286 | A | G | 1 | a0001c0001t0005g0268 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.919-262T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382286 | |||||||
| chr11:134382306 | A | AGT | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.919-284_919-283dup others(2): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382306 | |||||||
| chr11:134382306 | A | AGTGT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.919-286_919-283dup others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382306 | |||||||
| chr11:134382325 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0002g0031 a0001c0001t0002g0296 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.919-301C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382325 | |||||||
| chr11:134382362 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0085 others(12): Show |
18 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-338A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382362 | |||||||
| chr11:134382377 | C | G | 19 | a0001c0001t0001g0020 a0001c0001t0010g0011 a0001c0001t0010g0075 others(16): Show |
21 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.918+333G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382377 | |||||||
| chr11:134382409 | ATG | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.918+299_918+300del others(2): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382409 | |||||||
| chr11:134382418 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+292A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382418 | |||||||
| chr11:134382452 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.918+258A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382452 | |||||||
| chr11:134382527 | T | G | 5 | a0001c0001t0001g0203 a0001c0001t0002g0031 a0001c0001t0002g0296 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+183A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382527 | |||||||
| chr11:134382571 | A | G | 1 | a0001c0001t0053g0294 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+139T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382571 | |||||||
| chr11:134382707 | C | A | 1 | a0001c0001t0014g0069 | 1 | NA19000.hp2 | splice_region_variant&intron_variant | LOW | c.918+3G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 4/5 | chr11 | 134382707 | |||||||
| chr11:134383012 | A | AG | 21 | a0001c0001t0002g0257 a0001c0001t0010g0011 a0001c0001t0010g0075 others(18): Show |
22 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.622-7dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383012 | |||||||
| chr11:134383118 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.622-112G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383118 | |||||||
| chr11:134383159 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-153C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383159 | |||||||
| chr11:134383335 | G | C | 8 | a0001c0001t0008g0019 a0001c0001t0008g0023 a0001c0001t0008g0138 others(5): Show |
10 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-329C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383335 | |||||||
| chr11:134383462 | T | C | 1 | a0001c0001t0046g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.621+218A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383462 | |||||||
| chr11:134383512 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.621+168T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383512 | |||||||
| chr11:134383669 | C | A | 1 | a0001c0003t0004g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.621+11G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 3/5 | chr11 | 134383669 | |||||||
| chr11:134384252 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0006g0063 |
3 | HG00738.hp2 HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.113-64C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384252 | |||||||
| chr11:134384455 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.113-267G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384455 | |||||||
| chr11:134384467 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.113-279T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384467 | |||||||
| chr11:134384496 | C | A | 7 | a0001c0001t0004g0223 a0001c0001t0012g0238 a0001c0003t0001g0212 others(4): Show |
7 | HG02258.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-308G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384496 | |||||||
| chr11:134384530 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0185 |
2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.113-342G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384530 | |||||||
| chr11:134384558 | G | A | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-370C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384558 | |||||||
| chr11:134384564 | C | T | 1 | a0001c0001t0011g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.113-376G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384564 | |||||||
| chr11:134384902 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(63): Show |
85 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.113-714G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384902 | |||||||
| chr11:134384919 | T | C | 3 | a0002c0002t0001g0175 a0002c0002t0001g0179 a0002c0002t0001g0206 |
3 | HG01891.hp2 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.113-731A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384919 | |||||||
| chr11:134384945 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(303): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.113-757A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134384945 | |||||||
| chr11:134385137 | C | A | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-949G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385137 | |||||||
| chr11:134385140 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.113-952C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385140 | |||||||
| chr11:134385295 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0076 others(48): Show |
55 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.113-1107C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385295 | |||||||
| chr11:134385299 | T | C | 1 | a0001c0003t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113-1111A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385299 | |||||||
| chr11:134385350 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.113-1162A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385350 | |||||||
| chr11:134385431 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0076 others(69): Show |
86 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-1243A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385431 | |||||||
| chr11:134385496 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.113-1308C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385496 | |||||||
| chr11:134385496 | G | C | 39 | a0001c0001t0001g0026 a0001c0001t0001g0196 a0001c0001t0001g0203 others(36): Show |
43 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.113-1308C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385496 | |||||||
| chr11:134385504 | T | C | 2 | a0001c0001t0031g0044 a0001c0001t0054g0260 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.113-1316A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385504 | |||||||
| chr11:134385543 | C | G | 2 | a0001c0001t0005g0298 a0001c0001t0007g0208 |
2 | HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.113-1355G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385543 | |||||||
| chr11:134385555 | C | T | 31 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0003g0074 others(28): Show |
34 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-1367G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385555 | |||||||
| chr11:134385558 | GATGGGTG others(39): Show |
G | 5 | a0001c0001t0002g0295 a0001c0001t0003g0180 a0001c0001t0012g0240 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1416_113-1371d others(48): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385558 | |||||||
| chr11:134385570 | G | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.113-1382C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385570 | |||||||
| chr11:134385703 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1515G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385703 | |||||||
| chr11:134385717 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.113-1529G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385717 | |||||||
| chr11:134385764 | C | T | 3 | a0001c0001t0003g0084 a0001c0001t0045g0202 a0001c0003t0048g0243 |
3 | HG02145.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.113-1576G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385764 | |||||||
| chr11:134385765 | G | A | 1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.113-1577C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385765 | |||||||
| chr11:134385940 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.112+1608A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134385940 | |||||||
| chr11:134386034 | CAAGATAA others(5): Show |
C | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1502_112+1513d others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386034 | |||||||
| chr11:134386085 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0001t0001g0114 others(17): Show |
22 | HG00408.hp1 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.112+1463G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386085 | |||||||
| chr11:134386147 | C | G | 1 | a0001c0001t0013g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+1401G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386147 | |||||||
| chr11:134386412 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1136T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386412 | |||||||
| chr11:134386413 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.112+1135C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386413 | |||||||
| chr11:134386423 | A | AAG | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.112+1123_112+1124d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386423 | |||||||
| chr11:134386729 | G | T | 1 | a0001c0003t0004g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112+819C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386729 | |||||||
| chr11:134386857 | A | G | 19 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0224 others(16): Show |
20 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+691T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386857 | |||||||
| chr11:134386887 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.112+661G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386887 | |||||||
| chr11:134386911 | C | T | 23 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0152 others(20): Show |
24 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.112+637G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386911 | |||||||
| chr11:134386925 | C | A | 13 | a0002c0002t0001g0027 a0002c0002t0001g0095 a0002c0002t0001g0175 others(10): Show |
14 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+623G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386925 | |||||||
| chr11:134386929 | C | A | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112+619G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386929 | |||||||
| chr11:134386960 | T | G | 6 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0224 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+588A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134386960 | |||||||
| chr11:134387008 | C | G | 1 | a0001c0001t0001g0188 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.112+540G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387008 | |||||||
| chr11:134387021 | G | A | 1 | a0001c0001t0008g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.112+527C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387021 | |||||||
| chr11:134387126 | G | A | 3 | a0001c0001t0004g0230 a0001c0001t0014g0071 a0001c0003t0048g0243 |
3 | HG02717.hp1 NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.112+422C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387126 | |||||||
| chr11:134387184 | C | G | 22 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0001t0001g0114 others(19): Show |
24 | HG00408.hp1 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.112+364G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387184 | |||||||
| chr11:134387458 | G | C | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112+90C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 2/5 | chr11 | 134387458 | |||||||
| chr11:134388078 | T | C | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-138A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388078 | |||||||
| chr11:134388248 | A | C | 19 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0224 others(16): Show |
20 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-281-308T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388248 | |||||||
| chr11:134388297 | A | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-357T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388297 | |||||||
| chr11:134388351 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-281-411C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388351 | |||||||
| chr11:134388429 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-489G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388429 | |||||||
| chr11:134388430 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-490A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388430 | |||||||
| chr11:134388503 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-281-563A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388503 | |||||||
| chr11:134388522 | T | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(241): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-281-582A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388522 | |||||||
| chr11:134388779 | C | T | 21 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0001t0045g0202 others(18): Show |
22 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-281-839G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388779 | |||||||
| chr11:134388838 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-281-898A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134388838 | |||||||
| chr11:134389055 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-281-1115T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389055 | |||||||
| chr11:134389519 | C | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-1579G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389519 | |||||||
| chr11:134389617 | G | A | 1 | a0001c0001t0003g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-281-1677C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389617 | |||||||
| chr11:134389664 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(301): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-281-1724T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389664 | |||||||
| chr11:134389669 | G | C | 39 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0132 others(36): Show |
42 | HG00438.hp1 HG00544.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.-281-1729C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389669 | |||||||
| chr11:134389732 | T | C | 4 | a0001c0001t0010g0011 a0001c0001t0019g0051 a0001c0001t0031g0044 others(1): Show |
5 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-281-1792A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389732 | |||||||
| chr11:134389826 | G | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0004g0235 others(5): Show |
10 | HG02109.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-281-1886C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389826 | |||||||
| chr11:134389931 | G | A | 2 | a0001c0001t0010g0174 a0001c0001t0047g0222 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-281-1991C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134389931 | |||||||
| chr11:134390032 | C | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0004g0235 others(5): Show |
10 | HG02109.hp1 HG02451.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-281-2092G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390032 | |||||||
| chr11:134390087 | GTT | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0081 others(73): Show |
83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2149_-281-214 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390087 | |||||||
| chr11:134390090 | C | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0081 others(73): Show |
83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2150G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390090 | |||||||
| chr11:134390091 | C | A | 76 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0081 others(73): Show |
83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2151G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390091 | |||||||
| chr11:134390092 | C | G | 76 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0081 others(73): Show |
83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2152G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390092 | |||||||
| chr11:134390093 | C | A | 76 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0081 others(73): Show |
83 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-281-2153G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390093 | |||||||
| chr11:134390132 | G | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0110 others(42): Show |
49 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-281-2192C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390132 | |||||||
| chr11:134390175 | C | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0110 others(29): Show |
34 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.-281-2235G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390175 | |||||||
| chr11:134390283 | C | T | 1 | a0001c0001t0010g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-281-2343G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390283 | |||||||
| chr11:134390284 | A | G | 38 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0110 others(35): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-281-2344T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390284 | |||||||
| chr11:134390350 | C | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-2410G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390350 | |||||||
| chr11:134390410 | T | TCTTCTCA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-2471_-281-247 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390410 | |||||||
| chr11:134390411 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-2471A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390411 | |||||||
| chr11:134390425 | G | T | 1 | a0001c0001t0007g0182 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-281-2485C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390425 | |||||||
| chr11:134390500 | G | A | 13 | a0001c0001t0001g0203 a0001c0001t0002g0031 a0001c0001t0002g0296 others(10): Show |
15 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-281-2560C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390500 | |||||||
| chr11:134390739 | C | G | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-2799G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390739 | |||||||
| chr11:134390995 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(8): Show |
14 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-3055G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134390995 | |||||||
| chr11:134391018 | T | C | 34 | a0001c0001t0001g0203 a0001c0001t0002g0031 a0001c0001t0002g0296 others(31): Show |
38 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-281-3078A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391018 | |||||||
| chr11:134391040 | C | T | 5 | a0001c0001t0002g0269 a0001c0001t0003g0112 a0001c0001t0003g0137 others(2): Show |
5 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-3100G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391040 | |||||||
| chr11:134391236 | C | G | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-3296G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391236 | |||||||
| chr11:134391256 | A | G | 55 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0002g0295 others(52): Show |
59 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-281-3316T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391256 | |||||||
| chr11:134391329 | T | C | 27 | a0001c0001t0004g0006 a0001c0001t0004g0223 a0001c0001t0004g0235 others(24): Show |
30 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-3389A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391329 | |||||||
| chr11:134391412 | C | T | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-3472G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391412 | |||||||
| chr11:134391502 | G | A | 11 | a0001c0001t0002g0295 a0001c0001t0009g0215 a0001c0001t0009g0216 others(8): Show |
11 | HG01243.hp2 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-3562C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391502 | |||||||
| chr11:134391531 | T | C | 1 | a0001c0001t0012g0240 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-281-3591A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391531 | |||||||
| chr11:134391627 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0093 |
2 | HG00280.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.-281-3687G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391627 | |||||||
| chr11:134391682 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0006g0008 |
3 | HG00735.hp2 HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-281-3742C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391682 | |||||||
| chr11:134391698 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-281-3758G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391698 | |||||||
| chr11:134391814 | A | T | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-3874T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391814 | |||||||
| chr11:134391879 | T | G | 20 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0224 others(17): Show |
21 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-281-3939A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391879 | |||||||
| chr11:134391889 | A | T | 1 | a0001c0001t0003g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-281-3949T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391889 | |||||||
| chr11:134391938 | G | A | 1 | a0001c0001t0011g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-281-3998C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391938 | |||||||
| chr11:134391951 | T | G | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-4011A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134391951 | |||||||
| chr11:134392018 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-281-4078G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392018 | |||||||
| chr11:134392100 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0005g0289 |
2 | HG00438.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-281-4160G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392100 | |||||||
| chr11:134392151 | A | G | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-4211T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392151 | |||||||
| chr11:134392189 | T | TCCGTGGA others(27): Show |
21 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0001t0047g0222 others(18): Show |
22 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-281-4283_-281-425 others(38): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392189 | |||||||
| chr11:134392260 | A | G | 68 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0203 others(65): Show |
74 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.-281-4320T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392260 | |||||||
| chr11:134392260 | ATGGAACT others(21): Show |
A | 1 | a0001c0001t0040g0133 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-281-4348_-281-432 others(32): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392260 | |||||||
| chr11:134392340 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-281-4400G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392340 | |||||||
| chr11:134392444 | T | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-281-4504A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392444 | |||||||
| chr11:134392461 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG01106.hp1 HG02109.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-4521G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392461 | |||||||
| chr11:134392468 | C | G | 20 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0224 others(17): Show |
21 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-281-4528G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392468 | |||||||
| chr11:134392639 | G | A | 6 | a0001c0001t0004g0239 a0001c0001t0010g0011 a0001c0001t0012g0238 others(3): Show |
7 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-281-4699C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392639 | |||||||
| chr11:134392674 | G | A | 22 | a0001c0001t0004g0223 a0001c0001t0005g0289 a0001c0001t0044g0073 others(19): Show |
23 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-4734C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392674 | |||||||
| chr11:134392676 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-281-4736T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392676 | |||||||
| chr11:134392705 | C | G | 40 | a0001c0001t0001g0203 a0001c0001t0002g0031 a0001c0001t0002g0296 others(37): Show |
45 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-281-4765G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392705 | |||||||
| chr11:134392706 | G | A | 1 | a0001c0001t0037g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-281-4766C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392706 | |||||||
| chr11:134392947 | T | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-5007A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134392947 | |||||||
| chr11:134393044 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0197 |
2 | NA18952.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-281-5104A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393044 | |||||||
| chr11:134393081 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-281-5141G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393081 | |||||||
| chr11:134393434 | C | G | 1 | a0001c0001t0010g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-281-5494G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393434 | |||||||
| chr11:134393444 | C | T | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-5504G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393444 | |||||||
| chr11:134393522 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-281-5582G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393522 | |||||||
| chr11:134393776 | C | T | 1 | a0001c0001t0019g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-281-5836G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393776 | |||||||
| chr11:134393792 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0099 others(6): Show |
11 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-5852G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393792 | |||||||
| chr11:134393831 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-281-5891G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393831 | |||||||
| chr11:134393834 | C | A | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-5894G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393834 | |||||||
| chr11:134393840 | A | C | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-5900T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393840 | |||||||
| chr11:134393842 | A | T | 6 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-5902T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393842 | |||||||
| chr11:134393866 | C | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-5926G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393866 | |||||||
| chr11:134393873 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-5933G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134393873 | |||||||
| chr11:134394087 | G | A | 6 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-6147C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394087 | |||||||
| chr11:134394248 | T | C | 56 | a0001c0001t0001g0077 a0001c0001t0001g0152 a0001c0001t0001g0203 others(53): Show |
59 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-281-6308A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394248 | |||||||
| chr11:134394290 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-281-6350C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394290 | |||||||
| chr11:134394306 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-281-6366G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394306 | |||||||
| chr11:134394319 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6379G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394319 | |||||||
| chr11:134394333 | A | G | 31 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0002g0295 others(28): Show |
33 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-281-6393T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394333 | |||||||
| chr11:134394361 | T | C | 30 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0002g0295 others(27): Show |
32 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-281-6421A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394361 | |||||||
| chr11:134394372 | C | A | 1 | a0001c0001t0039g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-281-6432G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394372 | |||||||
| chr11:134394557 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-281-6617G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394557 | |||||||
| chr11:134394597 | C | A | 22 | a0001c0001t0001g0152 a0001c0001t0004g0223 a0001c0001t0004g0227 others(19): Show |
22 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-281-6657G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394597 | |||||||
| chr11:134394597 | C | G | 1 | a0001c0001t0003g0090 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-281-6657G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394597 | |||||||
| chr11:134394612 | T | G | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6672A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394612 | |||||||
| chr11:134394635 | A | G | 16 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(13): Show |
17 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-281-6695T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394635 | |||||||
| chr11:134394690 | C | T | 1 | a0001c0001t0023g0272 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-281-6750G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394690 | |||||||
| chr11:134394702 | T | C | 21 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(18): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-6762A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394702 | |||||||
| chr11:134394835 | G | A | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-6895C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134394835 | |||||||
| chr11:134395063 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-281-7123T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395063 | |||||||
| chr11:134395066 | T | A | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-7126A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395066 | |||||||
| chr11:134395197 | C | CT | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(25): Show |
30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-7258dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395197 | |||||||
| chr11:134395200 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0185 |
2 | HG00673.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-281-7260C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395200 | |||||||
| chr11:134395215 | C | T | 13 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(10): Show |
14 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-281-7275G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395215 | |||||||
| chr11:134395219 | T | G | 1 | a0001c0001t0042g0168 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-281-7279A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395219 | |||||||
| chr11:134395227 | C | T | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(25): Show |
30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-7287G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395227 | |||||||
| chr11:134395279 | C | T | 22 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(19): Show |
24 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.-281-7339G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395279 | |||||||
| chr11:134395342 | C | T | 21 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(18): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7402G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395342 | |||||||
| chr11:134395360 | A | G | 21 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(18): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7420T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395360 | |||||||
| chr11:134395421 | T | C | 21 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(18): Show |
23 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-281-7481A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395421 | |||||||
| chr11:134395485 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 |
6 | NA18948.hp1 NA18951.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-281-7545C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395485 | |||||||
| chr11:134395643 | C | G | 6 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
7 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-7703G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395643 | |||||||
| chr11:134395829 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-7889G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395829 | |||||||
| chr11:134395895 | T | C | 11 | a0001c0001t0001g0152 a0001c0001t0005g0289 a0001c0001t0009g0215 others(8): Show |
11 | HG00438.hp1 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-281-7955A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395895 | |||||||
| chr11:134395964 | G | A | 2 | a0001c0001t0005g0279 a0001c0001t0015g0251 |
2 | HG01070.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-281-8024C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134395964 | |||||||
| chr11:134396068 | G | A | 9 | a0001c0001t0004g0223 a0001c0001t0004g0227 a0001c0001t0004g0244 others(6): Show |
9 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-281-8128C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396068 | |||||||
| chr11:134396073 | T | G | 34 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(31): Show |
36 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.-281-8133A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396073 | |||||||
| chr11:134396226 | G | A | 2 | a0001c0001t0044g0073 a0001c0003t0048g0243 |
2 | HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-281-8286C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396226 | |||||||
| chr11:134396350 | G | A | 15 | a0001c0001t0001g0203 a0001c0001t0010g0174 a0001c0001t0045g0202 others(12): Show |
16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-281-8410C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396350 | |||||||
| chr11:134396417 | C | T | 1 | a0001c0001t0041g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-281-8477G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396417 | |||||||
| chr11:134396455 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-281-8515C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396455 | |||||||
| chr11:134396478 | A | G | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(25): Show |
30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-281-8538T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396478 | |||||||
| chr11:134396624 | GA | G | 32 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0158 others(29): Show |
35 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-281-8685delT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396624 | |||||||
| chr11:134396695 | C | T | 1 | a0001c0001t0009g0219 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-281-8755G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396695 | |||||||
| chr11:134396722 | G | A | 1 | a0001c0001t0009g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-281-8782C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396722 | |||||||
| chr11:134396800 | C | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-8860G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396800 | |||||||
| chr11:134396886 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-281-8946G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396886 | |||||||
| chr11:134396898 | C | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-8958G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396898 | |||||||
| chr11:134396901 | C | T | 16 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(13): Show |
17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-8961G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396901 | |||||||
| chr11:134396944 | C | T | 2 | a0001c0001t0003g0104 a0001c0001t0021g0105 |
2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-281-9004G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134396944 | |||||||
| chr11:134397014 | C | T | 2 | a0001c0001t0008g0138 a0001c0001t0008g0139 |
2 | HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-281-9074G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397014 | |||||||
| chr11:134397070 | C | T | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-281-9130G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397070 | |||||||
| chr11:134397198 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(12): Show |
16 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-281-9258G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397198 | |||||||
| chr11:134397199 | A | G | 69 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0203 others(66): Show |
76 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.-281-9259T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397199 | |||||||
| chr11:134397278 | C | T | 15 | a0001c0001t0001g0203 a0001c0001t0010g0174 a0001c0001t0045g0202 others(12): Show |
16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-281-9338G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397278 | |||||||
| chr11:134397347 | G | A | 6 | a0001c0001t0005g0268 a0001c0001t0005g0298 a0001c0001t0005g0299 others(3): Show |
6 | HG03130.hp2 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-281-9407C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397347 | |||||||
| chr11:134397383 | T | C | 21 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(18): Show |
24 | HG01081.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-281-9443A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397383 | |||||||
| chr11:134397391 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0007g0022 a0001c0001t0007g0170 |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-281-9451G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397391 | |||||||
| chr11:134397397 | T | TCTCCTGT others(3): Show |
16 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(13): Show |
17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-9467_-281-945 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397397 | |||||||
| chr11:134397410 | G | A | 1 | a0001c0001t0007g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-281-9470C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397410 | |||||||
| chr11:134397424 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-281-9484G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397424 | |||||||
| chr11:134397534 | A | G | 16 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(13): Show |
17 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-281-9594T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397534 | |||||||
| chr11:134397541 | GCCAGAGG others(18): Show |
G | 16 | a0001c0001t0001g0091 a0001c0001t0003g0090 a0001c0001t0004g0006 others(13): Show |
18 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.-281-9626_-281-960 others(29): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397541 | |||||||
| chr11:134397623 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-281-9683C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397623 | |||||||
| chr11:134397653 | G | A | 1 | a0001c0001t0008g0023 | 2 | HG01433.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-281-9713C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397653 | |||||||
| chr11:134397653 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-281-9713C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397653 | |||||||
| chr11:134397744 | C | T | 5 | a0001c0001t0004g0223 a0001c0001t0044g0073 a0001c0003t0004g0225 others(2): Show |
5 | HG02717.hp2 HG02897.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-9804G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397744 | |||||||
| chr11:134397790 | C | T | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-281-9850G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397790 | |||||||
| chr11:134397832 | C | T | 7 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(4): Show |
8 | HG01081.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-9892G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397832 | |||||||
| chr11:134397876 | G | A | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-281-9936C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397876 | |||||||
| chr11:134397938 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-281-9998G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397938 | |||||||
| chr11:134397953 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-281-10013A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134397953 | |||||||
| chr11:134398038 | C | T | 1 | a0001c0001t0010g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-281-10098G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398038 | |||||||
| chr11:134398155 | ACACC | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10219_-281-10 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398155 | |||||||
| chr11:134398201 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(1): Show |
5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-281-10261G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398201 | |||||||
| chr11:134398216 | C | T | 18 | a0001c0001t0001g0077 a0001c0001t0001g0173 a0001c0001t0002g0295 others(15): Show |
19 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-281-10276G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398216 | |||||||
| chr11:134398367 | A | G | 2 | a0001c0001t0004g0239 a0001c0001t0012g0238 |
2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-281-10427T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398367 | |||||||
| chr11:134398379 | A | G | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10439T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398379 | |||||||
| chr11:134398502 | G | T | 1 | a0001c0003t0004g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-281-10562C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398502 | |||||||
| chr11:134398517 | T | C | 24 | a0001c0001t0001g0077 a0001c0001t0001g0173 a0001c0001t0002g0281 others(21): Show |
25 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-281-10577A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398517 | |||||||
| chr11:134398559 | T | C | 21 | a0001c0001t0001g0077 a0001c0001t0002g0295 a0001c0001t0004g0029 others(18): Show |
22 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-281-10619A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398559 | |||||||
| chr11:134398559 | T | TACAGATG others(71): Show |
5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-281-10620_-281-10 others(84): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398559 | |||||||
| chr11:134398593 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-281-10653C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398593 | |||||||
| chr11:134398615 | G | A | 15 | a0001c0001t0001g0143 a0001c0001t0002g0252 a0001c0001t0002g0282 others(12): Show |
15 | HG01496.hp2 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-281-10675C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398615 | |||||||
| chr11:134398740 | C | T | 42 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0002g0031 others(39): Show |
47 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-281-10800G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398740 | |||||||
| chr11:134398758 | C | G | 1 | a0001c0001t0005g0271 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-281-10818G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398758 | |||||||
| chr11:134398947 | A | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(3): Show |
8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-281-11007T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134398947 | |||||||
| chr11:134399197 | T | C | 43 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(40): Show |
48 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.-281-11257A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399197 | |||||||
| chr11:134399198 | G | A | 2 | a0001c0001t0004g0230 a0001c0001t0014g0071 |
2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-281-11258C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399198 | |||||||
| chr11:134399212 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-281-11272C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399212 | |||||||
| chr11:134399226 | G | A | 22 | a0001c0001t0001g0077 a0001c0001t0002g0267 a0001c0001t0002g0288 others(19): Show |
25 | HG01243.hp2 HG01256.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.-281-11286C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399226 | |||||||
| chr11:134399439 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-281-11499G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399439 | |||||||
| chr11:134399689 | C | G | 1 | a0001c0001t0002g0270 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-281-11749G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399689 | |||||||
| chr11:134399717 | G | A | 1 | a0001c0001t0013g0290 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-281-11777C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399717 | |||||||
| chr11:134399743 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-281-11803G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399743 | |||||||
| chr11:134399878 | G | C | 26 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0295 others(23): Show |
30 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+11929C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134399878 | |||||||
| chr11:134400109 | C | T | 39 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(36): Show |
43 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-282+11698G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400109 | |||||||
| chr11:134400171 | C | A | 2 | a0001c0001t0004g0239 a0001c0001t0012g0238 |
2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-282+11636G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400171 | |||||||
| chr11:134400176 | A | G | 44 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(41): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+11631T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400176 | |||||||
| chr11:134400353 | A | G | 1 | a0001c0001t0005g0268 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-282+11454T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400353 | |||||||
| chr11:134400387 | T | A | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+11420A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400387 | |||||||
| chr11:134400440 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+11367G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400440 | |||||||
| chr11:134400615 | A | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+11192T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400615 | |||||||
| chr11:134400653 | T | C | 3 | a0001c0001t0007g0101 a0001c0001t0007g0182 a0001c0001t0041g0107 |
3 | HG00544.hp1 HG00673.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-282+11154A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400653 | |||||||
| chr11:134400666 | G | A | 1 | a0001c0001t0005g0307 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-282+11141C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400666 | |||||||
| chr11:134400827 | G | A | 39 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(36): Show |
43 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-282+10980C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400827 | |||||||
| chr11:134400877 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-282+10930G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400877 | |||||||
| chr11:134400974 | G | A | 1 | a0001c0001t0007g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-282+10833C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134400974 | |||||||
| chr11:134401061 | G | A | 43 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(40): Show |
48 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.-282+10746C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401061 | |||||||
| chr11:134401128 | C | T | 2 | a0001c0001t0004g0228 a0001c0001t0014g0069 |
2 | NA19000.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-282+10679G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401128 | |||||||
| chr11:134401281 | C | CAT | 18 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(15): Show |
19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+10524_-282+10 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401281 | |||||||
| chr11:134401393 | G | A | 8 | a0001c0001t0001g0144 a0001c0001t0003g0012 a0001c0001t0003g0096 others(5): Show |
9 | HG00642.hp1 HG01192.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+10414C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401393 | |||||||
| chr11:134401584 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-282+10223T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401584 | |||||||
| chr11:134401751 | T | A | 38 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(35): Show |
42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+10056A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401751 | |||||||
| chr11:134401752 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0116 a0001c0001t0002g0031 others(4): Show |
9 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+10055T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401752 | |||||||
| chr11:134401771 | C | T | 18 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0007g0010 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+10036G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401771 | |||||||
| chr11:134401877 | T | C | 38 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(35): Show |
42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9930A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401877 | |||||||
| chr11:134401911 | A | G | 38 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(35): Show |
42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9896T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401911 | |||||||
| chr11:134401970 | C | CG | 30 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0183 others(27): Show |
31 | HG00408.hp1 HG00558.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-282+9836dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401970 | |||||||
| chr11:134401970 | C | T | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+9837G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401970 | |||||||
| chr11:134401973 | G | A | 2 | a0001c0001t0003g0146 a0001c0001t0029g0038 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-282+9834C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401973 | |||||||
| chr11:134401978 | GGC | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(16): Show |
27 | HG00140.hp2 HG00642.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-282+9827_-282+982 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401978 | |||||||
| chr11:134401979 | G | GT | 18 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(15): Show |
18 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-282+9827_-282+982 others(5): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | |||||||
| chr11:134401979 | G | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+9828C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | |||||||
| chr11:134401979 | GC | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(84): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-282+9827delG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401979 | |||||||
| chr11:134401980 | C | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(142): Show |
159 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.-282+9827G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401980 | |||||||
| chr11:134401982 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-282+9825C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401982 | |||||||
| chr11:134401999 | C | T | 20 | a0001c0001t0001g0077 a0001c0001t0004g0006 a0001c0001t0004g0029 others(17): Show |
23 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-282+9808G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134401999 | |||||||
| chr11:134402007 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-282+9800C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402007 | |||||||
| chr11:134402160 | T | A | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+9647A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402160 | |||||||
| chr11:134402250 | G | A | 21 | a0001c0001t0001g0077 a0001c0001t0004g0006 a0001c0001t0004g0029 others(18): Show |
24 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-282+9557C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402250 | |||||||
| chr11:134402268 | G | A | 2 | a0001c0001t0004g0239 a0001c0001t0012g0238 |
2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-282+9539C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402268 | |||||||
| chr11:134402316 | G | C | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+9491C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402316 | |||||||
| chr11:134402318 | C | T | 1 | a0001c0001t0006g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-282+9489G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402318 | |||||||
| chr11:134402355 | C | T | 1 | a0001c0001t0013g0290 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-282+9452G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402355 | |||||||
| chr11:134402557 | G | A | 38 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(35): Show |
42 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+9250C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402557 | |||||||
| chr11:134402735 | AAACCCTG others(9): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-282+9056_-282+907 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402735 | |||||||
| chr11:134402870 | G | A | 2 | a0001c0001t0033g0046 a0001c0001t0043g0149 |
2 | HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-282+8937C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402870 | |||||||
| chr11:134402911 | TC | T | 30 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(27): Show |
32 | HG01074.hp2 HG01243.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+8895delG | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402911 | |||||||
| chr11:134402911 | TCA | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(4): Show |
9 | HG02109.hp1 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+8894_-282+889 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402911 | |||||||
| chr11:134402912 | C | A | 1 | a0001c0001t0022g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-282+8895G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402912 | |||||||
| chr11:134402912 | CA | C | 7 | a0001c0001t0001g0189 a0001c0001t0002g0031 a0001c0001t0002g0296 others(4): Show |
8 | HG01081.hp2 HG01891.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+8894delT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134402912 | |||||||
| chr11:134403107 | C | CACA | 4 | a0001c0001t0012g0240 a0001c0001t0012g0241 a0001c0001t0012g0245 others(1): Show |
4 | HG02258.hp2 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+8697_-282+869 others(7): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403107 | |||||||
| chr11:134403139 | G | A | 5 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+8668C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403139 | |||||||
| chr11:134403150 | G | A | 3 | a0001c0001t0003g0009 a0001c0001t0003g0150 a0001c0001t0011g0049 |
4 | HG01255.hp1 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+8657C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403150 | |||||||
| chr11:134403200 | G | A | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+8607C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403200 | |||||||
| chr11:134403256 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0304 |
3 | HG01891.hp1 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-282+8551G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403256 | |||||||
| chr11:134403265 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-282+8542A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403265 | |||||||
| chr11:134403272 | C | T | 1 | a0001c0001t0008g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-282+8535G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403272 | |||||||
| chr11:134403273 | G | A | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+8534C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403273 | |||||||
| chr11:134403327 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-282+8480G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403327 | |||||||
| chr11:134403385 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+8422G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403385 | |||||||
| chr11:134403410 | A | G | 53 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(50): Show |
58 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.-282+8397T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403410 | |||||||
| chr11:134403450 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-282+8357G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403450 | |||||||
| chr11:134403521 | G | C | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+8286C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403521 | |||||||
| chr11:134403665 | C | T | 71 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0178 others(68): Show |
78 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(75): Show |
intron_variant | MODIFIER | c.-282+8142G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403665 | |||||||
| chr11:134403742 | G | A | 1 | a0002c0002t0002g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+8065C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403742 | |||||||
| chr11:134403847 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
5 | HG00639.hp2 HG01106.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7960T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403847 | |||||||
| chr11:134403879 | C | G | 1 | a0001c0001t0049g0246 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-282+7928G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403879 | |||||||
| chr11:134403973 | G | T | 37 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0003g0176 others(34): Show |
41 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.-282+7834C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403973 | |||||||
| chr11:134403977 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-282+7830G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403977 | |||||||
| chr11:134403979 | TTCTTTA | T | 5 | a0001c0001t0010g0174 a0001c0001t0045g0202 a0002c0002t0001g0175 others(2): Show |
5 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(1): Show |
T | 4 | a0001c0001t0001g0178 a0001c0001t0003g0177 a0001c0001t0003g0180 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(3): Show |
T | 3 | a0001c0001t0003g0176 a0002c0002t0006g0067 a0002c0002t0016g0036 |
3 | HG02055.hp2 HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(5): Show |
T | 1 | a0002c0002t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-282+7816_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(17): Show |
T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+7804_-282+782 others(28): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(19): Show |
T | 1 | a0002c0002t0001g0027 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+7802_-282+782 others(30): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(21): Show |
T | 4 | a0001c0001t0004g0029 a0001c0001t0004g0230 a0001c0001t0014g0069 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+7800_-282+782 others(32): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(23): Show |
T | 10 | a0001c0001t0001g0077 a0001c0001t0004g0228 a0001c0001t0004g0229 others(7): Show |
10 | HG01256.hp1 HG01261.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+7798_-282+782 others(34): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403979 | TTCTTTAT others(25): Show |
T | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+7796_-282+782 others(36): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403979 | |||||||
| chr11:134403981 | C | A | 2 | a0002c0002t0001g0211 a0002c0002t0006g0066 |
2 | HG01074.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-282+7826G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403981 | |||||||
| chr11:134403981 | CT | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0130 a0001c0001t0002g0267 others(1): Show |
4 | HG00609.hp1 HG00642.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7825delA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403981 | |||||||
| chr11:134403983 | T | A | 7 | a0001c0001t0001g0188 a0001c0001t0002g0267 a0001c0001t0006g0050 others(4): Show |
7 | HG01074.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+7824A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TA | 3 | a0001c0001t0001g0091 a0001c0001t0001g0172 a0001c0001t0020g0125 |
3 | HG00438.hp2 HG02083.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-282+7823_-282+782 others(5): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
42 | HG00597.hp2 HG00621.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATA | 38 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0021 others(35): Show |
43 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0088 others(10): Show |
13 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0003g0096 |
3 | HG02074.hp1 NA18612.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-282+7816_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0028 a0001c0001t0027g0034 |
2 | HG00544.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-282+7814_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0119 |
2 | HG00558.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-282+7812_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATAT others(9): Show |
1 | a0001c0001t0002g0281 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-282+7808_-282+782 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0274 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-282+7806_-282+782 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTA | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(28): Show |
34 | HG00438.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.-282+7822_-282+782 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATA | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(19): Show |
23 | HG00323.hp2 HG00408.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-282+7820_-282+782 others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATA | T | 13 | a0001c0001t0001g0121 a0001c0001t0001g0159 a0001c0001t0001g0197 others(10): Show |
13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+7818_-282+782 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(1): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0141 others(13): Show |
16 | HG00099.hp2 HG01109.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-282+7816_-282+782 others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(3): Show |
T | 4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0004g0244 others(1): Show |
4 | HG02698.hp1 HG02735.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7814_-282+782 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(5): Show |
T | 8 | a0001c0001t0001g0155 a0001c0001t0006g0052 a0001c0001t0006g0059 others(5): Show |
8 | HG00280.hp1 HG03017.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+7812_-282+782 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(7): Show |
T | 6 | a0001c0001t0009g0215 a0001c0001t0009g0219 a0001c0001t0026g0033 others(3): Show |
6 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+7810_-282+782 others(18): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0213 a0001c0001t0003g0201 others(1): Show |
4 | HG00099.hp1 HG02717.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+7808_-282+782 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0021g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-282+7806_-282+782 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403983 | TTATATAT others(25): Show |
T | 1 | a0001c0001t0005g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-282+7792_-282+782 others(36): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403983 | |||||||
| chr11:134403994 | T | C | 1 | a0001c0001t0009g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-282+7813A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403994 | |||||||
| chr11:134403996 | T | C | 2 | a0001c0001t0009g0216 a0001c0001t0009g0217 |
2 | NA18954.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-282+7811A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403996 | |||||||
| chr11:134403998 | T | C | 6 | a0001c0001t0009g0215 a0001c0001t0009g0219 a0001c0001t0026g0033 others(3): Show |
6 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+7809A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134403998 | |||||||
| chr11:134404019 | A | T | 1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+7788T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404019 | |||||||
| chr11:134404023 | A | T | 2 | a0001c0001t0004g0244 a0002c0002t0002g0305 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-282+7784T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404023 | |||||||
| chr11:134404027 | A | ATATATAT others(3): Show |
1 | a0001c0001t0039g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATATATAT others(11): Show |
1 | a0001c0003t0004g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(22): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATATATAT others(9): Show |
1 | a0001c0003t0004g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(20): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATATATT | 3 | a0001c0001t0001g0196 a0001c0001t0007g0108 a0001c0001t0019g0065 |
3 | HG02080.hp2 HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-282+7779_-282+778 others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATATTTAT others(5): Show |
1 | a0001c0003t0004g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(16): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATT | 2 | a0001c0001t0010g0011 a0001c0001t0019g0051 |
3 | HG01358.hp1 HG01952.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-282+7779_-282+778 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | ATTTATTT others(3): Show |
1 | a0001c0001t0044g0073 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+7779_-282+778 others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404027 | A | T | 19 | a0001c0001t0001g0089 a0001c0001t0004g0223 a0001c0001t0004g0239 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+7780T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404027 | |||||||
| chr11:134404031 | T | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0110 others(6): Show |
11 | HG00609.hp1 HG00639.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+7776A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404031 | |||||||
| chr11:134404039 | C | T | 28 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0004g0223 others(25): Show |
30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+7768G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404039 | |||||||
| chr11:134404040 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-282+7767C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404040 | |||||||
| chr11:134404111 | C | T | 23 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0004g0227 others(20): Show |
25 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-282+7696G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404111 | |||||||
| chr11:134404112 | T | G | 65 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0178 others(62): Show |
71 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.-282+7695A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404112 | |||||||
| chr11:134404113 | G | A | 16 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(13): Show |
17 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-282+7694C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404113 | |||||||
| chr11:134404117 | C | T | 65 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0178 others(62): Show |
71 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.-282+7690G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404117 | |||||||
| chr11:134404275 | G | GT | 18 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0007g0010 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+7531dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404275 | |||||||
| chr11:134404290 | G | A | 8 | a0001c0001t0001g0196 a0001c0001t0001g0213 a0001c0001t0003g0201 others(5): Show |
8 | HG02257.hp2 HG02809.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+7517C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404290 | |||||||
| chr11:134404445 | A | T | 1 | a0001c0001t0013g0291 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-282+7362T>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404445 | |||||||
| chr11:134404484 | C | T | 2 | a0001c0001t0009g0215 a0001c0001t0026g0033 |
2 | NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-282+7323G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404484 | |||||||
| chr11:134404656 | C | A | 17 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0007g0010 others(14): Show |
19 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+7151G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404656 | |||||||
| chr11:134404681 | G | A | 28 | a0001c0001t0001g0089 a0001c0001t0002g0295 a0001c0001t0004g0223 others(25): Show |
30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+7126C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404681 | |||||||
| chr11:134404694 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0003g0176 a0001c0001t0003g0177 |
3 | HG01884.hp1 HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-282+7113G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404694 | |||||||
| chr11:134404782 | A | G | 80 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0106 others(77): Show |
87 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.-282+7025T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404782 | |||||||
| chr11:134404816 | A | G | 79 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0106 others(76): Show |
86 | HG00544.hp1 HG00673.hp2 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.-282+6991T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404816 | |||||||
| chr11:134404820 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-282+6987C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404820 | |||||||
| chr11:134404831 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0003g0097 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-282+6976T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404831 | |||||||
| chr11:134404869 | C | T | 33 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(30): Show |
35 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.-282+6938G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404869 | |||||||
| chr11:134404885 | C | G | 1 | a0001c0001t0003g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-282+6922G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404885 | |||||||
| chr11:134404979 | T | C | 1 | a0001c0001t0008g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-282+6828A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134404979 | |||||||
| chr11:134405066 | G | C | 1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+6741C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405066 | |||||||
| chr11:134405095 | T | TG | 10 | a0001c0001t0001g0213 a0001c0001t0004g0236 a0001c0001t0006g0057 others(7): Show |
10 | HG00544.hp2 HG02602.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+6711dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405095 | |||||||
| chr11:134405101 | G | A | 1 | a0001c0001t0050g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-282+6706C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405101 | |||||||
| chr11:134405129 | G | A | 2 | a0001c0001t0031g0044 a0001c0001t0054g0260 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-282+6678C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405129 | |||||||
| chr11:134405559 | C | T | 28 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0002g0031 others(25): Show |
32 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+6248G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405559 | |||||||
| chr11:134405561 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-282+6246C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405561 | |||||||
| chr11:134405643 | C | A | 18 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(15): Show |
19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+6164G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405643 | |||||||
| chr11:134405675 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
8 | NA18948.hp1 NA18951.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+6132G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405675 | |||||||
| chr11:134405742 | AG | A | 14 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0228 others(11): Show |
15 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+6064delC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405742 | |||||||
| chr11:134405788 | T | A | 1 | a0001c0001t0009g0218 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-282+6019A>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405788 | |||||||
| chr11:134405850 | C | T | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-282+5957G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405850 | |||||||
| chr11:134405852 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(301): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-282+5955T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405852 | |||||||
| chr11:134405962 | C | T | 1 | a0001c0001t0007g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-282+5845G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134405962 | |||||||
| chr11:134406028 | C | T | 26 | a0001c0001t0001g0089 a0001c0001t0001g0100 a0001c0001t0002g0295 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-282+5779G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406028 | |||||||
| chr11:134406092 | G | A | 51 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0002g0295 others(48): Show |
56 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-282+5715C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406092 | |||||||
| chr11:134406167 | C | T | 1 | a0001c0001t0008g0023 | 2 | HG01433.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-282+5640G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406167 | |||||||
| chr11:134406248 | A | G | 74 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0178 others(71): Show |
81 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.-282+5559T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406248 | |||||||
| chr11:134406408 | A | G | 49 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0002g0031 others(46): Show |
53 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.-282+5399T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406408 | |||||||
| chr11:134406472 | C | A | 1 | a0001c0001t0001g0154 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-282+5335G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406472 | |||||||
| chr11:134406938 | A | AGGTCCAC others(51): Show |
50 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(47): Show |
55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+4868_-282+486 others(62): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406938 | |||||||
| chr11:134406970 | C | A | 9 | a0001c0001t0009g0215 a0001c0001t0009g0216 a0001c0001t0009g0217 others(6): Show |
9 | HG02015.hp2 HG02056.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+4837G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406970 | |||||||
| chr11:134406971 | G | A | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+4836C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134406971 | |||||||
| chr11:134407076 | C | T | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(25): Show |
30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+4731G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407076 | |||||||
| chr11:134407316 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0155 a0001c0001t0006g0059 |
3 | HG00408.hp2 NA18942.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-282+4491A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407316 | |||||||
| chr11:134407558 | C | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+4249G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407558 | |||||||
| chr11:134407603 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-282+4204T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407603 | |||||||
| chr11:134407635 | C | T | 1 | a0001c0001t0005g0264 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-282+4172G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407635 | |||||||
| chr11:134407736 | C | CA | 31 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0157 others(28): Show |
32 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-282+4070dupT | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407736 | |||||||
| chr11:134407736 | C | CAA | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+4069_-282+407 others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407736 | |||||||
| chr11:134407766 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0006g0062 |
5 | HG00609.hp1 NA18960.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+4041A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407766 | |||||||
| chr11:134407856 | G | A | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(25): Show |
30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+3951C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407856 | |||||||
| chr11:134407921 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(2): Show |
6 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3886G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407921 | |||||||
| chr11:134407972 | A | AT | 50 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(47): Show |
55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+3834dupA | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407972 | |||||||
| chr11:134407987 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-282+3820G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407987 | |||||||
| chr11:134407990 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-282+3817G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134407990 | |||||||
| chr11:134408084 | G | A | 67 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(64): Show |
72 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.-282+3723C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408084 | |||||||
| chr11:134408116 | G | T | 28 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(25): Show |
30 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-282+3691C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408116 | |||||||
| chr11:134408157 | C | CGGGTGAG others(75): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
9 | HG00735.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | |||||||
| chr11:134408157 | C | CGGGTGAG others(75): Show |
238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | |||||||
| chr11:134408157 | C | CGGGTGAG others(608): Show |
2 | a0001c0001t0001g0098 a0001c0001t0003g0097 |
2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.-282+3649_-282+365 others(619): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408157 | |||||||
| chr11:134408188 | C | CGATTCCA others(75): Show |
3 | a0001c0001t0003g0012 a0001c0001t0003g0096 a0002c0002t0001g0095 |
4 | HG01192.hp2 HG02723.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3618_-282+361 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408188 | |||||||
| chr11:134408225 | G | C | 9 | a0001c0001t0004g0223 a0001c0001t0004g0227 a0001c0001t0004g0244 others(6): Show |
9 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-282+3582C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408225 | G | GCACCGAC others(116): Show |
12 | a0001c0001t0003g0180 a0001c0001t0010g0174 a0001c0001t0045g0202 others(9): Show |
12 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3581_-282+358 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408225 | G | GCACCGAC others(1428): Show |
1 | a0001c0001t0001g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(1439): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408225 | G | GCACCGAC others(4134): Show |
1 | a0001c0001t0001g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(4145): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408225 | G | GCACCGAC others(1469): Show |
2 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-282+3581_-282+358 others(1480): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408225 | G | GCACCGAC others(1428): Show |
1 | a0002c0002t0001g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-282+3581_-282+358 others(1439): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408225 | |||||||
| chr11:134408230 | T | G | 33 | a0001c0001t0001g0165 a0001c0001t0003g0180 a0001c0001t0004g0006 others(30): Show |
36 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-282+3577A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408230 | |||||||
| chr11:134408230 | T | TATTCCAG others(198): Show |
1 | a0001c0001t0035g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-282+3576_-282+357 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408230 | |||||||
| chr11:134408232 | T | C | 11 | a0001c0001t0001g0165 a0001c0001t0004g0006 a0001c0001t0004g0235 others(8): Show |
13 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+3575A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408232 | |||||||
| chr11:134408235 | T | C | 58 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0001g0178 others(55): Show |
63 | HG01074.hp2 HG01081.hp2 HG01168.hp2 others(60): Show |
intron_variant | MODIFIER | c.-282+3572A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408235 | |||||||
| chr11:134408237 | G | A | 11 | a0001c0001t0001g0165 a0001c0001t0004g0006 a0001c0001t0004g0235 others(8): Show |
13 | HG01168.hp2 HG01169.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-282+3570C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408237 | |||||||
| chr11:134408246 | A | G | 57 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0001g0178 others(54): Show |
62 | HG01074.hp2 HG01081.hp2 HG01168.hp2 others(59): Show |
intron_variant | MODIFIER | c.-282+3561T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408246 | |||||||
| chr11:134408266 | G | GCACCGAC others(116): Show |
3 | a0001c0001t0018g0041 a0001c0001t0022g0232 a0001c0001t0022g0233 |
3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3540_-282+354 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408266 | |||||||
| chr11:134408271 | G | GATTCCAG others(116): Show |
1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+3535_-282+353 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408271 | |||||||
| chr11:134408271 | G | T | 12 | a0001c0001t0003g0180 a0001c0001t0010g0174 a0001c0001t0045g0202 others(9): Show |
12 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3536C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408271 | |||||||
| chr11:134408273 | T | C | 15 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(12): Show |
17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3534A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408273 | |||||||
| chr11:134408278 | G | C | 3 | a0001c0001t0013g0290 a0001c0001t0013g0291 a0001c0001t0013g0303 |
3 | HG01496.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-282+3529C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408278 | |||||||
| chr11:134408281 | G | C | 3 | a0001c0001t0018g0041 a0001c0001t0022g0232 a0001c0001t0022g0233 |
3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3526C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408281 | |||||||
| chr11:134408287 | G | GGAGGGAG others(34): Show |
4 | a0001c0001t0001g0165 a0001c0001t0005g0254 a0001c0001t0031g0044 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3519_-282+352 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408287 | |||||||
| chr11:134408312 | G | GATTCCAG others(280): Show |
1 | a0001c0003t0001g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-282+3208_-282+349 others(291): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408312 | |||||||
| chr11:134408312 | G | T | 2 | a0001c0001t0005g0292 a0001c0001t0024g0263 |
2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3495C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408312 | |||||||
| chr11:134408314 | T | C | 15 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(12): Show |
17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3493A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408314 | |||||||
| chr11:134408317 | C | T | 2 | a0001c0001t0005g0292 a0001c0001t0024g0263 |
2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3490G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408317 | |||||||
| chr11:134408328 | G | A | 2 | a0001c0001t0005g0292 a0001c0001t0024g0263 |
2 | HG02683.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-282+3479C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408328 | |||||||
| chr11:134408333 | G | C | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3474C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408333 | |||||||
| chr11:134408348 | G | C | 15 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(12): Show |
17 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-282+3459C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408348 | |||||||
| chr11:134408353 | G | T | 13 | a0001c0001t0003g0180 a0001c0001t0010g0174 a0001c0001t0035g0048 others(10): Show |
13 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-282+3454C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408353 | |||||||
| chr11:134408389 | C | CCACCTAT others(75): Show |
1 | a0001c0001t0044g0073 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3417_-282+341 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | |||||||
| chr11:134408389 | C | CCACCTAT others(321): Show |
4 | a0001c0001t0004g0223 a0001c0003t0004g0224 a0001c0003t0004g0225 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3417_-282+341 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | |||||||
| chr11:134408389 | C | G | 33 | a0001c0001t0001g0028 a0001c0001t0001g0165 a0001c0001t0001g0178 others(30): Show |
37 | HG01074.hp2 HG01243.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.-282+3418G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408389 | |||||||
| chr11:134408393 | C | CTATTCCA others(198): Show |
1 | a0002c0002t0002g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+3413_-282+341 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408393 | |||||||
| chr11:134408394 | G | GATTCCAG others(34): Show |
1 | a0001c0001t0044g0073 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3412_-282+341 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408394 | |||||||
| chr11:134408394 | G | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0214 a0001c0001t0004g0006 others(6): Show |
12 | HG02109.hp1 HG02451.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.-282+3413C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408394 | |||||||
| chr11:134408396 | T | C | 4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0025g0032 others(1): Show |
4 | HG02698.hp1 HG02735.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+3411A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | |||||||
| chr11:134408396 | T | TTCCAGTG others(239): Show |
10 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0228 others(7): Show |
11 | HG01257.hp1 HG01258.hp2 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+3410_-282+341 others(250): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | |||||||
| chr11:134408396 | T | TTCCAGTG others(116): Show |
3 | a0001c0001t0018g0041 a0001c0001t0022g0232 a0001c0001t0022g0233 |
3 | HG01256.hp1 HG01934.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-282+3410_-282+341 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408396 | |||||||
| chr11:134408404 | G | C | 1 | a0001c0001t0018g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3403C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408404 | |||||||
| chr11:134408430 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0005g0254 |
2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-282+3377C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408430 | |||||||
| chr11:134408430 | G | GCACCTAT others(280): Show |
1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3376_-282+337 others(291): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408430 | |||||||
| chr11:134408435 | G | T | 1 | a0001c0001t0004g0223 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-282+3372C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408435 | |||||||
| chr11:134408437 | C | T | 26 | a0001c0001t0001g0165 a0001c0001t0001g0178 a0001c0001t0001g0203 others(23): Show |
30 | HG01081.hp2 HG01243.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.-282+3370G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408437 | |||||||
| chr11:134408471 | G | C | 14 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0228 others(11): Show |
15 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+3336C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408471 | |||||||
| chr11:134408471 | G | GCACCGAT others(239): Show |
4 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(1): Show |
5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+3335_-282+333 others(250): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408471 | |||||||
| chr11:134408478 | T | C | 15 | a0001c0001t0001g0165 a0001c0001t0002g0295 a0001c0001t0003g0180 others(12): Show |
15 | HG01074.hp2 HG01243.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-282+3329A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408478 | |||||||
| chr11:134408512 | G | C | 2 | a0001c0001t0035g0048 a0001c0001t0044g0073 |
2 | HG02897.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-282+3295C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408512 | |||||||
| chr11:134408517 | G | GACTCCAG others(321): Show |
1 | a0002c0002t0001g0027 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3289_-282+329 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408517 | |||||||
| chr11:134408519 | T | C | 14 | a0001c0001t0002g0295 a0001c0001t0003g0180 a0001c0001t0005g0292 others(11): Show |
14 | HG01074.hp2 HG01243.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-282+3288A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408519 | |||||||
| chr11:134408547 | T | C | 55 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0001g0178 others(52): Show |
60 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-282+3260A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408547 | |||||||
| chr11:134408553 | G | GCACCGAT others(75): Show |
6 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0229 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3253_-282+325 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408553 | |||||||
| chr11:134408558 | T | G | 38 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0002g0031 others(35): Show |
41 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-282+3249A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | |||||||
| chr11:134408558 | T | TATTCCAG others(34): Show |
6 | a0001c0001t0004g0223 a0001c0001t0004g0227 a0001c0003t0004g0224 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+3248_-282+324 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | |||||||
| chr11:134408558 | T | TATTCCAG others(157): Show |
1 | a0001c0001t0018g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3248_-282+324 others(168): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408558 | |||||||
| chr11:134408560 | T | C | 2 | a0001c0001t0044g0073 a0002c0002t0001g0027 |
3 | HG01243.hp1 HG02055.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-282+3247A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408560 | |||||||
| chr11:134408588 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0005g0254 |
2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-282+3219G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408588 | |||||||
| chr11:134408599 | T | G | 34 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0002g0031 others(31): Show |
38 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.-282+3208A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408599 | |||||||
| chr11:134408601 | T | TTCCAGTG others(34): Show |
4 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(1): Show |
5 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+3205_-282+320 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408601 | |||||||
| chr11:134408609 | G | GGGTGAGG others(116): Show |
1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+3197_-282+319 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408609 | |||||||
| chr11:134408616 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-282+3191C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408616 | |||||||
| chr11:134408629 | C | T | 1 | a0001c0001t0005g0292 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-282+3178G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408629 | |||||||
| chr11:134408632 | C | T | 1 | a0001c0001t0018g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3175G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408632 | |||||||
| chr11:134408635 | G | C | 8 | a0001c0001t0004g0029 a0001c0001t0004g0228 a0001c0001t0004g0230 others(5): Show |
8 | HG01257.hp1 HG01934.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-282+3172C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408635 | |||||||
| chr11:134408635 | G | GCACCGTC others(444): Show |
1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+3171_-282+317 others(455): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408635 | |||||||
| chr11:134408640 | G | GATTCCAG others(75): Show |
1 | a0001c0001t0035g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-282+3166_-282+316 others(86): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | |||||||
| chr11:134408640 | G | GATTCCAG others(198): Show |
1 | a0001c0001t0055g0262 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-282+3166_-282+316 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | |||||||
| chr11:134408640 | G | T | 8 | a0001c0001t0001g0165 a0001c0001t0004g0006 a0001c0001t0004g0235 others(5): Show |
10 | HG02109.hp1 HG02683.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-282+3167C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408640 | |||||||
| chr11:134408642 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0229 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3165A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | |||||||
| chr11:134408642 | T | TTCCAGTG others(526): Show |
7 | a0002c0002t0001g0198 a0002c0002t0001g0204 a0002c0002t0001g0205 others(4): Show |
7 | HG01074.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+3164_-282+316 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | |||||||
| chr11:134408642 | T | TTCCAGTG others(526): Show |
1 | a0001c0001t0010g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+3164_-282+316 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408642 | |||||||
| chr11:134408665 | T | C | 1 | a0002c0002t0001g0027 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3142A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408665 | |||||||
| chr11:134408670 | T | C | 47 | a0001c0001t0001g0077 a0001c0001t0001g0165 a0001c0001t0001g0178 others(44): Show |
51 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(48): Show |
intron_variant | MODIFIER | c.-282+3137A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408670 | |||||||
| chr11:134408676 | G | C | 9 | a0001c0001t0010g0174 a0002c0002t0001g0027 a0002c0002t0001g0198 others(6): Show |
10 | HG01074.hp2 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-282+3131C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408676 | |||||||
| chr11:134408676 | G | GCACCGAT others(526): Show |
1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+3130_-282+313 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408676 | |||||||
| chr11:134408681 | T | G | 37 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0002g0031 others(34): Show |
40 | HG01081.hp2 HG01257.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.-282+3126A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408681 | |||||||
| chr11:134408706 | T | C | 1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+3101A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408706 | |||||||
| chr11:134408711 | C | T | 1 | a0001c0001t0005g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3096G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408711 | |||||||
| chr11:134408717 | G | C | 1 | a0001c0001t0018g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+3090C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | |||||||
| chr11:134408717 | G | GCACCGAC others(116): Show |
7 | a0001c0001t0004g0029 a0001c0001t0004g0228 a0001c0001t0004g0230 others(4): Show |
7 | HG01257.hp1 HG01934.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+3089_-282+309 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | |||||||
| chr11:134408717 | G | GCACCGAT others(34): Show |
6 | a0001c0001t0001g0077 a0001c0001t0004g0029 a0001c0001t0004g0229 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-282+3089_-282+309 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408717 | |||||||
| chr11:134408722 | G | GATTCCAG others(198): Show |
1 | a0001c0001t0001g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-282+3084_-282+308 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | |||||||
| chr11:134408722 | G | GATTCCAG others(198): Show |
1 | a0001c0001t0001g0094 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-282+2880_-282+308 others(209): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | |||||||
| chr11:134408722 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3085C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408722 | |||||||
| chr11:134408724 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0167 others(2): Show |
7 | HG01433.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-282+3083A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408724 | |||||||
| chr11:134408724 | T | TTCCAGTG others(321): Show |
1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+3082_-282+308 others(332): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408724 | |||||||
| chr11:134408758 | G | GCACCGAT others(1100): Show |
1 | a0002c0002t0001g0027 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+3048_-282+304 others(1111): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408758 | |||||||
| chr11:134408763 | T | G | 35 | a0001c0001t0001g0077 a0001c0001t0001g0172 a0001c0001t0001g0178 others(32): Show |
37 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.-282+3044A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | |||||||
| chr11:134408763 | T | TATTCCAG others(34): Show |
1 | a0001c0001t0044g0073 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-282+3003_-282+304 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | |||||||
| chr11:134408763 | T | TATTCCAG others(485): Show |
2 | a0001c0001t0004g0006 a0001c0001t0014g0070 |
2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-282+3043_-282+304 others(496): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408763 | |||||||
| chr11:134408804 | G | GATTCCAG others(362): Show |
1 | a0001c0001t0004g0234 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-282+3002_-282+300 others(373): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | |||||||
| chr11:134408804 | G | GATTCCAG others(608): Show |
4 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(1): Show |
5 | HG02109.hp1 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-282+3002_-282+300 others(619): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | |||||||
| chr11:134408804 | G | T | 1 | a0001c0001t0005g0254 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-282+3003C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408804 | |||||||
| chr11:134408806 | C | CTCCAGTG others(157): Show |
1 | a0001c0001t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-282+2837_-282+300 others(168): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408806 | |||||||
| chr11:134408806 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(18): Show |
22 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-282+3001G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408806 | |||||||
| chr11:134408834 | C | T | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+2973G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408834 | |||||||
| chr11:134408837 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-282+2970G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408837 | |||||||
| chr11:134408845 | T | G | 18 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-282+2962A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408845 | |||||||
| chr11:134408845 | T | TATTCCAG others(34): Show |
1 | a0001c0001t0018g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-282+2921_-282+296 others(45): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408845 | |||||||
| chr11:134408847 | T | C | 2 | a0001c0001t0004g0227 a0002c0002t0001g0027 |
3 | HG01243.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-282+2960A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408847 | |||||||
| chr11:134408886 | G | T | 2 | a0001c0001t0001g0196 a0002c0002t0001g0027 |
3 | HG01243.hp1 HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-282+2921C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408886 | |||||||
| chr11:134408911 | T | C | 11 | a0001c0001t0004g0006 a0001c0001t0010g0174 a0001c0001t0014g0070 others(8): Show |
11 | HG01074.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+2896A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408911 | |||||||
| chr11:134408916 | T | C | 23 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(20): Show |
25 | HG01243.hp1 HG01261.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-282+2891A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408916 | |||||||
| chr11:134408922 | C | G | 24 | a0001c0001t0001g0092 a0001c0001t0001g0178 a0001c0001t0001g0203 others(21): Show |
26 | HG00408.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-282+2885G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408922 | |||||||
| chr11:134408927 | T | G | 22 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(19): Show |
24 | HG01243.hp1 HG01261.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-282+2880A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | |||||||
| chr11:134408927 | T | TATTCCAG others(116): Show |
18 | a0001c0001t0001g0077 a0001c0001t0002g0031 a0001c0001t0002g0296 others(15): Show |
20 | HG01081.hp2 HG01256.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-282+2879_-282+288 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | |||||||
| chr11:134408927 | T | TATTCCAG others(116): Show |
1 | a0001c0001t0014g0069 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-282+2879_-282+288 others(127): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408927 | |||||||
| chr11:134408929 | T | C | 1 | a0002c0002t0001g0027 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.-282+2878A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1633): Show |
1 | a0002c0002t0001g0175 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1644): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1838): Show |
2 | a0001c0001t0003g0180 a0002c0002t0001g0179 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(1849): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(526): Show |
5 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(537): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1346): Show |
1 | a0002c0002t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1357): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1305): Show |
1 | a0001c0001t0010g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1316): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1346): Show |
6 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0211 others(3): Show |
6 | HG01074.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-282+2877_-282+287 others(1357): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134408929 | T | TTCCAGTG others(1305): Show |
1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+2877_-282+287 others(1316): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134408929 | |||||||
| chr11:134409226 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0003g0090 |
2 | NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-282+2581G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409226 | |||||||
| chr11:134409233 | G | C | 3 | a0001c0001t0001g0169 a0001c0001t0007g0022 a0001c0001t0007g0170 |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+2574C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409233 | |||||||
| chr11:134409234 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-282+2573G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409234 | |||||||
| chr11:134409268 | C | T | 6 | a0001c0001t0001g0089 a0001c0001t0007g0010 a0001c0001t0010g0011 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-282+2539G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409268 | |||||||
| chr11:134409297 | A | G | 11 | a0001c0001t0001g0088 a0001c0001t0002g0255 a0001c0001t0002g0256 others(8): Show |
11 | HG00558.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-282+2510T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409297 | |||||||
| chr11:134409458 | T | C | 50 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(47): Show |
55 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-282+2349A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409458 | |||||||
| chr11:134409547 | G | A | 2 | a0001c0001t0003g0171 a0001c0001t0049g0246 |
2 | HG00099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-282+2260C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409547 | |||||||
| chr11:134409595 | C | A | 1 | a0001c0001t0046g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-282+2212G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409595 | |||||||
| chr11:134409633 | C | T | 5 | a0001c0001t0004g0239 a0001c0001t0012g0238 a0001c0001t0012g0240 others(2): Show |
5 | HG02723.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+2174G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409633 | |||||||
| chr11:134409697 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-282+2110G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409697 | |||||||
| chr11:134409697 | C | T | 18 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0003g0176 others(15): Show |
19 | HG01074.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+2110G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409697 | |||||||
| chr11:134409815 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-282+1992C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409815 | |||||||
| chr11:134409830 | G | A | 1 | a0001c0003t0048g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-282+1977C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409830 | |||||||
| chr11:134409932 | G | C | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+1875C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409932 | |||||||
| chr11:134409935 | C | T | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+1872G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409935 | |||||||
| chr11:134409988 | T | C | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1819A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134409988 | |||||||
| chr11:134410036 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-282+1771T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410036 | |||||||
| chr11:134410094 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-282+1713G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410094 | |||||||
| chr11:134410156 | C | T | 1 | a0001c0001t0004g0223 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-282+1651G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410156 | |||||||
| chr11:134410170 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-282+1637C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410170 | |||||||
| chr11:134410173 | G | A | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1634C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410173 | |||||||
| chr11:134410176 | G | T | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+1631C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410176 | |||||||
| chr11:134410191 | A | C | 1 | a0001c0001t0004g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-282+1616T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410191 | |||||||
| chr11:134410232 | A | C | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1575T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410232 | |||||||
| chr11:134410397 | C | T | 4 | a0001c0001t0001g0181 a0001c0001t0003g0084 a0001c0001t0008g0023 others(1): Show |
5 | HG01109.hp1 HG01433.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-282+1410G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410397 | |||||||
| chr11:134410549 | T | C | 1 | a0001c0001t0004g0244 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-282+1258A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410549 | |||||||
| chr11:134410609 | G | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1198C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410609 | |||||||
| chr11:134410610 | C | T | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1197G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410610 | |||||||
| chr11:134410627 | T | C | 46 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(43): Show |
49 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-282+1180A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410627 | |||||||
| chr11:134410630 | C | T | 1 | a0002c0002t0002g0305 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-282+1177G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410630 | |||||||
| chr11:134410666 | G | A | 1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+1141C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410666 | |||||||
| chr11:134410668 | C | G | 1 | a0001c0001t0015g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-282+1139G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410668 | |||||||
| chr11:134410728 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-282+1079G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410728 | |||||||
| chr11:134410840 | G | A | 1 | a0001c0001t0010g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-282+967C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410840 | |||||||
| chr11:134410843 | C | T | 1 | a0001c0001t0020g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-282+964G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410843 | |||||||
| chr11:134410872 | A | G | 62 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(59): Show |
67 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.-282+935T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410872 | |||||||
| chr11:134410966 | C | A | 57 | a0001c0001t0001g0077 a0001c0001t0001g0178 a0001c0001t0001g0203 others(54): Show |
60 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-282+841G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134410966 | |||||||
| chr11:134411011 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-282+796C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411011 | |||||||
| chr11:134411031 | G | C | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+776C>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411031 | |||||||
| chr11:134411084 | G | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+723C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411084 | |||||||
| chr11:134411108 | A | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0006g0050 |
3 | HG00621.hp2 NA18984.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-282+699T>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411108 | |||||||
| chr11:134411137 | T | C | 3 | a0001c0001t0002g0295 a0001c0001t0003g0074 a0001c0001t0053g0294 |
3 | HG01243.hp2 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-282+670A>G | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411137 | |||||||
| chr11:134411249 | C | A | 9 | a0001c0001t0001g0196 a0001c0001t0001g0213 a0001c0001t0003g0201 others(6): Show |
9 | HG02257.hp2 HG02809.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.-282+558G>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411249 | |||||||
| chr11:134411309 | C | T | 1 | a0001c0001t0010g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-282+498G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411309 | |||||||
| chr11:134411326 | C | T | 34 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0002g0031 others(31): Show |
36 | HG01074.hp2 HG01081.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-282+481G>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411326 | |||||||
| chr11:134411435 | G | T | 10 | a0001c0001t0002g0031 a0001c0001t0002g0296 a0001c0001t0002g0297 others(7): Show |
11 | HG01081.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-282+372C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411435 | |||||||
| chr11:134411438 | T | G | 24 | a0001c0001t0001g0077 a0001c0001t0004g0006 a0001c0001t0004g0029 others(21): Show |
27 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.-282+369A>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411438 | |||||||
| chr11:134411601 | C | G | 1 | a0001c0001t0045g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-282+206G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411601 | |||||||
| chr11:134411619 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-282+188C>T | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411619 | |||||||
| chr11:134411663 | G | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0034g0047 |
3 | NA18998.hp1 NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-282+144C>A | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411663 | |||||||
| chr11:134411667 | A | AGC | 5 | a0001c0001t0004g0006 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
7 | HG02109.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+138_-282+139d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411667 | |||||||
| chr11:134411670 | G | GCA | 18 | a0001c0001t0001g0026 a0001c0001t0002g0304 a0001c0001t0002g0308 others(15): Show |
19 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-282+135_-282+136d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | G | GCACA | 15 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0214 others(12): Show |
16 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-282+133_-282+136d others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | G | GCACACA | 3 | a0001c0003t0001g0212 a0002c0002t0001g0211 a0002c0002t0016g0036 |
3 | HG02258.hp1 HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-282+131_-282+136d others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0213 a0001c0001t0012g0245 |
4 | HG02723.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+129_-282+136d others(10): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | GCA | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-282+135_-282+136d others(4): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | GCACA | G | 15 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0004g0227 others(12): Show |
15 | HG00642.hp2 HG01256.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-282+133_-282+136d others(6): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | GCACACA | G | 7 | a0001c0001t0002g0252 a0001c0001t0004g0223 a0001c0001t0044g0073 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+131_-282+136d others(8): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | GCACACAC others(3): Show |
G | 7 | a0001c0001t0009g0215 a0001c0001t0009g0216 a0001c0001t0009g0217 others(4): Show |
7 | HG03688.hp2 NA18954.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-282+127_-282+136d others(12): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411670 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0021g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-282+125_-282+136d others(14): Show |
B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411670 | |||||||
| chr11:134411674 | A | G | 3 | a0001c0001t0003g0009 a0001c0001t0003g0074 a0001c0001t0011g0049 |
4 | HG01255.hp1 HG02257.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-282+133T>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411674 | |||||||
| chr11:134411695 | C | G | 1 | a0001c0001t0047g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-282+112G>C | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411695 | |||||||
| chr11:134411765 | T | TG | 2 | a0001c0001t0001g0028 a0001c0001t0001g0214 |
3 | HG02922.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-282+41dupC | B3GAT1 | ENSG00000109956.13 | transcript | ENST00000312527.9 | protein_coding | 1/5 | chr11 | 134411765 |