| geneid | 2650 |
|---|---|
| ensemblid | ENSG00000187210.14 |
| hgncid | 4203 |
| symbol | GCNT1 |
| name | glucosaminyl (N-acetyl) transferase 1 |
| refseq_nuc | NM_001490.5 |
| refseq_prot | NP_001481.2 |
| ensembl_nuc | ENST00000376730.5 |
| ensembl_prot | ENSP00000365920.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 76459182 |
| end | 76507416 |
| strand | + |
| ver | v1.2 |
| region | chr9:76459182-76507416 |
| region5000 | chr9:76454182-76512416 |
| regionname0 | GCNT1_chr9_76459182_76507416 |
| regionname5000 | GCNT1_chr9_76454182_76512416 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 428 | 252 | 63 | 50 | 99 | 12 | 26 | 67 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002 | 0/0 | 428 | 111 | 21 | 21 | 46 | 5 | 18 | 34 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0003 | 0/0 | 428 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0004 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0005 | 0/0 | 428 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0006 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0007 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1287 | 251 | 63 | 50 | 99 | 12 | 25 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0002 | 0/0 | 1287 | 108 | 20 | 21 | 46 | 5 | 16 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0003 | 0/0 | 1287 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0004 | 0/0 | 1287 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0005 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0006 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0007 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0008 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0009 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| c0010 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4282 | 93 | 14 | 17 | 40 | 5 | 17 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0002 | 0/1 | 4280 | 78 | 1 | 11 | 55 | 4 | 6 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0003 | 1/0 | 4280 | 41 | 5 | 13 | 10 | 5 | 7 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0004 | 0/0 | 4280 | 26 | 8 | 9 | 2 | 0 | 7 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0005 | 0/0 | 4283 | 19 | 3 | 6 | 6 | 3 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0006 | 0/0 | 4284 | 17 | 2 | 2 | 11 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0007 | 0/0 | 4282 | 12 | 10 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0008 | 0/0 | 4280 | 10 | 9 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0009 | 0/0 | 4282 | 7 | 6 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0010 | 0/0 | 4280 | 6 | 0 | 0 | 6 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0011 | 0/0 | 4279 | 4 | 4 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0012 | 0/0 | 4283 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0013 | 0/0 | 4284 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0014 | 0/0 | 4282 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0015 | 0/0 | 4279 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0016 | 0/0 | 4282 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0017 | 0/0 | 4279 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0018 | 0/0 | 4282 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0019 | 0/0 | 4280 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0020 | 0/0 | 4279 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0021 | 0/0 | 4282 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0022 | 0/0 | 4282 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0023 | 0/0 | 4280 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0024 | 0/0 | 4280 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0025 | 0/0 | 4283 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0026 | 0/0 | 4280 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0027 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0028 | 0/0 | 4280 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0029 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0030 | 0/0 | 4280 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0031 | 0/0 | 4280 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0032 | 0/0 | 4280 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0033 | 0/0 | 4258 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0034 | 0/0 | 4280 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0035 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0036 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0037 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0038 | 0/0 | 4284 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0039 | 0/0 | 4280 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0040 | 0/0 | 4279 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0041 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0042 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0043 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0044 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0045 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0046 | 0/0 | 4279 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0047 | 0/0 | 4280 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| t0048 | 0/0 | 4280 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0011 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1287 | 251 | 63 | 50 | 99 | 12 | 25 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0007 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002 | 0/0 | 1287 | 108 | 20 | 21 | 46 | 5 | 16 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0004 | 0/0 | 1287 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0006 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0003c0003 | 0/0 | 1287 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0004c0005 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0005c0009 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0006c0008 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0007c0010 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 5566 | 77 | 1 | 11 | 54 | 4 | 6 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0003 | 1/0 | 5566 | 39 | 5 | 12 | 10 | 5 | 6 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0004 | 0/0 | 5566 | 25 | 7 | 9 | 2 | 0 | 7 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0005 | 0/0 | 5569 | 19 | 3 | 6 | 6 | 3 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0006 | 0/0 | 5570 | 17 | 2 | 2 | 11 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0007 | 0/0 | 5568 | 12 | 10 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0008 | 0/0 | 5566 | 10 | 9 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0010 | 0/0 | 5566 | 6 | 0 | 0 | 6 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0011 | 0/0 | 5565 | 4 | 4 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0012 | 0/0 | 5569 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0013 | 0/0 | 5570 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0014 | 0/0 | 5568 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0018 | 0/0 | 5568 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0019 | 0/0 | 5566 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0020 | 0/0 | 5565 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0021 | 0/0 | 5568 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0022 | 0/0 | 5568 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0023 | 0/0 | 5566 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0024 | 0/0 | 5566 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0025 | 0/0 | 5569 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0026 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0027 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0028 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0030 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0031 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0032 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0033 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0034 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0035 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0036 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0037 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0038 | 0/0 | 5570 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0039 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0041 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0046 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0047 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0001t0048 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0001c0007t0003 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0001 | 0/0 | 5568 | 92 | 14 | 17 | 40 | 5 | 16 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0009 | 0/0 | 5568 | 6 | 5 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0015 | 0/0 | 5565 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0016 | 0/0 | 5568 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0042 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0043 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0044 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0002t0045 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0004t0001 | 0/0 | 5568 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0004t0029 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0002c0006t0009 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0003c0003t0017 | 0/0 | 5565 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0004c0005t0002 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0005c0009t0003 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0006c0008t0004 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| a0007c0010t0040 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | copy fasta | chr9 | 76454182 | 76512416 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0011 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0013g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0013g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0020g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0020g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0021g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0022g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0022g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0023g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0024g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0024g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0025g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0026g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0027g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0028g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0030g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0031g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0032g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0033g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0034g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0035g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0036g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0037g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0038g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0039g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0041g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0046g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0047g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0048g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0007t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0015g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0015g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0016g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0042g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0043g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0044g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0045g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0004t0029g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0006t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0004c0005t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0005c0009t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0006c0008t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0007c0010t0040g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0263 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0328 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00408 | hp2 | a0001 | c0001 | t0031 | g0114 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0167 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0160 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0110 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01074 | hp2 | a0002 | c0002 | t0016 | g0004 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01099 | hp2 | a0005 | c0009 | t0003 | g0053 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01106 | hp2 | a0002 | c0002 | t0009 | g0271 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0307 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0024 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01168 | hp2 | a0002 | c0002 | t0016 | g0004 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01169 | hp1 | a0002 | c0002 | t0016 | g0026 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0024 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0296 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0177 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0302 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01257 | hp1 | a0001 | c0001 | t0013 | g0329 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0153 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0156 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0171 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01496 | hp1 | a0001 | c0001 | t0038 | g0327 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01496 | hp2 | a0001 | c0001 | t0030 | g0095 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0256 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0072 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0096 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0322 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0324 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01891 | hp2 | a0001 | c0001 | t0036 | g0197 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01928 | hp1 | a0001 | c0001 | t0047 | g0097 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02040 | hp2 | a0001 | c0001 | t0020 | g0219 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02055 | hp1 | a0003 | c0003 | t0017 | g0189 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0313 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02145 | hp2 | a0002 | c0002 | t0042 | g0278 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0031 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02572 | hp2 | a0001 | c0001 | t0041 | g0046 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0193 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02698 | hp1 | a0001 | c0001 | t0032 | g0155 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02698 | hp2 | a0001 | c0001 | t0026 | g0060 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02717 | hp1 | a0001 | c0001 | t0046 | g0036 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02717 | hp2 | a0007 | c0010 | t0040 | g0047 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0310 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0280 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0316 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0312 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0244 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0039 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0088 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02897 | hp2 | a0002 | c0002 | t0009 | g0045 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0027 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02965 | hp2 | a0001 | c0001 | t0035 | g0030 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02976 | hp1 | a0002 | c0006 | t0009 | g0040 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0087 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0180 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03453 | hp2 | a0001 | c0001 | t0023 | g0084 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0174 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0187 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0326 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0279 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0325 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03704 | hp2 | a0001 | c0007 | t0003 | g0008 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03710 | hp1 | a0002 | c0004 | t0001 | g0285 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0186 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03927 | hp1 | a0001 | c0001 | t0028 | g0102 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0294 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04184 | hp2 | a0002 | c0004 | t0029 | g0152 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0297 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0207 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0282 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0330 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18522 | hp2 | a0001 | c0001 | t0024 | g0179 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18906 | hp1 | a0002 | c0002 | t0009 | g0038 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18948 | hp1 | a0002 | c0002 | t0045 | g0290 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18949 | hp1 | a0001 | c0001 | t0033 | g0136 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18950 | hp2 | a0001 | c0001 | t0048 | g0291 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0242 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18960 | hp2 | a0004 | c0005 | t0002 | g0145 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0318 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18964 | hp2 | a0001 | c0001 | t0039 | g0144 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0320 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18966 | hp1 | a0002 | c0002 | t0015 | g0017 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0305 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18983 | hp2 | a0001 | c0001 | t0034 | g0085 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18986 | hp1 | a0001 | c0001 | t0019 | g0148 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18991 | hp1 | a0002 | c0002 | t0044 | g0283 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18999 | hp1 | a0002 | c0002 | t0015 | g0017 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19003 | hp2 | a0001 | c0001 | t0020 | g0208 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19004 | hp1 | a0002 | c0002 | t0043 | g0226 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19005 | hp2 | a0001 | c0001 | t0010 | g0215 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0188 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19012 | hp2 | a0001 | c0001 | t0037 | g0106 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0303 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19060 | hp2 | a0002 | c0002 | t0015 | g0018 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0218 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0217 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0319 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19089 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19091 | hp2 | a0001 | c0001 | t0010 | g0211 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19240 | hp2 | a0002 | c0002 | t0009 | g0272 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ASW | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ASW | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0159 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20752 | hp2 | a0003 | c0003 | t0017 | g0225 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | GIH | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0292 | SAS | GIH | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0311 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0083 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02486 | hp1 | a0001 | c0001 | t0022 | g0323 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0044 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0231 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0245 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0172 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03471 | hp2 | a0003 | c0003 | t0017 | g0239 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20300 | hp2 | a0001 | c0001 | t0018 | g0089 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA21309 | hp1 | a0006 | c0008 | t0004 | g0204 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0165 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0011 | REF | REF | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0183 | REF | REF | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76460061
|
G | T | 1 | a0001 | 2 | HG01884.hp1 HG02486.hp1 |
splice_region_variant | LOW | c.-406G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460061 | ||||||
| chr9:76460062
|
C | T | 1 | a0001 | 2 | HG01884.hp1 HG02486.hp1 |
splice_region_variant | LOW | c.-405C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460062 | ||||||
| chr9:76502475
|
T | A | 1 | a0004 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.94T>A | p.Leu32Ile | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 625/5566 | 94/1287 | 32/428 | chr9 | 76502475 | ||
| chr9:76502737
|
C | A | 1 | a0003 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.356C>A | p.Ala119Glu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 887/5566 | 356/1287 | 119/428 | chr9 | 76502737 | ||
| chr9:76502835
|
A | G | 2 | a0002a0007 | 112 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
missense_variant | MODERATE | c.454A>G | p.Ile152Val | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 985/5566 | 454/1287 | 152/428 | chr9 | 76502835 | ||
| chr9:76502854
|
C | G | 1 | a0005 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.473C>G | p.Ser158Cys | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1004/5566 | 473/1287 | 158/428 | chr9 | 76502854 | ||
| chr9:76503484
|
C | T | 1 | a0006 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1103C>T | p.Pro368Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1634/5566 | 1103/1287 | 368/428 | chr9 | 76503484 | ||
| chr9:76503612
|
A | T | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1231A>T | p.Ile411Phe | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1762/5566 | 1231/1287 | 411/428 | chr9 | 76503612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76502573
|
G | A | 1 | a0002c0006 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.192G>A | p.Gln64Gln | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 723/5566 | 192/1287 | 64/428 | chr9 | 76502573 | ||
| chr9:76503084
|
T | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.703T>C | p.Leu235Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1234/5566 | 703/1287 | 235/428 | chr9 | 76503084 | ||
| chr9:76503413
|
G | A | 3 | a0002c0002a0002c0006a0007c0010 | 110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
synonymous_variant | LOW | c.1032G>A | p.Leu344Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1563/5566 | 1032/1287 | 344/428 | chr9 | 76503413 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76459239
|
G | C | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-474G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/4 | 43143 | chr9 | 76459239 | |||||
| chr9:76459244
|
C | T | 2 | a0001c0001t0023a0001c0001t0024 | 4 | HG02109.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-469C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/4 | 43138 | chr9 | 76459244 | |||||
| chr9:76460114
|
C | T | 1 | a0001c0001t0048 | 1 | NA18950.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-353C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460114 | ||||||
| chr9:76500928
|
A | C | 40 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(37): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
5_prime_UTR_variant | MODIFIER | c.-277A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/4 | 1454 | chr9 | 76500928 | |||||
| chr9:76500965
|
A | G | 1 | a0001c0001t0047 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-240A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/4 | 1417 | chr9 | 76500965 | |||||
| chr9:76502376
|
T | C | 1 | a0001c0001t0047 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 6 | chr9 | 76502376 | |||||
| chr9:76503675
|
C | T | 1 | a0001c0001t0018 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 7 | chr9 | 76503675 | |||||
| chr9:76503681
|
A | G | 1 | a0003c0003t0017 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 13 | chr9 | 76503681 | |||||
| chr9:76503712
|
C | T | 6 | a0001c0001t0011a0001c0001t0018a0001c0001t0020others(3): Show | 15 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*44C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 44 | chr9 | 76503712 | |||||
| chr9:76503715
|
AC | A | 21 | a0001c0001t0007a0001c0001t0011a0001c0001t0014others(18): Show | 144 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*50delC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 50 | INFO_REALIGN_3_PRIME | chr9 | 76503715 | ||||
| chr9:76503745
|
A | G | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(35): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 77 | chr9 | 76503745 | |||||
| chr9:76503769
|
C | T | 1 | a0001c0001t0022 | 2 | HG01884.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*101C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 101 | chr9 | 76503769 | |||||
| chr9:76503962
|
G | A | 1 | a0001c0001t0030 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 294 | chr9 | 76503962 | |||||
| chr9:76503987
|
A | C | 8 | a0002c0002t0001a0002c0002t0015a0002c0002t0016others(5): Show | 103 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*319A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 319 | chr9 | 76503987 | |||||
| chr9:76504300
|
C | T | 1 | a0001c0001t0024 | 2 | HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*632C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 632 | chr9 | 76504300 | |||||
| chr9:76504363
|
C | T | 1 | a0001c0001t0039 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 695 | chr9 | 76504363 | |||||
| chr9:76504454
|
C | T | 1 | a0001c0001t0018 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 786 | chr9 | 76504454 | |||||
| chr9:76504548
|
A | T | 1 | a0001c0001t0038 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 880 | chr9 | 76504548 | |||||
| chr9:76504566
|
G | A | 6 | a0001c0001t0004a0001c0001t0008a0001c0001t0019others(3): Show | 41 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*898G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 898 | chr9 | 76504566 | |||||
| chr9:76504836
|
C | T | 20 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(17): Show | 81 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1168C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1168 | chr9 | 76504836 | |||||
| chr9:76504913
|
A | AT | 3 | a0001c0001t0006a0001c0001t0013a0001c0001t0038 | 21 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1256dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1257 | INFO_REALIGN_3_PRIME | chr9 | 76504913 | ||||
| chr9:76505052
|
G | T | 1 | a0002c0002t0016 | 3 | HG01074.hp2 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1384G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1384 | chr9 | 76505052 | |||||
| chr9:76505382
|
C | T | 4 | a0001c0001t0014a0001c0001t0018a0001c0001t0022others(1): Show | 9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1714C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1714 | chr9 | 76505382 | |||||
| chr9:76505438
|
T | C | 1 | a0001c0001t0012 | 3 | HG01891.hp1 NA19030.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1770 | chr9 | 76505438 | |||||
| chr9:76505543
|
A | G | 1 | a0001c0001t0034 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1875A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1875 | chr9 | 76505543 | |||||
| chr9:76505559
|
A | T | 21 | a0001c0001t0005a0001c0001t0007a0001c0001t0012others(18): Show | 156 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1891A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1891 | chr9 | 76505559 | |||||
| chr9:76505560
|
G | C | 1 | a0002c0002t0042 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1892G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1892 | chr9 | 76505560 | |||||
| chr9:76505636
|
C | CAGT | 26 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(23): Show | 179 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1971_*1973dupTAG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1974 | INFO_REALIGN_3_PRIME | chr9 | 76505636 | ||||
| chr9:76505821
|
C | T | 1 | a0001c0001t0010 | 6 | HG02135.hp1 NA18960.hp1 NA19005.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2153C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2153 | chr9 | 76505821 | |||||
| chr9:76505824
|
G | A | 2 | a0001c0001t0013a0001c0001t0038 | 4 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2156G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2156 | chr9 | 76505824 | |||||
| chr9:76505839
|
T | G | 1 | a0003c0003t0017 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2171T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2171 | chr9 | 76505839 | |||||
| chr9:76505889
|
C | T | 1 | a0001c0001t0036 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2221C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2221 | chr9 | 76505889 | |||||
| chr9:76506169
|
G | T | 46 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(43): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2501 | chr9 | 76506169 | |||||
| chr9:76506183
|
A | G | 1 | a0001c0001t0026 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2515 | chr9 | 76506183 | |||||
| chr9:76506266
|
AATCACAT others(15): Show |
A | 1 | a0001c0001t0033 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2599_*2620delATCA others(18): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2599 | chr9 | 76506266 | |||||
| chr9:76506282
|
T | A | 1 | a0001c0001t0011 | 4 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2614T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2614 | chr9 | 76506282 | |||||
| chr9:76506359
|
C | T | 1 | a0001c0001t0014 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2691C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2691 | chr9 | 76506359 | |||||
| chr9:76506360
|
G | A | 1 | a0001c0001t0046 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2692G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2692 | chr9 | 76506360 | |||||
| chr9:76506370
|
C | G | 9 | a0001c0001t0007a0001c0001t0011a0001c0001t0014others(6): Show | 31 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2702C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2702 | chr9 | 76506370 | |||||
| chr9:76506464
|
A | G | 11 | a0002c0002t0001a0002c0002t0009a0002c0002t0015others(8): Show | 111 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2796A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2796 | chr9 | 76506464 | |||||
| chr9:76506468
|
G | A | 13 | a0001c0001t0006a0001c0001t0035a0001c0001t0036others(10): Show | 129 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2800G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2800 | chr9 | 76506468 | |||||
| chr9:76506605
|
G | A | 1 | a0002c0002t0043 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2937 | chr9 | 76506605 | |||||
| chr9:76506795
|
A | G | 2 | a0002c0002t0043a0002c0002t0045 | 2 | NA18948.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3127A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3127 | chr9 | 76506795 | |||||
| chr9:76506840
|
G | A | 1 | a0001c0001t0019 | 2 | NA18986.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3172G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3172 | chr9 | 76506840 | |||||
| chr9:76506846
|
G | A | 1 | a0002c0002t0044 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3178G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3178 | chr9 | 76506846 | |||||
| chr9:76506866
|
C | T | 1 | a0001c0001t0032 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3198C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3198 | chr9 | 76506866 | |||||
| chr9:76506867
|
G | A | 3 | a0001c0001t0006a0001c0001t0035a0001c0001t0036 | 19 | HG01123.hp2 HG01257.hp2 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3199G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3199 | chr9 | 76506867 | |||||
| chr9:76506990
|
C | T | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*3322C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3322 | chr9 | 76506990 | |||||
| chr9:76507104
|
A | G | 1 | a0001c0001t0031 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3436A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3436 | chr9 | 76507104 | |||||
| chr9:76507263
|
T | C | 1 | a0001c0001t0007 | 12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3595T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3595 | chr9 | 76507263 | |||||
| chr9:76507329
|
G | A | 1 | a0001c0001t0007 | 12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3661G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3661 | chr9 | 76507329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76459429
|
C | T | 11 | a0001c0001t0003g0328a0001c0001t0003g0331a0001c0001t0003g0332others(8): Show | 14 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-408+124C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459429 | ||||||
| chr9:76459432
|
G | A | 11 | a0001c0001t0021g0027a0001c0001t0021g0031a0001c0001t0035g0030others(8): Show | 12 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-408+127G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459432 | ||||||
| chr9:76459509
|
T | A | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-408+204T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459509 | ||||||
| chr9:76459609
|
G | T | 1 | a0002c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-408+304G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459609 | ||||||
| chr9:76459610
|
C | A | 1 | a0002c0002t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-408+305C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459610 | ||||||
| chr9:76459618
|
G | T | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-408+313G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459618 | ||||||
| chr9:76459709
|
C | T | 1 | a0001c0001t0005g0321 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-407-351C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459709 | ||||||
| chr9:76459983
|
C | A | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-407-77C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459983 | ||||||
| chr9:76460332
|
A | C | 20 | a0001c0001t0002g0317a0001c0001t0003g0309a0001c0001t0004g0302others(17): Show | 21 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-290+155A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460332 | ||||||
| chr9:76460516
|
G | T | 3 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320 | 3 | NA18962.hp1 NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-290+339G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460516 | ||||||
| chr9:76460525
|
A | G | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-290+348A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460525 | ||||||
| chr9:76460657
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+480T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460657 | ||||||
| chr9:76460672
|
G | T | 1 | a0001c0001t0002g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-290+495G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460672 | ||||||
| chr9:76460736
|
A | G | 133 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(130): Show | 148 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-290+559A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460736 | ||||||
| chr9:76460738
|
A | T | 1 | a0002c0002t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-290+561A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460738 | ||||||
| chr9:76460739
|
CTA | C | 20 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(17): Show | 21 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+564_-290+565d others(4): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76460739 | |||||
| chr9:76460862
|
T | C | 38 | a0001c0001t0003g0041a0001c0001t0004g0016a0001c0001t0004g0190others(35): Show | 39 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-290+685T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460862 | ||||||
| chr9:76461011
|
C | T | 1 | a0001c0001t0019g0188 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-290+834C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461011 | ||||||
| chr9:76461194
|
CT | C | 226 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(223): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.-290+1038delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | |||||
| chr9:76461194
|
CTT | C | 54 | a0001c0001t0002g0073a0001c0001t0002g0212a0001c0001t0002g0213others(51): Show | 55 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.-290+1037_-290+103 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | |||||
| chr9:76461194
|
CTTT | C | 26 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(23): Show | 30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.-290+1036_-290+103 others(7): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | |||||
| chr9:76461277
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-290+1100G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461277 | ||||||
| chr9:76461376
|
A | G | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-290+1199A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461376 | ||||||
| chr9:76461444
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-290+1267G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461444 | ||||||
| chr9:76461456
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-290+1279C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461456 | ||||||
| chr9:76461473
|
A | G | 1 | a0001c0001t0003g0332 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-290+1296A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461473 | ||||||
| chr9:76461509
|
G | A | 12 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(9): Show | 12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+1332G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461509 | ||||||
| chr9:76461592
|
A | C | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+1415A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461592 | ||||||
| chr9:76461651
|
G | T | 36 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(33): Show | 37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+1474G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461651 | ||||||
| chr9:76461652
|
C | T | 36 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(33): Show | 37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+1475C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461652 | ||||||
| chr9:76461865
|
G | T | 1 | a0001c0001t0002g0150 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-290+1688G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461865 | ||||||
| chr9:76461883
|
C | T | 20 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(17): Show | 21 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+1706C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461883 | ||||||
| chr9:76461884
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-290+1707G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461884 | ||||||
| chr9:76462133
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-290+1956G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462133 | ||||||
| chr9:76462143
|
AT | A | 235 | a0001c0001t0002g0061a0001c0001t0002g0212a0001c0001t0002g0213others(232): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-290+1980delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76462143 | |||||
| chr9:76462363
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-290+2186C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462363 | ||||||
| chr9:76462580
|
G | A | 1 | a0002c0002t0001g0224 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-290+2403G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462580 | ||||||
| chr9:76462602
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-290+2425T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462602 | ||||||
| chr9:76462997
|
T | G | 1 | a0003c0003t0017g0225 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-290+2820T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462997 | ||||||
| chr9:76463028
|
C | T | 2 | a0001c0001t0019g0148a0001c0001t0019g0188 | 2 | NA18986.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-290+2851C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463028 | ||||||
| chr9:76463040
|
G | A | 1 | a0001c0001t0034g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-290+2863G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463040 | ||||||
| chr9:76463122
|
C | A | 246 | a0001c0001t0002g0061a0001c0001t0002g0212a0001c0001t0002g0213others(243): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-290+2945C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463122 | ||||||
| chr9:76463204
|
C | T | 12 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(9): Show | 12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+3027C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463204 | ||||||
| chr9:76463205
|
T | A | 1 | a0001c0001t0006g0325 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-290+3028T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463205 | ||||||
| chr9:76463265
|
G | C | 1 | a0001c0001t0046g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-290+3088G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463265 | ||||||
| chr9:76463275
|
T | TA | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3105dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76463275 | |||||
| chr9:76463371
|
G | A | 36 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(33): Show | 37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+3194G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463371 | ||||||
| chr9:76463372
|
G | A | 2 | a0001c0001t0007g0037a0002c0002t0009g0038 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-290+3195G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463372 | ||||||
| chr9:76463419
|
C | G | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3242C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463419 | ||||||
| chr9:76463425
|
T | C | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+3248T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463425 | ||||||
| chr9:76463496
|
A | G | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3319A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463496 | ||||||
| chr9:76463507
|
T | A | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3330T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463507 | ||||||
| chr9:76463673
|
A | T | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3496A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463673 | ||||||
| chr9:76463680
|
C | T | 1 | a0001c0001t0003g0070 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-290+3503C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463680 | ||||||
| chr9:76463687
|
G | T | 9 | a0002c0002t0001g0006a0002c0002t0001g0022a0002c0002t0001g0281others(6): Show | 12 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.-290+3510G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463687 | ||||||
| chr9:76463733
|
T | TTTATGAG others(1): Show |
217 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(214): Show | 237 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.-290+3565_-290+357 others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76463733 | |||||
| chr9:76463787
|
T | C | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3610T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463787 | ||||||
| chr9:76464038
|
G | GT | 12 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0185others(9): Show | 12 | HG02040.hp2 HG02071.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-290+3876dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76464038 | |||||
| chr9:76464038
|
G | T | 10 | a0001c0001t0002g0014a0001c0001t0002g0080a0001c0001t0002g0143others(7): Show | 11 | HG02074.hp2 HG02145.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-290+3861G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464038 | ||||||
| chr9:76464038
|
GT | G | 82 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(79): Show | 87 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.-290+3876delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76464038 | |||||
| chr9:76464048
|
T | G | 2 | a0002c0002t0043g0226a0002c0002t0045g0290 | 2 | NA18948.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-290+3871T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464048 | ||||||
| chr9:76464068
|
A | T | 1 | a0001c0001t0027g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+3891A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464068 | ||||||
| chr9:76464077
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3900G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464077 | ||||||
| chr9:76464155
|
A | G | 5 | a0001c0001t0002g0137a0001c0001t0002g0138a0001c0001t0002g0140others(2): Show | 5 | NA18946.hp2 NA18969.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+3978A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464155 | ||||||
| chr9:76464155
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3978A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464155 | ||||||
| chr9:76464251
|
C | G | 24 | a0001c0001t0003g0041a0001c0001t0003g0328a0001c0001t0003g0331others(21): Show | 27 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-290+4074C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464251 | ||||||
| chr9:76464417
|
A | G | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4240A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464417 | ||||||
| chr9:76464455
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-290+4278G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464455 | ||||||
| chr9:76464515
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+4338C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464515 | ||||||
| chr9:76464615
|
A | G | 2 | a0002c0002t0001g0074a0002c0002t0001g0075 | 2 | NA18961.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-290+4438A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464615 | ||||||
| chr9:76464676
|
G | A | 1 | a0001c0001t0002g0137 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-290+4499G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464676 | ||||||
| chr9:76464685
|
A | G | 1 | a0001c0001t0002g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-290+4508A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464685 | ||||||
| chr9:76464779
|
A | T | 2 | a0001c0001t0007g0037a0002c0002t0009g0038 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-290+4602A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464779 | ||||||
| chr9:76464975
|
A | T | 1 | a0002c0002t0001g0222 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-290+4798A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464975 | ||||||
| chr9:76465027
|
G | A | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4850G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465027 | ||||||
| chr9:76465130
|
C | A | 216 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(213): Show | 236 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-290+4953C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465130 | ||||||
| chr9:76465155
|
G | GT | 26 | a0001c0001t0003g0041a0001c0001t0003g0328a0001c0001t0003g0331others(23): Show | 29 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-290+4991dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76465155 | |||||
| chr9:76465155
|
G | GTT | 22 | a0001c0001t0004g0016a0001c0001t0004g0191a0001c0001t0004g0192others(19): Show | 23 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-290+4990_-290+499 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76465155 | |||||
| chr9:76465156
|
T | G | 1 | a0002c0002t0001g0209 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-290+4979T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465156 | ||||||
| chr9:76465169
|
A | T | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4992A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465169 | ||||||
| chr9:76465413
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+5236C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465413 | ||||||
| chr9:76465414
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-290+5237G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465414 | ||||||
| chr9:76465520
|
G | A | 27 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(24): Show | 28 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-290+5343G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465520 | ||||||
| chr9:76465547
|
T | C | 1 | a0001c0001t0003g0227 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-290+5370T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465547 | ||||||
| chr9:76465700
|
C | A | 24 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(21): Show | 28 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-290+5523C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465700 | ||||||
| chr9:76465979
|
T | C | 2 | a0002c0002t0009g0039a0002c0006t0009g0040 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-290+5802T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465979 | ||||||
| chr9:76466169
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-290+5992G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466169 | ||||||
| chr9:76466303
|
TTTTG | T | 7 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6134_-290+613 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76466303 | |||||
| chr9:76466513
|
G | A | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0011g0231 | 3 | HG02055.hp2 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-290+6336G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466513 | ||||||
| chr9:76466538
|
G | A | 203 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0212others(200): Show | 223 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-290+6361G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466538 | ||||||
| chr9:76466666
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-290+6489G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466666 | ||||||
| chr9:76466729
|
G | GGA | 7 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6556_-290+655 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76466729 | |||||
| chr9:76466928
|
A | G | 7 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6751A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466928 | ||||||
| chr9:76466994
|
C | A | 13 | a0002c0002t0001g0018a0002c0002t0001g0224a0002c0002t0001g0232others(10): Show | 14 | HG00438.hp1 HG00544.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-290+6817C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466994 | ||||||
| chr9:76467042
|
A | C | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+6865A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467042 | ||||||
| chr9:76467044
|
C | CT | 21 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0004g0016others(18): Show | 22 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-290+6879dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467044 | |||||
| chr9:76467105
|
C | T | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+6928C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467105 | ||||||
| chr9:76467109
|
C | T | 1 | a0001c0001t0024g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-290+6932C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467109 | ||||||
| chr9:76467232
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-290+7055T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467232 | ||||||
| chr9:76467264
|
A | G | 234 | a0001c0001t0002g0061a0001c0001t0002g0091a0001c0001t0002g0147others(231): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-290+7087A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467264 | ||||||
| chr9:76467277
|
A | C | 234 | a0001c0001t0002g0061a0001c0001t0002g0091a0001c0001t0002g0147others(231): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-290+7100A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467277 | ||||||
| chr9:76467332
|
T | A | 1 | a0001c0001t0004g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-290+7155T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467332 | ||||||
| chr9:76467450
|
G | A | 3 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0089 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+7273G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467450 | ||||||
| chr9:76467489
|
C | G | 124 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(121): Show | 139 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-290+7312C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467489 | ||||||
| chr9:76467494
|
A | T | 1 | a0001c0001t0003g0009 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-290+7317A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467494 | ||||||
| chr9:76467553
|
G | T | 3 | a0001c0001t0004g0190a0001c0001t0004g0206a0001c0001t0004g0207 | 3 | HG01069.hp2 HG01099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-290+7376G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467553 | ||||||
| chr9:76467763
|
G | A | 7 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(4): Show | 9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+7586G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467763 | ||||||
| chr9:76467796
|
G | A | 3 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0089 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+7619G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467796 | ||||||
| chr9:76467850
|
T | C | 6 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(3): Show | 6 | HG02056.hp1 HG02155.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+7673T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467850 | ||||||
| chr9:76467897
|
G | GT | 80 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0061others(77): Show | 88 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.-290+7749dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467897
|
G | GTT | 22 | a0001c0001t0002g0185a0001c0001t0003g0068a0001c0001t0004g0201others(19): Show | 22 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+7748_-290+774 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467897
|
GT | G | 79 | a0001c0001t0002g0092a0001c0001t0002g0212a0001c0001t0002g0213others(76): Show | 91 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-290+7749delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467897
|
GTT | G | 8 | a0001c0001t0003g0041a0001c0001t0004g0302a0001c0001t0007g0037others(5): Show | 8 | HG01256.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-290+7748_-290+774 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467897
|
GTTTT | G | 8 | a0001c0001t0003g0328a0001c0001t0003g0332a0001c0001t0006g0325others(5): Show | 9 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-290+7746_-290+774 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467897
|
GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0004g0240a0001c0001t0004g0241a0003c0003t0017g0225others(1): Show | 4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+7740_-290+774 others(14): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | |||||
| chr9:76467902
|
T | G | 1 | a0001c0001t0018g0089 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-290+7725T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467902 | ||||||
| chr9:76467903
|
T | G | 2 | a0001c0001t0018g0087a0001c0001t0018g0088 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-290+7726T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467903 | ||||||
| chr9:76467916
|
T | G | 1 | a0001c0001t0007g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-290+7739T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467916 | ||||||
| chr9:76468026
|
C | A | 1 | a0001c0001t0002g0093 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-290+7849C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468026 | ||||||
| chr9:76468115
|
C | T | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0134 | 3 | HG00099.hp1 HG01081.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-290+7938C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468115 | ||||||
| chr9:76468156
|
C | T | 21 | a0001c0001t0003g0041a0001c0001t0003g0328a0001c0001t0003g0331others(18): Show | 22 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-290+7979C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468156 | ||||||
| chr9:76468187
|
G | A | 28 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(25): Show | 31 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.-290+8010G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468187 | ||||||
| chr9:76468454
|
C | T | 2 | a0001c0001t0008g0043a0001c0001t0046g0036 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-290+8277C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468454 | ||||||
| chr9:76468550
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+8373C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468550 | ||||||
| chr9:76468556
|
C | T | 37 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(34): Show | 39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+8379C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468556 | ||||||
| chr9:76468609
|
A | G | 52 | a0001c0001t0002g0267a0001c0001t0002g0274a0001c0001t0003g0020others(49): Show | 62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-290+8432A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468609 | ||||||
| chr9:76468743
|
G | C | 1 | a0001c0001t0006g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-290+8566G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468743 | ||||||
| chr9:76468848
|
G | A | 1 | a0001c0001t0012g0324 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+8671G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468848 | ||||||
| chr9:76468855
|
G | C | 1 | a0001c0001t0004g0194 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-290+8678G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468855 | ||||||
| chr9:76468857
|
A | T | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8680A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468857 | ||||||
| chr9:76468898
|
A | G | 1 | a0001c0001t0026g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-290+8721A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468898 | ||||||
| chr9:76468904
|
G | T | 1 | a0002c0002t0001g0139 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-290+8727G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468904 | ||||||
| chr9:76468960
|
C | G | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+8783C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468960 | ||||||
| chr9:76468979
|
A | G | 2 | a0002c0002t0001g0074a0002c0002t0001g0075 | 2 | NA18961.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-290+8802A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468979 | ||||||
| chr9:76468981
|
T | A | 29 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(26): Show | 31 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-290+8804T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468981 | ||||||
| chr9:76469044
|
C | A | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8867C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469044 | ||||||
| chr9:76469051
|
A | G | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8874A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469051 | ||||||
| chr9:76469054
|
G | A | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+8877G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469054 | ||||||
| chr9:76469106
|
G | A | 1 | a0001c0001t0004g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-290+8929G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469106 | ||||||
| chr9:76469113
|
CTAAG | C | 23 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(20): Show | 27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.-290+8938_-290+894 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76469113 | |||||
| chr9:76469261
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+9084C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469261 | ||||||
| chr9:76469299
|
G | A | 28 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(25): Show | 32 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.-290+9122G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469299 | ||||||
| chr9:76469322
|
T | C | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+9145T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469322 | ||||||
| chr9:76469405
|
A | G | 22 | a0001c0001t0003g0041a0001c0001t0003g0328a0001c0001t0003g0331others(19): Show | 23 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-290+9228A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469405 | ||||||
| chr9:76469460
|
T | G | 1 | a0001c0001t0002g0317 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-290+9283T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469460 | ||||||
| chr9:76469508
|
C | T | 7 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(4): Show | 7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+9331C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469508 | ||||||
| chr9:76469564
|
C | T | 4 | a0001c0001t0023g0083a0001c0001t0023g0084a0001c0001t0024g0179others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+9387C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469564 | ||||||
| chr9:76469720
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-290+9543G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469720 | ||||||
| chr9:76469737
|
G | C | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+9560G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469737 | ||||||
| chr9:76469743
|
G | T | 10 | a0001c0001t0021g0027a0001c0001t0021g0031a0002c0002t0001g0004others(7): Show | 11 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-290+9566G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469743 | ||||||
| chr9:76469818
|
C | T | 7 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(4): Show | 9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+9641C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469818 | ||||||
| chr9:76469827
|
T | G | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+9650T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469827 | ||||||
| chr9:76470109
|
T | C | 1 | a0001c0001t0012g0324 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+9932T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470109 | ||||||
| chr9:76470208
|
C | T | 2 | a0002c0002t0001g0262a0002c0002t0001g0263 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-290+10031C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470208 | ||||||
| chr9:76470477
|
C | G | 1 | a0001c0001t0002g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-290+10300C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470477 | ||||||
| chr9:76470478
|
G | A | 2 | a0002c0002t0009g0271a0002c0002t0009g0272 | 2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-290+10301G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470478 | ||||||
| chr9:76470603
|
C | CA | 13 | a0001c0001t0002g0094a0001c0001t0002g0126a0001c0001t0002g0127others(10): Show | 14 | HG00438.hp2 HG00741.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+10447dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | |||||
| chr9:76470603
|
CA | C | 187 | a0001c0001t0002g0091a0001c0001t0002g0212a0001c0001t0002g0213others(184): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-290+10447delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | |||||
| chr9:76470603
|
CAA | C | 20 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(17): Show | 21 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-290+10446_-290+10 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | |||||
| chr9:76470814
|
G | A | 29 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0003g0328others(26): Show | 32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+10637G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470814 | ||||||
| chr9:76470840
|
G | A | 1 | a0001c0001t0004g0016 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-290+10663G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470840 | ||||||
| chr9:76470923
|
C | T | 37 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(34): Show | 39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+10746C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470923 | ||||||
| chr9:76471238
|
G | A | 5 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+11061G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471238 | ||||||
| chr9:76471245
|
A | G | 1 | a0001c0001t0002g0146 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-290+11068A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471245 | ||||||
| chr9:76471552
|
T | C | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+11375T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471552 | ||||||
| chr9:76471579
|
C | T | 20 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0004g0240others(17): Show | 22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+11402C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471579 | ||||||
| chr9:76471657
|
A | G | 2 | a0001c0001t0008g0043a0001c0001t0046g0036 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-290+11480A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471657 | ||||||
| chr9:76471667
|
TAA | T | 20 | a0001c0001t0003g0041a0001c0001t0003g0078a0001c0001t0004g0240others(17): Show | 22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+11491_-290+11 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471667 | ||||||
| chr9:76471818
|
A | G | 3 | a0002c0002t0001g0042a0002c0002t0009g0044a0002c0002t0009g0045 | 3 | HG02486.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-290+11641A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471818 | ||||||
| chr9:76472068
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-290+11891G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472068 | ||||||
| chr9:76472120
|
T | TA | 12 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(9): Show | 12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+11951dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472120 | |||||
| chr9:76472191
|
C | T | 1 | a0002c0002t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-290+12014C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472191 | ||||||
| chr9:76472281
|
T | G | 7 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(4): Show | 9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+12104T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472281 | ||||||
| chr9:76472577
|
A | G | 2 | a0002c0002t0009g0271a0002c0002t0009g0272 | 2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-290+12400A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472577 | ||||||
| chr9:76472650
|
T | C | 13 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(10): Show | 13 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-290+12473T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472650 | ||||||
| chr9:76472720
|
C | CTTTCT | 5 | a0001c0001t0002g0128a0001c0001t0002g0137a0001c0001t0002g0140others(2): Show | 5 | HG01928.hp1 HG03669.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(11): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472720 | |||||
| chr9:76472720
|
CTTTCT | C | 49 | a0001c0001t0002g0061a0001c0001t0002g0120a0001c0001t0002g0121others(46): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(11): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472720 | |||||
| chr9:76472744
|
CTTTTCTT others(1): Show |
C | 132 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(129): Show | 148 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(14): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472744 | |||||
| chr9:76472745
|
TTTTC | T | 32 | a0001c0001t0002g0300a0001c0001t0003g0041a0001c0001t0003g0328others(29): Show | 32 | HG00323.hp2 HG01257.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472745 | |||||
| chr9:76472746
|
TTTC | T | 29 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(26): Show | 31 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472746 | |||||
| chr9:76472749
|
C | CT | 7 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0092others(4): Show | 8 | HG01261.hp1 HG01358.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-290+12589dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472749 | |||||
| chr9:76472749
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+12572C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472749 | ||||||
| chr9:76472754
|
T | C | 3 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0089 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+12577T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472754 | ||||||
| chr9:76472761
|
TTTTTTGA others(4): Show |
T | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+12585_-290+12 others(17): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472761 | ||||||
| chr9:76472772
|
G | T | 3 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0089 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+12595G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472772 | ||||||
| chr9:76472937
|
C | T | 2 | a0001c0001t0006g0312a0002c0002t0001g0247 | 2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-290+12760C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472937 | ||||||
| chr9:76472958
|
G | A | 24 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(21): Show | 28 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-290+12781G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472958 | ||||||
| chr9:76473048
|
G | C | 137 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(134): Show | 154 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-290+12871G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473048 | ||||||
| chr9:76473373
|
G | T | 4 | a0001c0001t0004g0266a0002c0002t0001g0005a0002c0002t0001g0019others(1): Show | 7 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-290+13196G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473373 | ||||||
| chr9:76473401
|
TAAACTGG others(15): Show |
T | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-290+13225_-290+13 others(28): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473401 | ||||||
| chr9:76473571
|
A | T | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+13394A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473571 | ||||||
| chr9:76473607
|
A | C | 159 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(156): Show | 176 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-290+13430A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473607 | ||||||
| chr9:76473641
|
T | A | 1 | a0001c0001t0003g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-290+13464T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473641 | ||||||
| chr9:76473697
|
G | T | 4 | a0001c0001t0004g0240a0001c0001t0004g0241a0003c0003t0017g0225others(1): Show | 4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+13520G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473697 | ||||||
| chr9:76473743
|
C | A | 9 | a0001c0001t0003g0328a0001c0001t0003g0331a0001c0001t0003g0332others(6): Show | 10 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-290+13566C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473743 | ||||||
| chr9:76473771
|
T | C | 1 | a0002c0002t0001g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-290+13594T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473771 | ||||||
| chr9:76473816
|
T | A | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+13639T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473816 | ||||||
| chr9:76473832
|
G | A | 5 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+13655G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473832 | ||||||
| chr9:76474056
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+13879C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474056 | ||||||
| chr9:76474061
|
C | T | 1 | a0001c0001t0013g0329 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-290+13884C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474061 | ||||||
| chr9:76474076
|
G | T | 1 | a0001c0001t0027g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+13899G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474076 | ||||||
| chr9:76474147
|
T | C | 8 | a0001c0001t0007g0037a0002c0002t0001g0042a0002c0002t0009g0038others(5): Show | 8 | HG02486.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-290+13970T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474147 | ||||||
| chr9:76474193
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-290+14016C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474193 | ||||||
| chr9:76474194
|
G | A | 144 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(141): Show | 159 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.-290+14017G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474194 | ||||||
| chr9:76474207
|
A | T | 151 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(148): Show | 168 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-290+14030A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474207 | ||||||
| chr9:76474297
|
G | A | 1 | a0001c0001t0008g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-290+14120G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474297 | ||||||
| chr9:76474466
|
A | G | 2 | a0001c0001t0023g0083a0001c0001t0023g0084 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-290+14289A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474466 | ||||||
| chr9:76474537
|
C | G | 4 | a0001c0001t0008g0043a0001c0001t0023g0083a0001c0001t0023g0084others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+14360C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474537 | ||||||
| chr9:76474540
|
A | G | 1 | a0001c0001t0008g0049 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-290+14363A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474540 | ||||||
| chr9:76474586
|
C | G | 14 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(11): Show | 14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+14409C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474586 | ||||||
| chr9:76474648
|
C | T | 14 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(11): Show | 14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+14471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474648 | ||||||
| chr9:76474772
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-290+14595C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474772 | ||||||
| chr9:76474849
|
C | G | 137 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(134): Show | 154 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-290+14672C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474849 | ||||||
| chr9:76475060
|
C | T | 4 | a0001c0001t0004g0240a0001c0001t0004g0241a0003c0003t0017g0225others(1): Show | 4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+14883C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475060 | ||||||
| chr9:76475115
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-290+14938C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475115 | ||||||
| chr9:76475146
|
A | G | 3 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050 | 3 | HG02622.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-290+14969A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475146 | ||||||
| chr9:76475172
|
G | A | 1 | a0001c0001t0010g0214 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-290+14995G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475172 | ||||||
| chr9:76475280
|
C | T | 1 | a0002c0002t0001g0115 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-290+15103C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475280 | ||||||
| chr9:76475365
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-290+15188A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475365 | ||||||
| chr9:76475383
|
A | G | 1 | a0001c0001t0012g0324 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+15206A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475383 | ||||||
| chr9:76475402
|
G | A | 325 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(322): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-290+15225G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475402 | ||||||
| chr9:76475448
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+15271A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475448 | ||||||
| chr9:76475497
|
G | T | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15320G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475497 | ||||||
| chr9:76475537
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-290+15360T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475537 | ||||||
| chr9:76475544
|
T | A | 1 | a0001c0001t0012g0324 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+15367T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475544 | ||||||
| chr9:76475575
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-290+15398C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475575 | ||||||
| chr9:76475577
|
G | T | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+15400G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475577 | ||||||
| chr9:76475618
|
TAAG | T | 7 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(4): Show | 9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+15442_-290+15 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475618 | ||||||
| chr9:76475662
|
G | A | 1 | a0002c0002t0001g0074 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-290+15485G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475662 | ||||||
| chr9:76475857
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0094a0001c0001t0002g0099others(2): Show | 6 | HG00423.hp1 HG00438.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15680G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475857 | ||||||
| chr9:76475858
|
G | A | 1 | a0001c0001t0005g0090 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-290+15681G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475858 | ||||||
| chr9:76475877
|
GTAAC | G | 158 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(155): Show | 175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-290+15705_-290+15 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76475877 | |||||
| chr9:76476030
|
A | T | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+15853A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476030 | ||||||
| chr9:76476046
|
G | A | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15869G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476046 | ||||||
| chr9:76476259
|
A | G | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+16082A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476259 | ||||||
| chr9:76476443
|
A | T | 2 | a0002c0002t0001g0286a0002c0004t0001g0285 | 2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-290+16266A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476443 | ||||||
| chr9:76476456
|
C | T | 34 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(31): Show | 35 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-290+16279C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476456 | ||||||
| chr9:76476550
|
TA | T | 135 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(132): Show | 152 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-290+16384delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76476550 | |||||
| chr9:76476663
|
T | C | 14 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(11): Show | 14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+16486T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476663 | ||||||
| chr9:76476710
|
T | TG | 15 | a0001c0001t0002g0101a0001c0001t0002g0117a0001c0001t0003g0052others(12): Show | 15 | HG00423.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+16537dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76476710 | |||||
| chr9:76476822
|
G | T | 37 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(34): Show | 39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+16645G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476822 | ||||||
| chr9:76477185
|
G | T | 5 | a0001c0001t0004g0240a0001c0001t0004g0241a0003c0003t0017g0189others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+17008G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477185 | ||||||
| chr9:76477207
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-290+17030G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477207 | ||||||
| chr9:76477259
|
G | A | 1 | a0001c0001t0008g0244 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-290+17082G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477259 | ||||||
| chr9:76477295
|
A | AG | 8 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(5): Show | 10 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-290+17120dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477295 | |||||
| chr9:76477299
|
G | C | 1 | a0001c0001t0012g0324 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+17122G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477299 | ||||||
| chr9:76477310
|
G | A | 129 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(126): Show | 144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17133G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477310 | ||||||
| chr9:76477509
|
G | A | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+17332G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477509 | ||||||
| chr9:76477519
|
C | CT | 129 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17343dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477519 | |||||
| chr9:76477526
|
C | CA | 8 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(5): Show | 10 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-290+17360dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477526 | |||||
| chr9:76477526
|
CA | C | 129 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(126): Show | 144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17360delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477526 | |||||
| chr9:76477603
|
C | A | 2 | a0001c0001t0023g0083a0001c0001t0023g0084 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-290+17426C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477603 | ||||||
| chr9:76477611
|
G | A | 14 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(11): Show | 14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+17434G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477611 | ||||||
| chr9:76477739
|
T | G | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+17562T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477739 | ||||||
| chr9:76477767
|
C | A | 1 | a0001c0001t0020g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-290+17590C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477767 | ||||||
| chr9:76477790
|
C | T | 24 | a0001c0001t0004g0016a0001c0001t0004g0190a0001c0001t0004g0191others(21): Show | 25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+17613C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477790 | ||||||
| chr9:76477797
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-290+17620C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477797 | ||||||
| chr9:76477846
|
C | G | 129 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17669C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477846 | ||||||
| chr9:76477874
|
C | T | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-290+17697C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477874 | ||||||
| chr9:76477879
|
T | C | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-290+17702T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477879 | ||||||
| chr9:76477962
|
G | A | 326 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(323): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-290+17785G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477962 | ||||||
| chr9:76477969
|
G | A | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+17792G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477969 | ||||||
| chr9:76478073
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+17896A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478073 | ||||||
| chr9:76478179
|
T | C | 309 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(306): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-290+18002T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478179 | ||||||
| chr9:76478189
|
T | G | 129 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+18012T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478189 | ||||||
| chr9:76478190
|
A | G | 23 | a0001c0001t0008g0244a0001c0001t0008g0245a0002c0002t0001g0006others(20): Show | 26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-290+18013A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478190 | ||||||
| chr9:76478190
|
A | T | 129 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+18013A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478190 | ||||||
| chr9:76478213
|
C | G | 1 | a0001c0001t0002g0014 | 2 | NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-290+18036C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478213 | ||||||
| chr9:76478251
|
C | T | 21 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(18): Show | 21 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+18074C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478251 | ||||||
| chr9:76478351
|
T | C | 3 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050 | 3 | HG02622.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-290+18174T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478351 | ||||||
| chr9:76478385
|
G | A | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+18208G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478385 | ||||||
| chr9:76478388
|
T | G | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18211T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478388 | ||||||
| chr9:76478429
|
A | G | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+18252A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478429 | ||||||
| chr9:76478479
|
T | C | 324 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(321): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-290+18302T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478479 | ||||||
| chr9:76478506
|
G | A | 1 | a0002c0002t0001g0022 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-290+18329G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478506 | ||||||
| chr9:76478586
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18409C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478586 | ||||||
| chr9:76478587
|
T | G | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18410T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478587 | ||||||
| chr9:76478588
|
G | T | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18411G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478588 | ||||||
| chr9:76478694
|
G | A | 1 | a0001c0001t0007g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-290+18517G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478694 | ||||||
| chr9:76478711
|
C | G | 37 | a0001c0001t0002g0091a0001c0001t0002g0185a0001c0001t0002g0299others(34): Show | 39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+18534C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478711 | ||||||
| chr9:76478748
|
A | G | 166 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-290+18571A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478748 | ||||||
| chr9:76478833
|
T | C | 1 | a0001c0001t0006g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-290+18656T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478833 | ||||||
| chr9:76478870
|
TATTGTAT others(4): Show |
T | 1 | a0001c0001t0003g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-290+18695_-290+18 others(17): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76478870 | |||||
| chr9:76478877
|
T | G | 1 | a0001c0001t0002g0140 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-290+18700T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478877 | ||||||
| chr9:76478905
|
T | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(315): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-290+18728T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478905 | ||||||
| chr9:76478931
|
A | G | 1 | a0001c0001t0003g0021 | 2 | HG00544.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-290+18754A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478931 | ||||||
| chr9:76478984
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(163): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-290+18807T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478984 | ||||||
| chr9:76479306
|
G | A | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+19129G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479306 | ||||||
| chr9:76479309
|
A | G | 14 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(11): Show | 14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+19132A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479309 | ||||||
| chr9:76479315
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-290+19138C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479315 | ||||||
| chr9:76479319
|
G | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(126): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+19142G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479319 | ||||||
| chr9:76479392
|
G | A | 1 | a0001c0001t0028g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-290+19215G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479392 | ||||||
| chr9:76479528
|
A | T | 1 | a0002c0002t0001g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-290+19351A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479528 | ||||||
| chr9:76479688
|
G | A | 1 | a0001c0001t0027g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+19511G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479688 | ||||||
| chr9:76479730
|
G | C | 2 | a0001c0001t0010g0214a0001c0001t0010g0215 | 2 | HG02135.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-290+19553G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479730 | ||||||
| chr9:76480020
|
T | A | 1 | a0001c0001t0013g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-290+19843T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480020 | ||||||
| chr9:76480067
|
A | G | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-290+19890A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480067 | ||||||
| chr9:76480266
|
C | T | 145 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(142): Show | 160 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.-290+20089C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480266 | ||||||
| chr9:76480335
|
C | T | 129 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(126): Show | 144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+20158C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480335 | ||||||
| chr9:76480354
|
A | G | 130 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(127): Show | 145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-290+20177A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480354 | ||||||
| chr9:76480630
|
G | A | 6 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(3): Show | 6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-20286G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480630 | ||||||
| chr9:76480691
|
T | C | 1 | a0001c0001t0008g0245 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-289-20225T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480691 | ||||||
| chr9:76480730
|
C | T | 8 | a0002c0002t0001g0004a0002c0002t0001g0025a0002c0002t0001g0028others(5): Show | 9 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-289-20186C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480730 | ||||||
| chr9:76480788
|
C | T | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-20128C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480788 | ||||||
| chr9:76480797
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-289-20119A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480797 | ||||||
| chr9:76480923
|
T | C | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-19993T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480923 | ||||||
| chr9:76481133
|
G | A | 1 | a0003c0003t0017g0225 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-289-19783G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481133 | ||||||
| chr9:76481164
|
C | T | 2 | a0002c0002t0001g0262a0002c0002t0001g0263 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-289-19752C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481164 | ||||||
| chr9:76481200
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-289-19716C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481200 | ||||||
| chr9:76481304
|
G | T | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-19612G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481304 | ||||||
| chr9:76481411
|
AT | A | 97 | a0001c0001t0002g0091a0001c0001t0002g0103a0001c0001t0002g0185others(94): Show | 101 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.-289-19492delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76481411 | |||||
| chr9:76481460
|
A | G | 2 | a0002c0002t0009g0039a0002c0006t0009g0040 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-289-19456A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481460 | ||||||
| chr9:76481694
|
G | A | 3 | a0001c0001t0007g0077a0001c0001t0007g0173a0001c0001t0014g0174 | 3 | HG03195.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-289-19222G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481694 | ||||||
| chr9:76481743
|
C | T | 127 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(124): Show | 142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-289-19173C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481743 | ||||||
| chr9:76481794
|
G | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0120 | 3 | HG00323.hp1 HG00733.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-289-19122G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481794 | ||||||
| chr9:76481829
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0031 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-19087G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481829 | ||||||
| chr9:76482050
|
C | T | 1 | a0002c0002t0001g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-289-18866C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482050 | ||||||
| chr9:76482107
|
G | C | 2 | a0001c0001t0021g0027a0001c0001t0021g0031 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-18809G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482107 | ||||||
| chr9:76482129
|
C | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0129a0001c0001t0004g0182 | 3 | HG02083.hp1 HG02165.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-289-18787C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482129 | ||||||
| chr9:76482183
|
G | A | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-289-18733G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482183 | ||||||
| chr9:76482198
|
A | C | 1 | a0002c0002t0001g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-289-18718A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482198 | ||||||
| chr9:76482201
|
G | A | 34 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(31): Show | 35 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-289-18715G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482201 | ||||||
| chr9:76482228
|
T | C | 130 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(127): Show | 145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-18688T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482228 | ||||||
| chr9:76482245
|
C | G | 2 | a0002c0002t0043g0226a0002c0002t0045g0290 | 2 | NA18948.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-289-18671C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482245 | ||||||
| chr9:76482347
|
G | T | 2 | a0002c0002t0001g0292a0002c0002t0001g0297 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-289-18569G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482347 | ||||||
| chr9:76482393
|
G | A | 6 | a0001c0001t0003g0078a0001c0001t0004g0240a0001c0001t0004g0241others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-18523G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482393 | ||||||
| chr9:76482397
|
G | A | 1 | a0002c0002t0001g0252 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-289-18519G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482397 | ||||||
| chr9:76482410
|
A | G | 1 | a0001c0001t0003g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-289-18506A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482410 | ||||||
| chr9:76482437
|
C | T | 131 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(128): Show | 146 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-289-18479C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482437 | ||||||
| chr9:76482465
|
C | CA | 129 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(126): Show | 144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-289-18442dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482465 | |||||
| chr9:76482479
|
C | T | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-18437C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482479 | ||||||
| chr9:76482530
|
A | G | 130 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(127): Show | 145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-18386A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482530 | ||||||
| chr9:76482731
|
A | G | 1 | a0001c0001t0003g0331 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-289-18185A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482731 | ||||||
| chr9:76482811
|
A | AT | 136 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(133): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-289-18086dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | |||||
| chr9:76482811
|
A | ATT | 127 | a0001c0001t0002g0098a0001c0001t0002g0113a0001c0001t0002g0132others(124): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-289-18087_-289-18 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | |||||
| chr9:76482811
|
A | ATTT | 22 | a0001c0001t0003g0309a0001c0001t0004g0205a0001c0001t0004g0316others(19): Show | 22 | HG00544.hp1 HG01123.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-289-18088_-289-18 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | |||||
| chr9:76482831
|
G | T | 1 | a0001c0001t0002g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-289-18085G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482831 | ||||||
| chr9:76482832
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-289-18084G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482832 | ||||||
| chr9:76482840
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-289-18076G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482840 | ||||||
| chr9:76482872
|
A | G | 318 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(315): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-289-18044A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482872 | ||||||
| chr9:76482950
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-289-17966C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482950 | ||||||
| chr9:76482981
|
T | C | 130 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(127): Show | 145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-17935T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482981 | ||||||
| chr9:76483044
|
C | T | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-17872C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483044 | ||||||
| chr9:76483194
|
A | C | 1 | a0001c0001t0002g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-289-17722A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483194 | ||||||
| chr9:76483243
|
T | A | 128 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(125): Show | 143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-289-17673T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483243 | ||||||
| chr9:76483270
|
G | A | 1 | a0001c0001t0010g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-289-17646G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483270 | ||||||
| chr9:76483403
|
G | GT | 8 | a0001c0001t0003g0052a0001c0001t0003g0057a0001c0001t0003g0058others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289-17503dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76483403 | |||||
| chr9:76483403
|
G | T | 3 | a0002c0002t0001g0042a0002c0002t0009g0044a0002c0002t0009g0045 | 3 | HG02486.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-289-17513G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483403 | ||||||
| chr9:76483403
|
GT | G | 132 | a0001c0001t0002g0103a0001c0001t0002g0212a0001c0001t0002g0213others(129): Show | 147 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-289-17503delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76483403 | |||||
| chr9:76483554
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-289-17362A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483554 | ||||||
| chr9:76483575
|
C | A | 1 | a0001c0001t0006g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-17341C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483575 | ||||||
| chr9:76483609
|
G | A | 2 | a0001c0001t0002g0143a0004c0005t0002g0145 | 2 | NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-289-17307G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483609 | ||||||
| chr9:76483737
|
A | C | 2 | a0001c0001t0002g0140a0002c0002t0001g0139 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-289-17179A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483737 | ||||||
| chr9:76483926
|
C | T | 16 | a0001c0001t0032g0155a0002c0002t0001g0002a0002c0002t0001g0076others(13): Show | 20 | HG00621.hp2 HG00673.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-289-16990C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483926 | ||||||
| chr9:76483958
|
G | A | 20 | a0001c0001t0003g0309a0001c0001t0004g0133a0001c0001t0004g0302others(17): Show | 21 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-289-16958G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483958 | ||||||
| chr9:76484001
|
ACT | A | 15 | a0001c0001t0003g0041a0001c0001t0007g0037a0001c0001t0008g0043others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-16914_-289-16 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484001 | ||||||
| chr9:76484158
|
C | A | 142 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0221others(139): Show | 157 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-289-16758C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484158 | ||||||
| chr9:76484281
|
G | T | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-289-16635G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484281 | ||||||
| chr9:76484285
|
A | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(74): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-289-16631A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484285 | ||||||
| chr9:76484369
|
T | TA | 13 | a0001c0001t0003g0041a0001c0001t0007g0007a0001c0001t0007g0037others(10): Show | 15 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-16533dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484369 | |||||
| chr9:76484369
|
TA | T | 7 | a0001c0001t0002g0111a0001c0001t0024g0179a0001c0001t0024g0180others(4): Show | 7 | HG01975.hp2 HG02897.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-289-16533delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484369 | |||||
| chr9:76484651
|
G | C | 1 | a0001c0001t0028g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-289-16265G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484651 | ||||||
| chr9:76484710
|
T | A | 1 | a0001c0001t0002g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-289-16206T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484710 | ||||||
| chr9:76484724
|
C | A | 5 | a0001c0001t0004g0240a0001c0001t0004g0241a0003c0003t0017g0189others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-16192C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484724 | ||||||
| chr9:76484751
|
G | A | 249 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(246): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.-289-16165G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484751 | ||||||
| chr9:76484766
|
A | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0221 | 2 | NA18939.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-289-16150A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484766 | ||||||
| chr9:76484786
|
C | CT | 16 | a0001c0001t0002g0103a0001c0001t0002g0185a0001c0001t0004g0266others(13): Show | 16 | HG01175.hp2 HG01981.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-289-16112dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484786 | |||||
| chr9:76484786
|
C | CTT | 90 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(87): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-289-16113_-289-16 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484786 | |||||
| chr9:76484815
|
A | G | 289 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(286): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-289-16101A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484815 | ||||||
| chr9:76484886
|
T | A | 1 | a0001c0001t0010g0215 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-289-16030T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484886 | ||||||
| chr9:76484934
|
T | G | 327 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(324): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-289-15982T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484934 | ||||||
| chr9:76484994
|
G | A | 14 | a0001c0001t0003g0309a0001c0001t0006g0010a0001c0001t0006g0181others(11): Show | 18 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(15): Show |
intron_variant | MODIFIER | c.-289-15922G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484994 | ||||||
| chr9:76485003
|
T | G | 1 | a0001c0001t0002g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-289-15913T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485003 | ||||||
| chr9:76485074
|
G | A | 117 | a0001c0001t0002g0061a0001c0001t0002g0267a0001c0001t0003g0003others(114): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-289-15842G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485074 | ||||||
| chr9:76485076
|
C | T | 1 | a0001c0001t0004g0308 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-289-15840C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485076 | ||||||
| chr9:76485106
|
A | G | 151 | a0001c0001t0002g0012a0001c0001t0002g0061a0001c0001t0002g0086others(148): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-289-15810A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485106 | ||||||
| chr9:76485253
|
A | G | 2 | a0001c0001t0005g0161a0001c0001t0005g0162 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-289-15663A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485253 | ||||||
| chr9:76485318
|
G | A | 1 | a0001c0001t0035g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-15598G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485318 | ||||||
| chr9:76485480
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-289-15436C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485480 | ||||||
| chr9:76485511
|
A | T | 6 | a0001c0001t0005g0151a0001c0001t0005g0161a0001c0001t0005g0162others(3): Show | 6 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-15405A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485511 | ||||||
| chr9:76485580
|
A | G | 4 | a0002c0002t0001g0022a0002c0002t0001g0282a0002c0002t0001g0284others(1): Show | 5 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-15336A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485580 | ||||||
| chr9:76485736
|
CT | C | 108 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(105): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-289-15168delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76485736 | |||||
| chr9:76485831
|
C | T | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-15085C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485831 | ||||||
| chr9:76485855
|
C | G | 1 | a0001c0001t0005g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-289-15061C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485855 | ||||||
| chr9:76485879
|
T | C | 300 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(297): Show | 329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-15037T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485879 | ||||||
| chr9:76485881
|
C | T | 9 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 13 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-15035C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485881 | ||||||
| chr9:76485893
|
T | G | 1 | a0001c0001t0003g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-289-15023T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485893 | ||||||
| chr9:76486065
|
G | A | 300 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(297): Show | 329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-14851G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486065 | ||||||
| chr9:76486090
|
A | G | 300 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(297): Show | 329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-14826A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486090 | ||||||
| chr9:76486174
|
G | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(75): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-289-14742G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486174 | ||||||
| chr9:76486217
|
G | A | 11 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(8): Show | 13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-14699G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486217 | ||||||
| chr9:76486311
|
T | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-14605T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486311 | ||||||
| chr9:76486344
|
C | T | 1 | a0002c0002t0001g0250 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-289-14572C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486344 | ||||||
| chr9:76486384
|
G | A | 3 | a0001c0001t0002g0143a0001c0001t0037g0106a0004c0005t0002g0145 | 3 | NA18947.hp1 NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-289-14532G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486384 | ||||||
| chr9:76486471
|
A | G | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-289-14445A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486471 | ||||||
| chr9:76486490
|
C | G | 6 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(3): Show | 6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-14426C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486490 | ||||||
| chr9:76486501
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-289-14415C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486501 | ||||||
| chr9:76486894
|
G | C | 1 | a0001c0001t0041g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-14022G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486894 | ||||||
| chr9:76486916
|
A | AAAAC | 128 | a0001c0001t0002g0061a0001c0001t0003g0003a0001c0001t0003g0008others(125): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-289-13976_-289-13 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76486916 | |||||
| chr9:76486916
|
AAAAC | A | 3 | a0002c0002t0001g0233a0002c0002t0001g0282a0002c0002t0001g0287 | 3 | HG00438.hp1 HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-289-13976_-289-13 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76486916 | |||||
| chr9:76486940
|
C | A | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-13976C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486940 | ||||||
| chr9:76486947
|
A | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-13969A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486947 | ||||||
| chr9:76486962
|
G | A | 11 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(8): Show | 11 | HG02040.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-289-13954G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486962 | ||||||
| chr9:76487175
|
A | G | 1 | a0001c0001t0008g0245 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-289-13741A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487175 | ||||||
| chr9:76487203
|
C | G | 1 | a0001c0001t0008g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-289-13713C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487203 | ||||||
| chr9:76487233
|
C | T | 74 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(71): Show | 76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13683C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487233 | ||||||
| chr9:76487549
|
G | A | 1 | a0001c0001t0010g0211 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-289-13367G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487549 | ||||||
| chr9:76487550
|
C | T | 74 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(71): Show | 76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13366C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487550 | ||||||
| chr9:76487580
|
T | C | 74 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(71): Show | 76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13336T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487580 | ||||||
| chr9:76487656
|
T | C | 2 | a0001c0001t0004g0196a0001c0001t0004g0206 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-289-13260T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487656 | ||||||
| chr9:76487680
|
C | A | 1 | a0002c0002t0009g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-289-13236C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487680 | ||||||
| chr9:76487687
|
G | C | 4 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0294others(1): Show | 4 | HG03927.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-13229G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487687 | ||||||
| chr9:76487688
|
G | T | 4 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0294others(1): Show | 4 | HG03927.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-13228G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487688 | ||||||
| chr9:76487900
|
A | C | 2 | a0001c0001t0011g0229a0001c0001t0011g0231 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-289-13016A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487900 | ||||||
| chr9:76488000
|
C | G | 10 | a0001c0001t0004g0016a0001c0001t0004g0182a0001c0001t0004g0199others(7): Show | 11 | HG00639.hp1 HG01175.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.-289-12916C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488000 | ||||||
| chr9:76488027
|
C | T | 25 | a0001c0001t0004g0016a0001c0001t0004g0133a0001c0001t0004g0182others(22): Show | 26 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-289-12889C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488027 | ||||||
| chr9:76488132
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12784C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488132 | ||||||
| chr9:76488445
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488445 | ||||||
| chr9:76488446
|
G | A | 2 | a0001c0001t0004g0199a0001c0001t0004g0266 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-289-12470G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488446 | ||||||
| chr9:76488450
|
T | C | 197 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(194): Show | 213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-12466T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488450 | ||||||
| chr9:76488541
|
A | G | 1 | a0001c0001t0027g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-289-12375A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488541 | ||||||
| chr9:76488554
|
C | G | 334 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(331): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-289-12362C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488554 | ||||||
| chr9:76488579
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-289-12337G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488579 | ||||||
| chr9:76488728
|
T | A | 1 | a0001c0001t0023g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-289-12188T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488728 | ||||||
| chr9:76488786
|
A | C | 52 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(49): Show | 53 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-289-12130A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488786 | ||||||
| chr9:76488786
|
A | T | 23 | a0001c0001t0005g0015a0001c0001t0005g0071a0001c0001t0005g0072others(20): Show | 24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-12130A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488786 | ||||||
| chr9:76488792
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12124C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488792 | ||||||
| chr9:76488793
|
G | A | 1 | a0001c0001t0003g0331 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-289-12123G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488793 | ||||||
| chr9:76488879
|
C | T | 1 | a0002c0006t0009g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-289-12037C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488879 | ||||||
| chr9:76488953
|
T | A | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11963T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488953 | ||||||
| chr9:76488954
|
T | G | 24 | a0001c0001t0004g0016a0001c0001t0004g0133a0001c0001t0004g0182others(21): Show | 25 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-289-11962T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488954 | ||||||
| chr9:76489003
|
AC | A | 66 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(63): Show | 68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11912delC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489003 | ||||||
| chr9:76489005
|
T | A | 66 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(63): Show | 68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11911T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489005 | ||||||
| chr9:76489166
|
C | T | 11 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(8): Show | 13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-11750C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489166 | ||||||
| chr9:76489192
|
C | T | 22 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(19): Show | 24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-11724C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489192 | ||||||
| chr9:76489254
|
T | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11662T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489254 | ||||||
| chr9:76489283
|
C | T | 1 | a0002c0002t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-289-11633C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489283 | ||||||
| chr9:76489301
|
G | C | 9 | a0001c0001t0007g0037a0001c0001t0007g0077a0001c0001t0007g0164others(6): Show | 9 | HG01255.hp1 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-289-11615G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489301 | ||||||
| chr9:76489348
|
C | T | 66 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(63): Show | 68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11568C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489348 | ||||||
| chr9:76489456
|
G | A | 1 | a0002c0002t0001g0258 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-289-11460G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489456 | ||||||
| chr9:76489549
|
C | T | 5 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0089others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-11367C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489549 | ||||||
| chr9:76489683
|
G | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(80): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-289-11233G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489683 | ||||||
| chr9:76489734
|
C | T | 22 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(19): Show | 24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-11182C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489734 | ||||||
| chr9:76489744
|
T | TC | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11166dupC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76489744 | |||||
| chr9:76489769
|
A | G | 11 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(8): Show | 13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-11147A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489769 | ||||||
| chr9:76489891
|
T | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-11025T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489891 | ||||||
| chr9:76489892
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-289-11024G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489892 | ||||||
| chr9:76489898
|
G | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11018G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489898 | ||||||
| chr9:76489902
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0129 | 2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-289-11014A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489902 | ||||||
| chr9:76489957
|
T | C | 302 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(299): Show | 331 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.-289-10959T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489957 | ||||||
| chr9:76490088
|
C | T | 1 | a0001c0001t0021g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-289-10828C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490088 | ||||||
| chr9:76490121
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-289-10795C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490121 | ||||||
| chr9:76490192
|
A | G | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-10724A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490192 | ||||||
| chr9:76490364
|
C | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(84): Show | 97 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-289-10552C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490364 | ||||||
| chr9:76490401
|
T | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-10515T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490401 | ||||||
| chr9:76490445
|
C | T | 22 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(19): Show | 24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-10471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490445 | ||||||
| chr9:76490648
|
G | A | 1 | a0001c0001t0039g0144 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-289-10268G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490648 | ||||||
| chr9:76490668
|
A | T | 1 | a0001c0001t0005g0151 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-289-10248A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490668 | ||||||
| chr9:76490742
|
A | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-10174A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490742 | ||||||
| chr9:76490746
|
T | C | 4 | a0002c0002t0001g0232a0002c0002t0001g0234a0002c0002t0001g0236others(1): Show | 4 | NA18947.hp2 NA18982.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-10170T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490746 | ||||||
| chr9:76490762
|
A | ACT | 301 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(298): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-10153_-289-10 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76490762 | |||||
| chr9:76490934
|
T | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-9982T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490934 | ||||||
| chr9:76490941
|
G | A | 25 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(22): Show | 27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-9975G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490941 | ||||||
| chr9:76491116
|
CTTCT | C | 3 | a0001c0001t0008g0043a0001c0001t0023g0083a0001c0001t0023g0084 | 3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-9797_-289-979 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491116 | |||||
| chr9:76491158
|
C | CCT | 11 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(8): Show | 13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-9749_-289-974 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491158 | |||||
| chr9:76491177
|
G | T | 18 | a0001c0001t0006g0210a0002c0002t0001g0018a0002c0002t0001g0115others(15): Show | 19 | HG00438.hp1 HG00544.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-9739G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491177 | ||||||
| chr9:76491183
|
TTCTC | T | 25 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(22): Show | 27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-9727_-289-972 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491183 | |||||
| chr9:76491220
|
T | C | 1 | a0001c0001t0003g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-9696T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491220 | ||||||
| chr9:76491258
|
T | G | 1 | a0001c0001t0005g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-289-9658T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491258 | ||||||
| chr9:76491346
|
T | A | 3 | a0003c0003t0017g0189a0003c0003t0017g0225a0003c0003t0017g0239 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-9570T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491346 | ||||||
| chr9:76491357
|
T | C | 3 | a0001c0001t0014g0035a0001c0001t0014g0172a0001c0001t0041g0046 | 3 | HG02280.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-289-9559T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491357 | ||||||
| chr9:76491509
|
GT | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(82): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-289-9402delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491509 | |||||
| chr9:76491736
|
C | G | 100 | a0001c0001t0003g0331a0001c0001t0006g0210a0002c0002t0001g0002others(97): Show | 110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-289-9180C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491736 | ||||||
| chr9:76491741
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-9175C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491741 | ||||||
| chr9:76491797
|
G | A | 156 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(153): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-289-9119G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491797 | ||||||
| chr9:76491829
|
A | G | 66 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(63): Show | 68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-9087A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491829 | ||||||
| chr9:76491835
|
C | T | 156 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(153): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-289-9081C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491835 | ||||||
| chr9:76491940
|
A | G | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0227others(2): Show | 7 | HG00408.hp1 HG00544.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-289-8976A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491940 | ||||||
| chr9:76491994
|
C | T | 1 | a0001c0001t0021g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-289-8922C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491994 | ||||||
| chr9:76491998
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-289-8918G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491998 | ||||||
| chr9:76492023
|
A | G | 1 | a0001c0001t0035g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-8893A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492023 | ||||||
| chr9:76492025
|
C | G | 1 | a0001c0001t0006g0311 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-289-8891C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492025 | ||||||
| chr9:76492032
|
C | T | 1 | a0001c0001t0005g0015 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-289-8884C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492032 | ||||||
| chr9:76492051
|
A | C | 25 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(22): Show | 27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-8865A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492051 | ||||||
| chr9:76492102
|
G | A | 14 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(11): Show | 14 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-289-8814G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492102 | ||||||
| chr9:76492198
|
C | T | 1 | a0001c0001t0010g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-289-8718C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492198 | ||||||
| chr9:76492279
|
C | A | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8637C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492279 | ||||||
| chr9:76492593
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-8323C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492593 | ||||||
| chr9:76492660
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-289-8256G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492660 | ||||||
| chr9:76492661
|
C | T | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-8255C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492661 | ||||||
| chr9:76492679
|
T | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-8237T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492679 | ||||||
| chr9:76492706
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8210C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492706 | ||||||
| chr9:76492707
|
A | G | 302 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(299): Show | 331 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.-289-8209A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492707 | ||||||
| chr9:76492709
|
T | A | 1 | a0001c0001t0006g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8207T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492709 | ||||||
| chr9:76492710
|
C | A | 1 | a0001c0001t0006g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8206C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492710 | ||||||
| chr9:76492770
|
C | T | 42 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(39): Show | 43 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-289-8146C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492770 | ||||||
| chr9:76492774
|
A | AT | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8138dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76492774 | |||||
| chr9:76492833
|
T | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-8083T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492833 | ||||||
| chr9:76492879
|
G | A | 1 | a0001c0001t0006g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8037G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492879 | ||||||
| chr9:76492898
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-289-8018G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492898 | ||||||
| chr9:76493031
|
C | T | 25 | a0001c0001t0004g0016a0001c0001t0004g0133a0001c0001t0004g0182others(22): Show | 26 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-289-7885C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493031 | ||||||
| chr9:76493046
|
T | A | 1 | a0003c0003t0017g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-289-7870T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493046 | ||||||
| chr9:76493072
|
C | T | 25 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(22): Show | 27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-7844C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493072 | ||||||
| chr9:76493158
|
C | A | 3 | a0003c0003t0017g0189a0003c0003t0017g0225a0003c0003t0017g0239 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-7758C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493158 | ||||||
| chr9:76493199
|
T | G | 3 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301 | 3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-289-7717T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493199 | ||||||
| chr9:76493248
|
A | AT | 23 | a0001c0001t0005g0015a0001c0001t0005g0071a0001c0001t0005g0072others(20): Show | 24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-7667dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76493248 | |||||
| chr9:76493283
|
G | T | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-7633G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493283 | ||||||
| chr9:76493338
|
C | T | 1 | a0001c0001t0036g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-289-7578C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493338 | ||||||
| chr9:76493368
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-289-7548T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493368 | ||||||
| chr9:76493454
|
A | G | 87 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(84): Show | 91 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-289-7462A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493454 | ||||||
| chr9:76493466
|
G | A | 155 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(152): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-289-7450G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493466 | ||||||
| chr9:76493513
|
A | G | 1 | a0001c0001t0005g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-289-7403A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493513 | ||||||
| chr9:76493598
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-289-7318G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493598 | ||||||
| chr9:76493686
|
C | A | 1 | a0001c0001t0041g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-7230C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493686 | ||||||
| chr9:76493689
|
T | G | 1 | a0001c0001t0041g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-7227T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493689 | ||||||
| chr9:76493737
|
A | G | 79 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(76): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-289-7179A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493737 | ||||||
| chr9:76493823
|
C | T | 3 | a0001c0001t0008g0043a0001c0001t0023g0083a0001c0001t0023g0084 | 3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-7093C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493823 | ||||||
| chr9:76493836
|
T | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7080T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493836 | ||||||
| chr9:76493850
|
A | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7066A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493850 | ||||||
| chr9:76493882
|
A | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7034A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493882 | ||||||
| chr9:76493907
|
T | C | 2 | a0001c0001t0004g0196a0001c0001t0004g0206 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-289-7009T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493907 | ||||||
| chr9:76494069
|
C | T | 1 | a0001c0001t0004g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-289-6847C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494069 | ||||||
| chr9:76494095
|
C | A | 1 | a0001c0001t0008g0049 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-289-6821C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494095 | ||||||
| chr9:76494095
|
C | T | 1 | a0002c0002t0001g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-289-6821C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494095 | ||||||
| chr9:76494126
|
G | A | 2 | a0002c0002t0001g0286a0002c0004t0001g0285 | 2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-289-6790G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494126 | ||||||
| chr9:76494194
|
A | G | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-6722A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494194 | ||||||
| chr9:76494216
|
G | A | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-6700G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494216 | ||||||
| chr9:76494242
|
G | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-6674G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494242 | ||||||
| chr9:76494289
|
A | G | 42 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(39): Show | 43 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-289-6627A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494289 | ||||||
| chr9:76494444
|
G | A | 2 | a0002c0002t0001g0262a0002c0002t0001g0263 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-289-6472G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494444 | ||||||
| chr9:76494565
|
G | A | 65 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(62): Show | 67 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-289-6351G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494565 | ||||||
| chr9:76494618
|
G | T | 7 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(4): Show | 7 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-289-6298G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494618 | ||||||
| chr9:76494647
|
C | T | 6 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(3): Show | 6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-6269C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494647 | ||||||
| chr9:76494656
|
G | A | 2 | a0001c0001t0005g0072a0001c0001t0005g0096 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-289-6260G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494656 | ||||||
| chr9:76494788
|
C | T | 3 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320 | 3 | NA18962.hp1 NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-289-6128C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494788 | ||||||
| chr9:76494807
|
A | G | 1 | a0005c0009t0003g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-289-6109A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494807 | ||||||
| chr9:76494826
|
C | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(80): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-289-6090C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494826 | ||||||
| chr9:76494867
|
C | T | 1 | a0001c0001t0027g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-289-6049C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494867 | ||||||
| chr9:76494959
|
A | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-5957A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494959 | ||||||
| chr9:76495034
|
G | A | 1 | a0001c0001t0041g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-5882G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495034 | ||||||
| chr9:76495082
|
G | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(80): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-289-5834G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495082 | ||||||
| chr9:76495115
|
C | T | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-5801C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495115 | ||||||
| chr9:76495156
|
A | G | 23 | a0001c0001t0005g0015a0001c0001t0005g0071a0001c0001t0005g0072others(20): Show | 24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-5760A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495156 | ||||||
| chr9:76495162
|
C | T | 103 | a0001c0001t0003g0331a0001c0001t0006g0010a0001c0001t0006g0181others(100): Show | 116 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-289-5754C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495162 | ||||||
| chr9:76495227
|
G | A | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-5689G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495227 | ||||||
| chr9:76495244
|
A | G | 301 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(298): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-5672A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495244 | ||||||
| chr9:76495268
|
T | A | 1 | a0001c0001t0012g0165 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-289-5648T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495268 | ||||||
| chr9:76495320
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-289-5596T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495320 | ||||||
| chr9:76495338
|
T | G | 3 | a0001c0001t0014g0035a0001c0001t0014g0172a0001c0001t0041g0046 | 3 | HG02280.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-289-5578T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495338 | ||||||
| chr9:76495528
|
G | A | 8 | a0001c0001t0003g0052a0001c0001t0003g0057a0001c0001t0003g0058others(5): Show | 8 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289-5388G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495528 | ||||||
| chr9:76495565
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-289-5351T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495565 | ||||||
| chr9:76495733
|
G | A | 2 | a0001c0001t0004g0302a0001c0001t0004g0307 | 2 | HG01167.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-289-5183G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495733 | ||||||
| chr9:76495852
|
T | G | 1 | a0001c0001t0005g0321 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-289-5064T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495852 | ||||||
| chr9:76496085
|
T | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0031 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-4831T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496085 | ||||||
| chr9:76496164
|
G | C | 1 | a0001c0001t0006g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-4752G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496164 | ||||||
| chr9:76496278
|
G | C | 1 | a0001c0001t0002g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-289-4638G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496278 | ||||||
| chr9:76496331
|
C | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0253a0002c0002t0001g0264 | 3 | HG01168.hp1 HG01981.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-289-4585C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496331 | ||||||
| chr9:76496346
|
G | A | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-289-4570G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496346 | ||||||
| chr9:76496450
|
T | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-4466T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496450 | ||||||
| chr9:76496476
|
T | C | 1 | a0001c0001t0003g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-289-4440T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496476 | ||||||
| chr9:76496495
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-289-4421C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496495 | ||||||
| chr9:76496535
|
A | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-4381A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496535 | ||||||
| chr9:76496600
|
CTT | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(82): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-289-4313_-289-431 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76496600 | |||||
| chr9:76496612
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-289-4304A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496612 | ||||||
| chr9:76496759
|
A | C | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-4157A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496759 | ||||||
| chr9:76496870
|
A | G | 26 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(23): Show | 28 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-289-4046A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496870 | ||||||
| chr9:76496995
|
A | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3921A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496995 | ||||||
| chr9:76497004
|
G | A | 1 | a0001c0001t0002g0299 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-289-3912G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497004 | ||||||
| chr9:76497049
|
T | C | 1 | a0001c0001t0003g0082 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-3867T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497049 | ||||||
| chr9:76497172
|
C | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3744C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497172 | ||||||
| chr9:76497284
|
C | T | 155 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(152): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-289-3632C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497284 | ||||||
| chr9:76497358
|
G | A | 3 | a0003c0003t0017g0189a0003c0003t0017g0225a0003c0003t0017g0239 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-3558G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497358 | ||||||
| chr9:76497510
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3406C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497510 | ||||||
| chr9:76497706
|
A | C | 1 | a0001c0001t0035g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-3210A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497706 | ||||||
| chr9:76497772
|
A | C | 194 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(191): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-289-3144A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497772 | ||||||
| chr9:76497785
|
C | T | 154 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(151): Show | 166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-289-3131C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497785 | ||||||
| chr9:76497854
|
C | G | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3062C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497854 | ||||||
| chr9:76497901
|
CAA | C | 26 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(23): Show | 28 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-289-3014_-289-301 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497901 | ||||||
| chr9:76497908
|
T | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3008T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497908 | ||||||
| chr9:76497980
|
AT | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(82): Show | 95 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-289-2934delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76497980 | |||||
| chr9:76498118
|
A | C | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-2798A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498118 | ||||||
| chr9:76498158
|
T | A | 1 | a0002c0002t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-289-2758T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498158 | ||||||
| chr9:76498171
|
G | A | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-2745G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498171 | ||||||
| chr9:76498227
|
C | T | 17 | a0001c0001t0006g0023a0001c0001t0006g0304a0001c0001t0006g0305others(14): Show | 19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-2689C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498227 | ||||||
| chr9:76498389
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-289-2527C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498389 | ||||||
| chr9:76498581
|
A | T | 198 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(195): Show | 214 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.-289-2335A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498581 | ||||||
| chr9:76498614
|
A | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-289-2302A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498614 | ||||||
| chr9:76498638
|
G | T | 301 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(298): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-2278G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498638 | ||||||
| chr9:76498641
|
C | T | 2 | a0001c0001t0007g0007a0001c0001t0007g0326 | 4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-2275C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498641 | ||||||
| chr9:76498773
|
CA | C | 15 | a0001c0001t0005g0110a0001c0001t0007g0007a0001c0001t0007g0037others(12): Show | 17 | HG01070.hp2 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.-289-2126delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76498773 | |||||
| chr9:76498786
|
A | AG | 101 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-289-2130_-289-212 others(5): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498786 | ||||||
| chr9:76498786
|
A | G | 1 | a0001c0001t0006g0305 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-289-2130A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498786 | ||||||
| chr9:76498787
|
A | AG | 103 | a0001c0001t0003g0331a0001c0001t0006g0010a0001c0001t0006g0181others(100): Show | 116 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-289-2129_-289-212 others(5): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498787 | ||||||
| chr9:76498790
|
A | AG | 6 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(3): Show | 6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-2125dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76498790 | |||||
| chr9:76498790
|
A | G | 20 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(17): Show | 22 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-289-2126A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498790 | ||||||
| chr9:76498923
|
G | A | 319 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(316): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.-289-1993G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498923 | ||||||
| chr9:76499020
|
A | G | 2 | a0001c0001t0024g0179a0001c0001t0024g0180 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-1896A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499020 | ||||||
| chr9:76499050
|
A | AT | 107 | a0001c0001t0003g0082a0001c0001t0003g0331a0001c0001t0004g0192others(104): Show | 120 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-289-1856dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76499050 | |||||
| chr9:76499050
|
A | ATT | 195 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(192): Show | 211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-289-1857_-289-185 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76499050 | |||||
| chr9:76499309
|
G | A | 3 | a0003c0003t0017g0189a0003c0003t0017g0225a0003c0003t0017g0239 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-1607G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499309 | ||||||
| chr9:76499316
|
T | C | 301 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(298): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-1600T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499316 | ||||||
| chr9:76499416
|
C | T | 71 | a0001c0001t0003g0041a0001c0001t0003g0332a0001c0001t0004g0016others(68): Show | 73 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.-289-1500C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499416 | ||||||
| chr9:76499443
|
C | T | 4 | a0001c0001t0014g0035a0001c0001t0014g0172a0001c0001t0014g0174others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-1473C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499443 | ||||||
| chr9:76499468
|
T | C | 302 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(299): Show | 331 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.-289-1448T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499468 | ||||||
| chr9:76499605
|
C | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0267 | 2 | HG00609.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-289-1311C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499605 | ||||||
| chr9:76499743
|
C | T | 1 | a0001c0001t0021g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-289-1173C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499743 | ||||||
| chr9:76500138
|
T | A | 4 | a0001c0001t0014g0035a0001c0001t0014g0172a0001c0001t0014g0174others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-778T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500138 | ||||||
| chr9:76500140
|
A | AT | 98 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(95): Show | 110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-289-766dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76500140 | |||||
| chr9:76500148
|
T | G | 3 | a0001c0001t0008g0043a0001c0001t0023g0083a0001c0001t0023g0084 | 3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-768T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500148 | ||||||
| chr9:76500189
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-289-727A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500189 | ||||||
| chr9:76500241
|
T | C | 1 | a0001c0001t0006g0325 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-289-675T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500241 | ||||||
| chr9:76500261
|
T | C | 10 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(7): Show | 12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-289-655T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500261 | ||||||
| chr9:76500322
|
T | C | 4 | a0001c0001t0011g0193a0001c0001t0011g0229a0001c0001t0011g0230others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-594T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500322 | ||||||
| chr9:76500577
|
G | A | 1 | a0001c0001t0035g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-339G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500577 | ||||||
| chr9:76500653
|
T | G | 1 | a0001c0001t0003g0332 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-289-263T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500653 | ||||||
| chr9:76500682
|
C | T | 1 | a0002c0002t0001g0247 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-289-234C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500682 | ||||||
| chr9:76500729
|
C | A | 2 | a0002c0002t0009g0271a0002c0002t0009g0272 | 2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-289-187C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500729 | ||||||
| chr9:76500731
|
A | G | 3 | a0003c0003t0017g0189a0003c0003t0017g0225a0003c0003t0017g0239 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-185A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500731 | ||||||
| chr9:76500808
|
T | G | 24 | a0001c0001t0002g0112a0001c0001t0002g0127a0001c0001t0002g0150others(21): Show | 27 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-108T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500808 | ||||||
| chr9:76500813
|
A | G | 100 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(97): Show | 112 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-289-103A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500813 | ||||||
| chr9:76501192
|
C | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(102): Show | 118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-144+131C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501192 | ||||||
| chr9:76501249
|
T | A | 31 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(28): Show | 33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-144+188T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501249 | ||||||
| chr9:76501274
|
G | C | 70 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(67): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-144+213G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501274 | ||||||
| chr9:76501278
|
C | T | 3 | a0001c0001t0006g0010a0001c0001t0006g0181a0001c0001t0006g0210 | 4 | NA18963.hp2 NA18975.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.-144+217C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501278 | ||||||
| chr9:76501358
|
C | T | 135 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(132): Show | 150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-144+297C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501358 | ||||||
| chr9:76501402
|
G | A | 1 | a0002c0002t0001g0262 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-144+341G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501402 | ||||||
| chr9:76501429
|
A | G | 104 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(101): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-144+368A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501429 | ||||||
| chr9:76501452
|
C | T | 104 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(101): Show | 117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-144+391C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501452 | ||||||
| chr9:76501497
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0033g0136 | 2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-144+436G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501497 | ||||||
| chr9:76501512
|
A | C | 1 | a0001c0001t0002g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-144+451A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501512 | ||||||
| chr9:76501516
|
T | C | 1 | a0001c0001t0018g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-144+455T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501516 | ||||||
| chr9:76501637
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-144+576G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501637 | ||||||
| chr9:76501712
|
C | G | 2 | a0001c0001t0002g0109a0001c0001t0002g0123 | 2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-143-527C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501712 | ||||||
| chr9:76501714
|
T | G | 2 | a0001c0001t0022g0322a0001c0001t0022g0323 | 2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-143-525T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501714 | ||||||
| chr9:76501820
|
GA | G | 301 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(298): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-143-417delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76501820 | |||||
| chr9:76501839
|
T | C | 22 | a0001c0001t0006g0010a0001c0001t0006g0023a0001c0001t0006g0181others(19): Show | 25 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-143-400T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501839 | ||||||
| chr9:76501906
|
G | A | 1 | a0001c0001t0046g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-143-333G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501906 | ||||||
| chr9:76502059
|
A | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(315): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.-143-180A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502059 | ||||||
| chr9:76502061
|
T | C | 135 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(132): Show | 150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-143-178T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502061 | ||||||
| chr9:76502105
|
C | T | 31 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(28): Show | 33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143-134C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502105 | ||||||
| chr9:76502155
|
A | G | 31 | a0001c0001t0007g0007a0001c0001t0007g0037a0001c0001t0007g0077others(28): Show | 33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143-84A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502155 | ||||||
| chr9:76502169
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0005g0015 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-143-68_-143-53del others(16): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502169 | |||||
| chr9:76502173
|
CTCTCTGT others(5): Show |
C | 7 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050others(4): Show | 7 | HG00642.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143-64_-143-53del others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502173 | |||||
| chr9:76502175
|
CTCTGTAT others(5): Show |
C | 3 | a0001c0001t0002g0111a0001c0001t0002g0116a0001c0001t0031g0114 | 3 | HG00408.hp2 NA18965.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-143-62_-143-51del others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502175 | |||||
| chr9:76502177
|
CTGTATA | C | 97 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(94): Show | 109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-143-60_-143-55del others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502177 | |||||
| chr9:76502179
|
G | C | 21 | a0001c0001t0005g0071a0001c0001t0005g0072a0001c0001t0005g0090others(18): Show | 21 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-143-60G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502179 | ||||||
| chr9:76502179
|
GTATA | G | 81 | a0001c0001t0003g0003a0001c0001t0003g0008a0001c0001t0003g0009others(78): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-143-38_-143-35del others(4): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | |||||
| chr9:76502179
|
GTATATA | G | 43 | a0001c0001t0003g0082a0001c0001t0003g0331a0001c0001t0003g0332others(40): Show | 46 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143-40_-143-35del others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | |||||
| chr9:76502179
|
GTATATAT others(1): Show |
G | 58 | a0001c0001t0003g0041a0001c0001t0004g0016a0001c0001t0004g0133others(55): Show | 61 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-143-42_-143-35del others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | |||||
| chr9:76502179
|
GTATATAT others(3): Show |
G | 2 | a0001c0001t0002g0108a0001c0001t0002g0134 | 2 | HG01081.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-143-44_-143-35del others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | |||||
| chr9:76502181
|
A | C | 22 | a0001c0001t0005g0071a0001c0001t0005g0072a0001c0001t0005g0090others(19): Show | 22 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-143-58A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502181 | ||||||
| chr9:76502183
|
A | C | 23 | a0001c0001t0005g0071a0001c0001t0005g0072a0001c0001t0005g0090others(20): Show | 23 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143-56A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502183 | ||||||
| chr9:76502185
|
A | C | 119 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(116): Show | 131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-143-54A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502185 | ||||||
| chr9:76502185
|
A | G | 1 | a0001c0001t0025g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143-54A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502185 | ||||||
| chr9:76502187
|
A | C | 99 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(96): Show | 112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-143-52A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502187 | ||||||
| chr9:76502187
|
A | G | 29 | a0001c0001t0005g0015a0001c0001t0005g0071a0001c0001t0005g0072others(26): Show | 30 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-143-52A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502187 | ||||||
| chr9:76502189
|
A | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-143-50A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502189 | ||||||
| chr9:76502201
|
A | T | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-143-38A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502201 | ||||||
| chr9:76502205
|
T | A | 1 | a0001c0001t0003g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143-34T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502205 |