Item | Value |
---|---|
geneid | 51301 |
ensemblid | ENSG00000176928.7 |
hgncid | 17973 |
symbol | GCNT4 |
name | glucosaminyl (N-acetyl) transferase 4 |
refseq_nuc | NM_001366737.1 |
refseq_prot | NP_001353666.1 |
ensembl_nuc | ENST00000652361.2 |
ensembl_prot | ENSP00000498836.1 |
mane_status | MANE Select |
chr | chr5 |
start | 75025346 |
end | 75052558 |
strand | - |
ver | v1.2 |
region | chr5:75025346-75052558 |
region5000 | chr5:75020346-75057558 |
regionname0 | GCNT4_chr5_75025346_75052558 |
regionname5000 | GCNT4_chr5_75020346_75057558 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 453 | 215 | 25 | 37 | 105 | 14 | 32 | 79 | GCNT4_chr5_75020346_75057558 | GCNT4 | MKIFK others(448): Show |
chr5 | 75020346 | 75057558 |
a0002 | 0/0 | 453 | 133 | 37 | 27 | 55 | 2 | 12 | 42 | GCNT4_chr5_75020346_75057558 | GCNT4 | MKIFK others(448): Show |
chr5 | 75020346 | 75057558 |
a0003 | 0/0 | 453 | 33 | 27 | 2 | 4 | 0 | 0 | 3 | GCNT4_chr5_75020346_75057558 | GCNT4 | MKIFK others(448): Show |
chr5 | 75020346 | 75057558 |
a0004 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | MKIFK others(448): Show |
chr5 | 75020346 | 75057558 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1359 | 215 | 25 | 37 | 105 | 14 | 32 | GCNT4_chr5_75020346_75057558 | GCNT4 | ATGAA others(1354): Show |
chr5 | 75020346 | 75057558 | ||
a0002c0002 | 0/0 | 1359 | 133 | 37 | 27 | 55 | 2 | 12 | GCNT4_chr5_75020346_75057558 | GCNT4 | ATGAA others(1354): Show |
chr5 | 75020346 | 75057558 | ||
a0003c0003 | 0/0 | 1359 | 33 | 27 | 2 | 4 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | ATGAA others(1354): Show |
chr5 | 75020346 | 75057558 | ||
a0004c0004 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | ATGAA others(1354): Show |
chr5 | 75020346 | 75057558 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5022 | 49 | 4 | 10 | 17 | 6 | 12 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0003 | 0/0 | 5023 | 35 | 5 | 0 | 20 | 1 | 9 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5018): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0004 | 0/0 | 5023 | 31 | 3 | 5 | 20 | 1 | 2 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5018): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0005 | 0/0 | 5020 | 22 | 0 | 5 | 14 | 2 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0006 | 0/0 | 5024 | 14 | 0 | 0 | 13 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0007 | 0/0 | 5021 | 10 | 7 | 2 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0009 | 0/0 | 5022 | 9 | 3 | 1 | 4 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0010 | 0/0 | 5024 | 9 | 2 | 1 | 3 | 0 | 3 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0011 | 1/0 | 5022 | 8 | 0 | 6 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0016 | 0/0 | 5021 | 7 | 0 | 2 | 5 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0017 | 0/0 | 5021 | 6 | 0 | 1 | 4 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0028 | 0/0 | 5020 | 2 | 0 | 1 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0042 | 0/0 | 5023 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | ACAGC others(5018): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0044 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0045 | 0/0 | 5022 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0046 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0047 | 0/0 | 5022 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0048 | 0/0 | 5025 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5020): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0049 | 0/0 | 5024 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0050 | 0/1 | 5024 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0051 | 0/0 | 5022 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0054 | 0/0 | 5023 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5018): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0055 | 0/0 | 5023 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5018): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0069 | 0/0 | 5019 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5014): Show |
chr5 | 75020346 | 75057558 |
a0001c0001t0072 | 0/0 | 5021 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0002 | 0/0 | 4987 | 41 | 2 | 6 | 30 | 0 | 3 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4982): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0008 | 0/0 | 4988 | 10 | 0 | 2 | 7 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4983): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0013 | 0/0 | 5015 | 8 | 2 | 2 | 0 | 1 | 3 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5010): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0014 | 0/0 | 4986 | 8 | 2 | 1 | 5 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4981): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0018 | 0/0 | 5018 | 6 | 3 | 2 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5013): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0019 | 0/0 | 4987 | 5 | 0 | 5 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4982): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0021 | 0/0 | 5022 | 5 | 1 | 0 | 4 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5017): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0022 | 0/0 | 5020 | 5 | 2 | 3 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0023 | 0/0 | 5019 | 3 | 0 | 0 | 0 | 1 | 2 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5014): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0024 | 0/0 | 4987 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4982): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0025 | 0/0 | 5019 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5014): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0026 | 0/0 | 5018 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5013): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0027 | 0/0 | 5019 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5014): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0033 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0034 | 0/0 | 5016 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5011): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0035 | 0/0 | 5024 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0036 | 0/0 | 5025 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5020): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0037 | 0/0 | 5020 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0038 | 0/0 | 5021 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0039 | 0/0 | 4989 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4984): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0040 | 0/0 | 4985 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4980): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0041 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5012): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0043 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4984): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0052 | 0/0 | 4986 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4981): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0053 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4983): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0061 | 0/0 | 5024 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5019): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0062 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4980): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0063 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4982): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0064 | 0/0 | 4986 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4981): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0065 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4985): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0066 | 0/0 | 4988 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4983): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0067 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5012): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0068 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0070 | 0/0 | 5019 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5014): Show |
chr5 | 75020346 | 75057558 |
a0002c0002t0071 | 0/0 | 4986 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(4981): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0012 | 0/0 | 5360 | 8 | 8 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5355): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0015 | 0/0 | 5361 | 7 | 7 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5356): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0020 | 0/0 | 5353 | 5 | 5 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5348): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0029 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5015): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0030 | 0/0 | 5021 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5016): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0031 | 0/0 | 5357 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5352): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0032 | 0/0 | 5355 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5350): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0056 | 0/0 | 5354 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5349): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0057 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5353): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0058 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5348): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0059 | 0/0 | 5382 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5377): Show |
chr5 | 75020346 | 75057558 |
a0003c0003t0060 | 0/0 | 5360 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5355): Show |
chr5 | 75020346 | 75057558 |
a0004c0004t0041 | 0/0 | 5017 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | AGAGC others(5012): Show |
chr5 | 75020346 | 75057558 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 0 | 8 | 2 | 3 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0009 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0004 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0005 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0003 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0006g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0006g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0006g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0011g0017 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0011g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0011g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0016g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0016g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0016g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0028g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0028g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0042g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0044g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0045g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0046g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0047g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0048g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0049g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0050g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0051g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0054g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0055g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0069g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0001c0001t0072g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0008g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0013g0008 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0013g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0013g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0014g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0018g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0018g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0018g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0019g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0019g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0019g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0021g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0021g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0021g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0021g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0022g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0022g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0022g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0022g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0023g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0023g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0024g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0024g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0025g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0025g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0025g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0026g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0026g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0027g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0027g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0033g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0033g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0034g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0034g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0035g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0035g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0036g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0036g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0037g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0037g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0038g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0039g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0040g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0041g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0043g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0052g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0053g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0061g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0062g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0063g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0064g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0065g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0066g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0067g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0068g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0070g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0002c0002t0071g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0015g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0015g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0020g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0020g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0020g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0029g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0029g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0030g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0031g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0031g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0032g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0056g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0057g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0058g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0059g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0003c0003t0060g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
a0004c0004t0041g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00140 | hp2 | a0002 | c0002 | t0023 | g0030 | EUR | GBR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00280 | hp1 | a0001 | c0001 | t0017 | g0212 | EUR | FIN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00280 | hp2 | a0001 | c0001 | t0044 | g0197 | EUR | FIN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00323 | hp1 | a0001 | c0001 | t0028 | g0195 | EUR | FIN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00323 | hp2 | a0001 | c0001 | t0045 | g0179 | EUR | FIN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00558 | hp2 | a0002 | c0002 | t0063 | g0109 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0214 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00609 | hp2 | a0001 | c0001 | t0016 | g0075 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00642 | hp2 | a0003 | c0003 | t0031 | g0257 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | CHS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00733 | hp1 | a0002 | c0002 | t0036 | g0132 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00733 | hp2 | a0002 | c0002 | t0014 | g0107 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00735 | hp1 | a0002 | c0002 | t0018 | g0015 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00735 | hp2 | a0001 | c0001 | t0069 | g0077 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00741 | hp1 | a0002 | c0002 | t0008 | g0014 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG00741 | hp2 | a0002 | c0002 | t0022 | g0046 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01069 | hp2 | a0002 | c0002 | t0013 | g0008 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01070 | hp1 | a0002 | c0002 | t0040 | g0027 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01071 | hp1 | a0002 | c0002 | t0013 | g0008 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01071 | hp2 | a0002 | c0002 | t0040 | g0027 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01074 | hp1 | a0001 | c0001 | t0011 | g0181 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01081 | hp1 | a0001 | c0001 | t0046 | g0209 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01081 | hp2 | a0002 | c0002 | t0022 | g0136 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01106 | hp1 | a0002 | c0002 | t0022 | g0046 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0147 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0052 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0052 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01175 | hp2 | a0002 | c0002 | t0066 | g0253 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01243 | hp1 | a0002 | c0002 | t0036 | g0248 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01243 | hp2 | a0003 | c0003 | t0032 | g0025 | AMR | PUR | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01256 | hp1 | a0002 | c0002 | t0018 | g0108 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01256 | hp2 | a0001 | c0001 | t0011 | g0041 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01258 | hp1 | a0001 | c0001 | t0011 | g0041 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0043 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01261 | hp2 | a0002 | c0002 | t0037 | g0255 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0196 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01361 | hp1 | a0001 | c0001 | t0016 | g0023 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0191 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01496 | hp2 | a0001 | c0001 | t0016 | g0023 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0081 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01516 | hp2 | a0002 | c0002 | t0013 | g0022 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0080 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01884 | hp2 | a0002 | c0002 | t0026 | g0024 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01891 | hp1 | a0002 | c0002 | t0033 | g0247 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01891 | hp2 | a0003 | c0003 | t0020 | g0060 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01934 | hp1 | a0002 | c0002 | t0019 | g0018 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0079 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01975 | hp1 | a0002 | c0002 | t0019 | g0018 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01978 | hp1 | a0001 | c0001 | t0017 | g0187 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01978 | hp2 | a0002 | c0002 | t0008 | g0220 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01981 | hp1 | a0002 | c0002 | t0019 | g0018 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01981 | hp2 | a0001 | c0001 | t0010 | g0038 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02004 | hp1 | a0002 | c0002 | t0019 | g0233 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02015 | hp1 | a0001 | c0001 | t0051 | g0206 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02027 | hp2 | a0002 | c0002 | t0021 | g0226 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02055 | hp2 | a0003 | c0003 | t0015 | g0138 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02056 | hp1 | a0003 | c0003 | t0029 | g0095 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02074 | hp2 | a0002 | c0002 | t0008 | g0114 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02129 | hp2 | a0002 | c0002 | t0052 | g0190 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0157 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02145 | hp2 | a0003 | c0003 | t0057 | g0155 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02148 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | CDX | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02257 | hp1 | a0001 | c0001 | t0049 | g0180 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02257 | hp2 | a0003 | c0003 | t0020 | g0021 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02258 | hp1 | a0003 | c0003 | t0031 | g0061 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0176 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02273 | hp1 | a0002 | c0002 | t0019 | g0232 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02273 | hp2 | a0001 | c0001 | t0072 | g0262 | AMR | PEL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02280 | hp2 | a0002 | c0002 | t0035 | g0183 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02451 | hp1 | a0002 | c0002 | t0025 | g0241 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02451 | hp2 | a0002 | c0002 | t0024 | g0028 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02572 | hp1 | a0002 | c0002 | t0037 | g0252 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02572 | hp2 | a0002 | c0002 | t0026 | g0024 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02602 | hp1 | a0002 | c0002 | t0018 | g0068 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02615 | hp2 | a0002 | c0002 | t0014 | g0218 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02622 | hp1 | a0002 | c0002 | t0035 | g0182 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02622 | hp2 | a0002 | c0002 | t0027 | g0091 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02647 | hp2 | a0003 | c0003 | t0020 | g0064 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0217 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02698 | hp2 | a0001 | c0001 | t0011 | g0043 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02717 | hp2 | a0002 | c0002 | t0033 | g0249 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02723 | hp1 | a0003 | c0003 | t0059 | g0093 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0085 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02738 | hp1 | a0002 | c0002 | t0013 | g0022 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0105 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02809 | hp2 | a0002 | c0002 | t0064 | g0115 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02895 | hp1 | a0002 | c0002 | t0027 | g0090 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02895 | hp2 | a0003 | c0003 | t0012 | g0175 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02896 | hp1 | a0003 | c0003 | t0012 | g0059 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02896 | hp2 | a0003 | c0003 | t0015 | g0020 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02897 | hp1 | a0003 | c0003 | t0012 | g0258 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02897 | hp2 | a0003 | c0003 | t0012 | g0101 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02965 | hp1 | a0002 | c0002 | t0067 | g0261 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02965 | hp2 | a0003 | c0003 | t0015 | g0055 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02970 | hp1 | a0002 | c0002 | t0061 | g0221 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02970 | hp2 | a0003 | c0003 | t0056 | g0063 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03041 | hp1 | a0002 | c0002 | t0013 | g0240 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03041 | hp2 | a0003 | c0003 | t0060 | g0256 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0153 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03098 | hp2 | a0002 | c0002 | t0024 | g0104 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03139 | hp2 | a0003 | c0003 | t0015 | g0139 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03209 | hp1 | a0002 | c0002 | t0018 | g0015 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03209 | hp2 | a0003 | c0003 | t0020 | g0021 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0260 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03225 | hp2 | a0002 | c0002 | t0071 | g0088 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03453 | hp1 | a0003 | c0003 | t0020 | g0062 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03453 | hp2 | a0003 | c0003 | t0012 | g0103 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03486 | hp1 | a0003 | c0003 | t0058 | g0065 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03486 | hp2 | a0003 | c0003 | t0032 | g0025 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0235 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03516 | hp1 | a0003 | c0003 | t0015 | g0020 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | ESN | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0254 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03540 | hp2 | a0002 | c0002 | t0027 | g0092 | AFR | GWD | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03654 | hp2 | a0002 | c0002 | t0034 | g0236 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03669 | hp2 | a0001 | c0001 | t0054 | g0170 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03688 | hp2 | a0001 | c0001 | t0042 | g0056 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0172 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0168 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03927 | hp1 | a0002 | c0002 | t0034 | g0162 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03927 | hp2 | a0001 | c0001 | t0010 | g0163 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0038 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04184 | hp2 | a0001 | c0001 | t0010 | g0237 | SAS | BEB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04199 | hp1 | a0002 | c0002 | t0013 | g0069 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04199 | hp2 | a0002 | c0002 | t0008 | g0127 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04204 | hp2 | a0002 | c0002 | t0023 | g0030 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG04228 | hp2 | a0002 | c0002 | t0013 | g0008 | SAS | STU | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18522 | hp1 | a0002 | c0002 | t0022 | g0134 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | CHB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18906 | hp1 | a0002 | c0002 | t0025 | g0239 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0246 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18939 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18941 | hp1 | a0001 | c0001 | t0010 | g0166 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18941 | hp2 | a0003 | c0003 | t0029 | g0094 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18947 | hp1 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18949 | hp2 | a0001 | c0001 | t0016 | g0013 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18953 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18956 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18967 | hp2 | a0002 | c0002 | t0008 | g0014 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18970 | hp2 | a0003 | c0003 | t0030 | g0026 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18972 | hp1 | a0002 | c0002 | t0062 | g0259 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18974 | hp1 | a0002 | c0002 | t0014 | g0033 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18975 | hp1 | a0002 | c0002 | t0038 | g0053 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18977 | hp1 | a0002 | c0002 | t0014 | g0122 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18979 | hp1 | a0002 | c0002 | t0008 | g0111 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18983 | hp2 | a0001 | c0001 | t0047 | g0205 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18984 | hp2 | a0002 | c0002 | t0039 | g0049 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18986 | hp1 | a0001 | c0001 | t0016 | g0013 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18989 | hp2 | a0002 | c0002 | t0065 | g0231 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18990 | hp2 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18995 | hp1 | a0001 | c0001 | t0017 | g0186 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0150 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18997 | hp2 | a0002 | c0002 | t0021 | g0054 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18999 | hp1 | a0001 | c0001 | t0016 | g0013 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19000 | hp2 | a0002 | c0002 | t0008 | g0014 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19001 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19004 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19004 | hp2 | a0002 | c0002 | t0014 | g0033 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19005 | hp2 | a0003 | c0003 | t0030 | g0026 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19007 | hp1 | a0002 | c0002 | t0021 | g0250 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19007 | hp2 | a0001 | c0001 | t0017 | g0106 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19009 | hp2 | a0002 | c0002 | t0043 | g0057 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19011 | hp1 | a0002 | c0002 | t0038 | g0053 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19030 | hp1 | a0002 | c0002 | t0026 | g0087 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19030 | hp2 | a0002 | c0002 | t0018 | g0242 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19043 | hp1 | a0003 | c0003 | t0012 | g0222 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19043 | hp2 | a0002 | c0002 | t0018 | g0015 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19062 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19068 | hp2 | a0002 | c0002 | t0014 | g0125 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19070 | hp1 | a0002 | c0002 | t0039 | g0049 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19075 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19075 | hp2 | a0002 | c0002 | t0014 | g0126 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19077 | hp2 | a0002 | c0002 | t0021 | g0054 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19079 | hp2 | a0002 | c0002 | t0008 | g0118 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19080 | hp1 | a0002 | c0002 | t0008 | g0120 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19087 | hp2 | a0001 | c0001 | t0048 | g0199 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19088 | hp2 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19090 | hp2 | a0001 | c0001 | t0055 | g0124 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19091 | hp1 | a0002 | c0002 | t0008 | g0230 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19240 | hp1 | a0003 | c0003 | t0015 | g0020 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA19240 | hp2 | a0003 | c0003 | t0012 | g0102 | AFR | YRI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20129 | hp1 | a0002 | c0002 | t0041 | g0086 | AFR | ASW | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ASW | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0245 | EUR | TSI | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20905 | hp1 | a0002 | c0002 | t0023 | g0184 | SAS | GIH | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | GIH | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0211 | AMR | CLM | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02109 | hp2 | a0002 | c0002 | t0014 | g0219 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02486 | hp1 | a0004 | c0004 | t0041 | g0096 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02486 | hp2 | a0002 | c0002 | t0024 | g0028 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02559 | hp1 | a0002 | c0002 | t0070 | g0089 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG02559 | hp2 | a0003 | c0003 | t0012 | g0137 | AFR | ACB | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03471 | hp1 | a0002 | c0002 | t0022 | g0142 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG03471 | hp2 | a0002 | c0002 | t0021 | g0251 | AFR | MSL | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
HG06807 | hp2 | a0002 | c0002 | t0013 | g0008 | AFR | USA | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20300 | hp1 | a0002 | c0002 | t0053 | g0189 | AFR | USA | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA20300 | hp2 | a0002 | c0002 | t0025 | g0143 | AFR | USA | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA21309 | hp1 | a0002 | c0002 | t0068 | g0097 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
NA21309 | hp2 | a0003 | c0003 | t0015 | g0055 | AFR | LWK | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
homoSapiens | chm13v2 | a0001 | c0001 | t0050 | g0177 | REF | REF | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0017 | REF | REF | GCNT4_chr5_75020346_75057558 | GCNT4 | chr5 | 75020346 | 75057558 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75028723 | G | A | 3 | a0002 a0003 a0004 |
167 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(164): Show |
missense_variant | MODERATE | c.1315C>T | p.Pro439Ser | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1646/5023 | 1315/1362 | 439/453 | chr5 | 75028723 | |||
chr5:75029077 | C | T | 2 | a0002 a0004 |
134 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(131): Show |
missense_variant | MODERATE | c.961G>A | p.Val321Ile | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1292/5023 | 961/1362 | 321/453 | chr5 | 75029077 | |||
chr5:75029922 | G | A | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.116C>T | p.Pro39Leu | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 447/5023 | 116/1362 | 39/453 | chr5 | 75029922 | |||
chr5:75052168 | CAT | C | 3 | a0001 a0002 a0004 |
43 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(40): Show |
splice_region_variant | LOW | c.-144_-143delAT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/4 | chr5 | 75052168 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75025505 | G | A | 1 | a0001c0001t0047 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3171C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 3171 | chr5 | 75025505 | ||||||
chr5:75025582 | T | C | 1 | a0002c0002t0071 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3094A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 3094 | chr5 | 75025582 | ||||||
chr5:75025728 | C | T | 2 | a0002c0002t0040 a0002c0002t0064 |
3 | HG01070.hp1 HG01071.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2948G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2948 | chr5 | 75025728 | ||||||
chr5:75026135 | T | C | 1 | a0003c0003t0058 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2541A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2541 | chr5 | 75026135 | ||||||
chr5:75026242 | G | A | 1 | a0002c0002t0068 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2434C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2434 | chr5 | 75026242 | ||||||
chr5:75026268 | G | A | 2 | a0001c0001t0042 a0001c0001t0054 |
2 | HG03669.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2408C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2408 | chr5 | 75026268 | ||||||
chr5:75026481 | ACT | A | 2 | a0003c0003t0032 a0003c0003t0059 |
3 | HG01243.hp2 HG02723.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2193_*2194delAG | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2193 | chr5 | 75026481 | ||||||
chr5:75026647 | C | CA | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 others(10): Show |
88 | HG00140.hp2 HG00609.hp1 HG00609.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2028dupT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2028 | chr5 | 75026647 | ||||||
chr5:75026647 | C | CAA | 12 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0049 others(9): Show |
42 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2027_*2028dupTT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2028 | chr5 | 75026647 | ||||||
chr5:75026647 | C | CAAA | 6 | a0001c0001t0048 a0002c0002t0027 a0002c0002t0036 others(3): Show |
17 | HG00733.hp1 HG01243.hp1 HG02559.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2026_*2028dupTTT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2028 | chr5 | 75026647 | ||||||
chr5:75026647 | C | CAAAA | 3 | a0002c0002t0021 a0003c0003t0015 a0003c0003t0060 |
13 | HG02027.hp2 HG02055.hp2 HG02896.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2025_*2028dupTTTT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2028 | chr5 | 75026647 | ||||||
chr5:75026647 | CA | C | 11 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0069 others(8): Show |
74 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2028delT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2028 | chr5 | 75026647 | ||||||
chr5:75026647 | CAA | C | 5 | a0001c0001t0046 a0002c0002t0013 a0002c0002t0014 others(2): Show |
19 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2027_*2028delTT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2027 | chr5 | 75026647 | ||||||
chr5:75026647 | CAAAA | C | 3 | a0003c0003t0020 a0003c0003t0056 a0003c0003t0058 |
7 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2025_*2028delTTTT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2025 | chr5 | 75026647 | ||||||
chr5:75026661 | A | C | 1 | a0002c0002t0024 | 3 | HG02451.hp2 HG02486.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2015T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2015 | chr5 | 75026661 | ||||||
chr5:75026664 | A | C | 1 | a0002c0002t0063 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 2012 | chr5 | 75026664 | ||||||
chr5:75026679 | T | C | 1 | a0002c0002t0066 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1997A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1997 | chr5 | 75026679 | ||||||
chr5:75026721 | C | G | 25 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(22): Show |
104 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1955G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1955 | chr5 | 75026721 | ||||||
chr5:75026861 | T | A | 25 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(22): Show |
104 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1815A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1815 | chr5 | 75026861 | ||||||
chr5:75027014 | TA | T | 2 | a0003c0003t0029 a0003c0003t0030 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1661delT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1661 | chr5 | 75027014 | ||||||
chr5:75027157 | A | G | 1 | a0001c0001t0028 | 2 | HG00323.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1519T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1519 | chr5 | 75027157 | ||||||
chr5:75027226 | TTTTACTT others(28): Show |
T | 1 | a0002c0002t0062 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1415_*1449delTATT others(31): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1415 | chr5 | 75027226 | ||||||
chr5:75027278 | TATATA | T | 2 | a0002c0002t0013 a0002c0002t0034 |
10 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1393_*1397delTATA others(1): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1393 | chr5 | 75027278 | ||||||
chr5:75027283 | A | T | 43 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(40): Show |
152 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1393T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1393 | chr5 | 75027283 | ||||||
chr5:75027292 | TTA | T | 2 | a0001c0001t0028 a0001c0001t0044 |
3 | HG00280.hp2 HG00323.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1382_*1383delTA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1382 | chr5 | 75027292 | ||||||
chr5:75027302 | ATAATTAT others(23): Show |
A | 15 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(12): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1344_*1373delATGA others(26): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1344 | chr5 | 75027302 | ||||||
chr5:75027306 | T | TAATA | 12 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(9): Show |
33 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1369_*1370insTATT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1369 | chr5 | 75027306 | ||||||
chr5:75027307 | T | A | 20 | a0002c0002t0013 a0002c0002t0018 a0002c0002t0021 others(17): Show |
54 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1369A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1369 | chr5 | 75027307 | ||||||
chr5:75027309 | TATGTATA others(21): Show |
T | 20 | a0002c0002t0013 a0002c0002t0018 a0002c0002t0021 others(17): Show |
54 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1339_*1366delTGTA others(24): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1339 | chr5 | 75027309 | ||||||
chr5:75027336 | C | A | 15 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(12): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1340G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1340 | chr5 | 75027336 | ||||||
chr5:75027336 | C | T | 11 | a0002c0002t0062 a0003c0003t0012 a0003c0003t0015 others(8): Show |
30 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1340G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1340 | chr5 | 75027336 | ||||||
chr5:75027337 | A | ATGTATAT others(15): Show |
9 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(6): Show |
28 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1338_*1339insATGA others(18): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1338 | chr5 | 75027337 | ||||||
chr5:75027337 | A | ATGTATAT others(42): Show |
1 | a0003c0003t0059 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1338_*1339insATGA others(45): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1338 | chr5 | 75027337 | ||||||
chr5:75027337 | A | T | 15 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(12): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1339T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1339 | chr5 | 75027337 | ||||||
chr5:75027344 | G | A | 1 | a0002c0002t0062 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1332 | chr5 | 75027344 | ||||||
chr5:75027362 | T | A | 1 | a0002c0002t0062 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1314 | chr5 | 75027362 | ||||||
chr5:75027443 | TTATA | T | 7 | a0002c0002t0021 a0002c0002t0023 a0002c0002t0033 others(4): Show |
16 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1229_*1232delTATA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1229 | chr5 | 75027443 | ||||||
chr5:75027546 | T | C | 10 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(7): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1130A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1130 | chr5 | 75027546 | ||||||
chr5:75027659 | T | G | 5 | a0002c0002t0021 a0002c0002t0023 a0002c0002t0037 others(2): Show |
13 | HG00140.hp2 HG01261.hp2 HG02027.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1017A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 1017 | chr5 | 75027659 | ||||||
chr5:75027704 | G | C | 49 | a0001c0001t0055 a0002c0002t0002 a0002c0002t0008 others(46): Show |
168 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*972C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 972 | chr5 | 75027704 | ||||||
chr5:75027764 | C | T | 69 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(66): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*912G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 912 | chr5 | 75027764 | ||||||
chr5:75027838 | GGTGT | G | 24 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0014 others(21): Show |
103 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*837delACAC | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 834 | chr5 | 75027838 | ||||||
chr5:75027968 | T | TCCCTTCG others(305): Show |
1 | a0003c0003t0060 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707_*708insGGCCGG others(306): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 707 | chr5 | 75027968 | ||||||
chr5:75027968 | T | TCCCTTCG others(306): Show |
7 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(4): Show |
26 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*707_*708insGGCCGG others(307): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 707 | chr5 | 75027968 | ||||||
chr5:75027968 | T | TCCCTTCG others(307): Show |
2 | a0003c0003t0056 a0003c0003t0057 |
2 | HG02145.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*707_*708insGGCCGG others(308): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 707 | chr5 | 75027968 | ||||||
chr5:75027974 | C | T | 1 | a0001c0001t0045 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 702 | chr5 | 75027974 | ||||||
chr5:75028178 | G | A | 10 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(7): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 498 | chr5 | 75028178 | ||||||
chr5:75028248 | A | C | 10 | a0003c0003t0012 a0003c0003t0015 a0003c0003t0020 others(7): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*428T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 428 | chr5 | 75028248 | ||||||
chr5:75028307 | A | G | 48 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0013 others(45): Show |
167 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*369T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 369 | chr5 | 75028307 | ||||||
chr5:75028361 | G | A | 1 | a0001c0001t0051 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 315 | chr5 | 75028361 | ||||||
chr5:75028612 | G | A | 48 | a0002c0002t0002 a0002c0002t0008 a0002c0002t0013 others(45): Show |
167 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*64C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 64 | chr5 | 75028612 | ||||||
chr5:75028626 | C | T | 2 | a0001c0001t0028 a0001c0001t0044 |
3 | HG00280.hp2 HG00323.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*50G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 4/4 | 50 | chr5 | 75028626 | ||||||
chr5:75047921 | C | T | 2 | a0003c0003t0029 a0003c0003t0030 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-26G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/4 | 17884 | chr5 | 75047921 | ||||||
chr5:75047944 | G | A | 52 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(49): Show |
226 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(223): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/4 | chr5 | 75047944 | |||||||
chr5:75052505 | G | A | 1 | a0002c0002t0043 | 1 | NA19009.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-278C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/4 | chr5 | 75052505 | |||||||
chr5:75052534 | C | T | 1 | a0002c0002t0043 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-307G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/4 | 22497 | chr5 | 75052534 | ||||||
chr5:75052536 | G | A | 1 | a0001c0001t0072 | 1 | HG02273.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/4 | chr5 | 75052536 | |||||||
chr5:75052557 | C | G | 1 | a0001c0001t0042 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-330G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/4 | 22520 | chr5 | 75052557 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:75030136 | TG | T | 3 | a0002c0002t0027g0092 a0002c0002t0041g0086 a0002c0002t0061g0221 |
3 | HG02970.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-99delC | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030136 | |||||||
chr5:75030314 | T | G | 6 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(3): Show |
10 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-276A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030314 | |||||||
chr5:75030362 | G | C | 1 | a0002c0002t0024g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-324C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030362 | |||||||
chr5:75030448 | G | A | 2 | a0001c0001t0005g0080 a0001c0001t0005g0081 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-1-410C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030448 | |||||||
chr5:75030510 | G | A | 1 | a0002c0002t0002g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-472C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030510 | |||||||
chr5:75030705 | T | C | 13 | a0002c0002t0021g0054 a0002c0002t0021g0226 a0002c0002t0021g0250 others(10): Show |
16 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-667A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030705 | |||||||
chr5:75030719 | G | A | 1 | a0001c0001t0003g0238 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-1-681C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030719 | |||||||
chr5:75030803 | C | T | 1 | a0002c0002t0014g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-1-765G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030803 | |||||||
chr5:75030848 | T | C | 2 | a0002c0002t0018g0068 a0002c0002t0018g0108 |
2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-1-810A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030848 | |||||||
chr5:75030974 | C | G | 1 | a0002c0002t0025g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-1-936G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75030974 | |||||||
chr5:75031055 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1-1017G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031055 | |||||||
chr5:75031079 | C | CTTT | 22 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(19): Show |
26 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1-1044_-1-1042dup others(3): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031079 | |||||||
chr5:75031257 | G | A | 1 | a0002c0002t0026g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-1-1219C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031257 | |||||||
chr5:75031457 | G | A | 7 | a0003c0003t0012g0101 a0003c0003t0012g0102 a0003c0003t0012g0103 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-1419C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031457 | |||||||
chr5:75031532 | A | G | 1 | a0002c0002t0002g0112 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-1-1494T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031532 | |||||||
chr5:75031591 | A | G | 5 | a0002c0002t0002g0110 a0002c0002t0002g0116 a0002c0002t0002g0229 others(2): Show |
5 | HG00558.hp2 NA18969.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1553T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031591 | |||||||
chr5:75031611 | G | A | 125 | a0002c0002t0002g0002 a0002c0002t0002g0029 a0002c0002t0002g0031 others(122): Show |
167 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.-1-1573C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031611 | |||||||
chr5:75031735 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-1697A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031735 | |||||||
chr5:75031738 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-1700C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031738 | |||||||
chr5:75031799 | C | T | 1 | a0001c0001t0010g0166 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-1-1761G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031799 | |||||||
chr5:75031800 | G | A | 7 | a0003c0003t0012g0101 a0003c0003t0012g0102 a0003c0003t0012g0103 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-1762C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031800 | |||||||
chr5:75031845 | A | G | 1 | a0004c0004t0041g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-1-1807T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031845 | |||||||
chr5:75031981 | T | C | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-1-1943A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75031981 | |||||||
chr5:75032026 | T | C | 23 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(20): Show |
30 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1-1988A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032026 | |||||||
chr5:75032067 | C | T | 1 | a0002c0002t0014g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-1-2029G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032067 | |||||||
chr5:75032086 | C | T | 30 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(27): Show |
39 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-2048G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032086 | |||||||
chr5:75032163 | A | C | 1 | a0001c0001t0009g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-1-2125T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032163 | |||||||
chr5:75032187 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0004g0191 others(1): Show |
7 | HG00140.hp1 HG01069.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-2149G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032187 | |||||||
chr5:75032243 | C | T | 125 | a0002c0002t0002g0002 a0002c0002t0002g0029 a0002c0002t0002g0031 others(122): Show |
167 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.-1-2205G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032243 | |||||||
chr5:75032351 | T | C | 2 | a0002c0002t0027g0092 a0002c0002t0041g0086 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-2313A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032351 | |||||||
chr5:75032729 | T | G | 1 | a0001c0001t0049g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1-2691A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032729 | |||||||
chr5:75032818 | A | G | 31 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(28): Show |
40 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1-2780T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032818 | |||||||
chr5:75032846 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-1-2808A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032846 | |||||||
chr5:75032869 | AGGGGTGT others(3): Show |
A | 1 | a0002c0002t0019g0233 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-1-2841_-1-2832del others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032869 | |||||||
chr5:75032870 | G | GGGGT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0210 others(25): Show |
35 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1-2836_-1-2833dup others(4): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032870 | |||||||
chr5:75032871 | G | GGGTGGGT others(4): Show |
1 | a0001c0001t0004g0005 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-1-2834_-1-2833ins others(11): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032871 | |||||||
chr5:75032872 | G | GGTGGGGG others(3): Show |
1 | a0001c0001t0009g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(18): Show |
24 | HG01261.hp1 HG01346.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(6): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGTG others(3): Show |
1 | a0001c0001t0046g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGTG others(1): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0058 others(15): Show |
21 | HG00140.hp1 HG01069.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(8): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGTG others(3): Show |
8 | a0001c0001t0001g0202 a0001c0001t0003g0161 a0001c0001t0003g0174 others(5): Show |
8 | NA18942.hp1 NA18968.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGTG others(5): Show |
2 | a0001c0001t0001g0001 a0001c0001t0007g0167 |
2 | NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(12): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGGGTG others(13): Show |
2 | a0001c0001t0001g0012 a0001c0001t0004g0191 |
2 | HG01361.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-2835_-1-2834ins others(20): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGTGT | 3 | a0001c0001t0011g0041 a0001c0001t0045g0179 a0001c0001t0049g0180 |
4 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-2840_-1-2835dup others(6): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGTGTG others(3): Show |
1 | a0003c0003t0030g0026 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-1-2844_-1-2835dup others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGTGTG others(7): Show |
2 | a0001c0001t0004g0005 a0003c0003t0029g0094 |
2 | NA18941.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-1-2848_-1-2835dup others(14): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | G | GGTGTGTG others(13): Show |
1 | a0003c0003t0029g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1-2854_-1-2835dup others(20): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGT | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0185 a0001c0001t0001g0198 others(24): Show |
30 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-2836_-1-2835del others(2): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGT | G | 23 | a0001c0001t0001g0201 a0001c0001t0003g0099 a0001c0001t0003g0160 others(20): Show |
25 | HG00673.hp1 HG01123.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1-2838_-1-2835del others(4): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGT | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0048 others(16): Show |
25 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1-2840_-1-2835del others(6): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(1): Show |
G | 36 | a0002c0002t0002g0002 a0002c0002t0002g0031 a0002c0002t0002g0032 others(33): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-1-2842_-1-2835del others(8): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(3): Show |
G | 10 | a0002c0002t0002g0002 a0002c0002t0002g0047 a0002c0002t0002g0135 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-2844_-1-2835del others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(5): Show |
G | 12 | a0002c0002t0002g0119 a0002c0002t0014g0219 a0002c0002t0022g0136 others(9): Show |
15 | HG00642.hp2 HG01081.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-2846_-1-2835del others(12): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(7): Show |
G | 5 | a0001c0001t0003g0171 a0002c0002t0014g0107 a0002c0002t0018g0242 others(2): Show |
6 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-2848_-1-2835del others(14): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(9): Show |
G | 4 | a0001c0001t0048g0199 a0002c0002t0014g0218 a0002c0002t0019g0232 others(1): Show |
4 | HG02273.hp1 HG02615.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2850_-1-2835del others(16): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(13): Show |
G | 2 | a0002c0002t0022g0134 a0002c0002t0068g0097 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-1-2854_-1-2835del others(20): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(15): Show |
G | 7 | a0003c0003t0012g0101 a0003c0003t0012g0102 a0003c0003t0012g0103 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-2856_-1-2835del others(22): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(21): Show |
G | 13 | a0002c0002t0021g0054 a0002c0002t0021g0226 a0002c0002t0021g0250 others(10): Show |
16 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-2862_-1-2835del others(28): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032872 | GGTGTGTG others(23): Show |
G | 10 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(7): Show |
14 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-2864_-1-2835del others(30): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032872 | |||||||
chr5:75032874 | T | TG | 3 | a0001c0001t0003g0016 a0001c0001t0005g0079 a0001c0001t0011g0043 |
3 | HG01952.hp2 HG02040.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-2837dupC | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032874 | |||||||
chr5:75032874 | T | TGG | 19 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0051 others(16): Show |
30 | HG00735.hp2 HG01258.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1-2837_-1-2836ins others(2): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032874 | |||||||
chr5:75032876 | T | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0223 others(14): Show |
20 | HG00558.hp1 HG01175.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-2838A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032876 | |||||||
chr5:75032878 | T | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0185 a0001c0001t0001g0198 others(20): Show |
26 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1-2840A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032878 | |||||||
chr5:75032880 | T | G | 14 | a0001c0001t0001g0198 a0001c0001t0001g0201 a0001c0001t0003g0099 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-2842A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032880 | |||||||
chr5:75032882 | T | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0048 others(2): Show |
8 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-2844A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032882 | |||||||
chr5:75032884 | T | G | 1 | a0001c0001t0001g0040 | 2 | HG00642.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-1-2846A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032884 | |||||||
chr5:75032890 | T | G | 1 | a0001c0001t0003g0171 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-1-2852A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032890 | |||||||
chr5:75032892 | T | G | 1 | a0001c0001t0048g0199 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-1-2854A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032892 | |||||||
chr5:75032922 | T | A | 8 | a0002c0002t0018g0068 a0002c0002t0018g0108 a0002c0002t0025g0143 others(5): Show |
8 | HG01256.hp1 HG02486.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-2884A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032922 | |||||||
chr5:75032924 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-1-2886T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032924 | |||||||
chr5:75032925 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-1-2887A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75032925 | |||||||
chr5:75033126 | C | G | 1 | a0001c0001t0003g0158 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-1-3088G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033126 | |||||||
chr5:75033151 | C | T | 4 | a0002c0002t0035g0182 a0002c0002t0035g0183 a0002c0002t0036g0132 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-3113G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033151 | |||||||
chr5:75033291 | A | T | 50 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(47): Show |
63 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-1-3253T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033291 | |||||||
chr5:75033339 | T | C | 2 | a0002c0002t0018g0068 a0002c0002t0018g0108 |
2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-1-3301A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033339 | |||||||
chr5:75033435 | G | C | 8 | a0002c0002t0018g0068 a0002c0002t0018g0108 a0002c0002t0025g0143 others(5): Show |
8 | HG01256.hp1 HG02486.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-3397C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033435 | |||||||
chr5:75033490 | C | T | 1 | a0002c0002t0013g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-1-3452G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033490 | |||||||
chr5:75033510 | C | T | 2 | a0003c0003t0020g0021 a0003c0003t0031g0061 |
3 | HG02257.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-3472G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033510 | |||||||
chr5:75033616 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-1-3578A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033616 | |||||||
chr5:75033647 | A | C | 1 | a0001c0001t0003g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-1-3609T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033647 | |||||||
chr5:75033653 | C | CTTTA | 14 | a0003c0003t0012g0101 a0003c0003t0012g0102 a0003c0003t0012g0103 others(11): Show |
15 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-3619_-1-3616dup others(4): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033653 | |||||||
chr5:75033653 | C | CTTTATTT others(1): Show |
3 | a0002c0002t0035g0182 a0002c0002t0036g0132 a0002c0002t0036g0248 |
3 | HG00733.hp1 HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-1-3623_-1-3616dup others(8): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033653 | |||||||
chr5:75033653 | C | CTTTATTT others(5): Show |
1 | a0002c0002t0035g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1-3627_-1-3616dup others(12): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033653 | |||||||
chr5:75033669 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-1-3631T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033669 | |||||||
chr5:75033672 | T | A | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-3634A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033672 | |||||||
chr5:75033673 | A | T | 22 | a0001c0001t0001g0223 a0001c0001t0003g0099 a0001c0001t0003g0159 others(19): Show |
25 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1-3635T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033673 | |||||||
chr5:75033673 | ATTTTTTT others(1): Show |
A | 18 | a0002c0002t0021g0054 a0002c0002t0021g0226 a0002c0002t0021g0251 others(15): Show |
24 | HG00140.hp2 HG00642.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1-3643_-1-3636del others(8): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033673 | |||||||
chr5:75033674 | T | TTTA | 5 | a0002c0002t0022g0046 a0002c0002t0022g0134 a0002c0002t0022g0142 others(2): Show |
6 | HG00741.hp2 HG01106.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-3637_-1-3636ins others(3): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033674 | |||||||
chr5:75033675 | T | A | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-3637A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033675 | |||||||
chr5:75033677 | T | A | 49 | a0001c0001t0001g0044 a0001c0001t0001g0200 a0001c0001t0001g0201 others(46): Show |
56 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1-3639A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033677 | |||||||
chr5:75033678 | T | A | 1 | a0002c0002t0022g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-3640A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033678 | |||||||
chr5:75033681 | T | A | 32 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(29): Show |
38 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.-1-3643A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033681 | |||||||
chr5:75033750 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-1-3712A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033750 | |||||||
chr5:75033770 | C | T | 1 | a0002c0002t0002g0032 | 2 | NA18991.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-1-3732G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033770 | |||||||
chr5:75033797 | G | A | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-3759C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75033797 | |||||||
chr5:75034083 | G | A | 2 | a0002c0002t0067g0261 a0004c0004t0041g0096 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-1-4045C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034083 | |||||||
chr5:75034167 | T | C | 1 | a0002c0002t0018g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1-4129A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034167 | |||||||
chr5:75034687 | T | C | 1 | a0001c0001t0009g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-1-4649A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034687 | |||||||
chr5:75034760 | A | G | 18 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(15): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-4722T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034760 | |||||||
chr5:75034898 | G | GCACCCCA others(28): Show |
4 | a0002c0002t0002g0119 a0002c0002t0014g0107 a0002c0002t0014g0218 others(1): Show |
4 | HG00733.hp2 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-4895_-1-4861dup others(35): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034898 | |||||||
chr5:75034898 | G | GCACCCCA others(98): Show |
27 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(24): Show |
33 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-4965_-1-4861dup others(105): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034898 | |||||||
chr5:75034898 | G | GCACCCCA others(62): Show |
6 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(3): Show |
10 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-4861_-1-4860ins others(69): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034898 | |||||||
chr5:75034898 | GCACCCCA others(28): Show |
G | 6 | a0001c0001t0003g0009 a0001c0001t0003g0165 a0001c0001t0003g0173 others(3): Show |
10 | HG01515.hp1 HG01981.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-4895_-1-4861del others(35): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034898 | |||||||
chr5:75034926 | T | C | 8 | a0002c0002t0018g0068 a0002c0002t0018g0108 a0002c0002t0025g0143 others(5): Show |
8 | HG01256.hp1 HG02486.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-4888A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034926 | |||||||
chr5:75034929 | A | AGGGACAC others(27): Show |
7 | a0002c0002t0018g0015 a0002c0002t0018g0242 a0002c0002t0022g0046 others(4): Show |
10 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-4925_-1-4892dup others(34): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034929 | |||||||
chr5:75034958 | G | A | 1 | a0002c0002t0052g0190 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1-4920C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034958 | |||||||
chr5:75034963 | CA | C | 11 | a0002c0002t0021g0054 a0002c0002t0021g0226 a0002c0002t0021g0251 others(8): Show |
14 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-4926delT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034963 | |||||||
chr5:75034963 | CAGGGACA others(29): Show |
C | 6 | a0002c0002t0021g0250 a0002c0002t0035g0182 a0002c0002t0035g0183 others(3): Show |
6 | HG00733.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-4961_-1-4926del others(36): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75034963 | |||||||
chr5:75035097 | CGCATTCA others(28): Show |
C | 13 | a0002c0002t0018g0068 a0002c0002t0018g0108 a0002c0002t0021g0054 others(10): Show |
16 | HG00140.hp2 HG01256.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1-5094_-1-5060del others(35): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035097 | |||||||
chr5:75035132 | T | C | 2 | a0002c0002t0021g0250 a0004c0004t0041g0096 |
2 | HG02486.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-1-5094A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035132 | |||||||
chr5:75035148 | T | C | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-5110A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035148 | |||||||
chr5:75035157 | T | C | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-5119A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035157 | |||||||
chr5:75035184 | C | T | 14 | a0001c0001t0003g0141 a0001c0001t0007g0052 a0001c0001t0007g0144 others(11): Show |
15 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-5146G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035184 | |||||||
chr5:75035220 | G | A | 1 | a0002c0002t0002g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-1-5182C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035220 | |||||||
chr5:75035287 | A | G | 1 | a0002c0002t0025g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1-5249T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035287 | |||||||
chr5:75035349 | G | C | 2 | a0002c0002t0067g0261 a0004c0004t0041g0096 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-1-5311C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035349 | |||||||
chr5:75035461 | G | A | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-5423C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035461 | |||||||
chr5:75035606 | T | C | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-5568A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035606 | |||||||
chr5:75035693 | C | T | 1 | a0002c0002t0034g0162 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-1-5655G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035693 | |||||||
chr5:75035703 | G | A | 54 | a0002c0002t0002g0002 a0002c0002t0002g0029 a0002c0002t0002g0031 others(51): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-1-5665C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035703 | |||||||
chr5:75035757 | C | T | 1 | a0002c0002t0021g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-1-5719G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035757 | |||||||
chr5:75035791 | C | A | 3 | a0002c0002t0013g0022 a0002c0002t0013g0069 a0002c0002t0034g0236 |
4 | HG01516.hp2 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-5753G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035791 | |||||||
chr5:75035868 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-1-5830A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035868 | |||||||
chr5:75035875 | G | A | 2 | a0002c0002t0002g0113 a0002c0002t0008g0114 |
2 | HG00438.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-1-5837C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035875 | |||||||
chr5:75035946 | G | C | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-5908C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035946 | |||||||
chr5:75035991 | C | A | 2 | a0002c0002t0018g0068 a0002c0002t0018g0108 |
2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-1-5953G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75035991 | |||||||
chr5:75036110 | G | A | 4 | a0002c0002t0035g0182 a0002c0002t0035g0183 a0002c0002t0036g0132 others(1): Show |
4 | HG00733.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6072C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036110 | |||||||
chr5:75036155 | G | GA | 23 | a0001c0001t0007g0146 a0001c0001t0009g0147 a0003c0003t0012g0059 others(20): Show |
28 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-6118dupT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036155 | |||||||
chr5:75036166 | A | C | 54 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(51): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-1-6128T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036166 | |||||||
chr5:75036184 | C | A | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6146G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036184 | |||||||
chr5:75036241 | A | C | 69 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(66): Show |
96 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-1-6203T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036241 | |||||||
chr5:75036347 | T | TA | 2 | a0002c0002t0018g0015 a0002c0002t0018g0242 |
4 | HG00735.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6310dupT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036347 | |||||||
chr5:75036400 | G | A | 1 | a0002c0002t0064g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1-6362C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036400 | |||||||
chr5:75036475 | T | C | 1 | a0001c0001t0010g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-6437A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036475 | |||||||
chr5:75036579 | G | A | 22 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(19): Show |
26 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1-6541C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036579 | |||||||
chr5:75036633 | CCT | C | 22 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(19): Show |
26 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1-6597_-1-6596del others(2): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036633 | |||||||
chr5:75036744 | G | C | 60 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(57): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1-6706C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036744 | |||||||
chr5:75036761 | GC | G | 3 | a0002c0002t0002g0047 a0002c0002t0008g0220 a0002c0002t0066g0253 |
4 | HG00738.hp1 HG01070.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6724delG | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036761 | |||||||
chr5:75036774 | A | G | 8 | a0002c0002t0018g0015 a0002c0002t0018g0242 a0002c0002t0022g0046 others(5): Show |
11 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-6736T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036774 | |||||||
chr5:75036783 | A | G | 1 | a0001c0001t0001g0048 | 2 | NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-1-6745T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036783 | |||||||
chr5:75036833 | C | T | 1 | a0001c0001t0005g0070 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-1-6795G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036833 | |||||||
chr5:75036857 | G | A | 2 | a0002c0002t0067g0261 a0004c0004t0041g0096 |
2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-1-6819C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036857 | |||||||
chr5:75036981 | A | G | 5 | a0002c0002t0022g0136 a0002c0002t0026g0024 a0002c0002t0026g0087 others(2): Show |
6 | HG01081.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-6943T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75036981 | |||||||
chr5:75037124 | G | T | 5 | a0002c0002t0018g0068 a0002c0002t0018g0108 a0002c0002t0027g0092 others(2): Show |
5 | HG01256.hp1 HG02602.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-7086C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037124 | |||||||
chr5:75037152 | T | C | 27 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(24): Show |
35 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-1-7114A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037152 | |||||||
chr5:75037218 | T | C | 4 | a0002c0002t0002g0029 a0002c0002t0002g0105 a0002c0002t0024g0028 others(1): Show |
6 | HG01167.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-7180A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037218 | |||||||
chr5:75037299 | T | C | 2 | a0003c0003t0032g0025 a0003c0003t0059g0093 |
3 | HG01243.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-1-7261A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037299 | |||||||
chr5:75037328 | T | C | 4 | a0002c0002t0002g0029 a0002c0002t0002g0105 a0002c0002t0024g0028 others(1): Show |
6 | HG01167.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-7290A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037328 | |||||||
chr5:75037328 | T | G | 33 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
44 | HG00609.hp1 HG00673.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.-1-7290A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037328 | |||||||
chr5:75037552 | C | A | 2 | a0001c0001t0005g0080 a0001c0001t0005g0081 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-1-7514G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037552 | |||||||
chr5:75037948 | TA | T | 85 | a0001c0001t0001g0202 a0001c0001t0003g0165 a0001c0001t0004g0228 others(82): Show |
110 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-1-7911delT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037948 | |||||||
chr5:75037948 | TAA | T | 35 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(32): Show |
47 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-1-7912_-1-7911del others(2): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75037948 | |||||||
chr5:75038031 | T | C | 3 | a0002c0002t0002g0117 a0002c0002t0002g0119 a0002c0002t0008g0118 |
3 | NA18999.hp2 NA19054.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-1-7993A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038031 | |||||||
chr5:75038306 | G | A | 2 | a0002c0002t0035g0182 a0002c0002t0035g0183 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-1-8268C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038306 | |||||||
chr5:75038412 | C | T | 5 | a0002c0002t0022g0136 a0002c0002t0026g0024 a0002c0002t0026g0087 others(2): Show |
6 | HG01081.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-8374G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038412 | |||||||
chr5:75038424 | G | C | 1 | a0001c0001t0003g0159 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-1-8386C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038424 | |||||||
chr5:75038496 | C | T | 22 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(19): Show |
26 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1-8458G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038496 | |||||||
chr5:75038577 | G | T | 1 | a0001c0001t0003g0164 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-1-8539C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038577 | |||||||
chr5:75038579 | C | T | 1 | a0002c0002t0036g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-1-8541G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038579 | |||||||
chr5:75038647 | C | T | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-8609G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038647 | |||||||
chr5:75038648 | G | A | 2 | a0002c0002t0002g0121 a0002c0002t0008g0120 |
2 | NA19080.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-1-8610C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038648 | |||||||
chr5:75038735 | A | C | 1 | a0001c0001t0010g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1-8697T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038735 | |||||||
chr5:75038827 | T | C | 1 | a0001c0001t0003g0160 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-1-8789A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75038827 | |||||||
chr5:75039082 | G | T | 15 | a0002c0002t0002g0031 a0002c0002t0021g0054 a0002c0002t0021g0226 others(12): Show |
19 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2+8815C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039082 | |||||||
chr5:75039147 | C | A | 55 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(52): Show |
80 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-2+8750G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039147 | |||||||
chr5:75039148 | A | T | 55 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(52): Show |
80 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-2+8749T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039148 | |||||||
chr5:75039149 | A | G | 3 | a0002c0002t0013g0022 a0002c0002t0013g0069 a0002c0002t0034g0236 |
4 | HG01516.hp2 HG02738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+8748T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039149 | |||||||
chr5:75039246 | C | T | 66 | a0002c0002t0002g0002 a0002c0002t0002g0029 a0002c0002t0002g0031 others(63): Show |
92 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-2+8651G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039246 | |||||||
chr5:75039276 | C | A | 56 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(53): Show |
71 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-2+8621G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039276 | |||||||
chr5:75039294 | A | G | 9 | a0002c0002t0018g0015 a0002c0002t0018g0242 a0002c0002t0022g0046 others(6): Show |
12 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+8603T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039294 | |||||||
chr5:75039370 | A | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0048 others(18): Show |
39 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2+8527T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039370 | |||||||
chr5:75039454 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-2+8443C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039454 | |||||||
chr5:75039894 | G | A | 2 | a0001c0001t0003g0099 a0001c0001t0003g0160 |
2 | HG00673.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-2+8003C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75039894 | |||||||
chr5:75040179 | A | G | 8 | a0001c0001t0007g0052 a0001c0001t0007g0144 a0001c0001t0007g0145 others(5): Show |
9 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+7718T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040179 | |||||||
chr5:75040183 | CT | C | 36 | a0001c0001t0001g0225 a0001c0001t0003g0154 a0001c0001t0003g0173 others(33): Show |
41 | HG00642.hp2 HG01256.hp1 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.-2+7713delA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040183 | |||||||
chr5:75040338 | G | T | 1 | a0002c0002t0018g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-2+7559C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040338 | |||||||
chr5:75040433 | T | C | 1 | a0001c0001t0011g0041 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-2+7464A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040433 | |||||||
chr5:75040446 | C | T | 3 | a0002c0002t0027g0092 a0002c0002t0041g0086 a0002c0002t0061g0221 |
3 | HG02970.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+7451G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040446 | |||||||
chr5:75040509 | A | AAAATTCT others(15): Show |
1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+7366_-2+7387dup others(22): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040509 | |||||||
chr5:75040534 | A | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0067 others(4): Show |
11 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+7363T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040534 | |||||||
chr5:75040641 | T | C | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2+7256A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040641 | |||||||
chr5:75040699 | G | C | 1 | a0002c0002t0002g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-2+7198C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040699 | |||||||
chr5:75040726 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-2+7171T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040726 | |||||||
chr5:75040765 | C | T | 13 | a0002c0002t0021g0054 a0002c0002t0021g0226 a0002c0002t0021g0250 others(10): Show |
16 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+7132G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040765 | |||||||
chr5:75040835 | T | C | 1 | a0002c0002t0026g0087 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2+7062A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040835 | |||||||
chr5:75040944 | G | GTTGT | 126 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0029 others(123): Show |
168 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.-2+6952_-2+6953ins others(4): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040944 | |||||||
chr5:75040978 | G | A | 1 | a0001c0001t0017g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-2+6919C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75040978 | |||||||
chr5:75041056 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-2+6841G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041056 | |||||||
chr5:75041058 | C | T | 61 | a0002c0002t0002g0002 a0002c0002t0002g0029 a0002c0002t0002g0031 others(58): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-2+6839G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041058 | |||||||
chr5:75041071 | T | G | 5 | a0002c0002t0022g0136 a0002c0002t0026g0024 a0002c0002t0026g0087 others(2): Show |
6 | HG01081.hp2 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+6826A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041071 | |||||||
chr5:75041118 | T | C | 32 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(29): Show |
42 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-2+6779A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041118 | |||||||
chr5:75041253 | C | A | 24 | a0003c0003t0012g0059 a0003c0003t0012g0101 a0003c0003t0012g0102 others(21): Show |
29 | HG00642.hp2 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2+6644G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041253 | |||||||
chr5:75041254 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0017g0106 a0001c0001t0017g0186 others(1): Show |
7 | HG01433.hp2 HG01928.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+6643G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041254 | |||||||
chr5:75041257 | ACCCAGGG others(3): Show |
A | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+6630_-2+6639del others(10): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041257 | |||||||
chr5:75041275 | T | A | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+6622A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041275 | |||||||
chr5:75041276 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+6621G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041276 | |||||||
chr5:75041277 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6620G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041277 | |||||||
chr5:75041277 | C | G | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+6620G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041277 | |||||||
chr5:75041279 | C | G | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-2+6618G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041279 | |||||||
chr5:75041280 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6617A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041280 | |||||||
chr5:75041289 | G | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6608C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041289 | |||||||
chr5:75041294 | C | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6603G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041294 | |||||||
chr5:75041299 | C | G | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6598G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041299 | |||||||
chr5:75041303 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6594C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041303 | |||||||
chr5:75041307 | C | G | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6590G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041307 | |||||||
chr5:75041314 | A | T | 92 | a0001c0001t0017g0187 a0001c0001t0055g0124 a0002c0002t0002g0002 others(89): Show |
126 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.-2+6583T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041314 | |||||||
chr5:75041336 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6561A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041336 | |||||||
chr5:75041339 | A | G | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6558T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041339 | |||||||
chr5:75041347 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6550T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041347 | |||||||
chr5:75041355 | T | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6542A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041355 | |||||||
chr5:75041365 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6532A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041365 | |||||||
chr5:75041369 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6528C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041369 | |||||||
chr5:75041371 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6526T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041371 | |||||||
chr5:75041381 | A | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6516T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041381 | |||||||
chr5:75041382 | T | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6515A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041382 | |||||||
chr5:75041385 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6512T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041385 | |||||||
chr5:75041387 | A | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6510T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041387 | |||||||
chr5:75041389 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6508G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041389 | |||||||
chr5:75041390 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6507A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041390 | |||||||
chr5:75041392 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6505A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041392 | |||||||
chr5:75041397 | C | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6500G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041397 | |||||||
chr5:75041416 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6481G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041416 | |||||||
chr5:75041419 | C | G | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6478G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041419 | |||||||
chr5:75041424 | T | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6473A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041424 | |||||||
chr5:75041425 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6472G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041425 | |||||||
chr5:75041427 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6470A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041427 | |||||||
chr5:75041429 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6468G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041429 | |||||||
chr5:75041436 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6461T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041436 | |||||||
chr5:75041438 | A | G | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6459T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041438 | |||||||
chr5:75041440 | G | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6457C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041440 | |||||||
chr5:75041442 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6455G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041442 | |||||||
chr5:75041445 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6452G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041445 | |||||||
chr5:75041448 | T | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6449A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041448 | |||||||
chr5:75041449 | A | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6448T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041449 | |||||||
chr5:75041450 | C | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6447G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041450 | |||||||
chr5:75041461 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6436A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041461 | |||||||
chr5:75041466 | A | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6431T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041466 | |||||||
chr5:75041477 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6420T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041477 | |||||||
chr5:75041478 | A | T | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6419T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041478 | |||||||
chr5:75041500 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6397T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041500 | |||||||
chr5:75041523 | A | C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6374T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041523 | |||||||
chr5:75041550 | T | A | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6347A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041550 | |||||||
chr5:75041559 | CCTCTCAC others(19): Show |
C | 1 | a0001c0001t0017g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+6312_-2+6337del others(26): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041559 | |||||||
chr5:75041727 | A | G | 26 | a0001c0001t0001g0227 a0002c0002t0002g0029 a0002c0002t0013g0008 others(23): Show |
35 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2+6170T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75041727 | |||||||
chr5:75042021 | T | C | 2 | a0002c0002t0014g0125 a0002c0002t0014g0126 |
2 | NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-2+5876A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042021 | |||||||
chr5:75042114 | C | T | 1 | a0002c0002t0013g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2+5783G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042114 | |||||||
chr5:75042358 | A | G | 1 | a0002c0002t0068g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+5539T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042358 | |||||||
chr5:75042630 | T | C | 2 | a0003c0003t0032g0025 a0003c0003t0059g0093 |
3 | HG01243.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-2+5267A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042630 | |||||||
chr5:75042727 | G | A | 7 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(4): Show |
12 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+5170C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042727 | |||||||
chr5:75042728 | T | C | 1 | a0001c0001t0011g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-2+5169A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042728 | |||||||
chr5:75042747 | A | C | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+5150T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042747 | |||||||
chr5:75042765 | G | A | 28 | a0001c0001t0010g0066 a0002c0002t0021g0054 a0002c0002t0021g0226 others(25): Show |
35 | HG00140.hp2 HG00642.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+5132C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042765 | |||||||
chr5:75042876 | C | A | 1 | a0002c0002t0021g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2+5021G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042876 | |||||||
chr5:75042969 | G | A | 29 | a0001c0001t0010g0066 a0002c0002t0021g0054 a0002c0002t0021g0226 others(26): Show |
36 | HG00140.hp2 HG00642.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2+4928C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042969 | |||||||
chr5:75042976 | T | C | 1 | a0001c0001t0003g0174 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-2+4921A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75042976 | |||||||
chr5:75043112 | T | A | 1 | a0002c0002t0002g0034 | 2 | NA18983.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-2+4785A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043112 | |||||||
chr5:75043112 | T | C | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-2+4785A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043112 | |||||||
chr5:75043153 | G | A | 8 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(5): Show |
13 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+4744C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043153 | |||||||
chr5:75043184 | T | C | 1 | a0002c0002t0014g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-2+4713A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043184 | |||||||
chr5:75043195 | T | C | 38 | a0001c0001t0055g0124 a0002c0002t0002g0002 a0002c0002t0002g0031 others(35): Show |
57 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2+4702A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043195 | |||||||
chr5:75043222 | T | A | 11 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(8): Show |
13 | HG00733.hp1 HG01167.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+4675A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043222 | |||||||
chr5:75043235 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-2+4662G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043235 | |||||||
chr5:75043325 | G | T | 1 | a0001c0001t0003g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-2+4572C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043325 | |||||||
chr5:75043366 | A | C | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+4531T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043366 | |||||||
chr5:75043651 | G | A | 1 | a0002c0002t0013g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2+4246C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043651 | |||||||
chr5:75043747 | G | A | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+4150C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043747 | |||||||
chr5:75043795 | A | G | 8 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(5): Show |
13 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+4102T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75043795 | |||||||
chr5:75044005 | T | C | 2 | a0003c0003t0032g0025 a0003c0003t0059g0093 |
3 | HG01243.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-2+3892A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044005 | |||||||
chr5:75044361 | T | C | 3 | a0003c0003t0012g0137 a0003c0003t0015g0138 a0003c0003t0015g0139 |
3 | HG02055.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-2+3536A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044361 | |||||||
chr5:75044470 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-2+3427T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044470 | |||||||
chr5:75044502 | A | C | 117 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0016 others(114): Show |
147 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(144): Show |
intron_variant | MODIFIER | c.-2+3395T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044502 | |||||||
chr5:75044502 | A | T | 7 | a0001c0001t0003g0037 a0001c0001t0003g0099 a0001c0001t0003g0158 others(4): Show |
8 | HG00609.hp1 HG00673.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+3395T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044502 | |||||||
chr5:75044719 | C | T | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-2+3178G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044719 | |||||||
chr5:75044720 | G | A | 1 | a0001c0001t0004g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-2+3177C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044720 | |||||||
chr5:75044721 | G | A | 1 | a0001c0001t0042g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-2+3176C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044721 | |||||||
chr5:75044734 | T | C | 1 | a0001c0001t0005g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-2+3163A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044734 | |||||||
chr5:75044888 | G | A | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+3009C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75044888 | |||||||
chr5:75045242 | G | T | 58 | a0001c0001t0009g0176 a0001c0001t0010g0066 a0002c0002t0002g0029 others(55): Show |
74 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.-2+2655C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045242 | |||||||
chr5:75045367 | A | G | 1 | a0001c0001t0006g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2+2530T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045367 | |||||||
chr5:75045400 | C | T | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+2497G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045400 | |||||||
chr5:75045440 | G | T | 1 | a0003c0003t0060g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2+2457C>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045440 | |||||||
chr5:75045492 | T | C | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+2405A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045492 | |||||||
chr5:75045631 | G | A | 1 | a0001c0001t0005g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-2+2266C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045631 | |||||||
chr5:75045691 | G | A | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+2206C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045691 | |||||||
chr5:75045780 | T | C | 2 | a0002c0002t0061g0221 a0003c0003t0012g0222 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-2+2117A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045780 | |||||||
chr5:75045817 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-2+2080C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045817 | |||||||
chr5:75045852 | C | G | 1 | a0003c0003t0029g0094 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-2+2045G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045852 | |||||||
chr5:75045890 | A | C | 1 | a0002c0002t0040g0027 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-2+2007T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045890 | |||||||
chr5:75045931 | TG | T | 6 | a0003c0003t0012g0059 a0003c0003t0012g0258 a0003c0003t0015g0020 others(3): Show |
9 | HG00642.hp2 HG02896.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+1965delC | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045931 | |||||||
chr5:75045932 | G | GT | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+1964dupA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045932 | |||||||
chr5:75045976 | G | GGATGTTC others(12): Show |
1 | a0001c0001t0016g0074 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-2+1902_-2+1920dup others(19): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75045976 | |||||||
chr5:75046032 | T | C | 1 | a0002c0002t0037g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-2+1865A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046032 | |||||||
chr5:75046211 | C | T | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+1686G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046211 | |||||||
chr5:75046355 | A | C | 2 | a0001c0001t0003g0141 a0001c0001t0009g0131 |
2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-2+1542T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046355 | |||||||
chr5:75046426 | G | A | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+1471C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046426 | |||||||
chr5:75046468 | C | T | 2 | a0002c0002t0035g0182 a0002c0002t0035g0183 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-2+1429G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046468 | |||||||
chr5:75046488 | G | A | 65 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0016 others(62): Show |
80 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-2+1409C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046488 | |||||||
chr5:75046562 | C | T | 31 | a0001c0001t0010g0066 a0002c0002t0021g0054 a0002c0002t0021g0226 others(28): Show |
39 | HG00140.hp2 HG00642.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2+1335G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046562 | |||||||
chr5:75046712 | T | G | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+1185A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046712 | |||||||
chr5:75046807 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0017g0106 a0001c0001t0017g0186 others(1): Show |
7 | HG01433.hp2 HG01928.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+1090G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046807 | |||||||
chr5:75046815 | T | C | 1 | a0001c0001t0004g0217 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-2+1082A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046815 | |||||||
chr5:75046825 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2+1072T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046825 | |||||||
chr5:75046872 | C | T | 2 | a0002c0002t0035g0182 a0002c0002t0035g0183 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-2+1025G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046872 | |||||||
chr5:75046877 | C | T | 18 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(15): Show |
25 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2+1020G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046877 | |||||||
chr5:75046951 | T | C | 33 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
43 | HG00609.hp1 HG00673.hp1 HG01515.hp1 others(40): Show |
intron_variant | MODIFIER | c.-2+946A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75046951 | |||||||
chr5:75047071 | T | G | 6 | a0002c0002t0018g0015 a0002c0002t0018g0242 a0002c0002t0022g0136 others(3): Show |
8 | HG00735.hp1 HG01081.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+826A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047071 | |||||||
chr5:75047100 | A | G | 1 | a0001c0001t0005g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-2+797T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047100 | |||||||
chr5:75047164 | T | G | 74 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0016 others(71): Show |
91 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.-2+733A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047164 | |||||||
chr5:75047169 | T | C | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+728A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047169 | |||||||
chr5:75047532 | T | A | 10 | a0002c0002t0018g0015 a0002c0002t0018g0242 a0002c0002t0022g0134 others(7): Show |
12 | HG00735.hp1 HG01081.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+365A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047532 | |||||||
chr5:75047677 | T | C | 1 | a0003c0003t0012g0103 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2+220A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047677 | |||||||
chr5:75047719 | A | T | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-2+178T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047719 | |||||||
chr5:75047772 | T | C | 2 | a0002c0002t0027g0092 a0002c0002t0036g0132 |
2 | HG00733.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-2+125A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047772 | |||||||
chr5:75047784 | CT | C | 17 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(14): Show |
24 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2+112delA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047784 | |||||||
chr5:75047790 | G | A | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+107C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 3/3 | chr5 | 75047790 | |||||||
chr5:75048147 | C | T | 1 | a0002c0002t0025g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-142-110G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048147 | |||||||
chr5:75048390 | G | A | 5 | a0001c0001t0001g0223 a0001c0001t0004g0224 a0002c0002t0002g0129 others(2): Show |
5 | HG02132.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-142-353C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048390 | |||||||
chr5:75048397 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-142-360C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048397 | |||||||
chr5:75048421 | G | C | 1 | a0002c0002t0036g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-142-384C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048421 | |||||||
chr5:75048488 | A | G | 32 | a0001c0001t0010g0066 a0002c0002t0021g0054 a0002c0002t0021g0226 others(29): Show |
40 | HG00140.hp2 HG00642.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-142-451T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048488 | |||||||
chr5:75048599 | A | G | 1 | a0001c0001t0003g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-142-562T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048599 | |||||||
chr5:75048640 | T | C | 53 | a0001c0001t0009g0176 a0001c0001t0010g0066 a0002c0002t0002g0029 others(50): Show |
69 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.-142-603A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048640 | |||||||
chr5:75048640 | T | G | 1 | a0001c0001t0001g0048 | 2 | NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-142-603A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048640 | |||||||
chr5:75048667 | A | G | 44 | a0001c0001t0010g0066 a0002c0002t0013g0008 a0002c0002t0013g0022 others(41): Show |
58 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.-142-630T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048667 | |||||||
chr5:75048728 | T | C | 1 | a0002c0002t0002g0035 | 2 | HG02148.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-142-691A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048728 | |||||||
chr5:75048732 | C | T | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-695G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048732 | |||||||
chr5:75048785 | G | A | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-748C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048785 | |||||||
chr5:75048935 | A | G | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-898T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048935 | |||||||
chr5:75048975 | T | C | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-142-938A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75048975 | |||||||
chr5:75049141 | T | TTA | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.-142-1105_-142-110 others(6): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049141 | |||||||
chr5:75049154 | C | G | 1 | a0002c0002t0040g0027 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-142-1117G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049154 | |||||||
chr5:75049160 | A | G | 1 | a0002c0002t0022g0134 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-142-1123T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049160 | |||||||
chr5:75049212 | T | C | 4 | a0002c0002t0026g0024 a0002c0002t0027g0090 a0002c0002t0027g0091 others(1): Show |
5 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-142-1175A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049212 | |||||||
chr5:75049344 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0004g0178 |
3 | HG00642.hp1 HG01496.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-142-1307T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049344 | |||||||
chr5:75049451 | C | T | 4 | a0003c0003t0012g0101 a0003c0003t0012g0102 a0003c0003t0012g0103 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-1414G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049451 | |||||||
chr5:75049544 | C | A | 58 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0016 others(55): Show |
71 | HG00609.hp1 HG00673.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-142-1507G>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049544 | |||||||
chr5:75049546 | C | T | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-142-1509G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049546 | |||||||
chr5:75049568 | T | C | 1 | a0001c0001t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-142-1531A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049568 | |||||||
chr5:75049595 | G | C | 2 | a0001c0001t0003g0050 a0001c0001t0003g0238 |
3 | NA18948.hp1 NA18991.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-142-1558C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049595 | |||||||
chr5:75049636 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-142-1599C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049636 | |||||||
chr5:75049749 | G | GACACTTG others(24): Show |
1 | a0001c0001t0005g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-142-1743_-142-171 others(35): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049749 | |||||||
chr5:75049770 | T | C | 5 | a0002c0002t0013g0008 a0002c0002t0013g0022 a0002c0002t0013g0069 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-1733A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049770 | |||||||
chr5:75049821 | T | A | 9 | a0001c0001t0009g0176 a0002c0002t0002g0029 a0002c0002t0002g0105 others(6): Show |
11 | HG01167.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-142-1784A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049821 | |||||||
chr5:75049950 | T | C | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1913A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049950 | |||||||
chr5:75049951 | T | A | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1914A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049951 | |||||||
chr5:75049952 | A | C | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1915T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049952 | |||||||
chr5:75049953 | T | C | 51 | a0001c0001t0001g0227 a0001c0001t0004g0228 a0001c0001t0055g0124 others(48): Show |
76 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-142-1916A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049953 | |||||||
chr5:75049953 | T | G | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1916A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049953 | |||||||
chr5:75049954 | G | A | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1917C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049954 | |||||||
chr5:75049955 | T | C | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1918A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049955 | |||||||
chr5:75049956 | G | A | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1919C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049956 | |||||||
chr5:75049958 | T | G | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1921A>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049958 | |||||||
chr5:75049959 | T | A | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1922A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049959 | |||||||
chr5:75049960 | G | C | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1923C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049960 | |||||||
chr5:75049961 | C | G | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1924G>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049961 | |||||||
chr5:75049964 | A | G | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1927T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049964 | |||||||
chr5:75049965 | A | T | 1 | a0001c0001t0009g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-142-1928T>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049965 | |||||||
chr5:75049967 | G | A | 2 | a0002c0002t0019g0232 a0002c0002t0019g0233 |
2 | HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-142-1930C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75049967 | |||||||
chr5:75050055 | CTG | C | 3 | a0003c0003t0029g0094 a0003c0003t0029g0095 a0003c0003t0030g0026 |
4 | HG02056.hp1 NA18941.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-142-2020_-142-201 others(6): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050055 | |||||||
chr5:75050125 | C | T | 79 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0016 others(76): Show |
96 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.-143+2044G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050125 | |||||||
chr5:75050259 | A | C | 1 | a0002c0002t0036g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-143+1910T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050259 | |||||||
chr5:75050292 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-143+1877A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050292 | |||||||
chr5:75050305 | A | G | 1 | a0002c0002t0068g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-143+1864T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050305 | |||||||
chr5:75050415 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-143+1754A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050415 | |||||||
chr5:75050566 | G | C | 2 | a0002c0002t0002g0129 a0002c0002t0002g0235 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-143+1603C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050566 | |||||||
chr5:75050712 | ACTCTCAC others(21): Show |
A | 6 | a0001c0001t0001g0067 a0002c0002t0013g0008 a0002c0002t0013g0022 others(3): Show |
10 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-143+1429_-143+145 others(32): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050712 | |||||||
chr5:75050745 | C | T | 1 | a0001c0001t0005g0072 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-143+1424G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050745 | |||||||
chr5:75050877 | C | T | 1 | a0002c0002t0025g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-143+1292G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75050877 | |||||||
chr5:75051039 | G | A | 1 | a0001c0001t0010g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-143+1130C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051039 | |||||||
chr5:75051184 | G | C | 2 | a0001c0001t0003g0050 a0001c0001t0003g0238 |
3 | NA18948.hp1 NA18991.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-143+985C>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051184 | |||||||
chr5:75051486 | CT | C | 28 | a0001c0001t0005g0003 a0001c0001t0005g0072 a0001c0001t0005g0073 others(25): Show |
41 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-143+682delA | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051486 | |||||||
chr5:75051558 | G | A | 1 | a0001c0001t0001g0051 | 2 | NA19077.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-143+611C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051558 | |||||||
chr5:75051616 | T | A | 1 | a0002c0002t0027g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-143+553A>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051616 | |||||||
chr5:75051700 | T | C | 1 | a0002c0002t0002g0130 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-143+469A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051700 | |||||||
chr5:75051776 | A | G | 1 | a0001c0001t0009g0131 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-143+393T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 2/3 | chr5 | 75051776 | |||||||
chr5:75052238 | T | C | 1 | a0002c0002t0002g0036 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-201-11A>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052238 | |||||||
chr5:75052244 | C | CA | 9 | a0001c0001t0001g0244 a0001c0001t0004g0245 a0001c0001t0007g0052 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-201-18dupT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052244 | |||||||
chr5:75052244 | CA | C | 65 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0004g0128 others(62): Show |
89 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-201-18delT | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052244 | |||||||
chr5:75052244 | CAAAA | C | 7 | a0002c0002t0040g0027 a0003c0003t0029g0094 a0003c0003t0029g0095 others(4): Show |
10 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.-201-21_-201-18del others(4): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052244 | |||||||
chr5:75052244 | CAAAAA | C | 28 | a0001c0001t0005g0003 a0001c0001t0005g0070 a0001c0001t0005g0071 others(25): Show |
40 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-201-22_-201-18del others(5): Show |
GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052244 | |||||||
chr5:75052251 | A | C | 20 | a0001c0001t0005g0003 a0001c0001t0005g0070 a0001c0001t0005g0071 others(17): Show |
31 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-201-24T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052251 | |||||||
chr5:75052256 | A | C | 5 | a0001c0001t0001g0067 a0002c0002t0013g0008 a0002c0002t0013g0022 others(2): Show |
9 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-201-29T>G | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052256 | |||||||
chr5:75052274 | A | G | 9 | a0001c0001t0010g0066 a0003c0003t0012g0059 a0003c0003t0020g0021 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-201-47T>C | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052274 | |||||||
chr5:75052307 | G | A | 19 | a0001c0001t0007g0246 a0001c0001t0007g0254 a0001c0001t0007g0260 others(16): Show |
24 | HG00642.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-201-80C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052307 | |||||||
chr5:75052328 | G | A | 1 | a0002c0002t0067g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-202+101C>T | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052328 | |||||||
chr5:75052428 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03579.hp1 | splice_donor_variant&intron_variant | HIGH | c.-202+1G>A | GCNT4 | ENSG00000176928.7 | transcript | ENST00000652361.2 | protein_coding | 1/3 | chr5 | 75052428 |