Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 60558 |
| ensemblid | ENSG00000151806.14 |
| hgncid | 25799 |
| symbol | GUF1 |
| name | GTP binding elongation factor GUF1 |
| refseq_nuc | NM_021927.3 |
| refseq_prot | NP_068746.2 |
| ensembl_nuc | ENST00000281543.6 |
| ensembl_prot | ENSP00000281543.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 44678420 |
| end | 44700928 |
| strand | + |
| ver | v1.2 |
| region | chr4:44678420-44700928 |
| region5000 | chr4:44673420-44705928 |
| regionname0 | GUF1_chr4_44678420_44700928 |
| regionname5000 | GUF1_chr4_44673420_44705928 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 669 | 241 | 60 | 33 | 126 | 4 | 16 | 91 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0002 | 0/0 | 669 | 137 | 25 | 37 | 55 | 6 | 14 | 46 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0003 | 0/0 | 669 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0004 | 0/0 | 512 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(507): Show |
chr4 | 44673420 | 44705928 |
| a0005 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0006 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0007 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| a0008 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | MWTLV others(664): Show |
chr4 | 44673420 | 44705928 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2007 | 239 | 59 | 33 | 125 | 4 | 16 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0001c0004 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0001c0009 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0002c0002 | 0/0 | 2007 | 137 | 25 | 37 | 55 | 6 | 14 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0003c0003 | 0/0 | 2007 | 7 | 5 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0004c0008 | 0/0 | 2029 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2024): Show |
chr4 | 44673420 | 44705928 | ||
| a0005c0007 | 0/0 | 2007 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0006c0005 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0007c0006 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 | ||
| a0008c0010 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | ATGTG others(2002): Show |
chr4 | 44673420 | 44705928 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 4460 | 89 | 19 | 16 | 52 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0003 | 0/1 | 4460 | 60 | 1 | 8 | 38 | 2 | 10 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0004 | 0/0 | 4458 | 51 | 7 | 6 | 33 | 1 | 4 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4453): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0005 | 0/0 | 4460 | 19 | 17 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0007 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0008 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0009 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0010 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0011 | 0/0 | 4460 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0012 | 0/0 | 4460 | 2 | 0 | 1 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0014 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0015 | 0/0 | 4460 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0018 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0019 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0020 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0001c0001t0022 | 0/0 | 4458 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4453): Show |
chr4 | 44673420 | 44705928 |
| a0001c0004t0004 | 0/0 | 4458 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4453): Show |
chr4 | 44673420 | 44705928 |
| a0001c0009t0002 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0001 | 0/0 | 4460 | 127 | 22 | 31 | 55 | 6 | 13 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0007 | 0/0 | 4460 | 5 | 2 | 2 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0013 | 0/0 | 4460 | 2 | 0 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0016 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0017 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0002c0002t0021 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0003c0003t0006 | 0/0 | 4460 | 7 | 5 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0004c0008t0003 | 0/0 | 4482 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4477): Show |
chr4 | 44673420 | 44705928 |
| a0005c0007t0005 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0006c0005t0008 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0007c0006t0006 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4455): Show |
chr4 | 44673420 | 44705928 |
| a0008c0010t0004 | 0/0 | 4458 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | AGACG others(4453): Show |
chr4 | 44673420 | 44705928 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 25 | 1 | 10 | 14 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0005 | 0/0 | 22 | 0 | 5 | 17 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0002 | 0/0 | 43 | 0 | 4 | 33 | 0 | 6 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0003 | 0/0 | 30 | 2 | 1 | 22 | 1 | 4 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0011 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0002 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0008g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0009g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0010g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0011g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0012g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0020g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0001t0022g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0004t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0001c0009t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0001 | 0/0 | 83 | 7 | 22 | 45 | 4 | 5 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0008 | 0/0 | 8 | 0 | 4 | 0 | 0 | 4 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0007g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0013g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0017g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0002c0002t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0003c0003t0006g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0003c0003t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0003c0003t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0004c0008t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0005c0007t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0006c0005t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0007c0006t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| a0008c0010t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | GBR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0005 | EUR | GBR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00639 | hp1 | a0003 | c0003 | t0006 | g0010 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00642 | hp1 | a0002 | c0002 | t0017 | g0090 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01167 | hp1 | a0003 | c0003 | t0006 | g0010 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01168 | hp2 | a0004 | c0008 | t0003 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01175 | hp2 | a0001 | c0001 | t0012 | g0005 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01192 | hp2 | a0002 | c0002 | t0013 | g0033 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01255 | hp1 | a0005 | c0007 | t0005 | g0002 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01346 | hp1 | a0002 | c0002 | t0007 | g0032 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01361 | hp1 | a0002 | c0002 | t0013 | g0033 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01496 | hp2 | a0002 | c0002 | t0016 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0087 | EUR | IBS | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CDX | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0096 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PEL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02451 | hp2 | a0003 | c0003 | t0006 | g0010 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02572 | hp2 | a0003 | c0003 | t0006 | g0010 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0005 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02809 | hp2 | a0002 | c0002 | t0007 | g0031 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03017 | hp1 | a0002 | c0002 | t0007 | g0076 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03130 | hp2 | a0003 | c0003 | t0006 | g0047 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0060 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03195 | hp1 | a0001 | c0009 | t0002 | g0013 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | ESN | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03540 | hp1 | a0002 | c0002 | t0021 | g0012 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03579 | hp2 | a0007 | c0006 | t0006 | g0010 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | BEB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | STU | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18522 | hp1 | a0001 | c0001 | t0020 | g0041 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18906 | hp1 | a0003 | c0003 | t0006 | g0010 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18950 | hp2 | a0008 | c0010 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18978 | hp1 | a0001 | c0001 | t0019 | g0029 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19054 | hp2 | a0001 | c0001 | t0022 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19068 | hp2 | a0001 | c0004 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | YRI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | ASW | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20129 | hp2 | a0002 | c0002 | t0007 | g0031 | AFR | ASW | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0030 | EUR | TSI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | TSI | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG01123 | hp2 | a0002 | c0002 | t0007 | g0032 | AMR | CLM | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03471 | hp1 | a0003 | c0003 | t0006 | g0048 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG03471 | hp2 | a0006 | c0005 | t0008 | g0021 | AFR | MSL | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | USA | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | LWK | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0067 | REF | REF | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0050 | REF | REF | GUF1_chr4_44673420_44705928 | GUF1 | chr4 | 44673420 | 44705928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44680448 | T | C | 1 | a0002 | 137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
missense_variant | MODERATE | c.173T>C | p.Leu58Pro | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 2/17 | 376/4460 | 173/2010 | 58/669 | chr4 | 44680448 | |||
| chr4:44680751 | G | A | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.335G>A | p.Arg112Gln | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 3/17 | 538/4460 | 335/2010 | 112/669 | chr4 | 44680751 | |||
| chr4:44683311 | G | C | 1 | a0007 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.662G>C | p.Cys221Ser | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/17 | 865/4460 | 662/2010 | 221/669 | chr4 | 44683311 | |||
| chr4:44686023 | C | T | 1 | a0008 | 1 | NA18950.hp2 | missense_variant&splice_region_variant | MODERATE | c.734C>T | p.Pro245Leu | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/17 | 937/4460 | 734/2010 | 245/669 | chr4 | 44686023 | |||
| chr4:44691693 | A | G | 2 | a0003 a0007 |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
missense_variant | MODERATE | c.1507A>G | p.Ile503Val | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/17 | 1710/4460 | 1507/2010 | 503/669 | chr4 | 44691693 | |||
| chr4:44691698 | T | TATTGATC others(15): Show |
1 | a0004 | 1 | HG01168.hp2 | frameshift_variant&stop_gained | HIGH | c.1527_1528insTATCAT others(16): Show |
p.Val510fs | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/17 | 1731/4460 | 1528/2010 | 510/669 | INFO_REALIGN_3_PRIME | chr4 | 44691698 | ||
| chr4:44698573 | G | C | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1902G>C | p.Lys634Asn | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 2105/4460 | 1902/2010 | 634/669 | chr4 | 44698573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44680695 | G | A | 1 | a0001c0004 | 1 | NA19068.hp2 | splice_region_variant&synonymous_variant | LOW | c.279G>A | p.Gly93Gly | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 3/17 | 482/4460 | 279/2010 | 93/669 | chr4 | 44680695 | |||
| chr4:44690764 | C | T | 1 | a0001c0009 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1383C>T | p.Pro461Pro | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/17 | 1586/4460 | 1383/2010 | 461/669 | chr4 | 44690764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44678519 | TGA | T | 4 | a0001c0001t0004 a0001c0001t0022 a0001c0004t0004 others(1): Show |
54 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-102_-101delAG | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/17 | 101 | INFO_REALIGN_3_PRIME | chr4 | 44678519 | |||||
| chr4:44698735 | A | C | 4 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0010 others(1): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*54A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 54 | chr4 | 44698735 | ||||||
| chr4:44698823 | G | A | 3 | a0001c0001t0008 a0001c0001t0009 a0006c0005t0008 |
7 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*142G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 142 | chr4 | 44698823 | ||||||
| chr4:44698867 | A | G | 1 | a0002c0002t0021 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 186 | chr4 | 44698867 | ||||||
| chr4:44698895 | G | A | 1 | a0001c0001t0022 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 214 | chr4 | 44698895 | ||||||
| chr4:44698959 | A | G | 1 | a0001c0001t0009 | 3 | HG02145.hp1 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*278A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 278 | chr4 | 44698959 | ||||||
| chr4:44699067 | C | T | 1 | a0001c0001t0020 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 386 | chr4 | 44699067 | ||||||
| chr4:44699068 | G | A | 1 | a0001c0001t0014 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 387 | chr4 | 44699068 | ||||||
| chr4:44699239 | G | T | 3 | a0001c0001t0003 a0001c0001t0019 a0004c0008t0003 |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*558G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 558 | chr4 | 44699239 | ||||||
| chr4:44699263 | C | T | 1 | a0001c0001t0018 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 582 | chr4 | 44699263 | ||||||
| chr4:44699328 | G | A | 1 | a0001c0001t0011 | 2 | HG03453.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*647G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 647 | chr4 | 44699328 | ||||||
| chr4:44699330 | G | C | 4 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0010 others(1): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*649G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 649 | chr4 | 44699330 | ||||||
| chr4:44699429 | A | G | 7 | a0001c0001t0007 a0002c0002t0001 a0002c0002t0007 others(4): Show |
138 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*748A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 748 | chr4 | 44699429 | ||||||
| chr4:44699479 | C | T | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 798 | chr4 | 44699479 | ||||||
| chr4:44699564 | C | T | 1 | a0002c0002t0013 | 2 | HG01192.hp2 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*883C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 883 | chr4 | 44699564 | ||||||
| chr4:44699683 | C | T | 1 | a0001c0001t0012 | 2 | HG00140.hp1 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1002C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1002 | chr4 | 44699683 | ||||||
| chr4:44699733 | A | C | 7 | a0001c0001t0007 a0002c0002t0001 a0002c0002t0007 others(4): Show |
138 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1052 | chr4 | 44699733 | ||||||
| chr4:44699747 | T | G | 4 | a0002c0002t0001 a0002c0002t0013 a0002c0002t0016 others(1): Show |
131 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1066 | chr4 | 44699747 | ||||||
| chr4:44699883 | A | G | 2 | a0003c0003t0006 a0007c0006t0006 |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1202A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1202 | chr4 | 44699883 | ||||||
| chr4:44700007 | C | T | 1 | a0001c0001t0011 | 2 | HG03453.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1326C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1326 | chr4 | 44700007 | ||||||
| chr4:44700522 | C | T | 1 | a0001c0001t0019 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1841 | chr4 | 44700522 | ||||||
| chr4:44700644 | A | C | 1 | a0002c0002t0016 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1963A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 1963 | chr4 | 44700644 | ||||||
| chr4:44700703 | T | C | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0014 others(3): Show |
82 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2022T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 2022 | chr4 | 44700703 | ||||||
| chr4:44700900 | G | A | 1 | a0002c0002t0017 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2219G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 17/17 | 2219 | chr4 | 44700900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44678839 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.165+52C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44678839 | |||||||
| chr4:44678897 | A | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+110A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44678897 | |||||||
| chr4:44679014 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.165+227A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679014 | |||||||
| chr4:44679154 | A | G | 1 | a0001c0001t0018g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.165+367A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679154 | |||||||
| chr4:44679521 | A | G | 2 | a0001c0001t0008g0098 a0001c0001t0009g0022 |
4 | HG02145.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+734A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679521 | |||||||
| chr4:44679605 | G | A | 20 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(17): Show |
78 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.165+818G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679605 | |||||||
| chr4:44679778 | CA | C | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.166-657delA | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 44679778 | ||||||
| chr4:44679806 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-635C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679806 | |||||||
| chr4:44679958 | C | A | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-483C>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44679958 | |||||||
| chr4:44680000 | A | G | 39 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(36): Show |
147 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.166-441A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44680000 | |||||||
| chr4:44680093 | A | G | 2 | a0001c0001t0008g0021 a0006c0005t0008g0021 |
3 | HG02723.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.166-348A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44680093 | |||||||
| chr4:44680108 | TTACTAGA others(5): Show |
T | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-330_166-319del others(12): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr4 | 44680108 | ||||||
| chr4:44680181 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-260A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44680181 | |||||||
| chr4:44680354 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.166-87C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 1/16 | chr4 | 44680354 | |||||||
| chr4:44680614 | CTTAAATT | C | 1 | a0001c0001t0010g0020 | 3 | HG02965.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.277+67_278-69delAT others(5): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr4 | 44680614 | ||||||
| chr4:44681273 | A | C | 6 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
13 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+70A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681273 | |||||||
| chr4:44681518 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.507+315T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681518 | |||||||
| chr4:44681524 | A | G | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.507+321A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681524 | |||||||
| chr4:44681544 | A | G | 104 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(101): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.507+341A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681544 | |||||||
| chr4:44681742 | C | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
13 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.507+539C>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681742 | |||||||
| chr4:44681745 | C | CT | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+550dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr4 | 44681745 | ||||||
| chr4:44681819 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508-515A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681819 | |||||||
| chr4:44681855 | ACTACCT | A | 2 | a0001c0001t0004g0015 a0001c0001t0004g0058 |
4 | HG02145.hp2 HG02559.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-478_508-473del others(6): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44681855 | |||||||
| chr4:44682049 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.508-285G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44682049 | |||||||
| chr4:44682149 | A | T | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-185A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44682149 | |||||||
| chr4:44682200 | G | A | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-134G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44682200 | |||||||
| chr4:44682232 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508-102G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 4/16 | chr4 | 44682232 | |||||||
| chr4:44682421 | A | G | 16 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0015 others(13): Show |
54 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.585+10A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | chr4 | 44682421 | |||||||
| chr4:44682438 | C | T | 104 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(101): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.585+27C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | chr4 | 44682438 | |||||||
| chr4:44682574 | A | T | 1 | a0001c0001t0004g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.585+163A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | chr4 | 44682574 | |||||||
| chr4:44683018 | G | GT | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.586-209dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr4 | 44683018 | ||||||
| chr4:44683207 | T | TA | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.586-28_586-27insA | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | chr4 | 44683207 | |||||||
| chr4:44683208 | T | A | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.586-27T>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | chr4 | 44683208 | |||||||
| chr4:44683219 | AT | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0037 others(6): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.586-5delT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr4 | 44683219 | ||||||
| chr4:44683463 | C | G | 1 | a0001c0001t0003g0018 | 3 | HG01981.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.669+145C>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44683463 | |||||||
| chr4:44683478 | T | G | 1 | a0002c0002t0001g0072 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.669+160T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44683478 | |||||||
| chr4:44683784 | C | T | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.669+466C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44683784 | |||||||
| chr4:44684075 | A | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+757A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684075 | |||||||
| chr4:44684235 | CTT | C | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+922_669+923del others(2): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr4 | 44684235 | ||||||
| chr4:44684301 | G | T | 1 | a0001c0001t0005g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.669+983G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684301 | |||||||
| chr4:44684337 | G | A | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+1019G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684337 | |||||||
| chr4:44684468 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.669+1150G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684468 | |||||||
| chr4:44684501 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.669+1183T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684501 | |||||||
| chr4:44684603 | A | G | 2 | a0002c0002t0001g0093 a0002c0002t0013g0033 |
3 | HG01192.hp2 HG01255.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.669+1285A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684603 | |||||||
| chr4:44684689 | A | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.670-1270A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684689 | |||||||
| chr4:44684728 | G | A | 1 | a0001c0001t0018g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.670-1231G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684728 | |||||||
| chr4:44684847 | T | C | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-1112T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684847 | |||||||
| chr4:44684871 | T | G | 2 | a0001c0001t0005g0016 a0001c0001t0005g0028 |
5 | HG01993.hp2 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1088T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684871 | |||||||
| chr4:44684947 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.670-1012A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44684947 | |||||||
| chr4:44685035 | A | T | 36 | a0001c0001t0004g0056 a0001c0001t0007g0051 a0002c0002t0001g0001 others(33): Show |
139 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.670-924A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685035 | |||||||
| chr4:44685111 | C | G | 2 | a0001c0001t0008g0098 a0001c0001t0009g0022 |
4 | HG02145.hp1 HG02622.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-848C>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685111 | |||||||
| chr4:44685146 | A | G | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.670-813A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685146 | |||||||
| chr4:44685213 | A | G | 1 | a0001c0001t0003g0017 | 3 | HG01256.hp2 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.670-746A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685213 | |||||||
| chr4:44685346 | G | C | 1 | a0001c0001t0008g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.670-613G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685346 | |||||||
| chr4:44685384 | A | G | 82 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(79): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.670-575A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685384 | |||||||
| chr4:44685424 | G | T | 1 | a0001c0001t0011g0023 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.670-535G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685424 | |||||||
| chr4:44685545 | A | T | 1 | a0001c0001t0003g0030 | 2 | HG01243.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.670-414A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685545 | |||||||
| chr4:44685599 | T | C | 1 | a0001c0001t0020g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.670-360T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685599 | |||||||
| chr4:44685794 | A | G | 1 | a0002c0002t0007g0032 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.670-165A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 6/16 | chr4 | 44685794 | |||||||
| chr4:44686024 | G | A | 2 | a0001c0001t0004g0011 a0001c0001t0004g0053 |
6 | HG01433.hp2 HG01952.hp2 HG01975.hp2 others(3): Show |
splice_donor_variant&intron_variant | HIGH | c.734+1G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/16 | chr4 | 44686024 | |||||||
| chr4:44686050 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
13 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.734+27G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/16 | chr4 | 44686050 | |||||||
| chr4:44686092 | G | T | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.734+69G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/16 | chr4 | 44686092 | |||||||
| chr4:44686253 | A | G | 1 | a0001c0001t0004g0027 | 2 | HG02135.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.734+230A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/16 | chr4 | 44686253 | |||||||
| chr4:44686400 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735-110T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 7/16 | chr4 | 44686400 | |||||||
| chr4:44686721 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.938+8A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44686721 | |||||||
| chr4:44686753 | T | C | 1 | a0002c0002t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.938+40T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44686753 | |||||||
| chr4:44687009 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.938+296A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687009 | |||||||
| chr4:44687069 | T | C | 2 | a0002c0002t0001g0012 a0002c0002t0021g0012 |
5 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.938+356T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687069 | |||||||
| chr4:44687251 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.938+538G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687251 | |||||||
| chr4:44687253 | A | G | 4 | a0003c0003t0006g0010 a0003c0003t0006g0047 a0003c0003t0006g0048 others(1): Show |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.938+540A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687253 | |||||||
| chr4:44687344 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.938+631T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687344 | |||||||
| chr4:44687379 | TC | T | 15 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0015 others(12): Show |
53 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.939-627delC | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687379 | |||||||
| chr4:44687507 | A | AT | 5 | a0001c0001t0007g0051 a0001c0001t0008g0021 a0001c0001t0008g0098 others(2): Show |
8 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.939-489dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr4 | 44687507 | ||||||
| chr4:44687590 | G | A | 1 | a0001c0001t0002g0024 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.939-417G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687590 | |||||||
| chr4:44687610 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.939-397G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687610 | |||||||
| chr4:44687636 | G | A | 1 | a0001c0001t0018g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.939-371G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687636 | |||||||
| chr4:44687829 | G | C | 1 | a0001c0001t0003g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.939-178G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687829 | |||||||
| chr4:44687850 | G | A | 1 | a0002c0002t0001g0019 | 3 | HG01257.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.939-157G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 8/16 | chr4 | 44687850 | |||||||
| chr4:44688303 | A | T | 40 | a0001c0001t0007g0051 a0001c0001t0008g0021 a0001c0001t0008g0098 others(37): Show |
148 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1078+157A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688303 | |||||||
| chr4:44688322 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1078+176A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688322 | |||||||
| chr4:44688380 | A | T | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078+234A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688380 | |||||||
| chr4:44688384 | A | G | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078+238A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688384 | |||||||
| chr4:44688393 | A | G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
13 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078+247A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688393 | |||||||
| chr4:44688460 | A | T | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078+314A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688460 | |||||||
| chr4:44688513 | C | T | 1 | a0003c0003t0006g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078+367C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688513 | |||||||
| chr4:44688600 | A | T | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1078+454A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688600 | |||||||
| chr4:44688827 | A | G | 1 | a0002c0002t0017g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1079-459A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44688827 | |||||||
| chr4:44689004 | C | T | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1079-282C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689004 | |||||||
| chr4:44689009 | GT | G | 40 | a0001c0001t0007g0051 a0001c0001t0008g0021 a0001c0001t0008g0098 others(37): Show |
148 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1079-266delT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr4 | 44689009 | ||||||
| chr4:44689014 | T | G | 1 | a0002c0002t0001g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1079-272T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689014 | |||||||
| chr4:44689081 | A | C | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1079-205A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689081 | |||||||
| chr4:44689112 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1079-174C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689112 | |||||||
| chr4:44689181 | T | G | 1 | a0001c0001t0018g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1079-105T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689181 | |||||||
| chr4:44689189 | TA | T | 29 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(26): Show |
130 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1079-94delA | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr4 | 44689189 | ||||||
| chr4:44689256 | C | T | 1 | a0001c0001t0004g0026 | 2 | HG00741.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1079-30C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 9/16 | chr4 | 44689256 | |||||||
| chr4:44689619 | C | A | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+210C>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 10/16 | chr4 | 44689619 | |||||||
| chr4:44689662 | G | C | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203-181G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 10/16 | chr4 | 44689662 | |||||||
| chr4:44689678 | T | C | 1 | a0001c0001t0014g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1203-165T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 10/16 | chr4 | 44689678 | |||||||
| chr4:44689737 | GACTTAAT others(3): Show |
G | 1 | a0002c0002t0001g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1203-104_1203-95de others(11): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 44689737 | ||||||
| chr4:44689778 | T | TA | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.1203-51dupA | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr4 | 44689778 | ||||||
| chr4:44690047 | A | C | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1335+72A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | chr4 | 44690047 | |||||||
| chr4:44690153 | TGAA | T | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1335+182_1335+184d others(5): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr4 | 44690153 | ||||||
| chr4:44690402 | T | C | 1 | a0001c0001t0002g0014 | 3 | NA18944.hp2 NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1336-315T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | chr4 | 44690402 | |||||||
| chr4:44690404 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1336-313C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | chr4 | 44690404 | |||||||
| chr4:44690425 | A | C | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1336-292A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | chr4 | 44690425 | |||||||
| chr4:44690532 | A | G | 2 | a0001c0001t0002g0006 a0001c0001t0002g0046 |
11 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.1336-185A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 11/16 | chr4 | 44690532 | |||||||
| chr4:44690907 | G | A | 1 | a0001c0001t0005g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1479+47G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44690907 | |||||||
| chr4:44690995 | A | C | 1 | a0002c0002t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1479+135A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44690995 | |||||||
| chr4:44691030 | T | C | 4 | a0003c0003t0006g0010 a0003c0003t0006g0047 a0003c0003t0006g0048 others(1): Show |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1479+170T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691030 | |||||||
| chr4:44691075 | A | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1479+215A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691075 | |||||||
| chr4:44691136 | G | A | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1479+276G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691136 | |||||||
| chr4:44691195 | A | C | 1 | a0001c0001t0005g0016 | 3 | HG03209.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1479+335A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691195 | |||||||
| chr4:44691225 | T | G | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1479+365T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691225 | |||||||
| chr4:44691364 | G | C | 1 | a0001c0001t0005g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1480-302G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691364 | |||||||
| chr4:44691482 | G | T | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1480-184G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 12/16 | chr4 | 44691482 | |||||||
| chr4:44692037 | CAAA | C | 2 | a0001c0001t0004g0015 a0001c0001t0004g0058 |
4 | HG02145.hp2 HG02559.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+243_1613+245d others(5): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr4 | 44692037 | ||||||
| chr4:44692060 | A | C | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1613+261A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692060 | |||||||
| chr4:44692065 | G | C | 1 | a0001c0001t0004g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1613+266G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692065 | |||||||
| chr4:44692166 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1613+367G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692166 | |||||||
| chr4:44692407 | T | G | 14 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0034 others(11): Show |
38 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1613+608T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692407 | |||||||
| chr4:44692407 | TTTG | T | 3 | a0002c0002t0001g0009 a0002c0002t0001g0074 a0002c0002t0001g0078 |
9 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1613+627_1613+629d others(5): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr4 | 44692407 | ||||||
| chr4:44692432 | C | A | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1613+633C>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692432 | |||||||
| chr4:44692456 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1613+657A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692456 | |||||||
| chr4:44692489 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1613+690T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692489 | |||||||
| chr4:44692654 | A | G | 1 | a0002c0002t0001g0078 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1613+855A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692654 | |||||||
| chr4:44692702 | A | T | 36 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(33): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1613+903A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44692702 | |||||||
| chr4:44693059 | A | G | 5 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(2): Show |
10 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613+1260A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693059 | |||||||
| chr4:44693136 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1614-1276A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693136 | |||||||
| chr4:44693255 | T | C | 1 | a0001c0001t0018g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1614-1157T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693255 | |||||||
| chr4:44693280 | A | G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
13 | HG01891.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1614-1132A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693280 | |||||||
| chr4:44693504 | GAAGA | G | 21 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1614-900_1614-897d others(6): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr4 | 44693504 | ||||||
| chr4:44693819 | T | C | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1614-593T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693819 | |||||||
| chr4:44693861 | A | G | 4 | a0003c0003t0006g0010 a0003c0003t0006g0047 a0003c0003t0006g0048 others(1): Show |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614-551A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693861 | |||||||
| chr4:44693875 | T | C | 2 | a0001c0001t0004g0015 a0001c0001t0004g0058 |
4 | HG02145.hp2 HG02559.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-537T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693875 | |||||||
| chr4:44693924 | A | G | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1614-488A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44693924 | |||||||
| chr4:44694272 | A | G | 1 | a0001c0001t0004g0026 | 2 | HG00741.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1614-140A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44694272 | |||||||
| chr4:44694294 | CAT | C | 2 | a0002c0002t0001g0008 a0002c0002t0001g0088 |
9 | HG01192.hp1 HG01928.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1614-115_1614-114d others(4): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr4 | 44694294 | ||||||
| chr4:44694381 | A | C | 1 | a0002c0002t0007g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1614-31A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 13/16 | chr4 | 44694381 | |||||||
| chr4:44694521 | C | G | 108 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(105): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
splice_region_variant&intron_variant | LOW | c.1715+8C>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694521 | |||||||
| chr4:44694543 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0071 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1715+30G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694543 | |||||||
| chr4:44694571 | T | A | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1715+58T>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694571 | |||||||
| chr4:44694572 | T | TCAAAAAA others(11): Show |
1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1715+59_1715+60ins others(18): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694572 | |||||||
| chr4:44694573 | A | T | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1715+60A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694573 | |||||||
| chr4:44694797 | G | GT | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1715+291dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 44694797 | ||||||
| chr4:44694815 | G | GT | 18 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0015 others(15): Show |
56 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1715+312dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr4 | 44694815 | ||||||
| chr4:44694815 | G | T | 4 | a0002c0002t0007g0031 a0002c0002t0007g0032 a0002c0002t0007g0076 others(1): Show |
6 | HG00642.hp1 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1715+302G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694815 | |||||||
| chr4:44694930 | C | G | 1 | a0003c0003t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1715+417C>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44694930 | |||||||
| chr4:44695027 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1715+514G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695027 | |||||||
| chr4:44695096 | G | A | 4 | a0002c0002t0007g0031 a0002c0002t0007g0032 a0002c0002t0007g0076 others(1): Show |
6 | HG00642.hp1 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716-519G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695096 | |||||||
| chr4:44695162 | G | A | 4 | a0001c0001t0008g0021 a0001c0001t0008g0098 a0001c0001t0009g0022 others(1): Show |
7 | HG02145.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716-453G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695162 | |||||||
| chr4:44695238 | A | C | 1 | a0002c0002t0001g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1716-377A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695238 | |||||||
| chr4:44695367 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1716-248G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695367 | |||||||
| chr4:44695410 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1716-205G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695410 | |||||||
| chr4:44695452 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1716-163C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695452 | |||||||
| chr4:44695533 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1716-82C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695533 | |||||||
| chr4:44695541 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1716-74A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695541 | |||||||
| chr4:44695548 | T | C | 1 | a0001c0001t0004g0025 | 2 | NA18971.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1716-67T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695548 | |||||||
| chr4:44695583 | G | T | 1 | a0001c0001t0004g0054 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1716-32G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 14/16 | chr4 | 44695583 | |||||||
| chr4:44695804 | T | C | 1 | a0002c0002t0001g0080 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1835+70T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44695804 | |||||||
| chr4:44695904 | A | G | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1835+170A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44695904 | |||||||
| chr4:44695958 | G | A | 1 | a0002c0002t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1835+224G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44695958 | |||||||
| chr4:44696085 | G | GT | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1835+355dupT | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr4 | 44696085 | ||||||
| chr4:44696271 | C | A | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1835+537C>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44696271 | |||||||
| chr4:44696487 | A | C | 4 | a0003c0003t0006g0010 a0003c0003t0006g0047 a0003c0003t0006g0048 others(1): Show |
8 | HG00639.hp1 HG01167.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1835+753A>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44696487 | |||||||
| chr4:44696639 | A | G | 1 | a0001c0001t0002g0024 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1836-769A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44696639 | |||||||
| chr4:44696669 | C | T | 1 | a0001c0001t0003g0063 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1836-739C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44696669 | |||||||
| chr4:44697044 | G | T | 2 | a0002c0002t0001g0093 a0002c0002t0013g0033 |
3 | HG01192.hp2 HG01255.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1836-364G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44697044 | |||||||
| chr4:44697117 | A | G | 1 | a0001c0001t0004g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1836-291A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44697117 | |||||||
| chr4:44697388 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1836-20C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 15/16 | chr4 | 44697388 | |||||||
| chr4:44697467 | T | G | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1872+23T>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697467 | |||||||
| chr4:44697475 | A | G | 1 | a0001c0001t0007g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1872+31A>G | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697475 | |||||||
| chr4:44697489 | C | T | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1872+45C>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697489 | |||||||
| chr4:44697516 | T | C | 1 | a0002c0002t0001g0081 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1872+72T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697516 | |||||||
| chr4:44697568 | G | T | 16 | a0001c0001t0004g0003 a0001c0001t0004g0011 a0001c0001t0004g0015 others(13): Show |
54 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1872+124G>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697568 | |||||||
| chr4:44697569 | A | T | 1 | a0001c0001t0002g0045 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1872+125A>T | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697569 | |||||||
| chr4:44697616 | T | C | 1 | a0002c0002t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1872+172T>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697616 | |||||||
| chr4:44697710 | ACAG | A | 34 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(31): Show |
137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1872+267_1872+269d others(5): Show |
GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44697710 | |||||||
| chr4:44698436 | G | C | 30 | a0002c0002t0001g0001 a0002c0002t0001g0008 a0002c0002t0001g0009 others(27): Show |
131 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1873-108G>C | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44698436 | |||||||
| chr4:44698437 | G | A | 1 | a0002c0002t0013g0033 | 2 | HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1873-107G>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44698437 | |||||||
| chr4:44698497 | T | A | 1 | a0002c0002t0001g0082 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1873-47T>A | GUF1 | ENSG00000151806.14 | transcript | ENST00000281543.6 | protein_coding | 16/16 | chr4 | 44698497 |