Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2110 |
| ensemblid | ENSG00000171503.13 |
| hgncid | 3483 |
| symbol | ETFDH |
| name | electron transfer flavoprotein dehydrogenase |
| refseq_nuc | NM_004453.4 |
| refseq_prot | NP_004444.2 |
| ensembl_nuc | ENST00000511912.6 |
| ensembl_prot | ENSP00000426638.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 158672296 |
| end | 158709623 |
| strand | + |
| ver | v1.2 |
| region | chr4:158672296-158709623 |
| region5000 | chr4:158667296-158714623 |
| regionname0 | ETFDH_chr4_158672296_158709623 |
| regionname5000 | ETFDH_chr4_158667296_158714623 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 617 | 174 | 8 | 39 | 85 | 11 | 30 | 68 | ETFDH_chr4_158667296_158714623 | ETFDH | MLVPL others(612): Show |
chr4 | 158667296 | 158714623 |
| a0002 | 1/0 | 617 | 123 | 81 | 15 | 13 | 3 | 10 | 12 | ETFDH_chr4_158667296_158714623 | ETFDH | MLVPL others(612): Show |
chr4 | 158667296 | 158714623 |
| a0003 | 0/0 | 617 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | MLVPL others(612): Show |
chr4 | 158667296 | 158714623 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1851 | 173 | 8 | 38 | 85 | 11 | 30 | ETFDH_chr4_158667296_158714623 | ETFDH | ATGCT others(1846): Show |
chr4 | 158667296 | 158714623 | ||
| a0001c0004 | 0/0 | 1851 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | ATGCT others(1846): Show |
chr4 | 158667296 | 158714623 | ||
| a0002c0002 | 1/0 | 1851 | 123 | 81 | 15 | 13 | 3 | 10 | ETFDH_chr4_158667296_158714623 | ETFDH | ATGCT others(1846): Show |
chr4 | 158667296 | 158714623 | ||
| a0003c0003 | 0/0 | 1851 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | ATGCT others(1846): Show |
chr4 | 158667296 | 158714623 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3111 | 110 | 5 | 32 | 52 | 8 | 13 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0002 | 0/0 | 3111 | 55 | 3 | 5 | 29 | 3 | 15 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0003 | 0/0 | 3111 | 2 | 0 | 0 | 2 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0005 | 0/0 | 3111 | 2 | 0 | 0 | 0 | 0 | 2 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0006 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0007 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0008 | 0/0 | 3093 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3088): Show |
chr4 | 158667296 | 158714623 |
| a0001c0001t0010 | 0/1 | 3119 | 1 | 0 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3114): Show |
chr4 | 158667296 | 158714623 |
| a0001c0004t0001 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0002c0002t0001 | 1/0 | 3111 | 96 | 66 | 14 | 4 | 3 | 8 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0002c0002t0002 | 0/0 | 3111 | 12 | 12 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0002c0002t0003 | 0/0 | 3111 | 12 | 0 | 1 | 9 | 0 | 2 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0002c0002t0004 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0002c0002t0009 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| a0003c0003t0001 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | GTGAA others(3106): Show |
chr4 | 158667296 | 158714623 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0001t0010g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0001 | 0/0 | 7 | 0 | 4 | 0 | 0 | 3 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0001g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0002c0002t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| a0003c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0106 | EUR | GBR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | GBR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0107 | EUR | FIN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0216 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0105 | EUR | IBS | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0097 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0023 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0231 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0065 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0096 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0109 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0075 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0054 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ESN | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0210 | SAS | PJL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0148 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0076 | SAS | STU | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0155 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0234 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0108 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0084 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19072 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | ASW | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ASW | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | TSI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | GIH | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | MSL | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | USA | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | USA | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | LWK | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0215 | REF | REF | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0232 | REF | REF | ETFDH_chr4_158667296_158714623 | ETFDH | chr4 | 158667296 | 158714623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158680524 | C | T | 1 | a0001 | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
missense_variant | MODERATE | c.92C>T | p.Thr31Ile | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/13 | 253/3111 | 92/1854 | 31/617 | chr4 | 158680524 | |||
| chr4:158699063 | G | A | 1 | a0003 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1049G>A | p.Arg350Gln | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/13 | 1210/3111 | 1049/1854 | 350/617 | chr4 | 158699063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158690392 | C | T | 1 | a0001c0004 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.651C>T | p.Asn217Asn | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/13 | 812/3111 | 651/1854 | 217/617 | chr4 | 158690392 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158672321 | G | C | 1 | a0001c0001t0006 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/13 | 136 | chr4 | 158672321 | ||||||
| chr4:158708662 | A | C | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(1): Show |
70 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 135 | chr4 | 158708662 | ||||||
| chr4:158708901 | T | C | 1 | a0001c0001t0007 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*374T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 374 | chr4 | 158708901 | ||||||
| chr4:158708929 | G | T | 1 | a0002c0002t0004 | 2 | HG02258.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*402G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 402 | chr4 | 158708929 | ||||||
| chr4:158708994 | G | A | 1 | a0002c0002t0004 | 2 | HG02258.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*467G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 467 | chr4 | 158708994 | ||||||
| chr4:158709000 | T | A | 1 | a0001c0001t0005 | 2 | HG03710.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*473T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 473 | chr4 | 158709000 | ||||||
| chr4:158709016 | AGTTTGTG others(11): Show |
A | 1 | a0001c0001t0008 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492_*509delTTGTGT others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 492 | INFO_REALIGN_3_PRIME | chr4 | 158709016 | |||||
| chr4:158709019 | T | TGTGTGTG others(2): Show |
3 | a0001c0001t0001 a0001c0001t0002 a0002c0002t0001 |
3 | HG00738.hp2 HG03130.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492_*493insGTGTGT others(3): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 493 | chr4 | 158709019 | ||||||
| chr4:158709019 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0002 a0002c0002t0001 |
2 | HG02809.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492_*493insGTGTGT others(5): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 493 | chr4 | 158709019 | ||||||
| chr4:158709019 | T | TGTGTGTG others(10): Show |
1 | a0002c0002t0002 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492_*493insGTGTGT others(11): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 493 | chr4 | 158709019 | ||||||
| chr4:158709019 | T | TTG | 5 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0001 others(2): Show |
27 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*530_*531dupGT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTG | 5 | a0001c0001t0002 a0001c0001t0006 a0002c0002t0001 others(2): Show |
17 | HG01123.hp1 HG01943.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*531dupGTGT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTG | 3 | a0001c0001t0001 a0001c0001t0002 a0002c0002t0001 |
22 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*531dupGTGTGT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(1): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(1): Show |
31 | HG01123.hp2 HG01167.hp1 HG02027.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*524_*531dupGTGTGT others(2): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0002 a0001c0001t0005 a0002c0002t0001 |
17 | HG02055.hp1 HG02055.hp2 HG02129.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*522_*531dupGTGTGT others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0002c0002t0001 others(1): Show |
8 | HG00438.hp2 HG02683.hp2 HG03130.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*531dupGTGTGT others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0002 a0002c0002t0001 |
4 | HG00140.hp2 HG02074.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*518_*531dupGTGTGT others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0002 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516_*531dupGTGTGT others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0002 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512_*531dupGTGTGT others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 532 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0001 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518_*531delGTGTGT others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 518 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0001 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516_*531delGTGTGT others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 516 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709019 | TTGTGTGT others(11): Show |
T | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(3): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*514_*531delGTGTGT others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 514 | INFO_REALIGN_3_PRIME | chr4 | 158709019 | |||||
| chr4:158709023 | G | T | 1 | a0002c0002t0004 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 496 | chr4 | 158709023 | ||||||
| chr4:158709027 | G | T | 1 | a0002c0002t0004 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 500 | chr4 | 158709027 | ||||||
| chr4:158709249 | C | T | 1 | a0002c0002t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*722C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 722 | chr4 | 158709249 | ||||||
| chr4:158709383 | T | G | 2 | a0001c0001t0003 a0002c0002t0003 |
14 | HG01943.hp2 HG02735.hp2 HG04228.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*856T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 13/13 | 856 | chr4 | 158709383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:158672547 | C | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+57C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158672547 | |||||||
| chr4:158672599 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.34+109A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158672599 | |||||||
| chr4:158672636 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+146T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158672636 | |||||||
| chr4:158672756 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+266A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158672756 | |||||||
| chr4:158672897 | G | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+407G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158672897 | |||||||
| chr4:158673005 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+515C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673005 | |||||||
| chr4:158673029 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
8 | HG00408.hp1 HG01978.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+539C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673029 | |||||||
| chr4:158673033 | G | C | 1 | a0002c0002t0001g0043 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.34+543G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673033 | |||||||
| chr4:158673075 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.34+585G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673075 | |||||||
| chr4:158673094 | A | G | 1 | a0002c0002t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.34+604A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673094 | |||||||
| chr4:158673257 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+767C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673257 | |||||||
| chr4:158673341 | C | A | 1 | a0001c0001t0002g0045 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.34+851C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673341 | |||||||
| chr4:158673387 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.34+897G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673387 | |||||||
| chr4:158673598 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1108G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673598 | |||||||
| chr4:158673665 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1175T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673665 | |||||||
| chr4:158673739 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.34+1249G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673739 | |||||||
| chr4:158673909 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1419T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673909 | |||||||
| chr4:158673940 | C | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1450C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673940 | |||||||
| chr4:158673941 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1451A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673941 | |||||||
| chr4:158673965 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1475G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158673965 | |||||||
| chr4:158674077 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1587G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674077 | |||||||
| chr4:158674168 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.34+1678A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674168 | |||||||
| chr4:158674434 | T | A | 1 | a0002c0002t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.34+1944T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674434 | |||||||
| chr4:158674527 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.34+2037C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674527 | |||||||
| chr4:158674532 | C | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2042C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674532 | |||||||
| chr4:158674535 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2045A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674535 | |||||||
| chr4:158674723 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.34+2233T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674723 | |||||||
| chr4:158674877 | T | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2387T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158674877 | |||||||
| chr4:158675202 | G | GC | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2716dupC | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158675202 | ||||||
| chr4:158675249 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2759A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675249 | |||||||
| chr4:158675480 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+2990C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675480 | |||||||
| chr4:158675520 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3030G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675520 | |||||||
| chr4:158675543 | T | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3053T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675543 | |||||||
| chr4:158675569 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.34+3079T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675569 | |||||||
| chr4:158675626 | G | A | 11 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(8): Show |
11 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+3136G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675626 | |||||||
| chr4:158675851 | A | G | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.34+3361A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675851 | |||||||
| chr4:158675942 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.34+3452C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675942 | |||||||
| chr4:158675966 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3476A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158675966 | |||||||
| chr4:158676187 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34+3697G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676187 | |||||||
| chr4:158676276 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3786A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676276 | |||||||
| chr4:158676287 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3797C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676287 | |||||||
| chr4:158676336 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.34+3846C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676336 | |||||||
| chr4:158676407 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG00741.hp1 HG01192.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+3917G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676407 | |||||||
| chr4:158676453 | C | G | 1 | a0002c0002t0001g0226 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.34+3963C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676453 | |||||||
| chr4:158676470 | C | T | 1 | a0002c0002t0001g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.34+3980C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676470 | |||||||
| chr4:158676763 | A | AAG | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3704_35-3703ins others(2): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676763 | |||||||
| chr4:158676892 | T | C | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35-3575T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158676892 | |||||||
| chr4:158677087 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.35-3380C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677087 | |||||||
| chr4:158677122 | C | T | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35-3345C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677122 | |||||||
| chr4:158677131 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.35-3336A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677131 | |||||||
| chr4:158677163 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3304A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677163 | |||||||
| chr4:158677227 | A | G | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35-3240A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677227 | |||||||
| chr4:158677286 | T | C | 1 | a0002c0002t0003g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.35-3181T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677286 | |||||||
| chr4:158677294 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3173A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677294 | |||||||
| chr4:158677323 | C | T | 1 | a0001c0001t0003g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.35-3144C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677323 | |||||||
| chr4:158677378 | G | A | 3 | a0002c0002t0001g0077 a0002c0002t0001g0078 a0002c0002t0001g0226 |
3 | HG02055.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.35-3089G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677378 | |||||||
| chr4:158677438 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3029G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677438 | |||||||
| chr4:158677642 | G | A | 2 | a0002c0002t0001g0049 a0002c0002t0001g0050 |
2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.35-2825G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677642 | |||||||
| chr4:158677782 | A | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.35-2685A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677782 | |||||||
| chr4:158677853 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.35-2614G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677853 | |||||||
| chr4:158677869 | G | GT | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-2597dupT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158677869 | ||||||
| chr4:158677924 | C | T | 1 | a0002c0002t0001g0230 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.35-2543C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158677924 | |||||||
| chr4:158678516 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1951A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678516 | |||||||
| chr4:158678535 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0222 |
5 | HG01361.hp1 HG01433.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1932A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678535 | |||||||
| chr4:158678556 | A | G | 2 | a0002c0002t0001g0014 a0002c0002t0002g0037 |
3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.35-1911A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678556 | |||||||
| chr4:158678653 | C | CT | 208 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.35-1798dupT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158678653 | ||||||
| chr4:158678653 | C | CTT | 7 | a0001c0001t0001g0042 a0001c0001t0001g0220 a0001c0001t0001g0221 others(4): Show |
7 | HG01071.hp1 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-1799_35-1798dup others(2): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158678653 | ||||||
| chr4:158678793 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1674G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678793 | |||||||
| chr4:158678794 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.35-1673C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678794 | |||||||
| chr4:158678805 | A | C | 1 | a0002c0002t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.35-1662A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678805 | |||||||
| chr4:158678879 | T | G | 5 | a0002c0002t0001g0043 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1588T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678879 | |||||||
| chr4:158678977 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1490A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678977 | |||||||
| chr4:158678994 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1473G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158678994 | |||||||
| chr4:158679054 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1413C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679054 | |||||||
| chr4:158679293 | C | T | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.35-1174C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679293 | |||||||
| chr4:158679314 | C | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-1153C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679314 | |||||||
| chr4:158679473 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 |
5 | HG00408.hp1 HG02027.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-994C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679473 | |||||||
| chr4:158679755 | A | G | 1 | a0001c0001t0007g0219 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.35-712A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679755 | |||||||
| chr4:158679774 | T | C | 1 | a0002c0002t0003g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.35-693T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679774 | |||||||
| chr4:158679898 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-569C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158679898 | |||||||
| chr4:158680078 | C | CT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.35-388dupT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680078 | ||||||
| chr4:158680084 | C | CAAAAAAA others(3): Show |
37 | a0001c0001t0008g0216 a0002c0002t0001g0001 a0002c0002t0001g0017 others(34): Show |
47 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.35-375_35-366dupAA others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680084 | ||||||
| chr4:158680084 | C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0034 a0002c0002t0001g0046 a0002c0002t0001g0086 others(11): Show |
15 | HG00642.hp1 HG01517.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.35-376_35-366dupAA others(9): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680084 | ||||||
| chr4:158680084 | C | CAAAAAAA others(5): Show |
107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.35-377_35-366dupAA others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680084 | ||||||
| chr4:158680084 | C | CAAAAAAA others(6): Show |
34 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0044 others(31): Show |
37 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.35-378_35-366dupAA others(11): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680084 | ||||||
| chr4:158680084 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0002g0227 a0002c0002t0001g0077 a0002c0002t0001g0123 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-379_35-366dupAA others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680084 | ||||||
| chr4:158680092 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0217 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.35-366_35-365insAA others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 158680092 | ||||||
| chr4:158680182 | G | A | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35-285G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 1/12 | chr4 | 158680182 | |||||||
| chr4:158680705 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+98T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158680705 | |||||||
| chr4:158680770 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.175+163A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158680770 | |||||||
| chr4:158680809 | G | GA | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+206dupA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 158680809 | ||||||
| chr4:158680959 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.175+352C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158680959 | |||||||
| chr4:158681043 | TCTTA | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.175+441_175+444del others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 158681043 | ||||||
| chr4:158681177 | G | A | 7 | a0002c0002t0001g0053 a0002c0002t0001g0055 a0002c0002t0001g0056 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+570G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681177 | |||||||
| chr4:158681195 | G | A | 3 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 |
3 | HG02280.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.175+588G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681195 | |||||||
| chr4:158681387 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.175+780T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681387 | |||||||
| chr4:158681410 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-785A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681410 | |||||||
| chr4:158681817 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-378T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681817 | |||||||
| chr4:158681946 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.176-249T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 2/12 | chr4 | 158681946 | |||||||
| chr4:158682597 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+173G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158682597 | |||||||
| chr4:158682905 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405+481T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158682905 | |||||||
| chr4:158683072 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.405+648G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683072 | |||||||
| chr4:158683143 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+719A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683143 | |||||||
| chr4:158683193 | G | A | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.405+769G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683193 | |||||||
| chr4:158683262 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+838T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683262 | |||||||
| chr4:158683309 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.405+885G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683309 | |||||||
| chr4:158683409 | C | T | 1 | a0002c0002t0003g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.405+985C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683409 | |||||||
| chr4:158683465 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.405+1041A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683465 | |||||||
| chr4:158683605 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-987G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683605 | |||||||
| chr4:158683634 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-958C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683634 | |||||||
| chr4:158683707 | G | A | 1 | a0002c0002t0001g0043 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.406-885G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158683707 | |||||||
| chr4:158684028 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0041 |
4 | HG00408.hp1 HG02027.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-564C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684028 | |||||||
| chr4:158684029 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-563G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684029 | |||||||
| chr4:158684063 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.406-529T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684063 | |||||||
| chr4:158684095 | A | G | 2 | a0002c0002t0001g0120 a0002c0002t0003g0119 |
2 | NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.406-497A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684095 | |||||||
| chr4:158684389 | C | CA | 5 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0001g0066 others(2): Show |
6 | HG01884.hp1 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.406-185dupA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 158684389 | ||||||
| chr4:158684389 | CA | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.406-185delA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 158684389 | ||||||
| chr4:158684444 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-148G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684444 | |||||||
| chr4:158684553 | A | G | 2 | a0001c0001t0005g0148 a0001c0001t0005g0210 |
2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.406-39A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 3/12 | chr4 | 158684553 | |||||||
| chr4:158684723 | G | A | 3 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 |
3 | HG02280.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+50G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 4/12 | chr4 | 158684723 | |||||||
| chr4:158684838 | C | G | 1 | a0002c0002t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.487+165C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 4/12 | chr4 | 158684838 | |||||||
| chr4:158685233 | T | C | 1 | a0002c0002t0001g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.606+14T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685233 | |||||||
| chr4:158685340 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+121A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685340 | |||||||
| chr4:158685503 | G | C | 1 | a0002c0002t0003g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.606+284G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685503 | |||||||
| chr4:158685715 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.606+496G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685715 | |||||||
| chr4:158685716 | A | C | 1 | a0001c0001t0002g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.606+497A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685716 | |||||||
| chr4:158685750 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+531A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685750 | |||||||
| chr4:158685764 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0002g0032 a0001c0001t0002g0147 others(4): Show |
9 | HG02698.hp1 HG02738.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+545C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685764 | |||||||
| chr4:158685772 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.606+553C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158685772 | |||||||
| chr4:158686129 | A | G | 1 | a0001c0001t0006g0206 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.606+910A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686129 | |||||||
| chr4:158686236 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.606+1017T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686236 | |||||||
| chr4:158686263 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1044A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686263 | |||||||
| chr4:158686578 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1359T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686578 | |||||||
| chr4:158686579 | C | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1360C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686579 | |||||||
| chr4:158686712 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1493A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686712 | |||||||
| chr4:158686720 | C | A | 1 | a0001c0001t0002g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606+1501C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686720 | |||||||
| chr4:158686837 | C | G | 1 | a0002c0002t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.606+1618C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686837 | |||||||
| chr4:158686918 | G | A | 2 | a0002c0002t0002g0094 a0002c0002t0002g0155 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.606+1699G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686918 | |||||||
| chr4:158686930 | A | C | 2 | a0002c0002t0001g0204 a0002c0002t0001g0205 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.606+1711A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158686930 | |||||||
| chr4:158687010 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.606+1791G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687010 | |||||||
| chr4:158687049 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0004t0001g0023 |
3 | HG01081.hp2 HG01109.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.606+1830G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687049 | |||||||
| chr4:158687054 | T | A | 1 | a0002c0002t0001g0017 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.606+1835T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687054 | |||||||
| chr4:158687055 | C | A | 1 | a0002c0002t0001g0017 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.606+1836C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687055 | |||||||
| chr4:158687056 | A | G | 1 | a0002c0002t0001g0017 | 2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.606+1837A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687056 | |||||||
| chr4:158687256 | G | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.606+2037G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687256 | |||||||
| chr4:158687437 | A | T | 3 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 |
3 | HG02280.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.606+2218A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687437 | |||||||
| chr4:158687458 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+2239A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687458 | |||||||
| chr4:158687563 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+2344A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687563 | |||||||
| chr4:158687574 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.606+2355C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687574 | |||||||
| chr4:158687773 | G | T | 2 | a0002c0002t0001g0049 a0002c0002t0001g0050 |
2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.606+2554G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687773 | |||||||
| chr4:158687828 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.607-2520C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158687828 | |||||||
| chr4:158688081 | C | A | 1 | a0002c0002t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.607-2267C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688081 | |||||||
| chr4:158688131 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.607-2217T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688131 | |||||||
| chr4:158688136 | G | C | 3 | a0002c0002t0001g0012 a0002c0002t0001g0212 a0002c0002t0001g0213 |
5 | HG01891.hp1 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-2212G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688136 | |||||||
| chr4:158688169 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2179G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688169 | |||||||
| chr4:158688175 | C | T | 1 | a0002c0002t0001g0116 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.607-2173C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688175 | |||||||
| chr4:158688176 | G | A | 1 | a0002c0002t0004g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.607-2172G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688176 | |||||||
| chr4:158688302 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.607-2046G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688302 | |||||||
| chr4:158688365 | C | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0137 others(6): Show |
13 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.607-1983C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688365 | |||||||
| chr4:158688390 | CA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.607-1941delA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158688390 | ||||||
| chr4:158688469 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-1879A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688469 | |||||||
| chr4:158688500 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-1848T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688500 | |||||||
| chr4:158688546 | A | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.607-1802A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688546 | |||||||
| chr4:158688546 | A | T | 1 | a0002c0002t0002g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.607-1802A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688546 | |||||||
| chr4:158688589 | C | T | 4 | a0001c0001t0001g0180 a0002c0002t0001g0057 a0002c0002t0001g0058 others(1): Show |
4 | HG02280.hp2 HG02970.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-1759C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688589 | |||||||
| chr4:158688668 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-1680A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688668 | |||||||
| chr4:158688672 | C | G | 49 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(46): Show |
59 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.607-1676C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688672 | |||||||
| chr4:158688689 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.607-1659A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688689 | |||||||
| chr4:158688731 | C | CTA | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-1616_607-1615i others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158688731 | ||||||
| chr4:158688782 | G | A | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.607-1566G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688782 | |||||||
| chr4:158688807 | C | T | 4 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 others(1): Show |
5 | HG03139.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-1541C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688807 | |||||||
| chr4:158688816 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.607-1532T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158688816 | |||||||
| chr4:158689150 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.607-1198G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689150 | |||||||
| chr4:158689251 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.607-1097A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689251 | |||||||
| chr4:158689272 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.607-1076C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689272 | |||||||
| chr4:158689352 | G | T | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.607-996G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689352 | |||||||
| chr4:158689431 | C | G | 1 | a0002c0002t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.607-917C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689431 | |||||||
| chr4:158689434 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-914G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689434 | |||||||
| chr4:158689577 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.607-771G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689577 | |||||||
| chr4:158689595 | C | CATATACA others(7): Show |
1 | a0001c0001t0001g0158 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.607-748_607-747ins others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(3): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0002g0186 others(1): Show |
5 | HG03490.hp2 HG03492.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-720_607-711dup others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(5): Show |
5 | a0001c0001t0002g0139 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG00735.hp2 HG02027.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-722_607-711dup others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(7): Show |
6 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0001c0001t0002g0147 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-724_607-711dup others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(9): Show |
2 | a0001c0001t0001g0061 a0001c0001t0002g0032 |
3 | HG01192.hp2 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.607-726_607-711dup others(16): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(13): Show |
2 | a0001c0001t0002g0081 a0001c0001t0002g0208 |
2 | HG03491.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.607-730_607-711dup others(20): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0188 a0001c0001t0002g0207 |
2 | HG04228.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.607-732_607-711dup others(22): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CAT | C | 17 | a0001c0001t0001g0187 a0001c0001t0001g0221 a0001c0001t0002g0013 others(14): Show |
21 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.607-712_607-711del others(2): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATAT | C | 7 | a0002c0002t0001g0068 a0002c0002t0001g0078 a0002c0002t0001g0086 others(4): Show |
7 | HG01081.hp1 HG02129.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-714_607-711del others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATAT | C | 10 | a0002c0002t0001g0017 a0002c0002t0001g0051 a0002c0002t0001g0057 others(7): Show |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.607-716_607-711del others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0047 a0002c0002t0001g0043 a0002c0002t0001g0052 others(3): Show |
6 | HG01109.hp1 HG03041.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-718_607-711del others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(3): Show |
C | 12 | a0001c0001t0002g0202 a0002c0002t0001g0015 a0002c0002t0001g0035 others(9): Show |
14 | HG01123.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-720_607-711del others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(5): Show |
C | 7 | a0001c0001t0002g0203 a0002c0002t0001g0016 a0002c0002t0001g0072 others(4): Show |
12 | HG00735.hp1 HG01981.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.607-722_607-711del others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(7): Show |
C | 1 | a0001c0001t0001g0178 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.607-724_607-711del others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(11): Show |
C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0082 |
3 | HG01071.hp2 HG01192.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.607-728_607-711del others(18): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689595 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0179 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.607-734_607-711del others(24): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689595 | ||||||
| chr4:158689636 | A | ATATATAT others(33): Show |
1 | a0001c0001t0002g0195 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.607-711_607-710ins others(40): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0120 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.607-711_607-710ins others(30): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(15): Show |
3 | a0002c0002t0001g0009 a0002c0002t0001g0142 a0002c0002t0001g0153 |
3 | HG02630.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.607-711_607-710ins others(22): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0137 |
2 | NA18945.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.607-711_607-710ins others(20): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(11): Show |
2 | a0002c0002t0001g0116 a0002c0002t0001g0214 |
2 | HG03453.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.607-711_607-710ins others(18): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(7): Show |
10 | a0001c0001t0001g0131 a0001c0001t0001g0170 a0002c0002t0001g0009 others(7): Show |
11 | HG01099.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(5): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0024 others(11): Show |
16 | HG00280.hp2 HG00323.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(7): Show |
1 | a0001c0001t0008g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.607-711_607-710ins others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(3): Show |
12 | a0001c0001t0001g0034 a0001c0001t0001g0157 a0001c0001t0001g0159 others(9): Show |
12 | HG00621.hp2 HG00642.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATAT others(1): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0028 others(4): Show |
7 | HG00741.hp2 HG01928.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATATT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(13): Show |
17 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATATT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(21): Show |
29 | HG00408.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.607-711_607-710ins others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | ATT | 34 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.607-711_607-710dup others(2): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 158689636 | ||||||
| chr4:158689636 | A | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.607-712A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689636 | |||||||
| chr4:158689849 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0151 |
3 | HG01928.hp1 HG02004.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.607-499T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689849 | |||||||
| chr4:158689971 | C | T | 7 | a0002c0002t0001g0001 a0002c0002t0001g0020 a0002c0002t0001g0090 others(4): Show |
14 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-377C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158689971 | |||||||
| chr4:158690013 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.607-335C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158690013 | |||||||
| chr4:158690020 | A | G | 1 | a0002c0002t0009g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.607-328A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158690020 | |||||||
| chr4:158690059 | G | A | 2 | a0002c0002t0001g0018 a0002c0002t0001g0095 |
3 | HG02976.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.607-289G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158690059 | |||||||
| chr4:158690150 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.607-198G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158690150 | |||||||
| chr4:158690264 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.607-84A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 5/12 | chr4 | 158690264 | |||||||
| chr4:158690438 | A | C | 2 | a0002c0002t0001g0056 a0002c0002t0009g0054 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.684+13A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158690438 | |||||||
| chr4:158690543 | G | A | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+118G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158690543 | |||||||
| chr4:158690565 | G | C | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.684+140G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158690565 | |||||||
| chr4:158690679 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.684+254T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158690679 | |||||||
| chr4:158690689 | A | AAAG | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.684+273_684+275dup others(3): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158690689 | ||||||
| chr4:158690797 | A | G | 3 | a0002c0002t0001g0043 a0002c0002t0001g0051 a0002c0002t0001g0052 |
3 | HG02109.hp1 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.684+372A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158690797 | |||||||
| chr4:158690879 | A | AAAATAAA others(1): Show |
2 | a0002c0002t0001g0014 a0002c0002t0002g0037 |
3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.684+474_684+481dup others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158690879 | ||||||
| chr4:158690879 | A | AAAATAAA others(5): Show |
1 | a0002c0002t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.684+470_684+481dup others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158690879 | ||||||
| chr4:158691150 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.684+725G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691150 | |||||||
| chr4:158691166 | T | C | 32 | a0002c0002t0001g0001 a0002c0002t0001g0019 a0002c0002t0001g0020 others(29): Show |
40 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.684+741T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691166 | |||||||
| chr4:158691182 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.684+757A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691182 | |||||||
| chr4:158691315 | C | CGTGT | 5 | a0002c0002t0001g0019 a0002c0002t0001g0087 a0002c0002t0001g0098 others(2): Show |
6 | HG01884.hp2 HG01943.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+890_684+891ins others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691315 | |||||||
| chr4:158691316 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.684+891A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691316 | |||||||
| chr4:158691316 | A | T | 5 | a0002c0002t0001g0019 a0002c0002t0001g0087 a0002c0002t0001g0098 others(2): Show |
6 | HG01884.hp2 HG01943.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+891A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691316 | |||||||
| chr4:158691320 | T | G | 1 | a0002c0002t0001g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.684+895T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691320 | |||||||
| chr4:158691450 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+1025G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691450 | |||||||
| chr4:158691603 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0008g0216 |
2 | HG00639.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.684+1178G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691603 | |||||||
| chr4:158691613 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.684+1188G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691613 | |||||||
| chr4:158691729 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+1304G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691729 | |||||||
| chr4:158691730 | G | A | 1 | a0002c0002t0003g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.684+1305G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691730 | |||||||
| chr4:158691781 | A | C | 2 | a0001c0001t0002g0199 a0001c0001t0002g0201 |
2 | HG00438.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.684+1356A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691781 | |||||||
| chr4:158691782 | A | T | 2 | a0001c0001t0002g0199 a0001c0001t0002g0201 |
2 | HG00438.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.684+1357A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691782 | |||||||
| chr4:158691881 | A | G | 1 | a0002c0002t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.684+1456A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158691881 | |||||||
| chr4:158692150 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.684+1725T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692150 | |||||||
| chr4:158692162 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00423.hp2 NA18945.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1737G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692162 | |||||||
| chr4:158692374 | T | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG00140.hp2 HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.684+1949T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692374 | |||||||
| chr4:158692399 | C | CA | 10 | a0002c0002t0001g0020 a0002c0002t0001g0050 a0002c0002t0001g0072 others(7): Show |
11 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+1999dupA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692399 | ||||||
| chr4:158692399 | CA | C | 5 | a0002c0002t0001g0019 a0002c0002t0001g0098 a0002c0002t0001g0112 others(2): Show |
6 | HG01123.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+1999delA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692399 | ||||||
| chr4:158692399 | CAAAAAA | C | 28 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0033 others(25): Show |
32 | HG00735.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.684+1994_684+1999d others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692399 | ||||||
| chr4:158692399 | CAAAAAAA | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.684+1993_684+1999d others(9): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692399 | ||||||
| chr4:158692399 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.684+1984_684+1999d others(18): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692399 | ||||||
| chr4:158692467 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2042A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692467 | |||||||
| chr4:158692489 | T | G | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.684+2064T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692489 | |||||||
| chr4:158692633 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2208C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692633 | |||||||
| chr4:158692709 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.684+2284A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692709 | |||||||
| chr4:158692809 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2384A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692809 | |||||||
| chr4:158692837 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2412A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692837 | |||||||
| chr4:158692858 | TA | T | 16 | a0002c0002t0001g0009 a0002c0002t0001g0012 a0002c0002t0001g0077 others(13): Show |
20 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.684+2447delA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692858 | ||||||
| chr4:158692876 | TAA | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(99): Show |
129 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.684+2463_684+2464d others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692876 | ||||||
| chr4:158692886 | A | ATAT | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0230 |
3 | HG01123.hp1 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.684+2461_684+2462i others(5): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692886 | |||||||
| chr4:158692888 | A | T | 17 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0044 others(14): Show |
17 | HG00280.hp1 HG00621.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.684+2463A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692888 | |||||||
| chr4:158692888 | AAC | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(90): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.684+2465_684+2466d others(4): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692888 | ||||||
| chr4:158692889 | AC | A | 3 | a0001c0001t0002g0045 a0002c0002t0001g0050 a0002c0002t0001g0052 |
3 | HG02647.hp2 HG03041.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.684+2465delC | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692889 | |||||||
| chr4:158692890 | C | A | 3 | a0002c0002t0001g0049 a0002c0002t0001g0051 a0002c0002t0001g0055 |
3 | HG02109.hp1 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.684+2465C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692890 | |||||||
| chr4:158692890 | C | CATAT | 3 | a0002c0002t0001g0016 a0002c0002t0001g0072 a0002c0002t0001g0073 |
4 | HG01981.hp2 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+2480_684+2483d others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158692890 | ||||||
| chr4:158692890 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.684+2465C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692890 | |||||||
| chr4:158692892 | T | A | 26 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0061 others(23): Show |
29 | HG00735.hp2 HG00741.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.684+2467T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692892 | |||||||
| chr4:158692894 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0002g0125 |
2 | NA18999.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.684+2469T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158692894 | |||||||
| chr4:158693156 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.685-2341C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693156 | |||||||
| chr4:158693210 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.685-2287G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693210 | |||||||
| chr4:158693252 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.685-2245G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693252 | |||||||
| chr4:158693766 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-1731A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693766 | |||||||
| chr4:158693795 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-1702G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693795 | |||||||
| chr4:158693819 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.685-1678T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693819 | |||||||
| chr4:158693886 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.685-1611G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693886 | |||||||
| chr4:158693913 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.685-1584G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158693913 | |||||||
| chr4:158694006 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00741.hp1 HG01192.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.685-1491G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694006 | |||||||
| chr4:158694022 | A | T | 16 | a0001c0001t0001g0033 a0001c0001t0002g0032 a0001c0001t0002g0045 others(13): Show |
18 | HG00735.hp2 HG02027.hp2 HG02698.hp1 others(15): Show |
intron_variant | MODIFIER | c.685-1475A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694022 | |||||||
| chr4:158694164 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.685-1333C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694164 | |||||||
| chr4:158694290 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0235 |
5 | HG00323.hp2 HG01258.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-1207G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694290 | |||||||
| chr4:158694322 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-1175A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694322 | |||||||
| chr4:158694542 | C | T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0205 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.685-955C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694542 | |||||||
| chr4:158694594 | CA | C | 8 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0053 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-888delA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 158694594 | ||||||
| chr4:158694678 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.685-819T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694678 | |||||||
| chr4:158694856 | T | C | 1 | a0002c0002t0004g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-641T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694856 | |||||||
| chr4:158694899 | T | C | 3 | a0002c0002t0001g0043 a0002c0002t0001g0051 a0002c0002t0001g0052 |
3 | HG02109.hp1 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.685-598T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694899 | |||||||
| chr4:158694964 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-533G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158694964 | |||||||
| chr4:158695014 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-483T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695014 | |||||||
| chr4:158695034 | A | G | 1 | a0002c0002t0009g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-463A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695034 | |||||||
| chr4:158695056 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.685-441G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695056 | |||||||
| chr4:158695140 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-357G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695140 | |||||||
| chr4:158695169 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.685-328G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695169 | |||||||
| chr4:158695294 | A | G | 1 | a0002c0002t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.685-203A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695294 | |||||||
| chr4:158695348 | A | G | 1 | a0001c0001t0002g0196 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.685-149A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695348 | |||||||
| chr4:158695364 | G | C | 1 | a0002c0002t0001g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.685-133G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695364 | |||||||
| chr4:158695438 | G | A | 1 | a0001c0001t0008g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.685-59G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 6/12 | chr4 | 158695438 | |||||||
| chr4:158695829 | A | G | 1 | a0002c0002t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.831+186A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158695829 | |||||||
| chr4:158695867 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.831+224C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158695867 | |||||||
| chr4:158695937 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0009g0054 |
2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.831+294G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158695937 | |||||||
| chr4:158696492 | T | C | 2 | a0002c0002t0001g0053 a0002c0002t0001g0055 |
2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.831+849T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696492 | |||||||
| chr4:158696631 | G | A | 1 | a0001c0001t0002g0022 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.832-928G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696631 | |||||||
| chr4:158696725 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-834T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696725 | |||||||
| chr4:158696746 | G | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.832-813G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696746 | |||||||
| chr4:158696782 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-777A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696782 | |||||||
| chr4:158696979 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.832-580T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158696979 | |||||||
| chr4:158697013 | G | A | 1 | a0002c0002t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832-546G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158697013 | |||||||
| chr4:158697059 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0036 a0002c0002t0002g0037 |
4 | HG03139.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-500T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158697059 | |||||||
| chr4:158697241 | T | C | 6 | a0002c0002t0001g0017 a0002c0002t0001g0086 a0002c0002t0001g0113 others(3): Show |
7 | HG02129.hp2 HG03239.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-318T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158697241 | |||||||
| chr4:158697374 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.832-185C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 7/12 | chr4 | 158697374 | |||||||
| chr4:158698091 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.972+392C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698091 | |||||||
| chr4:158698144 | T | A | 1 | a0002c0002t0001g0090 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.972+445T>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698144 | |||||||
| chr4:158698190 | C | T | 8 | a0002c0002t0001g0060 a0002c0002t0001g0086 a0002c0002t0001g0089 others(5): Show |
8 | HG02129.hp2 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.972+491C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698190 | |||||||
| chr4:158698274 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.972+575T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698274 | |||||||
| chr4:158698365 | C | G | 1 | a0002c0002t0001g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.973-622C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698365 | |||||||
| chr4:158698495 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.973-492T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698495 | |||||||
| chr4:158698526 | G | T | 2 | a0001c0001t0002g0172 a0001c0001t0002g0186 |
2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.973-461G>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698526 | |||||||
| chr4:158698788 | TCCTTTTC others(4): Show |
T | 1 | a0002c0002t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.973-188_973-178del others(11): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr4 | 158698788 | ||||||
| chr4:158698883 | A | C | 96 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.973-104A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698883 | |||||||
| chr4:158698890 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.973-97T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 8/12 | chr4 | 158698890 | |||||||
| chr4:158699202 | T | C | 8 | a0001c0001t0001g0137 a0001c0001t0001g0167 a0002c0002t0001g0001 others(5): Show |
15 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1116+72T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699202 | |||||||
| chr4:158699271 | A | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1116+141A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699271 | |||||||
| chr4:158699438 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1116+308C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699438 | |||||||
| chr4:158699505 | G | A | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1116+375G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699505 | |||||||
| chr4:158699634 | A | T | 1 | a0002c0002t0001g0014 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+504A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699634 | |||||||
| chr4:158699730 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1116+600A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158699730 | |||||||
| chr4:158700033 | A | T | 57 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(54): Show |
70 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1116+903A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700033 | |||||||
| chr4:158700098 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1116+968C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700098 | |||||||
| chr4:158700113 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1116+983A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700113 | |||||||
| chr4:158700222 | TTATAAA | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0182 others(5): Show |
8 | HG02129.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116+1098_1116+110 others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700222 | ||||||
| chr4:158700330 | G | GAAATA | 3 | a0001c0001t0002g0144 a0001c0001t0002g0145 a0001c0001t0002g0197 |
3 | HG00140.hp2 HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1116+1201_1116+120 others(9): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700330 | ||||||
| chr4:158700530 | CAGG | C | 33 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(30): Show |
42 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1116+1403_1116+140 others(7): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700530 | ||||||
| chr4:158700556 | C | CCA | 3 | a0002c0002t0001g0014 a0002c0002t0001g0117 a0002c0002t0003g0102 |
4 | HG01081.hp1 HG03139.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+1440_1116+144 others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700556 | ||||||
| chr4:158700570 | ACG | A | 56 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(53): Show |
69 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1116+1442_1116+144 others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700570 | ||||||
| chr4:158700572 | G | A | 29 | a0001c0001t0002g0130 a0001c0001t0002g0152 a0001c0001t0002g0195 others(26): Show |
33 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1116+1442G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700572 | |||||||
| chr4:158700572 | G | GCA | 4 | a0002c0002t0001g0016 a0002c0002t0001g0036 a0002c0002t0001g0073 others(1): Show |
5 | HG02630.hp1 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+1470_1116+147 others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700572 | GCA | G | 16 | a0001c0001t0001g0028 a0001c0001t0001g0192 a0002c0002t0001g0009 others(13): Show |
19 | HG01123.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1116+1470_1116+147 others(6): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700572 | GCACA | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
9 | HG01261.hp1 HG02129.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1116+1468_1116+147 others(8): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700572 | GCACACA | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1116+1466_1116+147 others(10): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700572 | GCACACAC others(1): Show |
G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0149 others(3): Show |
7 | HG00621.hp1 HG01255.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+1464_1116+147 others(12): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700572 | GCACACAC others(3): Show |
G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1116+1462_1116+147 others(14): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700572 | ||||||
| chr4:158700574 | A | G | 28 | a0001c0001t0002g0130 a0001c0001t0002g0195 a0001c0001t0003g0175 others(25): Show |
32 | HG00597.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.1116+1444A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700574 | |||||||
| chr4:158700576 | A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0014 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+1461_1116+146 others(20): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158700576 | ||||||
| chr4:158700576 | A | G | 57 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(54): Show |
70 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1116+1446A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700576 | |||||||
| chr4:158700580 | A | G | 1 | a0001c0001t0008g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1116+1450A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700580 | |||||||
| chr4:158700845 | G | A | 79 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(76): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1116+1715G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700845 | |||||||
| chr4:158700907 | G | A | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1116+1777G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158700907 | |||||||
| chr4:158701045 | T | C | 2 | a0002c0002t0001g0036 a0002c0002t0001g0117 |
2 | HG01081.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1116+1915T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701045 | |||||||
| chr4:158701093 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1116+1963C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701093 | |||||||
| chr4:158701094 | G | A | 9 | a0002c0002t0001g0012 a0002c0002t0001g0018 a0002c0002t0001g0092 others(6): Show |
12 | HG01891.hp1 HG02109.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116+1964G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701094 | |||||||
| chr4:158701268 | G | C | 1 | a0001c0001t0002g0203 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1116+2138G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701268 | |||||||
| chr4:158701315 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0160 |
2 | HG00423.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1117-2108C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701315 | |||||||
| chr4:158701553 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1117-1870A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701553 | |||||||
| chr4:158701672 | C | T | 11 | a0001c0001t0001g0192 a0002c0002t0001g0009 a0002c0002t0001g0077 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-1751C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701672 | |||||||
| chr4:158701758 | A | T | 57 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(54): Show |
70 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1117-1665A>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701758 | |||||||
| chr4:158701794 | C | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-1629C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701794 | |||||||
| chr4:158701854 | C | T | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-1569C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158701854 | |||||||
| chr4:158702014 | T | C | 2 | a0002c0002t0001g0099 a0002c0002t0001g0105 |
2 | HG01517.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1117-1409T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702014 | |||||||
| chr4:158702155 | G | GT | 20 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0187 others(17): Show |
20 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1117-1256dupT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158702155 | ||||||
| chr4:158702155 | GT | G | 10 | a0001c0001t0001g0132 a0001c0001t0002g0022 a0001c0001t0002g0029 others(7): Show |
12 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.1117-1256delT | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 158702155 | ||||||
| chr4:158702404 | T | G | 11 | a0001c0001t0001g0192 a0002c0002t0001g0009 a0002c0002t0001g0077 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-1019T>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702404 | |||||||
| chr4:158702422 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1117-1001A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702422 | |||||||
| chr4:158702444 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1117-979C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702444 | |||||||
| chr4:158702463 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1117-960G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702463 | |||||||
| chr4:158702575 | C | A | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-848C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702575 | |||||||
| chr4:158702692 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1117-731T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702692 | |||||||
| chr4:158702875 | GC | G | 3 | a0002c0002t0001g0066 a0002c0002t0001g0069 a0002c0002t0001g0089 |
3 | HG01884.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1117-547delC | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702875 | |||||||
| chr4:158702912 | G | A | 10 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0182 others(7): Show |
11 | HG02129.hp2 HG02647.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.1117-511G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702912 | |||||||
| chr4:158702940 | A | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-483A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158702940 | |||||||
| chr4:158703139 | C | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-284C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158703139 | |||||||
| chr4:158703191 | G | A | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-232G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158703191 | |||||||
| chr4:158703230 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0141 a0001c0001t0002g0146 |
5 | HG00423.hp1 NA18966.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-193T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158703230 | |||||||
| chr4:158703311 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0001c0001t0001g0193 |
4 | HG01109.hp2 HG01943.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-112A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 9/12 | chr4 | 158703311 | |||||||
| chr4:158703762 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1285+171T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158703762 | |||||||
| chr4:158703855 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1285+264G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158703855 | |||||||
| chr4:158703967 | C | T | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1285+376C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158703967 | |||||||
| chr4:158703976 | G | A | 1 | a0002c0002t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1285+385G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158703976 | |||||||
| chr4:158704097 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1285+506C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704097 | |||||||
| chr4:158704107 | C | CA | 3 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 |
3 | HG02280.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1285+522dupA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 158704107 | ||||||
| chr4:158704240 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1285+649A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704240 | |||||||
| chr4:158704296 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1285+705T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704296 | |||||||
| chr4:158704432 | C | T | 8 | a0002c0002t0001g0056 a0002c0002t0001g0057 a0002c0002t0001g0058 others(5): Show |
8 | HG01123.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1285+841C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704432 | |||||||
| chr4:158704501 | G | A | 33 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0022 others(30): Show |
42 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1285+910G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704501 | |||||||
| chr4:158704605 | A | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0055 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1285+1014A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704605 | |||||||
| chr4:158704616 | G | A | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1285+1025G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704616 | |||||||
| chr4:158704692 | A | G | 4 | a0002c0002t0001g0018 a0002c0002t0001g0068 a0002c0002t0001g0092 others(1): Show |
5 | HG02280.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1285+1101A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158704692 | |||||||
| chr4:158705017 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1286-1172T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705017 | |||||||
| chr4:158705267 | T | C | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1286-922T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705267 | |||||||
| chr4:158705495 | C | G | 1 | a0001c0001t0001g0028 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1286-694C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705495 | |||||||
| chr4:158705618 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1286-571G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705618 | |||||||
| chr4:158705657 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1286-532A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705657 | |||||||
| chr4:158705659 | G | C | 1 | a0002c0002t0004g0065 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1286-530G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705659 | |||||||
| chr4:158705744 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1286-445G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705744 | |||||||
| chr4:158705931 | G | A | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1286-258G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158705931 | |||||||
| chr4:158706035 | C | T | 2 | a0002c0002t0001g0108 a0002c0002t0001g0204 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1286-154C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 10/12 | chr4 | 158706035 | |||||||
| chr4:158706386 | A | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0055 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1468+15A>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 11/12 | chr4 | 158706386 | |||||||
| chr4:158706588 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1469-41A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 11/12 | chr4 | 158706588 | |||||||
| chr4:158706865 | C | T | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1690+15C>T | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158706865 | |||||||
| chr4:158707038 | C | CA | 12 | a0001c0001t0001g0028 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
14 | HG02129.hp2 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1690+203dupA | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 158707038 | ||||||
| chr4:158707142 | C | A | 21 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0001t0002g0062 others(18): Show |
21 | HG00735.hp2 HG00738.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.1690+292C>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707142 | |||||||
| chr4:158707370 | A | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0001g0165 others(2): Show |
5 | HG00597.hp2 HG01099.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690+520A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707370 | |||||||
| chr4:158707371 | C | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1690+521C>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707371 | |||||||
| chr4:158707508 | C | CG | 2 | a0002c0002t0002g0003 a0002c0002t0002g0075 |
6 | HG02895.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+658_1690+659i others(3): Show |
ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707508 | |||||||
| chr4:158707512 | T | C | 2 | a0002c0002t0002g0003 a0002c0002t0002g0075 |
6 | HG02895.hp2 HG02897.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+662T>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707512 | |||||||
| chr4:158707747 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1691-617G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707747 | |||||||
| chr4:158707899 | A | AG | 1 | a0001c0001t0001g0011 | 3 | NA18950.hp1 NA18968.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1691-464dupG | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 158707899 | ||||||
| chr4:158707926 | G | A | 6 | a0001c0001t0002g0032 a0001c0001t0002g0147 a0001c0001t0002g0207 others(3): Show |
7 | HG02698.hp1 HG02738.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1691-438G>A | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707926 | |||||||
| chr4:158707999 | G | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1691-365G>C | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158707999 | |||||||
| chr4:158708114 | A | G | 2 | a0002c0002t0004g0065 a0002c0002t0004g0231 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1691-250A>G | ETFDH | ENSG00000171503.13 | transcript | ENST00000511912.6 | protein_coding | 12/12 | chr4 | 158708114 |