Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3033 |
| ensemblid | ENSG00000138796.18 |
| hgncid | 4799 |
| symbol | HADH |
| name | hydroxyacyl-CoA dehydrogenase |
| refseq_nuc | NM_005327.7 |
| refseq_prot | NP_005318.6 |
| ensembl_nuc | ENST00000309522.8 |
| ensembl_prot | ENSP00000312288.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 107989889 |
| end | 108035171 |
| strand | + |
| ver | v1.2 |
| region | chr4:107989889-108035171 |
| region5000 | chr4:107984889-108040171 |
| regionname0 | HADH_chr4_107989889_108035171 |
| regionname5000 | HADH_chr4_107984889_108040171 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 314 | 249 | 50 | 59 | 90 | 15 | 35 | 62 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0002 | 1/1 | 314 | 45 | 30 | 3 | 5 | 0 | 5 | 4 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0003 | 0/0 | 314 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0004 | 0/0 | 314 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0005 | 0/0 | 314 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0006 | 0/0 | 314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| a0007 | 0/0 | 314 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | MAFVT others(309): Show |
chr4 | 107984889 | 108040171 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 942 | 249 | 50 | 59 | 90 | 15 | 35 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0002c0002 | 1/1 | 942 | 45 | 30 | 3 | 5 | 0 | 5 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0003c0004 | 0/0 | 942 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0004c0003 | 0/0 | 942 | 3 | 3 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0005c0005 | 0/0 | 942 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0006c0007 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 | ||
| a0007c0006 | 0/0 | 942 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | ATGGC others(937): Show |
chr4 | 107984889 | 108040171 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1803 | 222 | 48 | 50 | 81 | 14 | 29 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0001c0001t0003 | 0/0 | 1803 | 21 | 2 | 9 | 4 | 1 | 5 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0001c0001t0004 | 0/0 | 1803 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0001c0001t0006 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0001c0001t0007 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0001c0001t0008 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0002c0002t0001 | 1/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0002c0002t0002 | 0/1 | 1803 | 44 | 30 | 3 | 5 | 0 | 5 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0003c0004t0001 | 0/0 | 1803 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0004c0003t0001 | 0/0 | 1803 | 3 | 3 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0005c0005t0005 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0006c0007t0002 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| a0007c0006t0001 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | CTTCC others(1798): Show |
chr4 | 107984889 | 108040171 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 2 | 10 | 0 | 8 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 4 | 9 | 0 | 2 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0002 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0008 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0003c0004t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0004c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0004c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0004c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0005c0005t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0006c0007t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| a0007c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0113 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0173 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02056 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0175 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0185 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02572 | hp1 | a0005 | c0005 | t0005 | g0031 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02630 | hp2 | a0005 | c0005 | t0005 | g0031 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02895 | hp1 | a0004 | c0003 | t0001 | g0041 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02897 | hp1 | a0004 | c0003 | t0001 | g0037 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03041 | hp2 | a0004 | c0003 | t0001 | g0040 | AFR | GWD | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0164 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03225 | hp2 | a0006 | c0007 | t0002 | g0182 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0171 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0001 | SAS | STU | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18945 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0170 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19076 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19082 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0176 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | ASW | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20805 | hp2 | a0007 | c0006 | t0001 | g0190 | EUR | TSI | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0172 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | USA | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0163 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0166 | REF | REF | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0071 | REF | REF | HADH_chr4_107984889_108040171 | HADH | chr4 | 107984889 | 108040171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107990031 | C | G | 1 | a0003 | 3 | HG02056.hp2 NA18945.hp1 NA19082.hp1 |
missense_variant | MODERATE | c.99C>G | p.Ile33Met | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/8 | 143/1803 | 99/945 | 33/314 | chr4 | 107990031 | |||
| chr4:108009883 | T | C | 5 | a0001 a0003 a0004 others(2): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
missense_variant | MODERATE | c.257T>C | p.Leu86Pro | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/8 | 301/1803 | 257/945 | 86/314 | chr4 | 108009883 | |||
| chr4:108014444 | T | G | 1 | a0007 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.275T>G | p.Phe92Cys | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/8 | 319/1803 | 275/945 | 92/314 | chr4 | 108014444 | |||
| chr4:108023541 | G | C | 1 | a0004 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.614G>C | p.Gly205Ala | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/8 | 658/1803 | 614/945 | 205/314 | chr4 | 108023541 | |||
| chr4:108027713 | G | A | 1 | a0006 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.662G>A | p.Arg221His | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/8 | 706/1803 | 662/945 | 221/314 | chr4 | 108027713 | |||
| chr4:108034293 | A | G | 1 | a0005 | 2 | HG02572.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.881A>G | p.Asn294Ser | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 925/1803 | 881/945 | 294/314 | chr4 | 108034293 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107989895 | T | C | 2 | a0002c0002t0002 a0006c0007t0002 |
44 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(41): Show |
5_prime_UTR_variant | MODIFIER | c.-38T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/8 | 38 | chr4 | 107989895 | ||||||
| chr4:108034416 | G | A | 1 | a0001c0001t0006 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 59 | chr4 | 108034416 | ||||||
| chr4:108034466 | T | A | 1 | a0001c0001t0003 | 21 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*109T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 109 | chr4 | 108034466 | ||||||
| chr4:108034733 | C | T | 1 | a0001c0001t0008 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*376C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 376 | chr4 | 108034733 | ||||||
| chr4:108034734 | G | A | 1 | a0001c0001t0007 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 377 | chr4 | 108034734 | ||||||
| chr4:108034867 | T | C | 1 | a0005c0005t0005 | 2 | HG02572.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 510 | chr4 | 108034867 | ||||||
| chr4:108034871 | A | G | 1 | a0001c0001t0004 | 3 | HG00609.hp2 HG02027.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 514 | chr4 | 108034871 | ||||||
| chr4:108034889 | C | T | 1 | a0001c0001t0008 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*532C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 8/8 | 532 | chr4 | 108034889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:107990085 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+21C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990085 | |||||||
| chr4:107990153 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG00735.hp2 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.132+89A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990153 | |||||||
| chr4:107990157 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.132+93G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990157 | |||||||
| chr4:107990190 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+126C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990190 | |||||||
| chr4:107990390 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.132+326G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990390 | |||||||
| chr4:107990605 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+541T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990605 | |||||||
| chr4:107990621 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.132+557A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990621 | |||||||
| chr4:107990711 | G | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+647G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107990711 | |||||||
| chr4:107990735 | GTCTC | G | 3 | a0002c0002t0002g0200 a0002c0002t0002g0201 a0002c0002t0002g0202 |
3 | HG01891.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.132+677_132+680del others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107990735 | ||||||
| chr4:107990743 | C | CT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0032 others(21): Show |
29 | HG01069.hp2 HG01071.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.132+702dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107990743 | ||||||
| chr4:107990743 | C | CTT | 9 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
12 | HG01192.hp1 HG01978.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.132+701_132+702dup others(2): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107990743 | ||||||
| chr4:107990743 | CT | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG00558.hp2 HG01255.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+702delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107990743 | ||||||
| chr4:107991022 | T | A | 1 | a0002c0002t0002g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.132+958T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991022 | |||||||
| chr4:107991083 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.132+1019A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991083 | |||||||
| chr4:107991091 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.132+1027G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991091 | |||||||
| chr4:107991111 | C | G | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1047C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991111 | |||||||
| chr4:107991121 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.132+1057A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991121 | |||||||
| chr4:107991155 | C | CT | 9 | a0001c0001t0001g0055 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG00323.hp1 HG01496.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.132+1102dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107991155 | ||||||
| chr4:107991166 | T | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(10): Show |
19 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.132+1102T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991166 | |||||||
| chr4:107991167 | A | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 others(30): Show |
46 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.132+1103A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991167 | |||||||
| chr4:107991168 | A | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 others(30): Show |
46 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.132+1104A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991168 | |||||||
| chr4:107991169 | A | T | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+1105A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991169 | |||||||
| chr4:107991268 | G | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
15 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+1204G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991268 | |||||||
| chr4:107991512 | A | T | 68 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(65): Show |
86 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.132+1448A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991512 | |||||||
| chr4:107991541 | C | A | 3 | a0001c0001t0001g0034 a0002c0002t0002g0185 a0002c0002t0002g0192 |
3 | HG02055.hp2 HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.132+1477C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991541 | |||||||
| chr4:107991558 | AC | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+1496delC | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107991558 | ||||||
| chr4:107991560 | C | T | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+1496C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991560 | |||||||
| chr4:107991586 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.132+1522T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991586 | |||||||
| chr4:107991627 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.132+1563C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991627 | |||||||
| chr4:107991884 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.132+1820A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107991884 | |||||||
| chr4:107992327 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02630.hp1 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+2263G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992327 | |||||||
| chr4:107992450 | A | G | 1 | a0002c0002t0002g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+2386A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992450 | |||||||
| chr4:107992471 | C | A | 3 | a0002c0002t0002g0162 a0002c0002t0002g0163 a0002c0002t0002g0183 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.132+2407C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992471 | |||||||
| chr4:107992677 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.132+2613A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992677 | |||||||
| chr4:107992785 | G | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+2721G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992785 | |||||||
| chr4:107992927 | C | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
14 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+2863C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107992927 | |||||||
| chr4:107993065 | G | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
15 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+3001G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993065 | |||||||
| chr4:107993339 | A | G | 2 | a0002c0002t0002g0185 a0002c0002t0002g0192 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.132+3275A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993339 | |||||||
| chr4:107993420 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0158 |
3 | HG00408.hp1 NA18951.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.132+3356A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993420 | |||||||
| chr4:107993422 | T | C | 32 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(29): Show |
44 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.132+3358T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993422 | |||||||
| chr4:107993676 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+3612T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993676 | |||||||
| chr4:107993733 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+3669A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993733 | |||||||
| chr4:107993896 | G | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+3832G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993896 | |||||||
| chr4:107993906 | G | GT | 69 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(66): Show |
87 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.132+3849dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107993906 | ||||||
| chr4:107993969 | C | G | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+3905C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993969 | |||||||
| chr4:107993981 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.132+3917C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107993981 | |||||||
| chr4:107994247 | C | G | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+4183C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994247 | |||||||
| chr4:107994390 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.132+4326C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994390 | |||||||
| chr4:107994494 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+4430A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994494 | |||||||
| chr4:107994680 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.132+4616C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994680 | |||||||
| chr4:107994754 | G | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0066 |
3 | HG00609.hp2 HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.132+4690G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994754 | |||||||
| chr4:107994816 | C | T | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+4752C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107994816 | |||||||
| chr4:107995100 | C | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+5036C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995100 | |||||||
| chr4:107995262 | T | C | 66 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(63): Show |
84 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.132+5198T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995262 | |||||||
| chr4:107995263 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.132+5199G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995263 | |||||||
| chr4:107995391 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.132+5327C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995391 | |||||||
| chr4:107995400 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG00099.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.132+5336A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995400 | |||||||
| chr4:107995473 | C | T | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+5409C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995473 | |||||||
| chr4:107995549 | T | TAATCTC | 68 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(65): Show |
86 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.132+5486_132+5487i others(8): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107995549 | ||||||
| chr4:107995951 | A | G | 3 | a0002c0002t0002g0162 a0002c0002t0002g0163 a0002c0002t0002g0183 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.132+5887A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995951 | |||||||
| chr4:107995962 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.132+5898A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995962 | |||||||
| chr4:107995973 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.132+5909C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995973 | |||||||
| chr4:107995993 | T | A | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+5929T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107995993 | |||||||
| chr4:107996088 | T | G | 30 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(27): Show |
42 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.132+6024T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996088 | |||||||
| chr4:107996500 | A | AAAAATGG others(8): Show |
2 | a0002c0002t0002g0185 a0002c0002t0002g0192 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.132+6437_132+6451d others(17): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107996500 | ||||||
| chr4:107996509 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.132+6445C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996509 | |||||||
| chr4:107996510 | G | A | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+6446G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996510 | |||||||
| chr4:107996564 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.132+6500A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996564 | |||||||
| chr4:107996758 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
5 | HG01109.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+6694G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996758 | |||||||
| chr4:107996767 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.132+6703G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996767 | |||||||
| chr4:107996818 | C | T | 2 | a0001c0001t0003g0057 a0001c0001t0003g0150 |
2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.132+6754C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107996818 | |||||||
| chr4:107996893 | CA | C | 23 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0034 others(20): Show |
28 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.132+6846delA | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107996893 | ||||||
| chr4:107996893 | CAA | C | 21 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0009 others(18): Show |
33 | HG00558.hp1 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.132+6845_132+6846d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107996893 | ||||||
| chr4:107996893 | CAAA | C | 8 | a0002c0002t0002g0162 a0002c0002t0002g0163 a0002c0002t0002g0183 others(5): Show |
8 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.132+6844_132+6846d others(5): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 107996893 | ||||||
| chr4:107997085 | ACT | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+7022_132+7023d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997085 | |||||||
| chr4:107997088 | T | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+7024T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997088 | |||||||
| chr4:107997213 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.132+7149A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997213 | |||||||
| chr4:107997314 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | NA18968.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.132+7250G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997314 | |||||||
| chr4:107997381 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.132+7317G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997381 | |||||||
| chr4:107997437 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.132+7373T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997437 | |||||||
| chr4:107997449 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA19004.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.132+7385C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997449 | |||||||
| chr4:107997793 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.132+7729G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997793 | |||||||
| chr4:107997827 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+7763G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997827 | |||||||
| chr4:107997891 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0003g0191 |
2 | HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.132+7827G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997891 | |||||||
| chr4:107997971 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.132+7907C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107997971 | |||||||
| chr4:107998364 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.132+8300C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998364 | |||||||
| chr4:107998508 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(38): Show |
63 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.132+8444G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998508 | |||||||
| chr4:107998544 | C | T | 3 | a0004c0003t0001g0037 a0004c0003t0001g0040 a0004c0003t0001g0041 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.132+8480C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998544 | |||||||
| chr4:107998552 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.132+8488G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998552 | |||||||
| chr4:107998564 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+8500T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998564 | |||||||
| chr4:107998569 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+8505C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998569 | |||||||
| chr4:107998682 | T | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+8618T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998682 | |||||||
| chr4:107998940 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.132+8876G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998940 | |||||||
| chr4:107998988 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+8924A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998988 | |||||||
| chr4:107998996 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+8932T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107998996 | |||||||
| chr4:107999018 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01175.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.132+8954A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107999018 | |||||||
| chr4:107999511 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(8): Show |
11 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+9447C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107999511 | |||||||
| chr4:107999544 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132+9480C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107999544 | |||||||
| chr4:107999837 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.132+9773T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107999837 | |||||||
| chr4:107999982 | T | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG00735.hp2 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.133-9777T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 107999982 | |||||||
| chr4:108000012 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | NA18968.hp2 NA19004.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.133-9747T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000012 | |||||||
| chr4:108000174 | A | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.133-9585A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000174 | |||||||
| chr4:108000211 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(60): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.133-9548G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000211 | |||||||
| chr4:108000395 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.133-9364G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000395 | |||||||
| chr4:108000508 | G | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133-9251G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000508 | |||||||
| chr4:108000563 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.133-9196G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000563 | |||||||
| chr4:108000615 | A | G | 1 | a0002c0002t0002g0181 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133-9144A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000615 | |||||||
| chr4:108000652 | T | C | 1 | a0001c0001t0008g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133-9107T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000652 | |||||||
| chr4:108000685 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.133-9074T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000685 | |||||||
| chr4:108000836 | A | T | 1 | a0001c0001t0003g0144 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.133-8923A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108000836 | |||||||
| chr4:108001065 | T | G | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-8694T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001065 | |||||||
| chr4:108001087 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.133-8672T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001087 | |||||||
| chr4:108001302 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.133-8457G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001302 | |||||||
| chr4:108001310 | G | A | 1 | a0002c0002t0002g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.133-8449G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001310 | |||||||
| chr4:108001414 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.133-8345A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001414 | |||||||
| chr4:108001471 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.133-8288T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001471 | |||||||
| chr4:108001574 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.133-8185G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001574 | |||||||
| chr4:108001609 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.133-8150T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001609 | |||||||
| chr4:108001638 | TA | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG00735.hp2 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.133-8120delA | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001638 | |||||||
| chr4:108001642 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.133-8117C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001642 | |||||||
| chr4:108001759 | T | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.133-8000T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001759 | |||||||
| chr4:108001948 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.133-7811T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108001948 | |||||||
| chr4:108002185 | C | T | 10 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-7574C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002185 | |||||||
| chr4:108002186 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.133-7573G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002186 | |||||||
| chr4:108002358 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.133-7401G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002358 | |||||||
| chr4:108002555 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.133-7204C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002555 | |||||||
| chr4:108002749 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.133-7010G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002749 | |||||||
| chr4:108002927 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.133-6832A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002927 | |||||||
| chr4:108002967 | C | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.133-6792C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108002967 | |||||||
| chr4:108003053 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.133-6706G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003053 | |||||||
| chr4:108003105 | C | CT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.133-6635dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 108003105 | ||||||
| chr4:108003105 | C | CTT | 28 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
28 | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.133-6636_133-6635d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 108003105 | ||||||
| chr4:108003136 | C | G | 1 | a0002c0002t0002g0176 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133-6623C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003136 | |||||||
| chr4:108003194 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133-6565G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003194 | |||||||
| chr4:108003224 | A | G | 1 | a0002c0002t0002g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.133-6535A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003224 | |||||||
| chr4:108003302 | A | G | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-6457A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003302 | |||||||
| chr4:108003401 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(62): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.133-6358C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003401 | |||||||
| chr4:108003410 | C | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.133-6349C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003410 | |||||||
| chr4:108003521 | T | C | 1 | a0001c0001t0003g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.133-6238T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003521 | |||||||
| chr4:108003597 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0155 |
3 | HG02615.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.133-6162C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003597 | |||||||
| chr4:108003811 | TAA | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(10): Show |
19 | HG00673.hp1 HG01891.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.133-5934_133-5933d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 108003811 | ||||||
| chr4:108003811 | TAAA | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.133-5935_133-5933d others(5): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 108003811 | ||||||
| chr4:108003820 | A | C | 1 | a0002c0002t0002g0175 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.133-5939A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003820 | |||||||
| chr4:108003824 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.133-5935A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003824 | |||||||
| chr4:108003826 | A | AC | 2 | a0002c0002t0002g0003 a0002c0002t0002g0058 |
3 | HG02451.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.133-5932dupC | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 108003826 | ||||||
| chr4:108003837 | A | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.133-5922A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003837 | |||||||
| chr4:108003856 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.133-5903G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003856 | |||||||
| chr4:108003931 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-5828T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108003931 | |||||||
| chr4:108004097 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-5662T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004097 | |||||||
| chr4:108004111 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133-5648C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004111 | |||||||
| chr4:108004301 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.133-5458A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004301 | |||||||
| chr4:108004490 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-5269C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004490 | |||||||
| chr4:108004762 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-4997C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004762 | |||||||
| chr4:108004838 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-4921A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004838 | |||||||
| chr4:108004948 | G | A | 1 | a0006c0007t0002g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.133-4811G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004948 | |||||||
| chr4:108004952 | T | G | 3 | a0004c0003t0001g0037 a0004c0003t0001g0040 a0004c0003t0001g0041 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.133-4807T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108004952 | |||||||
| chr4:108005002 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.133-4757A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005002 | |||||||
| chr4:108005014 | T | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.133-4745T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005014 | |||||||
| chr4:108005049 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01358.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.133-4710C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005049 | |||||||
| chr4:108005053 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133-4706C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005053 | |||||||
| chr4:108005143 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-4616C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005143 | |||||||
| chr4:108005227 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.133-4532G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005227 | |||||||
| chr4:108005339 | G | T | 1 | a0001c0001t0003g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.133-4420G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005339 | |||||||
| chr4:108005461 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-4298G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005461 | |||||||
| chr4:108005642 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.133-4117G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005642 | |||||||
| chr4:108005657 | A | G | 3 | a0004c0003t0001g0037 a0004c0003t0001g0040 a0004c0003t0001g0041 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.133-4102A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108005657 | |||||||
| chr4:108006225 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0193 |
3 | HG01069.hp2 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.133-3534G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006225 | |||||||
| chr4:108006351 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0064 a0001c0001t0001g0143 |
5 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-3408G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006351 | |||||||
| chr4:108006375 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-3384C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006375 | |||||||
| chr4:108006584 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.133-3175C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006584 | |||||||
| chr4:108006685 | A | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.133-3074A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006685 | |||||||
| chr4:108006834 | A | C | 1 | a0002c0002t0002g0174 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.133-2925A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006834 | |||||||
| chr4:108006889 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-2870C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006889 | |||||||
| chr4:108006913 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.133-2846G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108006913 | |||||||
| chr4:108007018 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.133-2741G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007018 | |||||||
| chr4:108007099 | G | C | 1 | a0006c0007t0002g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.133-2660G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007099 | |||||||
| chr4:108007244 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.133-2515C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007244 | |||||||
| chr4:108007263 | C | T | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-2496C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007263 | |||||||
| chr4:108007267 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.133-2492C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007267 | |||||||
| chr4:108007308 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.133-2451C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007308 | |||||||
| chr4:108007578 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.133-2181C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007578 | |||||||
| chr4:108007579 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.133-2180G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007579 | |||||||
| chr4:108007640 | C | G | 1 | a0007c0006t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.133-2119C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007640 | |||||||
| chr4:108007727 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.133-2032A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108007727 | |||||||
| chr4:108008109 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.133-1650G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008109 | |||||||
| chr4:108008188 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-1571C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008188 | |||||||
| chr4:108008189 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.133-1570G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008189 | |||||||
| chr4:108008262 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.133-1497C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008262 | |||||||
| chr4:108008402 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.133-1357A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008402 | |||||||
| chr4:108008631 | T | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
15 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-1128T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008631 | |||||||
| chr4:108008725 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133-1034G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008725 | |||||||
| chr4:108008815 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-944C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008815 | |||||||
| chr4:108008823 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-936A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008823 | |||||||
| chr4:108008893 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.133-866C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108008893 | |||||||
| chr4:108009281 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.133-478G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009281 | |||||||
| chr4:108009454 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.133-305C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009454 | |||||||
| chr4:108009455 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.133-304A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009455 | |||||||
| chr4:108009608 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.133-151G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009608 | |||||||
| chr4:108009627 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133-132C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009627 | |||||||
| chr4:108009690 | G | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0047 others(5): Show |
8 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-69G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009690 | |||||||
| chr4:108009744 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.133-15C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 1/7 | chr4 | 108009744 | |||||||
| chr4:108009968 | T | G | 1 | a0006c0007t0002g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.261+81T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108009968 | |||||||
| chr4:108009977 | C | CT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.261+107dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 108009977 | ||||||
| chr4:108009977 | CT | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0001c0001t0001g0199 others(2): Show |
7 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+107delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 108009977 | ||||||
| chr4:108010022 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+135C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010022 | |||||||
| chr4:108010048 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+161A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010048 | |||||||
| chr4:108010359 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.261+472G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010359 | |||||||
| chr4:108010395 | A | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(62): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.261+508A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010395 | |||||||
| chr4:108010422 | G | GT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.261+540dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 108010422 | ||||||
| chr4:108010481 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.261+594C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010481 | |||||||
| chr4:108010600 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.261+713T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010600 | |||||||
| chr4:108010631 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.261+744G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010631 | |||||||
| chr4:108010747 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.261+860T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010747 | |||||||
| chr4:108010764 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261+877A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010764 | |||||||
| chr4:108010849 | CT | C | 27 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
28 | HG00642.hp2 HG01070.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.261+981delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 108010849 | ||||||
| chr4:108010991 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.261+1104G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010991 | |||||||
| chr4:108010994 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1107G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010994 | |||||||
| chr4:108010997 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0194 others(1): Show |
5 | HG01106.hp2 HG01515.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+1110C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108010997 | |||||||
| chr4:108011006 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 |
6 | HG01074.hp1 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+1119G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011006 | |||||||
| chr4:108011014 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.261+1127A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011014 | |||||||
| chr4:108011126 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.261+1239T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011126 | |||||||
| chr4:108011127 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.261+1240G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011127 | |||||||
| chr4:108011372 | G | A | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1485G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011372 | |||||||
| chr4:108011595 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.261+1708T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011595 | |||||||
| chr4:108011773 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261+1886G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108011773 | |||||||
| chr4:108012119 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.261+2232A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012119 | |||||||
| chr4:108012234 | C | T | 1 | a0002c0002t0002g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-2197C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012234 | |||||||
| chr4:108012244 | TTTA | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0196 a0001c0001t0001g0199 |
3 | HG02055.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.262-2186_262-2184d others(5): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012244 | |||||||
| chr4:108012249 | A | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0196 a0001c0001t0001g0199 |
3 | HG02055.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.262-2182A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012249 | |||||||
| chr4:108012420 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.262-2011G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012420 | |||||||
| chr4:108012425 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.262-2006C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012425 | |||||||
| chr4:108012482 | C | T | 1 | a0002c0002t0002g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-1949C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012482 | |||||||
| chr4:108012642 | T | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.262-1789T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012642 | |||||||
| chr4:108012737 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.262-1694G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108012737 | |||||||
| chr4:108013019 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.262-1412A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013019 | |||||||
| chr4:108013025 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.262-1406C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013025 | |||||||
| chr4:108013059 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.262-1372A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013059 | |||||||
| chr4:108013153 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-1278G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013153 | |||||||
| chr4:108013174 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.262-1257G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013174 | |||||||
| chr4:108013209 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.262-1222G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013209 | |||||||
| chr4:108013741 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.262-690A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013741 | |||||||
| chr4:108013745 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.262-686T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013745 | |||||||
| chr4:108013807 | A | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-624A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108013807 | |||||||
| chr4:108014315 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262-116T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108014315 | |||||||
| chr4:108014397 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0196 a0001c0001t0001g0199 |
3 | HG02055.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.262-34G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108014397 | |||||||
| chr4:108014397 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262-34G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 2/7 | chr4 | 108014397 | |||||||
| chr4:108014609 | C | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.419+21C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014609 | |||||||
| chr4:108014612 | CT | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0123 others(5): Show |
8 | HG00099.hp2 HG00558.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.419+39delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 108014612 | ||||||
| chr4:108014614 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.419+26T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014614 | |||||||
| chr4:108014615 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0123 others(2): Show |
5 | HG00099.hp2 HG02922.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.419+27T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014615 | |||||||
| chr4:108014645 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.419+57T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014645 | |||||||
| chr4:108014652 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0194 |
3 | HG03490.hp2 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.419+64T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014652 | |||||||
| chr4:108014715 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+127G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014715 | |||||||
| chr4:108014750 | C | G | 6 | a0001c0001t0003g0007 a0001c0001t0003g0057 a0001c0001t0003g0112 others(3): Show |
9 | HG00558.hp2 HG01433.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.419+162C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014750 | |||||||
| chr4:108014814 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+226C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014814 | |||||||
| chr4:108014838 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.419+250C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014838 | |||||||
| chr4:108014953 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0151 |
3 | HG02080.hp2 NA18971.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.419+365A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108014953 | |||||||
| chr4:108015167 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.419+579G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015167 | |||||||
| chr4:108015227 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.419+639T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015227 | |||||||
| chr4:108015301 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.419+713G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015301 | |||||||
| chr4:108015378 | T | C | 4 | a0001c0001t0003g0026 a0001c0001t0003g0138 a0001c0001t0003g0141 others(1): Show |
5 | HG00741.hp1 HG01361.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.419+790T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015378 | |||||||
| chr4:108015482 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0142 |
2 | HG01070.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.419+894G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015482 | |||||||
| chr4:108015523 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+935C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015523 | |||||||
| chr4:108015613 | G | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0066 |
3 | HG00609.hp2 HG02027.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.419+1025G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015613 | |||||||
| chr4:108015626 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+1038C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015626 | |||||||
| chr4:108015780 | A | G | 1 | a0002c0002t0002g0162 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.419+1192A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015780 | |||||||
| chr4:108015782 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.419+1194G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015782 | |||||||
| chr4:108015790 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.419+1202G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015790 | |||||||
| chr4:108015814 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+1226T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015814 | |||||||
| chr4:108015967 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.419+1379A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108015967 | |||||||
| chr4:108016065 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.419+1477G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108016065 | |||||||
| chr4:108016305 | T | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.419+1717T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108016305 | |||||||
| chr4:108016398 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.419+1810G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108016398 | |||||||
| chr4:108016677 | C | T | 38 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0032 others(35): Show |
44 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.419+2089C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108016677 | |||||||
| chr4:108017141 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0008g0113 |
2 | HG00408.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.420-2399T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017141 | |||||||
| chr4:108017201 | A | C | 1 | a0002c0002t0002g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.420-2339A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017201 | |||||||
| chr4:108017206 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.420-2334G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017206 | |||||||
| chr4:108017300 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.420-2240G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017300 | |||||||
| chr4:108017345 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.420-2195G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017345 | |||||||
| chr4:108017369 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0003g0103 |
2 | HG00280.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.420-2171A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017369 | |||||||
| chr4:108017379 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.420-2161A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017379 | |||||||
| chr4:108017556 | CT | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
27 | HG00558.hp1 HG01070.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.420-1969delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 108017556 | ||||||
| chr4:108017684 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.420-1856G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017684 | |||||||
| chr4:108017744 | G | A | 1 | a0002c0002t0002g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.420-1796G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017744 | |||||||
| chr4:108017768 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.420-1772C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017768 | |||||||
| chr4:108017771 | A | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0039 |
2 | HG01192.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.420-1769A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017771 | |||||||
| chr4:108017818 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-1722G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017818 | |||||||
| chr4:108017833 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.420-1707G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017833 | |||||||
| chr4:108017839 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.420-1701G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017839 | |||||||
| chr4:108017909 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.420-1631C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017909 | |||||||
| chr4:108017926 | G | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.420-1614G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108017926 | |||||||
| chr4:108018177 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.420-1363T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018177 | |||||||
| chr4:108018181 | C | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.420-1359C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018181 | |||||||
| chr4:108018429 | A | AT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0034 others(11): Show |
15 | HG01255.hp1 HG01358.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.420-1101dupT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 108018429 | ||||||
| chr4:108018440 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG01358.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.420-1100A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018440 | |||||||
| chr4:108018544 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.420-996G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018544 | |||||||
| chr4:108018682 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.420-858G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018682 | |||||||
| chr4:108018703 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.420-837T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018703 | |||||||
| chr4:108018768 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01358.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.420-772C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018768 | |||||||
| chr4:108018873 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0116 |
4 | HG00280.hp1 HG00738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-667T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018873 | |||||||
| chr4:108018883 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18952.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.420-657T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018883 | |||||||
| chr4:108018988 | T | C | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.420-552T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108018988 | |||||||
| chr4:108019067 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.420-473C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108019067 | |||||||
| chr4:108019179 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.420-361G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108019179 | |||||||
| chr4:108019247 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.420-293A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108019247 | |||||||
| chr4:108019473 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.420-67C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 3/7 | chr4 | 108019473 | |||||||
| chr4:108020018 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.546+352G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020018 | |||||||
| chr4:108020038 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.546+372G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020038 | |||||||
| chr4:108020111 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.546+445G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020111 | |||||||
| chr4:108020127 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.546+461G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020127 | |||||||
| chr4:108020190 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.546+524T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020190 | |||||||
| chr4:108020201 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.546+535G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020201 | |||||||
| chr4:108020229 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG00642.hp2 HG02451.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.546+563G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020229 | |||||||
| chr4:108020383 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+717T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020383 | |||||||
| chr4:108020511 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.546+845T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020511 | |||||||
| chr4:108020524 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546+858C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020524 | |||||||
| chr4:108020536 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.546+870A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020536 | |||||||
| chr4:108020734 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+1068G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108020734 | |||||||
| chr4:108021061 | TA | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+1397delA | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108021061 | ||||||
| chr4:108021383 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.546+1717A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108021383 | |||||||
| chr4:108021447 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546+1781G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108021447 | |||||||
| chr4:108021491 | TG | T | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+1827delG | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108021491 | ||||||
| chr4:108021555 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.546+1889T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108021555 | |||||||
| chr4:108021703 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547-1771A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108021703 | |||||||
| chr4:108021829 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.547-1645C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108021829 | |||||||
| chr4:108022009 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.547-1465C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022009 | |||||||
| chr4:108022018 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0194 |
3 | HG03490.hp2 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.547-1456C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022018 | |||||||
| chr4:108022126 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-1348G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022126 | |||||||
| chr4:108022158 | CAT | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0068 others(10): Show |
17 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.547-1307_547-1306d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022158 | ||||||
| chr4:108022163 | ATATATGT others(17): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.547-1307_547-1284d others(26): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022163 | ||||||
| chr4:108022165 | A | ATG | 6 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
8 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.547-1308_547-1307i others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022165 | ||||||
| chr4:108022165 | A | ATGTG | 3 | a0001c0001t0001g0042 a0003c0004t0001g0010 a0004c0003t0001g0040 |
3 | HG02056.hp2 HG02486.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.547-1308_547-1307i others(6): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022165 | ||||||
| chr4:108022165 | A | G | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1309A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022165 | |||||||
| chr4:108022165 | ATATG | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.547-1307_547-1304d others(6): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022165 | ||||||
| chr4:108022165 | ATATGTG | A | 12 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0075 others(9): Show |
12 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.547-1307_547-1302d others(8): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022165 | ||||||
| chr4:108022165 | ATATGTGT others(23): Show |
A | 1 | a0001c0001t0003g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.547-1307_547-1278d others(32): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022165 | ||||||
| chr4:108022167 | A | G | 40 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0033 others(37): Show |
44 | HG00642.hp2 HG01175.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.547-1307A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022167 | |||||||
| chr4:108022181 | GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.547-1285_547-1266d others(22): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022181 | ||||||
| chr4:108022189 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.547-1285A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022189 | |||||||
| chr4:108022191 | G | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0046 others(9): Show |
13 | HG01515.hp2 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.547-1283G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022191 | |||||||
| chr4:108022191 | G | GTA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01175.hp1 HG01255.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-1282_547-1281i others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022191 | ||||||
| chr4:108022193 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG00642.hp2 HG00738.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1281G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022193 | |||||||
| chr4:108022195 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.547-1279G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022195 | |||||||
| chr4:108022195 | G | GTGTATGT others(43): Show |
1 | a0001c0001t0001g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.547-1276_547-1275i others(52): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022195 | ||||||
| chr4:108022197 | G | A | 13 | a0001c0001t0001g0070 a0001c0001t0001g0075 a0001c0001t0001g0079 others(10): Show |
13 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-1277G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022197 | |||||||
| chr4:108022199 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.547-1275G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022199 | |||||||
| chr4:108022201 | A | ATGTG | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1253_547-1250d others(6): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022201 | ||||||
| chr4:108022201 | A | ATGTGTGT others(45): Show |
1 | a0001c0001t0001g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.547-1250_547-1249i others(54): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022201 | ||||||
| chr4:108022201 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.547-1273A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022201 | |||||||
| chr4:108022203 | G | A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(14): Show |
18 | HG01255.hp1 HG01515.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-1271G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022203 | |||||||
| chr4:108022205 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.547-1269G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022205 | |||||||
| chr4:108022205 | G | GTATGTGT others(7): Show |
2 | a0004c0003t0001g0037 a0004c0003t0001g0041 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.547-1268_547-1267i others(16): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022205 | ||||||
| chr4:108022205 | G | GTGTGTGT others(1): Show |
8 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
11 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-1262_547-1261i others(10): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022205 | ||||||
| chr4:108022207 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0005c0005t0005g0031 |
5 | HG01069.hp2 HG01071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-1267G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022207 | |||||||
| chr4:108022225 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.547-1249A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022225 | |||||||
| chr4:108022240 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.547-1234A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022240 | |||||||
| chr4:108022252 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0198 |
5 | HG01934.hp2 HG01978.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-1222C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022252 | |||||||
| chr4:108022267 | TA | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0106 a0001c0001t0001g0189 |
4 | HG00140.hp1 HG01099.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1202delA | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022267 | ||||||
| chr4:108022271 | AAT | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.547-1189_547-1188d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022271 | ||||||
| chr4:108022277 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.547-1197T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022277 | |||||||
| chr4:108022285 | TAC | T | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
15 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-1188_547-1187d others(4): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022285 | |||||||
| chr4:108022312 | A | G | 3 | a0002c0002t0002g0162 a0002c0002t0002g0163 a0002c0002t0002g0183 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.547-1162A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022312 | |||||||
| chr4:108022356 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.547-1118C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022356 | |||||||
| chr4:108022376 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.547-1098A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022376 | |||||||
| chr4:108022466 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(59): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.547-1008G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022466 | |||||||
| chr4:108022525 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.547-949G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022525 | |||||||
| chr4:108022629 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-845T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022629 | |||||||
| chr4:108022630 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-844C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022630 | |||||||
| chr4:108022655 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.547-819G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022655 | |||||||
| chr4:108022662 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.547-812C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022662 | |||||||
| chr4:108022663 | G | A | 4 | a0002c0002t0002g0009 a0002c0002t0002g0164 a0002c0002t0002g0165 others(1): Show |
7 | HG01884.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-811G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022663 | |||||||
| chr4:108022682 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-792A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022682 | |||||||
| chr4:108022728 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547-746G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022728 | |||||||
| chr4:108022945 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.547-529C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108022945 | |||||||
| chr4:108022994 | CT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.547-463delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 108022994 | ||||||
| chr4:108023028 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0107 others(3): Show |
7 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-446C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023028 | |||||||
| chr4:108023062 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.547-412C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023062 | |||||||
| chr4:108023075 | C | A | 1 | a0002c0002t0002g0200 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.547-399C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023075 | |||||||
| chr4:108023101 | C | T | 1 | a0002c0002t0002g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.547-373C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023101 | |||||||
| chr4:108023181 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.547-293A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023181 | |||||||
| chr4:108023190 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.547-284C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023190 | |||||||
| chr4:108023423 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.547-51C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 4/7 | chr4 | 108023423 | |||||||
| chr4:108023576 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+13G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023576 | |||||||
| chr4:108023624 | C | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0044 others(12): Show |
15 | HG00642.hp2 HG01255.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+61C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023624 | |||||||
| chr4:108023665 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.636+102C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023665 | |||||||
| chr4:108023690 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.636+127A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023690 | |||||||
| chr4:108023782 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.636+219C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023782 | |||||||
| chr4:108023803 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.636+240G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023803 | |||||||
| chr4:108023804 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.636+241G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023804 | |||||||
| chr4:108023861 | T | G | 1 | a0001c0001t0004g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.636+298T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023861 | |||||||
| chr4:108023914 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.636+351C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023914 | |||||||
| chr4:108023927 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.636+364A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023927 | |||||||
| chr4:108023948 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.636+385A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108023948 | |||||||
| chr4:108024263 | G | A | 1 | a0006c0007t0002g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.636+700G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024263 | |||||||
| chr4:108024373 | T | C | 4 | a0002c0002t0002g0184 a0002c0002t0002g0200 a0002c0002t0002g0201 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+810T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024373 | |||||||
| chr4:108024408 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0136 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.636+845A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024408 | |||||||
| chr4:108024475 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.636+912T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024475 | |||||||
| chr4:108024745 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0188 |
2 | NA18963.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.636+1182A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024745 | |||||||
| chr4:108024911 | A | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0104 a0001c0001t0001g0107 others(3): Show |
7 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+1348A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024911 | |||||||
| chr4:108024985 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.636+1422T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108024985 | |||||||
| chr4:108025173 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0094 |
2 | NA18948.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.636+1610A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108025173 | |||||||
| chr4:108025222 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.636+1659T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108025222 | |||||||
| chr4:108025449 | GTTA | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.636+1891_636+1893d others(5): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 108025449 | ||||||
| chr4:108025488 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.636+1925T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108025488 | |||||||
| chr4:108025517 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0056 a0001c0001t0001g0110 |
5 | HG02622.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+1954A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108025517 | |||||||
| chr4:108025613 | G | A | 2 | a0001c0001t0001g0197 a0002c0002t0002g0174 |
2 | HG01515.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.636+2050G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108025613 | |||||||
| chr4:108026007 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.637-1681A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026007 | |||||||
| chr4:108026041 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.637-1647A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026041 | |||||||
| chr4:108026041 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.637-1647A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026041 | |||||||
| chr4:108026045 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637-1643A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026045 | |||||||
| chr4:108026082 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.637-1606C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026082 | |||||||
| chr4:108026102 | C | T | 1 | a0002c0002t0002g0009 | 4 | HG01975.hp2 HG02486.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1586C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026102 | |||||||
| chr4:108026230 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.637-1458A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026230 | |||||||
| chr4:108026258 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1430C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026258 | |||||||
| chr4:108026430 | A | G | 3 | a0002c0002t0002g0162 a0002c0002t0002g0163 a0002c0002t0002g0183 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.637-1258A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026430 | |||||||
| chr4:108026513 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-1175A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026513 | |||||||
| chr4:108026732 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637-956G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026732 | |||||||
| chr4:108026831 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.637-857A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026831 | |||||||
| chr4:108026935 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.637-753T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108026935 | |||||||
| chr4:108027014 | G | T | 1 | a0002c0002t0002g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.637-674G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027014 | |||||||
| chr4:108027099 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.637-589C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027099 | |||||||
| chr4:108027108 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.637-580C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027108 | |||||||
| chr4:108027128 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.637-560C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027128 | |||||||
| chr4:108027202 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.637-486C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027202 | |||||||
| chr4:108027236 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.637-452G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 5/7 | chr4 | 108027236 | |||||||
| chr4:108027807 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.709+47G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108027807 | |||||||
| chr4:108027849 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.709+89C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108027849 | |||||||
| chr4:108028029 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.709+269G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028029 | |||||||
| chr4:108028283 | C | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.709+523C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028283 | |||||||
| chr4:108028520 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0027 |
5 | HG02135.hp1 NA18954.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+760T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028520 | |||||||
| chr4:108028574 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.709+814C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028574 | |||||||
| chr4:108028661 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.709+901T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028661 | |||||||
| chr4:108028749 | CT | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0208 a0001c0001t0003g0057 others(3): Show |
7 | HG00558.hp2 HG00609.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.709+1003delT | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 108028749 | ||||||
| chr4:108028901 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.709+1141C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108028901 | |||||||
| chr4:108029099 | C | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.709+1339C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108029099 | |||||||
| chr4:108029187 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.709+1427C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108029187 | |||||||
| chr4:108029620 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.709+1860A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108029620 | |||||||
| chr4:108029902 | G | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.709+2142G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108029902 | |||||||
| chr4:108029993 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0194 a0001c0001t0001g0197 |
4 | HG01515.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+2233G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108029993 | |||||||
| chr4:108030134 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0002c0002t0002g0185 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+2374C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030134 | |||||||
| chr4:108030515 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.710-2661A>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030515 | |||||||
| chr4:108030583 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.710-2593C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030583 | |||||||
| chr4:108030637 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710-2539G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030637 | |||||||
| chr4:108030718 | T | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.710-2458T>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030718 | |||||||
| chr4:108030981 | A | T | 1 | a0002c0002t0002g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.710-2195A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108030981 | |||||||
| chr4:108031216 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.710-1960T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108031216 | |||||||
| chr4:108031223 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710-1953A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108031223 | |||||||
| chr4:108031513 | A | G | 1 | a0005c0005t0005g0031 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.710-1663A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108031513 | |||||||
| chr4:108031598 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02055.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710-1578A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108031598 | |||||||
| chr4:108031819 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.710-1357G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108031819 | |||||||
| chr4:108032106 | A | G | 1 | a0002c0002t0002g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.710-1070A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032106 | |||||||
| chr4:108032125 | CTCTTT | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.710-1045_710-1041d others(7): Show |
HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 108032125 | ||||||
| chr4:108032336 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.710-840C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032336 | |||||||
| chr4:108032470 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710-706A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032470 | |||||||
| chr4:108032520 | T | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.710-656T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032520 | |||||||
| chr4:108032779 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.710-397T>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032779 | |||||||
| chr4:108032857 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.710-319C>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032857 | |||||||
| chr4:108032914 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
13 | HG01192.hp1 HG01243.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.710-262G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032914 | |||||||
| chr4:108032925 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.710-251C>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032925 | |||||||
| chr4:108032975 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.710-201C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108032975 | |||||||
| chr4:108033158 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.710-18C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 6/7 | chr4 | 108033158 | |||||||
| chr4:108033326 | A | G | 1 | a0002c0002t0002g0163 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+34A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033326 | |||||||
| chr4:108033422 | A | T | 1 | a0002c0002t0002g0171 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.826+130A>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033422 | |||||||
| chr4:108033535 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA18954.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.826+243T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033535 | |||||||
| chr4:108033706 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0155 |
3 | HG02615.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.826+414T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033706 | |||||||
| chr4:108033759 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.826+467T>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033759 | |||||||
| chr4:108033881 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.827-358G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033881 | |||||||
| chr4:108033883 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.827-356G>A | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033883 | |||||||
| chr4:108033921 | C | T | 1 | a0002c0002t0002g0168 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.827-318C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033921 | |||||||
| chr4:108033964 | G | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.827-275G>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033964 | |||||||
| chr4:108033994 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.827-245C>T | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108033994 | |||||||
| chr4:108034007 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.827-232G>C | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108034007 | |||||||
| chr4:108034009 | A | G | 1 | a0001c0001t0003g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.827-230A>G | HADH | ENSG00000138796.18 | transcript | ENST00000309522.8 | protein_coding | 7/7 | chr4 | 108034009 |